首页 > 最新文献

Plant Gene最新文献

英文 中文
Chloroplast genomes of six Aloe species: Insights into genetic variation and evolutionary patterns 六种芦荟的叶绿体基因组:遗传变异和进化模式的见解
IF 2.2 Q3 GENETICS & HEREDITY Pub Date : 2025-09-01 Epub Date: 2025-07-13 DOI: 10.1016/j.plgene.2025.100530
Dede Kurniawan , Linzhou Li , Min Liu , Jose Marie Wynne Aquavita , Martha Britany Napitupulu , Manik Prabhu Narsing Rao , Turhadi Turhadi , Shouzhou Zhang , Tong Wei , Sunil Kumar Sahu
Aloe is a highly diverse genus of succulent plants with important pharmacological, medicinal, and commercial importance. However, the limited availability of genomic resources has constrained evolutionary and comparative genomics studies of this genus. To address this problem, we sequenced and assembled the first comprehensive chloroplast genome sequences of six Aloe species (Aloe barberae, Aloe excelsa, Aloe marlothii, Aloe perfoliata, Aloe glauca, and Aloe tenuifolia) using a high-throughput whole-genome sequencing approach. The total length of the assembled chloroplast genomes varied from 152,383 to 154,127 bp, exhibiting a conserved quadripartite structure comprising 131 genes. Comparative genomic analyses revealed the loss of the rpl32 and infA genes across all the sampled species except for Aloe arborescens, suggesting lineage-specific gene retention. Furthermore, we identified eight protein-coding genes under positive selection and five intergenic regions with significant variability, which hold potential for molecular species identification (DNA barcoding) and phylogenetic studies. Phylogenetic reconstruction revealed robust branch support values, validating the monophyletic status of the Aloe genus and updating the sister clade of Aloe vera, which was previously close to Aloe maculata. These findings offer insights into genetic variation, gene loss, and potential evolutionary patterns, contributing to future phylogenetic and conservation research.
芦荟是一种高度多样化的多肉植物属,具有重要的药理、药用和商业意义。然而,有限的基因组资源限制了该属的进化和比较基因组学研究。为了解决这个问题,我们使用高通量全基因组测序方法对6种芦荟(芦荟,芦荟excelsa,芦荟marlothii,芦荟perfoliata,芦荟glauca和芦荟tenuifolia)进行了首次全面的叶绿体基因组测序和组装。叶绿体基因组总长度在152,383 ~ 154,127 bp之间,呈现由131个基因组成的保守四部结构。比较基因组分析显示,除了芦荟外,所有样本物种的rpl32和infA基因都缺失,这表明谱系特异性基因保留。此外,我们还发现了8个正选择的蛋白质编码基因和5个具有显著变异的基因间区,这些基因具有分子物种鉴定(DNA条形码)和系统发育研究的潜力。系统发育重建显示了强大的分支支持值,验证了芦荟属的单系地位,并更新了芦荟的姐妹分支,该分支此前与芦荟接近。这些发现提供了对遗传变异、基因丢失和潜在进化模式的见解,有助于未来的系统发育和保护研究。
{"title":"Chloroplast genomes of six Aloe species: Insights into genetic variation and evolutionary patterns","authors":"Dede Kurniawan ,&nbsp;Linzhou Li ,&nbsp;Min Liu ,&nbsp;Jose Marie Wynne Aquavita ,&nbsp;Martha Britany Napitupulu ,&nbsp;Manik Prabhu Narsing Rao ,&nbsp;Turhadi Turhadi ,&nbsp;Shouzhou Zhang ,&nbsp;Tong Wei ,&nbsp;Sunil Kumar Sahu","doi":"10.1016/j.plgene.2025.100530","DOIUrl":"10.1016/j.plgene.2025.100530","url":null,"abstract":"<div><div><em>Aloe</em> is a highly diverse genus of succulent plants with important pharmacological, medicinal, and commercial importance. However, the limited availability of genomic resources has constrained evolutionary and comparative genomics studies of this genus. To address this problem, we sequenced and assembled the first comprehensive chloroplast genome sequences of six <em>A</em><em>loe</em> species (<em>Aloe barberae, Aloe excelsa, Aloe marlothii, Aloe perfoliata, Aloe glauca</em>, and <em>Aloe tenuifolia</em>) using a high-throughput whole-genome sequencing approach. The total length of the assembled chloroplast genomes varied from 152,383 to 154,127 bp, exhibiting a conserved quadripartite structure comprising 131 genes. Comparative genomic analyses revealed the loss of the <em>rpl32</em> and <em>infA</em> genes across all the sampled species except for <em>Aloe arborescens</em>, suggesting lineage-specific gene retention. Furthermore, we identified eight protein-coding genes under positive selection and five intergenic regions with significant variability, which hold potential for molecular species identification (DNA barcoding) and phylogenetic studies. Phylogenetic reconstruction revealed robust branch support values, validating the monophyletic status of the <em>Aloe</em> genus and updating the sister clade of <em>Aloe vera</em>, which was previously close to <em>Aloe maculata</em>. These findings offer insights into genetic variation, gene loss, and potential evolutionary patterns, contributing to future phylogenetic and conservation research.</div></div>","PeriodicalId":38041,"journal":{"name":"Plant Gene","volume":"43 ","pages":"Article 100530"},"PeriodicalIF":2.2,"publicationDate":"2025-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144655442","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Segregation distortion and linkage analysis in F2 populations of pumpkin (C.Moschata Duch) 南瓜(C.Moschata Duch) F2居群分离畸变及连锁分析
IF 2.2 Q3 GENETICS & HEREDITY Pub Date : 2025-09-01 Epub Date: 2025-04-08 DOI: 10.1016/j.plgene.2025.100508
Zixia Zhang, Yanfang Jiang, Hailong Zhu, Ziyao Chen, Zefa Liu
F2 materials derived from a cross between introgression lines B-5 × A-3 were used as mapping population in C. moschata. Duch. Among the 89 genetic markers (ls, yf, and 87 marker alleles) analyzed, 5 markers (5.6 % P<0.01) and 12 markers (13.5 % P<0.01) showed genetic distortion in the F2 population. Among these segregation distortion genetic markers, 11 genetic markers were skewed to the male parent B-5(64.70 %), 3 genetic markers were skewed to the heterozygote (17.65 %), and 3 genetic markers were skewed to both parents (17.65 %). These segregation distortion genetic markers were in the clusters of tight loci or single markers, which were distributed in 9 different chromosomes with 3 (SDR1, SDR2, and SDR3) hot regions in 3 (LGP2, LGP6, and LGP10) of them. In this research, reasons for segregation distortion were discussed, and the gametophyte selection may be the result of segregation distortion of genetic polymorphic loci.
