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Serotonin-Related Gene Polymorphisms and Asymptomatic Neurocognitive Impairment in HIV-Infected Alcohol Abusers. hiv感染酒精滥用者血清素相关基因多态性和无症状神经认知障碍
Q3 Biochemistry, Genetics and Molecular Biology Pub Date : 2016-01-01 Epub Date: 2016-03-16 DOI: 10.1155/2016/7169172
Karina Villalba, Jessy G Dévieux, Rhonda Rosenberg, Jean Lud Cadet

HIV-infected individuals continue to experience neurocognitive deterioration despite virologically successful treatments. While the cause remains unclear, evidence suggests that HIV-associated neurocognitive disorders (HAND) may be associated with neurobehavioral dysfunction. Genetic variants have been explored to identify risk markers to determine neuropathogenesis of neurocognitive deterioration. Memory deficits and executive dysfunction are highly prevalent among HIV-infected adults. These conditions can affect their quality of life and HIV risk-taking behaviors. Single nucleotide polymorphisms in the SLC6A4, TPH2, and GALM genes may affect the activity of serotonin and increase the risk of HAND. The present study explored the relationship between SLC6A4, TPH2, and GALM genes and neurocognitive impairment in HIV-infected alcohol abusers. A total of 267 individuals were genotyped for polymorphisms in SLC6A4 5-HTTLPR, TPH2 rs4570625, and GALM rs6741892. To assess neurocognitive functions, the Short Category and the Auditory Verbal Learning Tests were used. TPH2 SNP rs4570625 showed a significant association with executive function in African American males (odds ratio 4.8, 95% CI, 1.5-14.8; P = 0.005). Similarly, GALM SNP rs6741892 showed an increased risk with African American males (odds ratio 2.4, 95% CI, 1.2-4.9; P = 0.02). This study suggests that TPH2 rs4570625 and GALM rs6741892 polymorphisms may be risk factors for HAND.

尽管病毒学治疗取得了成功,但艾滋病毒感染者的神经认知能力继续恶化。虽然病因尚不清楚,但有证据表明,hiv相关的神经认知障碍(HAND)可能与神经行为功能障碍有关。遗传变异已被探索以确定神经认知退化的神经发病机制的风险标记。记忆缺陷和执行功能障碍在感染艾滋病毒的成年人中非常普遍。这些情况会影响他们的生活质量和艾滋病毒风险行为。SLC6A4、TPH2和GALM基因的单核苷酸多态性可能影响血清素的活性,增加HAND的风险。本研究探讨了SLC6A4、TPH2和GALM基因与hiv感染的酒精滥用者神经认知障碍的关系。对267个个体进行SLC6A4 5-HTTLPR、TPH2 rs4570625和GALM rs6741892多态性基因分型。为了评估神经认知功能,使用了短类别和听觉语言学习测试。TPH2 SNP rs4570625与非裔美国男性的执行功能显著相关(优势比4.8,95% CI, 1.5-14.8;P = 0.005)。同样,GALM SNP rs6741892显示非裔美国男性的风险增加(优势比2.4,95% CI, 1.2-4.9;P = 0.02)。本研究提示TPH2 rs4570625和GALM rs6741892多态性可能是HAND的危险因素。
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引用次数: 9
Altered Body Weight Regulation in CK1ε Null and tau Mutant Mice on Regular Chow and High Fat Diets. 正常饮食和高脂肪饮食改变CK1ε零和tau突变小鼠的体重调节
Q3 Biochemistry, Genetics and Molecular Biology Pub Date : 2016-01-01 Epub Date: 2016-04-06 DOI: 10.1155/2016/4973242
Lili Zhou, Keith C Summa, Christopher Olker, Martha H Vitaterna, Fred W Turek

Disruption of circadian rhythms results in metabolic dysfunction. Casein kinase 1 epsilon (CK1ε) is a canonical circadian clock gene. Null and tau mutations in CK1ε show distinct effects on circadian period. To investigate the role of CK1ε in body weight regulation under both regular chow (RC) and high fat (HF) diet conditions, we examined body weight on both RC and HF diets in CK1ε (-/-) and CK1ε (tau/tau) mice on a standard 24 hr light-dark (LD) cycle. Given the abnormal entrainment of CK1ε (tau/tau) mice on a 24 hr LD cycle, a separate set of CK1ε (tau/tau) mice were tested under both diet conditions on a 20 hr LD cycle, which more closely matches their endogenous period length. On the RC diet, both CK1ε (-/-) and CK1ε (tau/tau) mutants on a 24 hr LD cycle and CK1ε (tau/tau) mice on a 20 hr LD cycle exhibited significantly lower body weights, despite similar overall food intake and activity levels. On the HF diet, CK1ε (tau/tau) mice on a 20 hr LD cycle were protected against the development of HF diet-induced excess weight gain. These results provide additional evidence supporting a link between circadian rhythms and energy regulation at the genetic level, particularly highlighting CK1ε involved in the integration of circadian biology and metabolic physiology.

