Large-scale integration of meta-QTL and genome-wide association study identifies genomic regions and candidate genes for photosynthetic efficiency traits in bread wheat.

IF 3.7 2区 生物学 Q2 BIOTECHNOLOGY & APPLIED MICROBIOLOGY BMC Genomics Pub Date : 2025-03-22 DOI:10.1186/s12864-025-11472-6
Ming Chen, Tao Chen, Letong Yun, Zhuo Che, Jingfu Ma, Binxue Kong, Jiangying Long, Chunhua Cheng, Kaiqi Guo, Peipei Zhang, Lijian Guo, Delong Yang
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Abstract

Background: Improving photosynthetic efficiency is an essential strategy for advancing wheat breeding progress. Integrating wheat genetic resources provides an opportunity to discover pivotal genomic regions and candidate genes (CGs) for photosynthetic efficiency traits in wheat.

Results: A large-scale meta-QTL (MQTL) analysis was performed with 1363 initial quantitative trait loci (QTLs) for photosynthetic efficiency traits extracted from 66 independent QTL mapping studies over the past decades. Consequently, 718 initial QTLs were refined into 74 MQTLs, which were distributed on all wheat chromosomes except 1D, 3 A, 4B, and 5B. Compared with the confidence interval (CI) of the initial QTL, the CI of the identified MQTL was 0.03 to 10.97 cM, with an average of 1.46 cM, which was 20.46 times narrower than that of the original QTL. The maximum explained phenotypic variance (PVE) of the MQTL ranged from 7.43 to 20.42, with an average of 11.97, which was 1.07 times higher than that of the original QTL. Of these, 54 MQTLs were validated using genome-wide association study (GWAS) data from different natural populations in previous research. A total of 3,102 CGs were identified within the MQTL intervals, where 342 CGs share homology with rice, and 1,043 CGs are highly expressed in leaves, spikes, and stems. These CGs were mainly involved in porphyrin metabolism, glyoxylate, dicarboxylate metabolism, carbon metabolism and photosynthesis antenna proteins metabolism pathways by the in silico transcriptome assessment. For the key CG TaGGR-6A (TraesCS6A02G307700) involved in the porphyrin metabolism pathway, a functional kompetitive allele-specific PCR (KASP) marker was developed at 2464 bp (A/G) position within the 3' untranslated region, successfully distinguishing two haplotypes: TaGGR-6A-Hap I (type AA) and TaGGR-6A-Hap II (type GG). Varieties with the TaGGR-6A-Hap II allele exhibited approximately 13.42% and 11.45% higher flag leaf chlorophyll content than those carrying the TaGGR-6A-Hap I allele. The elite haplotype TaGGR-6A-Hap II was positively selected during wheat breeding, as evidenced by the geographical and annual frequency distributions of the two TaGGR-6A haplotypes.

Conclusion: The findings will give further insights into the genetic determinants of photosynthetic efficiency traits and provide some reliable MQTLs and putative CGs for the genetic improvement of photosynthetic efficiency in wheat.

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大规模整合meta-QTL和全基因组关联研究鉴定面包小麦光合效率性状的基因组区域和候选基因。
背景:提高小麦光合效率是推进小麦育种进程的重要策略。整合小麦遗传资源为发现小麦光合效率性状的关键基因组区域和候选基因(CGs)提供了机会。结果:利用过去几十年66个独立QTL定位研究中提取的1363个光合效率性状初始数量性状位点(QTL)进行了大规模meta-QTL分析。结果表明,718个初始qtl被精炼为74个,分布在除1D、3a、4B和5B外的所有小麦染色体上。与初始QTL的置信区间(CI)相比,鉴定出的MQTL CI为0.03 ~ 10.97 cM,平均CI为1.46 cM,比原始QTL窄20.46倍。MQTL的最大解释表型方差(PVE)为7.43 ~ 20.42,平均为11.97,是原QTL的1.07倍。其中,54个mqtl使用先前研究中来自不同自然种群的全基因组关联研究(GWAS)数据进行了验证。在MQTL区间内共鉴定出3102个基因,其中342个基因与水稻具有同源性,1043个基因在叶片、穗和茎中高度表达。这些基因主要参与卟啉代谢、乙醛酸盐、二羧酸盐代谢、碳代谢和光合作用天线蛋白代谢途径。针对参与卟啉代谢途径的关键CG TaGGR-6A (TraesCS6A02G307700),在3'非翻译区2464 bp (a /G)位置建立了功能性竞争等位基因特异性PCR (KASP)标记,成功区分了两种单倍型:TaGGR-6A- hap I (AA型)和TaGGR-6A- hap II (GG型)。与携带TaGGR-6A-Hap II等位基因的品种相比,携带TaGGR-6A-Hap II等位基因的品种旗叶叶绿素含量分别高出13.42%和11.45%。从两个TaGGR-6A单倍型的地理分布和年频率分布可以看出,在小麦育种过程中,精英单倍型TaGGR-6A- hap II被正向选择。结论:研究结果将进一步揭示小麦光合效率性状的遗传决定因素,为小麦光合效率的遗传改良提供可靠的mqtl和推测的CGs。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
BMC Genomics
BMC Genomics 生物-生物工程与应用微生物
CiteScore
7.40
自引率
4.50%
发文量
769
审稿时长
6.4 months
期刊介绍: BMC Genomics is an open access, peer-reviewed journal that considers articles on all aspects of genome-scale analysis, functional genomics, and proteomics. BMC Genomics is part of the BMC series which publishes subject-specific journals focused on the needs of individual research communities across all areas of biology and medicine. We offer an efficient, fair and friendly peer review service, and are committed to publishing all sound science, provided that there is some advance in knowledge presented by the work.
期刊最新文献
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