利用B-5 × a -3杂交获得的F2个材料作为莫夏塔的定位群体。杜赫。在分析的89个遗传标记(ls、yf和87个标记等位基因)中,F2群体中有5个标记(5.6% P<0.01)和12个标记(13.5% P<0.01)存在遗传畸变。在这些分离扭曲遗传标记中,有11个遗传标记偏向父本B-5(64.70%), 3个遗传标记偏向杂合子(17.65%),3个遗传标记偏向双亲(17.65%)。这些分离畸变遗传标记以紧密位点或单标记簇的形式分布在9条不同的染色体上,其中3条(LGP2、LGP6和LGP10)染色体上有3个(SDR1、SDR2和SDR3)热点区。本文讨论了分离扭曲的原因,认为配子体选择可能是遗传多态性位点分离扭曲的结果。
{"title":"Segregation distortion and linkage analysis in F2 populations of pumpkin (C.Moschata Duch)","authors":"Zixia Zhang,&nbsp;Yanfang Jiang,&nbsp;Hailong Zhu,&nbsp;Ziyao Chen,&nbsp;Zefa Liu","doi":"10.1016/j.plgene.2025.100508","DOIUrl":"10.1016/j.plgene.2025.100508","url":null,"abstract":"<div><div>F<sub>2</sub> materials derived from a cross between introgression lines B-5 × A-3 were used as mapping population in <em>C. moschata.</em> Duch. Among the 89 genetic markers (ls, yf, and 87 marker alleles) analyzed, 5 markers (5.6 % P&lt;0.01) and 12 markers (13.5 % P&lt;0.01) showed genetic distortion in the F<sub>2</sub> population. Among these segregation distortion genetic markers, 11 genetic markers were skewed to the male parent B-5(64.70 %), 3 genetic markers were skewed to the heterozygote (17.65 %), and 3 genetic markers were skewed to both parents (17.65 %). These segregation distortion genetic markers were in the clusters of tight loci or single markers, which were distributed in 9 different chromosomes with 3 (SDR1, SDR2, and SDR3) hot regions in 3 (LGP2, LGP6, and LGP10) of them. In this research, reasons for segregation distortion were discussed, and the gametophyte selection may be the result of segregation distortion of genetic polymorphic loci.</div></div>","PeriodicalId":38041,"journal":{"name":"Plant Gene","volume":"43 ","pages":"Article 100508"},"PeriodicalIF":2.2,"publicationDate":"2025-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143835254","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Identification of medicinal plant Solanum procumbens Lour. using DNA barcodes and morphology 药用植物天竺葵的鉴定。利用DNA条形码和形态学
IF 2.2 Q3 GENETICS & HEREDITY Pub Date : 2025-09-01 Epub Date: 2025-05-26 DOI: 10.1016/j.plgene.2025.100517
Lieu Thi Thuy Nguyen , Quyen Thi Thao Tran , Dan Thai Vo , Tri Minh Bui , Biet Van Huynh , Dung Minh Ha-Tran

Background

This study employed DNA barcoding to identify and differentiate Solanum procumbens, a potential medicinal plant used from other species in Solanaceae family. Eleven plant samples of Solanum spp. with morphological characteristics similar with those of S. procumbens and S. trilobatum were collected from various locations across Vietnam. Five DNA barcode markers were analyzed for identifying Solanum procumbens and its morphologically cryptic species Solanum trilobatum.

Results

Ten putative S. procumbens samples displayed a high identity (99.6–99.7 %) with the reference sequence within the transfer RNA leucine-transfer RNA phenylalanine (trnLtrnF) region. DNA sequences of the Internal Transcribed Spacer (ITS) region exhibited lower identity with the reference sequence, ranging from 94 % to 97.25 %. Despite this difference, DNA barcoding effectively differentiated these individuals, with both chloroplast trnLtrnF and nuclear ITS barcodes achieving high identification accuracy. The precision of trnLtrnF and ITS in species identification was validated using dried leaf samples of the putative S. procumbens and S. trilobatum. The consistency between fresh and dried samples confirms that our results are reliable and applicable in the pharmaceutical industry.

Conclusions

Phylogenetic analysis based on barcoding data aligned with morphology-based phenogram. These findings demonstrate the effectiveness of DNA barcoding for accurate identification of S. procumbens, particularly when morphological traits are ambiguous.
摘要本研究利用DNA条形码技术对茄科植物中具有潜在药用价值的原蛮茄(Solanum procumbens)进行鉴定和区分。在越南不同地点采集了11种形态特征与原藜和三叶草相似的茄属植物标本。对5种DNA条形码标记进行了分析,用于鉴别原甘菊及其形态隐种三叶甘菊。结果10份推定样品与参考序列在转移RNA亮氨酸-转移RNA苯丙氨酸(trnL-trnF)区具有较高的一致性(99.6 ~ 99.7%)。ITS区域的DNA序列与参考序列的一致性较低,在94% ~ 97.25%之间。尽管存在这种差异,但DNA条形码可以有效地区分这些个体,叶绿体trnL-trnF和核ITS条形码都具有很高的识别精度。利用推定的原藜和三叶草的干叶样品,验证了trnL-trnF和ITS在物种鉴定中的精度。新鲜和干燥样品之间的一致性证实了我们的结果是可靠的,适用于制药行业。结论基于条形码数据的系统发育分析与基于形态学的表型图一致。这些发现证明了DNA条形码在准确鉴定原藜的有效性,特别是在形态特征不明确的情况下。
{"title":"Identification of medicinal plant Solanum procumbens Lour. using DNA barcodes and morphology","authors":"Lieu Thi Thuy Nguyen ,&nbsp;Quyen Thi Thao Tran ,&nbsp;Dan Thai Vo ,&nbsp;Tri Minh Bui ,&nbsp;Biet Van Huynh ,&nbsp;Dung Minh Ha-Tran","doi":"10.1016/j.plgene.2025.100517","DOIUrl":"10.1016/j.plgene.2025.100517","url":null,"abstract":"<div><h3>Background</h3><div>This study employed DNA barcoding to identify and differentiate <em>Solanum procumbens</em>, a potential medicinal plant used from other species in Solanaceae family. Eleven plant samples of <em>Solanum</em> spp. with morphological characteristics similar with those of <em>S. procumbens</em> and <em>S. trilobatum</em> were collected from various locations across Vietnam. Five DNA barcode markers were analyzed for identifying <em>Solanum procumbens</em> and its morphologically cryptic species <em>Solanum trilobatum</em>.</div></div><div><h3>Results</h3><div>Ten putative <em>S. procumbens</em> samples displayed a high identity (99.6–99.7 %) with the reference sequence within the transfer RNA leucine-transfer RNA phenylalanine <em>(trnL</em>–<em>trnF)</em> region. DNA sequences of the Internal Transcribed Spacer (ITS) region exhibited lower identity with the reference sequence, ranging from 94 % to 97.25 %. Despite this difference, DNA barcoding effectively differentiated these individuals, with both chloroplast <em>trnL</em>–<em>trnF</em> and nuclear ITS barcodes achieving high identification accuracy. The precision of <em>trnL</em>–<em>trnF</em> and ITS in species identification was validated using dried leaf samples of the putative <em>S. procumbens</em> and <em>S. trilobatum</em>. The consistency between fresh and dried samples confirms that our results are reliable and applicable in the pharmaceutical industry.</div></div><div><h3>Conclusions</h3><div>Phylogenetic analysis based on barcoding data aligned with morphology-based phenogram. These findings demonstrate the effectiveness of DNA barcoding for accurate identification of <em>S. procumbens</em>, particularly when morphological traits are ambiguous.</div></div>","PeriodicalId":38041,"journal":{"name":"Plant Gene","volume":"43 ","pages":"Article 100517"},"PeriodicalIF":2.2,"publicationDate":"2025-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144166991","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Genome-wide identification and expression analysis of the OVATE gene family in melon (Cucumis melo L.) 甜瓜(Cucumis melo L.) OVATE基因家族全基因组鉴定及表达分析
IF 2.2 Q3 GENETICS & HEREDITY Pub Date : 2025-09-01 Epub Date: 2025-07-20 DOI: 10.1016/j.plgene.2025.100532
Zixuan Li , Shuaidong Wu , Wenxi Liu , Jiyuan Wang , Yanliang Guo , Congsheng Yan , Yan Wang , Huijun Zhang , Jie Liu
The OVATE gene family (OFP) is widely present in plants and plays a crucial role in regulating growth, development, and plant morphology, particularly in shaping fruit morphology. However, limited research has been conducted on the OFP gene in melon. In this study, we systematically identified and analyzed the entire OFP gene family in the melon genome. By comparing with 20 AtOFP protein sequences, 16 CmOFP genes were identified from the melon genome, and their physicochemical properties were characterized. Phylogenetic relationship analysis revealed that CmOFP and AtOFP could be classified into five subfamilies. Syntenic analysis demonstrated high synteny between Arabidopsis and melon OFP. Additionally, the gene structure and conserved domains of CmOFP were determined, and its predicted tertiary protein structure was elucidated. Through promoter analysis of CmOFP, a total of 30 regulatory elements were identified, showing significant differences in both number and classification among these elements. Expression pattern analysis indicated that the relative expression of CmOFP in the ovary was high and decreased post-pollination. Transcriptome analysis of different melon fruit pulps revealed that plant hormone signal transduction pathways were closely associated with fruit shape determination. Notably, four CmOFP genes exhibited significant differential expression across various fruit shapes, suggesting potential applications in fruit shape improvement. This study provides a theoretical foundation for further exploring the functional roles of CmOFP and their utilization in melon breeding programs.