昼夜节律紊乱会导致代谢功能紊乱。酪蛋白激酶1ε (CK1ε)是一个典型的生物钟基因。CK1ε的Null和tau突变对昼夜节律有明显的影响。为了研究CK1ε在正常饮食(RC)和高脂肪饮食(HF)条件下的体重调节中的作用,我们在标准的24小时光暗(LD)周期中检测了CK1ε(-/-)和CK1ε (tau/tau)小鼠在RC和HF饮食条件下的体重。考虑到在24小时LD周期中CK1ε (tau/tau)小鼠的异常携带,在20小时LD周期中对另一组CK1ε (tau/tau)小鼠进行了两种饮食条件下的测试,这与它们的内源性周期长度更接近。在RC饮食中,CK1ε(-/-)和CK1ε (tau/tau)突变体在24小时LD周期和CK1ε (tau/tau)突变体在20小时LD周期小鼠表现出显著降低的体重,尽管总体食物摄入量和活动水平相似。在HF饮食中,CK1ε (tau/tau)小鼠在20小时LD周期中免受HF饮食诱导的过度体重增加的影响。这些结果提供了额外的证据,支持昼夜节律和遗传水平上的能量调节之间的联系,特别强调了CK1ε参与昼夜节律生物学和代谢生理学的整合。
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引用次数: 6
Assessment of Functional EST-SSR Markers (Sugarcane) in Cross-Species Transferability, Genetic Diversity among Poaceae Plants, and Bulk Segregation Analysis. 功能EST-SSR标记(甘蔗)在禾科植物间的可转移性、遗传多样性及群体分离分析中的应用。
Q3 Biochemistry, Genetics and Molecular Biology Pub Date : 2016-01-01 Epub Date: 2016-06-01 DOI: 10.1155/2016/7052323
Shamshad Ul Haq, Pradeep Kumar, R K Singh, Kumar Sambhav Verma, Ritika Bhatt, Meenakshi Sharma, Sumita Kachhwaha, S L Kothari

Expressed sequence tags (ESTs) are important resource for gene discovery, gene expression and its regulation, molecular marker development, and comparative genomics. We procured 10000 ESTs and analyzed 267 EST-SSRs markers through computational approach. The average density was one SSR/10.45 kb or 6.4% frequency, wherein trinucleotide repeats (66.74%) were the most abundant followed by di- (26.10%), tetra- (4.67%), penta- (1.5%), and hexanucleotide (1.2%) repeats. Functional annotations were done and after-effect newly developed 63 EST-SSRs were used for cross transferability, genetic diversity, and bulk segregation analysis (BSA). Out of 63 EST-SSRs, 42 markers were identified owing to their expansion genetics across 20 different plants which amplified 519 alleles at 180 loci with an average of 2.88 alleles/locus and the polymorphic information content (PIC) ranged from 0.51 to 0.93 with an average of 0.83. The cross transferability ranged from 25% for wheat to 97.22% for Schlerostachya, with an average of 55.86%, and genetic relationships were established based on diversification among them. Moreover, 10 EST-SSRs were recognized as important markers between bulks of pooled DNA of sugarcane cultivars through BSA. This study highlights the employability of the markers in transferability, genetic diversity in grass species, and distinguished sugarcane bulks.