OVATE基因家族(OFP)广泛存在于植物中,在调节植物的生长发育和形态,特别是果实形态的形成中起着至关重要的作用。然而,对甜瓜中OFP基因的研究有限。在这项研究中,我们系统地鉴定和分析了甜瓜基因组中的整个OFP基因家族。通过比对20个AtOFP蛋白序列,从甜瓜基因组中鉴定出16个CmOFP基因,并对其理化性质进行了分析。系统发育关系分析表明,CmOFP和AtOFP可划分为5个亚科。同源性分析表明拟南芥与甜瓜OFP具有较高的同源性。此外,还确定了CmOFP的基因结构和保守结构域,并对其预测的三级蛋白结构进行了阐释。通过对CmOFP的启动子分析,共鉴定出30个调控元件,这些元件在数量和分类上都存在显著差异。表达谱分析表明,CmOFP在子房中的相对表达量较高,授粉后相对表达量降低。对不同甜瓜果肉的转录组分析表明,植物激素信号转导途径与果实形状的决定密切相关。值得注意的是,4个CmOFP基因在不同果实形状中表现出显著的差异表达,这表明CmOFP基因在改善果实形状方面具有潜在的应用前景。该研究为进一步探索CmOFP的功能作用及其在甜瓜育种中的应用提供了理论基础。
{"title":"Genome-wide identification and expression analysis of the OVATE gene family in melon (Cucumis melo L.)","authors":"Zixuan Li ,&nbsp;Shuaidong Wu ,&nbsp;Wenxi Liu ,&nbsp;Jiyuan Wang ,&nbsp;Yanliang Guo ,&nbsp;Congsheng Yan ,&nbsp;Yan Wang ,&nbsp;Huijun Zhang ,&nbsp;Jie Liu","doi":"10.1016/j.plgene.2025.100532","DOIUrl":"10.1016/j.plgene.2025.100532","url":null,"abstract":"<div><div>The OVATE gene family (OFP) is widely present in plants and plays a crucial role in regulating growth, development, and plant morphology, particularly in shaping fruit morphology. However, limited research has been conducted on the <em>OFP</em> gene in melon. In this study, we systematically identified and analyzed the entire <em>OFP</em> gene family in the melon genome. By comparing with 20 AtOFP protein sequences, 16 <em>CmOFP</em> genes were identified from the melon genome, and their physicochemical properties were characterized. Phylogenetic relationship analysis revealed that CmOFP and AtOFP could be classified into five subfamilies. Syntenic analysis demonstrated high synteny between Arabidopsis and melon <em>OFP</em>. Additionally, the gene structure and conserved domains of CmOFP were determined, and its predicted tertiary protein structure was elucidated. Through promoter analysis of <em>CmOFP</em>, a total of 30 regulatory elements were identified, showing significant differences in both number and classification among these elements. Expression pattern analysis indicated that the relative expression of <em>CmOFP</em> in the ovary was high and decreased post-pollination. Transcriptome analysis of different melon fruit pulps revealed that plant hormone signal transduction pathways were closely associated with fruit shape determination. Notably, four <em>CmOFP</em> genes exhibited significant differential expression across various fruit shapes, suggesting potential applications in fruit shape improvement. This study provides a theoretical foundation for further exploring the functional roles of <em>CmOFP</em> and their utilization in melon breeding programs.</div></div>","PeriodicalId":38041,"journal":{"name":"Plant Gene","volume":"43 ","pages":"Article 100532"},"PeriodicalIF":2.2,"publicationDate":"2025-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144704123","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Genetic diversity analysis in cytoplasmic male sterile ‘A’ lines and restorer ‘R’ lines of Indian mustard using SSR markers 利用SSR标记分析印度芥菜细胞质雄性不育系A和恢复系R的遗传多样性
IF 2.2 Q3 GENETICS & HEREDITY Pub Date : 2025-09-01 Epub Date: 2025-05-11 DOI: 10.1016/j.plgene.2025.100518
K.H. Singh, Lal Singh, Nehanjali Parmar, Deepika Sharma, J. Nanjundan, Ajay Kumar Thakur
Indian mustard (Brassica juncea L. Czern & Coss.) is a highly economically important oilseed crop of India. An accurate estimation of genetic diversity inherent in breeding material is a pre-requisite for the success of any hybrid breeding programme, as it leads to identification of genetically divergent parents for exploiting high heterotic levels. In the present study, 200 genome-wide spanned simple sequence repeat (SSR) markers were used for estimation of genetic diversity and identification of genetically divergent parental combinations in a panel of 28 parental lines of Indian mustard comprising of 21 cytoplasmic male sterile (CMS) ‘A' lines and 7 restrorer ‘R' lines. A total of 179 SSR markers resulted in positive amplification with 155 (81.57 %) SSRs producing polymorphic amplicons and 24 (13.41 %) SSRs resulted into monomorphic products. Allele number varied from 2 to 6 with a mean value of 3.27 alleles per SSR marker. PIC values ranged from 0.23 to 0.7 with a mean value of 0.38 per SSR marker. Gene diversity values were in the range of 0.27–0.75 with average value of 0.47, inferring the presence of a moderate level of genetic diversity in the plant material. Neighbor-Joining dendrogram could not exactly differentiate ‘A' and ‘R' lines into different groups. This study led to identification of few genetically diverse A and R lines, suitable for making crosses for heterotic hybrid development in Indian mustard. On the basis of Euclidean distances, various cross-combinations viz. MJA10 & MJR3/EC597313, MJA 14 & MJR3/EC597313, and MH 12–12/EC597313S & MJR9 were designated as genetically diverse genotypes. These cross-combinations may be used in hybrid breeding program to exploit heterosis in Indian mustard improvement.
印度芥菜(Brassica juncea L. Czern;是印度一种经济上非常重要的油籽作物。准确估计育种材料中固有的遗传多样性是任何杂交育种计划成功的先决条件,因为它导致鉴定遗传上不同的亲本,以利用高杂种优势水平。本研究利用200个全基因组跨简单序列重复(SSR)标记,对21个细胞质雄性不育(CMS)“a”系和7个恢复系“R”系28个亲本组合进行了遗传多样性估计和遗传分化鉴定。共有179个SSR标记产生阳性扩增,其中155个(81.57%)SSR标记产生多态性扩增,24个(13.41%)SSR标记产生单态扩增。等位基因数为2 ~ 6个,平均每个SSR标记有3.27个等位基因。PIC值为0.23 ~ 0.7,平均为0.38。基因多样性值在0.27 ~ 0.75之间,平均值为0.47,表明该植物材料具有中等水平的遗传多样性。Neighbor-Joining tree - plan不能准确区分A和R线。本研究鉴定出了少数遗传多样性较好的A、R系,适合用于印度芥菜杂种开发。在欧氏距离的基础上,各种交叉组合即MJA10 &;MJR3/EC597313, MJA 14 &;MJR3/EC597313和MH 12-12 /EC597313S &;MJR9基因型具有遗传多样性。这些杂交组合可用于杂交育种计划,利用杂种优势改良印度芥菜。
{"title":"Genetic diversity analysis in cytoplasmic male sterile ‘A’ lines and restorer ‘R’ lines of Indian mustard using SSR markers","authors":"K.H. Singh,&nbsp;Lal Singh,&nbsp;Nehanjali Parmar,&nbsp;Deepika Sharma,&nbsp;J. Nanjundan,&nbsp;Ajay Kumar Thakur","doi":"10.1016/j.plgene.2025.100518","DOIUrl":"10.1016/j.plgene.2025.100518","url":null,"abstract":"<div><div>Indian mustard (<em>Brassica juncea</em> L. Czern &amp; Coss.) is a highly economically important oilseed crop of India. An accurate estimation of genetic diversity inherent in breeding material is a pre-requisite for the success of any hybrid breeding programme, as it leads to identification of genetically divergent parents for exploiting high heterotic levels. In the present study, 200 genome-wide spanned simple sequence repeat (SSR) markers were used for estimation of genetic diversity and identification of genetically divergent parental combinations in a panel of 28 parental lines of Indian mustard comprising of 21 cytoplasmic male sterile (CMS) ‘A' lines and 7 restrorer ‘R' lines. A total of 179 SSR markers resulted in positive amplification with 155 (81.57 %) SSRs producing polymorphic amplicons and 24 (13.41 %) SSRs resulted into monomorphic products. Allele number varied from 2 to 6 with a mean value of 3.27 alleles per SSR marker. PIC values ranged from 0.23 to 0.7 with a mean value of 0.38 per SSR marker. Gene diversity values were in the range of 0.27–0.75 with average value of 0.47, inferring the presence of a moderate level of genetic diversity in the plant material. Neighbor-Joining dendrogram could not exactly differentiate ‘A' and ‘R' lines into different groups. This study led to identification of few genetically diverse A and R lines, suitable for making crosses for heterotic hybrid development in Indian mustard. On the basis of Euclidean distances, various cross-combinations viz. MJA10 &amp; MJR3/EC597313, MJA 14 &amp; MJR3/EC597313, and MH 12–12/EC597313S &amp; MJR9 were designated as genetically diverse genotypes. These cross-combinations may be used in hybrid breeding program to exploit heterosis in Indian mustard improvement.</div></div>","PeriodicalId":38041,"journal":{"name":"Plant Gene","volume":"43 ","pages":"Article 100518"},"PeriodicalIF":2.2,"publicationDate":"2025-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144068341","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Computational interference of gene regulatory networks on the growth and development of millets 基因调控网络对谷子生长发育的计算干扰
IF 2.2 Q3 GENETICS & HEREDITY Pub Date : 2025-09-01 Epub Date: 2025-07-15 DOI: 10.1016/j.plgene.2025.100531
Lipsa Leena Panigrahi , Gayatri Mishra , Dhaneswar Swain , Gyana Ranjan Rout
Millets are among the cereal crops cultivated for nutrient-rich food. They are generally considered as resilient crops in terms of growth requirements, as they can withstand harsh climatic factors such as unpredictable climate change and nutrient-depleted soils. The present review highlighted that gene regulatory networks are rewired to control the adaptable traits and to understand the transcriptional regulatory system against environmental stress. By combining machine learning, predictive modeling, and multi-omics data to unravel intricate regulatory relationships, computational methods have entirely changed the study of GRNs (gene regulatory networks), making and identifying important transcription factors, co-regulators, and signaling networks. Recent developments in artificial intelligence, systems biology, and bioinformatics have made reconstructing and analyzing millet GRNs, providing new information on blooming mechanisms, nutrient absorption,and drought resistance. Data scarcity, species-specific heterogeneity, and the requirement for high-throughput functional validation. Computational models incorporating transcriptomics, proteomics, and metabolomics help to improve crop improvement by enabling targeted genetic alterations and increasing predictive accuracy. This study discusses critical approaches, accessible datasets, and new developments in computational GRN investigations in millets. Deep learning, CRISPR-based gene editing, and synthetic biology in millet research are among the opportunities to develop new genotypes. By using computational methods to gain a thorough understanding of millet GRNs, it will be possible to create millet varieties that are more nutritious and climate-robust, promoting sustainable agriculture.