表达序列标签(est)是基因发现、基因表达调控、分子标记开发和比较基因组学的重要资源。我们获取了10000个est,并通过计算方法分析了267个EST-SSRs标记。平均密度为1个SSR/10.45 kb,频率为6.4%,其中三核苷酸(66.74%)最多,其次是二核苷酸(26.10%)、四核苷酸(4.67%)、五核苷酸(1.5%)和六核苷酸(1.2%)。对新开发的63个EST-SSRs进行了功能注释,并将其用于交叉可转移性、遗传多样性和体分离分析(BSA)。在63个EST-SSRs中,有42个标记在20个不同的植物上扩增了180个位点的519个等位基因,平均每个位点扩增2.88个等位基因,多态性信息含量(PIC)在0.51 ~ 0.93之间,平均为0.83。小麦的杂交可转性为25% ~ 97.22%,平均为55.86%,在多样化基础上建立了亲缘关系。此外,通过BSA鉴定出10个EST-SSRs是甘蔗品种混合DNA块间的重要标记。本研究强调了这些标记在草地物种的可转移性、遗传多样性和区分甘蔗块中的应用能力。
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引用次数: 23
SOD1 Gene +35A/C (exon3/intron3) Polymorphism in Type 2 Diabetes Mellitus among South Indian Population. 南印度人群中 2 型糖尿病的 SOD1 基因 +35A/C(外显子 3/内含子 3)多态性。
Q3 Biochemistry, Genetics and Molecular Biology Pub Date : 2016-01-01 Epub Date: 2016-04-17 DOI: 10.1155/2016/3787268
K Nithya, T Angeline, W Isabel, A J Asirvatham

Superoxide dismutase is an antioxidant enzyme that is involved in defence mechanisms against oxidative stress. Cu/Zn SOD is a variant that is located in exon3/intron3 boundary. The aim of the present study was to investigate whether the Cu/Zn SOD (+35A/C) gene polymorphism is associated with the susceptibility to type 2 diabetes mellitus among south Indian population. The study included patients with type 2 diabetes mellitus (n = 100) and healthy controls (n = 75). DNA was isolated from the blood and genotyping of Cu/Zn SOD gene polymorphism was done by polymerase chain reaction based restriction fragment length polymorphism method. Occurrence of different genotypes and normal (A) and mutant (C) allele frequencies were determined. The frequency of the three genotypes of the total subjects was as follows: homozygous wild-type A/A (95%), heterozygous genotype A/C (3%), and homozygous mutant C/C (2%). The mutant (C) allele and the mutant genotypes (AC/CC) were found to be completely absent among the patients with type 2 diabetes mellitus. Absence of mutant genotype (CC) shows that the Cu/Zn SOD gene polymorphism may not be associated with the susceptibility to type 2 diabetes mellitus among south Indian population.

超氧化物歧化酶是一种抗氧化酶,参与氧化应激的防御机制。Cu/Zn SOD是位于外显子3/内含子3边界的一个变体。本研究旨在调查 Cu/Zn SOD(+35A/C)基因多态性是否与南印度人群的 2 型糖尿病易感性有关。研究对象包括 2 型糖尿病患者(100 人)和健康对照组(75 人)。从血液中分离出 DNA,通过聚合酶链式反应限制性片段长度多态性方法对 Cu/Zn SOD 基因多态性进行基因分型。测定了不同基因型的出现情况以及正常(A)和突变(C)等位基因的频率。在所有受试者中,三种基因型的频率如下:同基因野生型 A/A(95%)、杂合子基因型 A/C(3%)和同基因突变型 C/C(2%)。在 2 型糖尿病患者中,完全不存在突变型(C)等位基因和突变基因型(AC/CC)。突变基因型(CC)的缺失表明,在南印度人群中,Cu/Zn SOD 基因多态性可能与 2 型糖尿病的易感性无关。
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引用次数: 0
De Novo Assembly and Transcriptome Characterization of Canine Retina Using High-Throughput Sequencing 利用高通量测序技术对犬视网膜进行从头组装和转录组表征
Q3 Biochemistry, Genetics and Molecular Biology Pub Date : 2015-12-16 DOI: 10.1155/2015/638679
B. Reddy, Amrutlal K. Patel, Krishna M. Singh, D. Patil, P. Parikh, D. N. Kelawala, P. Koringa, V. Bhatt, M. V. Rao, C. Joshi
We performed transcriptome sequencing of canine retinal tissue by 454 GS-FLX and Ion Torrent PGM platforms. RNA-Seq analysis by CLC Genomics Workbench mapped expression of 10,360 genes. Gene ontology analysis of retinal transcriptome revealed abundance of transcripts known to be involved in vision associated processes. The de novo assembly of the sequences using CAP3 generated 29,683 contigs with mean length of 560.9 and N50 of 619 bases. Further analysis of contigs predicted 3,827 full-length cDNAs and 29,481 (99%) open reading frames (ORFs). In addition, 3,782 contigs were assigned to 316 KEGG pathways which included melanogenesis, phototransduction, and retinol metabolism with 33, 15, and 11 contigs, respectively. Among the identified microsatellites, dinucleotide repeats were 68.84%, followed by trinucleotides, tetranucleotides, pentanucleotides, and hexanucleotides in proportions of 25.76, 9.40, 2.52, and 0.96%, respectively. This study will serve as a valuable resource for understanding the biology and function of canine retina.