小米是一种营养丰富的谷类作物。就生长需求而言,它们通常被认为是适应力强的作物,因为它们可以承受恶劣的气候因素,如不可预测的气候变化和营养枯竭的土壤。本文综述了基因调控网络的重新布线,以控制适应性性状,并了解对环境胁迫的转录调控系统。通过结合机器学习、预测建模和多组学数据来揭示复杂的调控关系,计算方法完全改变了grn(基因调控网络)的研究,制造和识别重要的转录因子、协同调控因子和信号网络。近年来,人工智能、系统生物学和生物信息学的发展使谷子grn得以重构和分析,为谷子开花机制、养分吸收和抗旱性提供了新的信息。数据稀缺性、物种特异性异质性以及对高通量功能验证的需求。结合转录组学、蛋白质组学和代谢组学的计算模型通过实现靶向遗传改变和提高预测准确性来帮助改善作物改良。本研究讨论了小米计算GRN研究的关键方法、可访问的数据集和新发展。小米研究中的深度学习、基于crispr的基因编辑和合成生物学都是开发新基因型的机会。通过使用计算方法来全面了解谷子grn,将有可能创造出更有营养、更适应气候变化的谷子品种,从而促进可持续农业。
{"title":"Computational interference of gene regulatory networks on the growth and development of millets","authors":"Lipsa Leena Panigrahi ,&nbsp;Gayatri Mishra ,&nbsp;Dhaneswar Swain ,&nbsp;Gyana Ranjan Rout","doi":"10.1016/j.plgene.2025.100531","DOIUrl":"10.1016/j.plgene.2025.100531","url":null,"abstract":"<div><div>Millets are among the cereal crops cultivated for nutrient-rich food. They are generally considered as resilient crops in terms of growth requirements, as they can withstand harsh climatic factors such as unpredictable climate change and nutrient-depleted soils. The present review highlighted that gene regulatory networks are rewired to control the adaptable traits and to understand the transcriptional regulatory system against environmental stress. By combining machine learning, predictive modeling, and multi-omics data to unravel intricate regulatory relationships, computational methods have entirely changed the study of GRNs (gene regulatory networks), making and identifying important transcription factors, co-regulators, and signaling networks. Recent developments in artificial intelligence, systems biology, and bioinformatics have made reconstructing and analyzing millet GRNs, providing new information on blooming mechanisms, nutrient absorption,and drought resistance. Data scarcity, species-specific heterogeneity, and the requirement for high-throughput functional validation. Computational models incorporating transcriptomics, proteomics, and metabolomics help to improve crop improvement by enabling targeted genetic alterations and increasing predictive accuracy. This study discusses critical approaches, accessible datasets, and new developments in computational GRN investigations in millets. Deep learning, CRISPR-based gene editing, and synthetic biology in millet research are among the opportunities to develop new genotypes. By using computational methods to gain a thorough understanding of millet GRNs, it will be possible to create millet varieties that are more nutritious and climate-robust, promoting sustainable agriculture.</div></div>","PeriodicalId":38041,"journal":{"name":"Plant Gene","volume":"43 ","pages":"Article 100531"},"PeriodicalIF":2.2,"publicationDate":"2025-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144655443","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
The 14-3-3 gene family in Nicotiana tabacum: Genome-wide identification, expression profiling, subcellular localization, and protein interaction analysis in response to cadmium stress 烟草14-3-3基因家族:全基因组鉴定、表达谱、亚细胞定位和镉胁迫下蛋白相互作用分析
IF 2.2 Q3 GENETICS & HEREDITY Pub Date : 2025-09-01 Epub Date: 2025-06-11 DOI: 10.1016/j.plgene.2025.100525
Tengfei Ma , Kunjian Yang , Fang Yang , Li Chen , Ji Chen , Shunqin Zhu , Wanhong Liu
Plant 14-3-3 proteins play a crucial role in the fine-tuning of growth and development, stress resistance, and nutrient metabolism. Tobacco is recognized as a hyperaccumulator of cadmium (Cd), yet the understanding of the Nt14-3-3 gene family remains limited in tobacco (Nicotiana tabacum L.). This study systematically identified 28 members (designated as NtGRF1 through NtGRF28) of the Nt14-3-3 family in the cultivated variety TN90 and categorized them into ε and non-ε groups. Genes within the same evolutionary branch exhibited similar conserved motif patterns and intron-exon structures. Promoter cis-acting element analysis indicated that the expression of NtGRF genes is regulated by plant hormones, particularly abscisic acid (ABA) and jasmonic acid (JA), as well as various stress factors. RNA-seq-based analysis revealed three expression patterns for the Nt14-3-3 family genes: constitutively high-expressing, low-expressing, and tissue-specific expression groups, corroborating these findings with qPCR results. Cd stress significantly enhanced the expression levels of six out of eight randomly screened NtGRF genes (NtGRF8, NtGRF15, NtGRF16, NtGRF21, NtGRF22, and NtGRF28). Subcellular localization analysis showed that NtGRF8, NtGRF16, and NtGRF22 were expressed in the cytoplasm and nucleus, while NtGRF26 was restricted to the cytoplasm. Yeast two-hybrid assays demonstrated that NtGRF16 and NtGRF22 formed homodimers, with heterodimer formation also prevalent. These results offer important insights into the potential biological functions of the Nt14-3-3 gene family, emphasizing their role in various biological processes, particularly in the response of tobacco to cadmium stress.
植物14-3-3蛋白在植物生长发育、抗逆性和养分代谢的调控中起着至关重要的作用。烟草被认为是镉(Cd)的高蓄积者,但对烟草(Nicotiana tabacum L.) Nt14-3-3基因家族的了解仍然有限。本研究系统鉴定了栽培品种TN90中Nt14-3-3家族的28个成员(指定为NtGRF1 ~ NtGRF28),并将其分为ε族和非ε族。同一进化分支内的基因表现出相似的保守基序模式和内含子-外显子结构。启动子顺式作用元件分析表明,NtGRF基因的表达受植物激素,特别是脱落酸(ABA)和茉莉酸(JA)以及各种胁迫因子的调控。基于rna序列的分析揭示了Nt14-3-3家族基因的三种表达模式:组成性高表达、低表达和组织特异性表达组,与qPCR结果证实了这些发现。Cd胁迫显著提高了随机筛选的8个NtGRF基因中的6个(NtGRF8、NtGRF15、NtGRF16、NtGRF21、NtGRF22和NtGRF28)的表达水平。亚细胞定位分析显示,NtGRF8、NtGRF16和NtGRF22在细胞质和细胞核中表达,而NtGRF26仅限于细胞质中表达。酵母双杂交实验表明,NtGRF16和NtGRF22形成同型二聚体,异源二聚体也普遍存在。这些结果为Nt14-3-3基因家族的潜在生物学功能提供了重要的见解,强调了它们在各种生物过程中的作用,特别是在烟草对镉胁迫的反应中。
{"title":"The 14-3-3 gene family in Nicotiana tabacum: Genome-wide identification, expression profiling, subcellular localization, and protein interaction analysis in response to cadmium stress","authors":"Tengfei Ma ,&nbsp;Kunjian Yang ,&nbsp;Fang Yang ,&nbsp;Li Chen ,&nbsp;Ji Chen ,&nbsp;Shunqin Zhu ,&nbsp;Wanhong Liu","doi":"10.1016/j.plgene.2025.100525","DOIUrl":"10.1016/j.plgene.2025.100525","url":null,"abstract":"<div><div>Plant 14-3-3 proteins play a crucial role in the fine-tuning of growth and development, stress resistance, and nutrient metabolism. Tobacco is recognized as a hyperaccumulator of cadmium (Cd), yet the understanding of the <em>Nt14-3-3</em> gene family remains limited in tobacco (<em>Nicotiana tabacum</em> L.). This study systematically identified 28 members (designated as NtGRF1 through NtGRF28) of the <em>Nt14-3-3</em> family in the cultivated variety TN90 and categorized them into ε and non-ε groups. Genes within the same evolutionary branch exhibited similar conserved motif patterns and intron-exon structures. Promoter <em>cis</em>-acting element analysis indicated that the expression of <em>NtGRF</em> genes is regulated by plant hormones, particularly abscisic acid (ABA) and jasmonic acid (JA), as well as various stress factors. RNA-seq-based analysis revealed three expression patterns for the <em>Nt14-3-3</em> family genes: constitutively high-expressing, low-expressing, and tissue-specific expression groups, corroborating these findings with qPCR results. Cd stress significantly enhanced the expression levels of six out of eight randomly screened <em>NtGRF</em> genes (<em>NtGRF8, NtGRF15, NtGRF16, NtGRF21, NtGRF22,</em> and <em>NtGRF28</em>). Subcellular localization analysis showed that <em>NtGRF8, NtGRF16,</em> and <em>NtGRF22</em> were expressed in the cytoplasm and nucleus, while <em>NtGRF26</em> was restricted to the cytoplasm. Yeast two-hybrid assays demonstrated that <em>NtGRF16</em> and <em>NtGRF22</em> formed homodimers, with heterodimer formation also prevalent. These results offer important insights into the potential biological functions of the <em>Nt14-3-3</em> gene family, emphasizing their role in various biological processes, particularly in the response of tobacco to cadmium stress.</div></div>","PeriodicalId":38041,"journal":{"name":"Plant Gene","volume":"43 ","pages":"Article 100525"},"PeriodicalIF":2.2,"publicationDate":"2025-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144279366","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Genome-wide analysis of receptor-like 2 kinase 1-like genes reveals involvement of a RLK1L member in tolerance to salt stress in Medicago sativa 受体样2激酶1样基因的全基因组分析揭示了RLK1L成员参与苜蓿对盐胁迫的耐受性
IF 2.2 Q3 GENETICS & HEREDITY Pub Date : 2025-09-01 Epub Date: 2025-05-23 DOI: 10.1016/j.plgene.2025.100520
Yiping Wei , Tian Zhang , Qinyan Bao, Zhaozhu Wen, Shuzhi Ma, Yanbo Zhang, Wenxuan Du
The Catharanthus roseus receptor-like kinase 1-like (CrRLK1L) family constitutes a specialized group within plant receptor-like protein kinases that has been detected in numerous plant varieties. However, RLK1L members have not been characterized in alfalfa. Through systematic analysis, this study examined the features and identification of RLK1L genes within alfalfa based on known gene sequences from the model plants within the Arabidopsis genus, specifically Arabidopsis thaliana, and those in the Medicago genus, such as Medicago truncatula. Phylogenetic analysis of AtCrRLK1Ls, MtCrRLK1Ls, and MsCrRLK1Ls led to the classification of 19 MsCrRLK1L genes in alfalfa into eight distinct clusters. Bioinformatic analyses revealed that the molecular masses of MsCrRLK1L proteins spanned from 29.17 to 167.36 kDa. Subcellular targeting predictions indicated predominant cell membrane localization for these polypeptides Conserved domain profiling demonstrated the ubiquitous presence of a malectin-like domain across all MsCrRLK1L members. Chromosome localization and collinearity analysis showed that the 19 MsCrRLK1L genes were unevenly distributed across five alfalfa chromosomes, with four gene pairs exhibiting intra-species collinearity. Cis-Acting element analysis identified stress- and hormone-responsive motifs, suggesting that MsCrRLK1Ls are involved in abiotic stress signaling. Gene expression profiling under salt stress (200 mM NaCl) demonstrated tissue-specific induction patterns, with six MsCrRLK1L genes significantly upregulated in aerial and root tissues. Furthermore, MsCrRLK1L2 overexpression in Arabidopsis improved the germination rate and growth status under salt stress. This study comprehensively profiles the MsCrRLK1L family in alfalfa, confirming its role in salt tolerance and suggesting genetic targets to boost crop resilience.
Catharanthus roseus receptor-like kinase 1-like (CrRLK1L)家族是植物受体样蛋白激酶中的一个特殊类群,已在许多植物品种中检测到。然而,RLK1L成员尚未在苜蓿中被表征。本研究通过系统分析,利用拟南芥属模式植物(特别是拟南芥)和紫花苜蓿属模式植物(如truncatula紫花苜蓿)的已知基因序列,对紫花苜蓿RLK1L基因的特征和鉴定进行了研究。通过对AtCrRLK1Ls、MtCrRLK1Ls和MsCrRLK1Ls的系统发育分析,将苜蓿中19个MsCrRLK1L基因分为8个不同的基因簇。生物信息学分析显示,MsCrRLK1L蛋白的分子质量在29.17 ~ 167.36 kDa之间。亚细胞靶向预测表明这些多肽的主要细胞膜定位保守结构域分析表明,在所有MsCrRLK1L成员中普遍存在雄性凝集素样结构域。染色体定位和共线性分析表明,19个MsCrRLK1L基因不均匀分布在5条苜蓿染色体上,其中4对基因在种内共线性。顺式作用元件分析确定了应激和激素反应基序,表明mscrrlk1l参与非生物应激信号传导。盐胁迫(200 mM NaCl)下的基因表达谱显示出组织特异性诱导模式,6个MsCrRLK1L基因在地上和根组织中显著上调。此外,MsCrRLK1L2在拟南芥中的过表达改善了盐胁迫下的发芽率和生长状况。本研究全面分析了苜蓿中MsCrRLK1L家族,证实了其在耐盐性中的作用,并提出了提高作物抗逆性的遗传靶点。
{"title":"Genome-wide analysis of receptor-like 2 kinase 1-like genes reveals involvement of a RLK1L member in tolerance to salt stress in Medicago sativa","authors":"Yiping Wei ,&nbsp;Tian Zhang ,&nbsp;Qinyan Bao,&nbsp;Zhaozhu Wen,&nbsp;Shuzhi Ma,&nbsp;Yanbo Zhang,&nbsp;Wenxuan Du","doi":"10.1016/j.plgene.2025.100520","DOIUrl":"10.1016/j.plgene.2025.100520","url":null,"abstract":"<div><div>The <em>Catharanthus roseus</em> receptor-like kinase 1-like (CrRLK1L) family constitutes a specialized group within plant receptor-like protein kinases that has been detected in numerous plant varieties. However, <em>RLK1L</em> members have not been characterized in alfalfa. Through systematic analysis, this study examined the features and identification of <em>RLK1L</em> genes within alfalfa based on known gene sequences from the model plants within the Arabidopsis genus, specifically <em>Arabidopsis thaliana</em>, and those in the Medicago genus, such as <em>Medicago truncatula</em>. Phylogenetic analysis of <em>AtCrRLK1Ls</em>, <em>MtCrRLK1Ls</em>, and <em>MsCrRLK1Ls</em> led to the classification of 19 <em>MsCrRLK1L</em> genes in alfalfa into eight distinct clusters<em>.</em> Bioinformatic analyses revealed that the molecular masses of MsCrRLK1L proteins spanned from 29.17 to 167.36 kDa. Subcellular targeting predictions indicated predominant cell membrane localization for these polypeptides Conserved domain profiling demonstrated the ubiquitous presence of a malectin-like domain across all MsCrRLK1L members. Chromosome localization and collinearity analysis showed that the 19 <em>MsCrRLK1L</em> genes were unevenly distributed across five alfalfa chromosomes, with four gene pairs exhibiting intra-species collinearity. <em>Cis</em>-Acting element analysis identified stress- and hormone-responsive motifs, suggesting that <em>MsCrRLK1Ls</em> are involved in abiotic stress signaling. Gene expression profiling under salt stress (200 mM NaCl) demonstrated tissue-specific induction patterns, with six <em>MsCrRLK1L</em> genes significantly upregulated in aerial and root tissues. Furthermore, <em>MsCrRLK1L2</em> overexpression in <em>Arabidopsis</em> improved the germination rate and growth status under salt stress. This study comprehensively profiles the <em>MsCrRLK1L</em> family in alfalfa, confirming its role in salt tolerance and suggesting genetic targets to boost crop resilience.</div></div>","PeriodicalId":38041,"journal":{"name":"Plant Gene","volume":"43 ","pages":"Article 100520"},"PeriodicalIF":2.2,"publicationDate":"2025-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144139563","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Effectiveness of KASP-SNP markers in selecting for grain quality traits in rice KASP-SNP标记在水稻品质性状选择中的有效性