我们利用454 GS-FLX和Ion Torrent PGM平台对犬视网膜组织进行转录组测序。CLC Genomics Workbench的RNA-Seq分析绘制了10360个基因的表达图谱。视网膜转录组的基因本体论分析揭示了大量已知参与视觉相关过程的转录本。利用CAP3对序列进行从头组装,得到29,683个contigs,平均长度为560.9,N50为619个碱基。进一步分析预测了3827个全长cdna和29481个(99%)开放阅读框(orf)。此外,3,782个contigs被分配到316个KEGG通路,包括黑色素生成,光导和视黄醇代谢,分别有33个,15个和11个contigs。在所鉴定的微卫星中,二核苷酸重复序列占68.84%,其次是三核苷酸、四核苷酸、五核苷酸和六核苷酸,分别占25.76%、9.40%、2.52%和0.96%。本研究为进一步了解犬视网膜的生物学和功能提供了宝贵的资源。
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引用次数: 3
Study of Cysteine-Rich Protein 61 Genetic Polymorphism in Predisposition to Fracture Nonunion: A Case Control 富半胱氨酸蛋白61基因多态性与骨折不愈合易感性的研究:一个病例对照
Q3 Biochemistry, Genetics and Molecular Biology Pub Date : 2015-12-10 DOI: 10.1155/2015/754872
Sabir Ali, Syed Rizwan Hussain, Ajai Pratap Singh, Vineet Kumar, S. Walliullah, N. Rizvi, M. Yadav, M. Ahmad, A. Mahdi
Background. Many factors are responsible for this impaired healing, especially in long bones, but a possible genetic predisposition for the development of this complication remains unknown till now. In the present study, we aim to examine the CYR61 gene polymorphism in fracture nonunion patients and the correlation with clinical findings. Materials and Methods. We performed SNP analysis of the CYR61 gene in 250 fracture nonunion patients and 250 healthy subjects were genotyped in this hospital-based case control study, and 56 cases were further evaluated for mRNA expression of CYR61 by real-time quantitative reverse-transcription PCR. Results. CYR61 gene TT, TG, and GG genotype frequencies of total fracture nonunion cases were 41.6%, 49.2%, and 9.20% and 54.4%, 39.2%, and 6.40% in healthy controls. Heterozygous TG genotype was found statistically significant in fracture nonunion cases compared with that in controls, whereas homozygous mutant GG genotype was not found significant. Moreover, we found that TG + GG genotypes were significantly different in serum expression of CYR61 mRNA when compared with cases (TT genotypes). Conclusions. Our result signifies that genotype of CYR61 affects the mRNA expression and acts as a risk factor that could synergistically increase the susceptibility of a patient to develop fracture nonunion.