IF 2.2 Q3 GENETICS & HEREDITY Pub Date : 2025-09-01 Epub Date: 2025-04-12 DOI: 10.1016/j.plgene.2025.100503
Maxwell Darko Asante , Kirpal Agyemang Ofosu , Felix Frimpong , Deladem Kwami Alphonso , Elizabeth Nartey , Agyei Elvis Obeng , Ralph K. Bam , Daniel D. Gamenyah , Priscilla F. Ribeiro , William Manilal
Grain quality is a crucial factor for rice consumers, and as such, it is a major focus for breeders. Phenotyping for grain quality traits can be a laborious and costly process. In this study, we evaluated the effectiveness of KASP-SNP markers in selecting for grain quality traits, including aroma, gelatinization temperature, grain length, grain width, and grain length: width ratio. We phenotyped 300 diverse rice genotypes for these four traits and genotyped them using their respective KASP-SNP markers. A regression analysis of the phenotype on the genotype was performed. The markers associated with the fgr-1 and GS3 genes explained 97 % and 94 % of the phenotypic variation for aroma and grain length, respectively. Two SNP markers (snpOS00440 and snpOS00441) associated with the GW5/SW5 gene each explained 82 % of the phenotypic variation for grain width, which increased marginally to 85 % when combined. However, two markers, snpOS00036 and snpOS00450, for gelatinization temperature explained only 2 % and 25 % of the phenotypic variation, respectively, indicating that these markers were not efficient in predicting this trait. Our findings suggest that the markers associated with aroma (fgr-1), grain length (GS3), and grain width (GW5/SW5) are highly efficient and reliable for marker-assisted selection.
粮食质量对大米消费者来说是一个至关重要的因素,因此,它也是育种者关注的重点。谷物品质性状的表型分析是一个费时费力的过程。在本研究中,我们评估了KASP-SNP标记在籽粒品质性状选择中的有效性,包括香气、糊化温度、粒长、粒宽和粒长:粒宽比。我们对这4个性状进行了300个不同的水稻基因型表型分析,并利用它们各自的KASP-SNP标记进行了基因型分型。表型对基因型进行回归分析。与fgr-1和GS3基因相关的标记分别解释了97%和94%的香气和粒长表型变异。与GW5/SW5基因相关的两个SNP标记(snpOS00440和snpOS00441)分别解释了82%的籽粒宽度表型变异,当组合在一起时,这一比例增加到85%。然而,糊化温度的两个标记snpOS00036和snpOS00450分别只解释了2%和25%的表型变异,表明这些标记在预测该性状方面效率不高。研究结果表明,与香气(fgr-1)、粒长(GS3)和粒宽(GW5/SW5)相关的标记在标记辅助选择中是高效可靠的。
{"title":"Effectiveness of KASP-SNP markers in selecting for grain quality traits in rice","authors":"Maxwell Darko Asante ,&nbsp;Kirpal Agyemang Ofosu ,&nbsp;Felix Frimpong ,&nbsp;Deladem Kwami Alphonso ,&nbsp;Elizabeth Nartey ,&nbsp;Agyei Elvis Obeng ,&nbsp;Ralph K. Bam ,&nbsp;Daniel D. Gamenyah ,&nbsp;Priscilla F. Ribeiro ,&nbsp;William Manilal","doi":"10.1016/j.plgene.2025.100503","DOIUrl":"10.1016/j.plgene.2025.100503","url":null,"abstract":"<div><div>Grain quality is a crucial factor for rice consumers, and as such, it is a major focus for breeders. Phenotyping for grain quality traits can be a laborious and costly process. In this study, we evaluated the effectiveness of KASP-SNP markers in selecting for grain quality traits, including aroma, gelatinization temperature, grain length, grain width, and grain length: width ratio. We phenotyped 300 diverse rice genotypes for these four traits and genotyped them using their respective KASP-SNP markers. A regression analysis of the phenotype on the genotype was performed. The markers associated with the <em>fgr-1</em> and <em>GS3</em> genes explained 97 % and 94 % of the phenotypic variation for aroma and grain length, respectively. Two SNP markers (snpOS00440 and snpOS00441) associated with the <em>GW5/SW5</em> gene each explained 82 % of the phenotypic variation for grain width, which increased marginally to 85 % when combined. However, two markers, snpOS00036 and snpOS00450, for gelatinization temperature explained only 2 % and 25 % of the phenotypic variation, respectively, indicating that these markers were not efficient in predicting this trait. Our findings suggest that the markers associated with aroma (<em>fgr-1</em>), grain length (<em>GS3)</em>, and grain width (<em>GW5/SW5</em>) are highly efficient and reliable for marker-assisted selection.</div></div>","PeriodicalId":38041,"journal":{"name":"Plant Gene","volume":"43 ","pages":"Article 100503"},"PeriodicalIF":2.2,"publicationDate":"2025-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143844127","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Molecular network, structural and expression analyses of NHX genes in Phaseolus vulgaris in response to salt stress 盐胁迫下菜豆NHX基因的分子网络、结构及表达分析
IF 2.2 Q3 GENETICS & HEREDITY Pub Date : 2025-09-01 Epub Date: 2025-06-18 DOI: 10.1016/j.plgene.2025.100526
Faten Mhadhbi, Hatem Boubakri
Salt stress is one of the most serious abiotic stresses limiting plant productivity worldwide. Here, we identified and characterized Sodium/Hydrogen antiporter (NHX) family in Phaseolus vulgaris genome and studied their expression in response to salt stress, for the first time, using RT q-PCR. In total, we identified 9 PvNHX genes from the common bean genome. Phylogeny, gene structure, motif patterns were performed and allowed the classification of these genes according to their subcellular localization into three subfamilies termed vacuolar (Vac-class), plasma membrane (PM-class) and endosomal (Endo-class). Conserved motifs and gene structures showed that most of which had an amiloride-binding site (FFI/LY/FLLPPI). RT q-PCR analysis revealed that salt stress induced the expression of specific PvNHX genes in both leaves (PvNHX1, PvNHX2, PvNHX3, and PvNHX7) and roots (PvNHX1, PvNHX2, PvNHX3, PvNHX4 and PvNHX7), suggesting their potential role in regulating salinity tolerance in P. vulgaris. Protein-protein interaction (PPI) network indicated that several PvNHX proteins interact with CIPK24 (CBL-interacting serine/threonine-protein kinase 24), CBL4 (Calcineurin B-like protein 4) and KEA4 (K+ efflux antiporter 4) proteins, implying their involvement in CBL-CIPK pathway during salinity adaptation. These findings provide valuable targets within the PvNHX family for genetic engineering aimed at improving salinity tolerance in Phaseolus vulgaris.
盐胁迫是世界范围内限制植物生产力的最严重的非生物胁迫之一。本研究首次利用RT - q-PCR技术,鉴定了菜豆(Phaseolus vulgaris)基因组中钠/氢反转运蛋白(Sodium/Hydrogen antiporter, NHX)家族,并对其在盐胁迫下的表达进行了研究。我们一共从普通豆基因组中鉴定出9个PvNHX基因。系统发育、基因结构、基序模式进行了分析,并根据亚细胞定位将这些基因分为三个亚家族,即空泡亚家族(vac类)、质膜亚家族(pm类)和内体亚家族(endo类)。保守的基序和基因结构表明,其中大部分具有一个酰胺结合位点(FFI/LY/FLLPPI)。RT - q-PCR分析结果显示,盐胁迫诱导PvNHX基因在植物叶片(PvNHX1、PvNHX2、PvNHX3和PvNHX7)和根系(PvNHX1、PvNHX2、PvNHX3、PvNHX4和PvNHX7)中表达,提示PvNHX基因可能在盐胁迫下调控植物耐盐性。蛋白质-蛋白质相互作用(PPI)网络表明,PvNHX蛋白与CIPK24 (cbl -相互作用丝氨酸/苏氨酸-蛋白激酶24)、CBL4(钙调磷酸酶b样蛋白4)和KEA4 (K+外排反转运蛋白4)蛋白相互作用,暗示它们在盐度适应过程中参与了CBL-CIPK途径。这些发现为提高菜豆耐盐性的基因工程提供了PvNHX家族有价值的靶点。
{"title":"Molecular network, structural and expression analyses of NHX genes in Phaseolus vulgaris in response to salt stress","authors":"Faten Mhadhbi,&nbsp;Hatem Boubakri","doi":"10.1016/j.plgene.2025.100526","DOIUrl":"10.1016/j.plgene.2025.100526","url":null,"abstract":"<div><div>Salt stress is one of the most serious abiotic stresses limiting plant productivity worldwide. Here, we identified and characterized Sodium/Hydrogen antiporter (NHX) family in <em>Phaseolus vulgaris</em> genome and studied their expression in response to salt stress, for the first time, using RT q-PCR. In total, we identified 9 <em>PvNHX</em> genes from the common bean genome. Phylogeny, gene structure, motif patterns were performed and allowed the classification of these genes according to their subcellular localization into three subfamilies termed vacuolar (Vac-class), plasma membrane (PM-class) and endosomal (Endo-class). Conserved motifs and gene structures showed that most of which had an amiloride-binding site (FFI/LY/FLLPPI). RT q-PCR analysis revealed that salt stress induced the expression of specific <em>PvNHX</em> genes in both leaves (<em>PvNHX1</em>, <em>PvNHX2</em>, Pv<em>NHX3</em>, and <em>PvNHX7</em>) and roots (<em>PvNHX1</em>, <em>PvNHX2</em>, <em>PvNHX3</em>, <em>PvNHX4</em> and <em>PvNHX7</em>), suggesting their potential role in regulating salinity tolerance in <em>P. vulgaris.</em> Protein-protein interaction (PPI) network indicated that several PvNHX proteins interact with CIPK24 (CBL-interacting serine/threonine-protein kinase 24), CBL4 (Calcineurin B-like protein 4) and KEA4 (K<sup>+</sup> efflux antiporter 4) proteins, implying their involvement in CBL-CIPK pathway during salinity adaptation. These findings provide valuable targets within the <em>PvNHX</em> family for genetic engineering aimed at improving salinity tolerance in <em>Phaseolus vulgaris</em>.</div></div>","PeriodicalId":38041,"journal":{"name":"Plant Gene","volume":"43 ","pages":"Article 100526"},"PeriodicalIF":2.2,"publicationDate":"2025-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144321044","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
期刊
Plant Gene
全部 Acc. Chem. Res. ACS Applied Bio Materials ACS Appl. Electron. Mater. ACS Appl. Energy Mater. ACS Appl. Mater. Interfaces ACS Appl. Nano Mater. ACS Appl. Polym. Mater. ACS BIOMATER-SCI ENG ACS Catal. ACS Cent. Sci. ACS Chem. Biol. ACS Chemical Health & Safety ACS Chem. Neurosci. ACS Comb. Sci. ACS Earth Space Chem. ACS Energy Lett. ACS Infect. Dis. ACS Macro Lett. ACS Mater. Lett. ACS Med. Chem. Lett. ACS Nano ACS Omega ACS Photonics ACS Sens. ACS Sustainable Chem. Eng. ACS Synth. Biol. Anal. Chem. BIOCHEMISTRY-US Bioconjugate Chem. BIOMACROMOLECULES Chem. Res. Toxicol. Chem. Rev. Chem. Mater. CRYST GROWTH DES ENERG FUEL Environ. Sci. Technol. Environ. Sci. Technol. Lett. Eur. J. Inorg. Chem. IND ENG CHEM RES Inorg. Chem. J. Agric. Food. Chem. J. Chem. Eng. Data J. Chem. Educ. J. Chem. Inf. Model. J. Chem. Theory Comput. J. Med. Chem. J. Nat. Prod. J PROTEOME RES J. Am. Chem. Soc. LANGMUIR MACROMOLECULES Mol. Pharmaceutics Nano Lett. Org. Lett. ORG PROCESS RES DEV ORGANOMETALLICS J. Org. Chem. J. Phys. Chem. J. Phys. Chem. A J. Phys. Chem. B J. Phys. Chem. C J. Phys. Chem. Lett. Analyst Anal. Methods Biomater. Sci. Catal. Sci. Technol. Chem. Commun. Chem. Soc. Rev. CHEM EDUC RES PRACT CRYSTENGCOMM Dalton Trans. Energy Environ. Sci. ENVIRON SCI-NANO ENVIRON SCI-PROC IMP ENVIRON SCI-WAT RES Faraday Discuss. Food Funct. Green Chem. Inorg. Chem. Front. Integr. Biol. J. Anal. At. Spectrom. J. Mater. Chem. A J. Mater. Chem. B J. Mater. Chem. C Lab Chip Mater. Chem. Front. Mater. Horiz. MEDCHEMCOMM Metallomics Mol. Biosyst. Mol. Syst. Des. Eng. Nanoscale Nanoscale Horiz. Nat. Prod. Rep. New J. Chem. Org. Biomol. Chem. Org. Chem. Front. PHOTOCH PHOTOBIO SCI PCCP Polym. Chem.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1