背景。许多因素导致这种愈合受损,尤其是长骨,但迄今为止,这种并发症的可能遗传易感性尚不清楚。在本研究中,我们旨在研究骨折不愈合患者的CYR61基因多态性及其与临床表现的相关性。材料与方法。在这项以医院为基础的病例对照研究中,我们对250例骨折不愈合患者和250名健康受试者的CYR61基因进行了SNP分析,并通过实时定量反转录PCR进一步评估了56例患者CYR61 mRNA的表达。结果。CYR61基因TT、TG和GG基因型频率在骨折不愈合病例中分别为41.6%、49.2%和9.20%,在健康对照中分别为54.4%、39.2%和6.40%。与对照组相比,杂合子TG基因型在骨折不愈合病例中有统计学意义,而纯合子突变GG基因型在骨折不愈合病例中无统计学意义。此外,我们发现TG + GG基因型与TT基因型相比,血清CYR61 mRNA的表达有显著差异。结论。我们的研究结果表明,CYR61基因型影响mRNA表达,并作为一个危险因素,可能协同增加患者发生骨折不愈合的易感性。
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引用次数: 9
Frequency Distribution of Mannose Binding Lectin-2 and Vitamin D Receptor Gene Variants: Putative Markers for Tuberculosis 甘露糖结合凝集素-2和维生素D受体基因变异的频率分布:结核病的推定标记
Q3 Biochemistry, Genetics and Molecular Biology Pub Date : 2015-11-26 DOI: 10.1155/2015/264120
Anuroopa Gupta, H. Padh
Genetic polymorphism in Mannose Binding Lectin-2 (MBL-2) and Vitamin D Receptor (VDR) is known to influence the susceptibility to tuberculosis. The objective of the present study was to evaluate the frequency distribution of the MBL-2 promoter and structural polymorphism (−550 H/L, −221 Y/X, and +4 P/Q; R52C, G54D, and G57F) and VDR polymorphism (FokI, BsmI, TaqI, and ApaI) in healthy individuals of Indian population and comparative analysis with the global population. In Indian population, the frequency of VDR mutant alleles “f” for FokI, “b” for BsmI, “t” for TaqI, and “a” for ApaI was 25%, 54%, 30%, and 61%, respectively. The allelic frequency of MBL-2 promoter polymorphism −550 H/L was H versus L: 32% versus 68%, −221 Y/X was Y versus X: 68% versus 32%, and +4 P/Q was P versus Q: 78% versus 22%. Mutant allelic frequencies of the MBL-2 exon 1 D, B, and C allele were 6%, 11%, and 3%, respectively. Comparative analysis with global populations showed a noteworthy difference for MBL-2 and VDR polymorphism frequency distribution, indicating the ethnic variability of Indians. The study signifies the differential distribution of susceptibility genes in Indian population, which can influence the understanding of the pathophysiology of tuberculosis in Indian population.
甘露糖结合凝集素-2 (MBL-2)和维生素D受体(VDR)的遗传多态性影响结核病的易感性。本研究的目的是评估MBL-2启动子的频率分布和结构多态性(- 550 H/L, - 221 Y/X和+4 P/Q;R52C、G54D和G57F)和VDR多态性(FokI、BsmI、TaqI和ApaI)在印度健康人群中的分布及其与全球人群的比较分析在印度人群中,FokI的VDR突变等位基因“f”、BsmI的“b”、TaqI的“t”和ApaI的“a”的频率分别为25%、54%、30%和61%。MBL-2启动子多态性的等位基因频率−550 H/L为H对L: 32%对68%,−221 Y/X为Y对X: 68%对32%,+4 P/Q为P对Q: 78%对Q: 22%。MBL-2外显子1 D、B和C等位基因的突变频率分别为6%、11%和3%。与全球人群的比较分析显示,MBL-2和VDR多态性频率分布存在显著差异,说明印度人存在民族变异性。该研究表明印度人群中易感基因的差异分布,可以影响对印度人群结核病病理生理的认识。
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引用次数: 3
Association of Polymorphisms of Phase I Metabolizing Genes with Sister Chromatid Exchanges in Occupational Workers Exposed to Toluene Used in Paint Thinners 接触油漆稀释剂中使用的甲苯的职业工人I期代谢基因多态性与姐妹染色单体交换的关系
Q3 Biochemistry, Genetics and Molecular Biology Pub Date : 2015-11-24 DOI: 10.1155/2015/630296
K. Priya, A. Yadav, Neeraj Kumar, Sachin Gulati, N. Aggarwal, Ranjan Gupta
This study investigated genetic damage in paint workers mainly exposed to toluene as it is a major solvent used in paint thinners. Sister chromatid exchange (SCE) assay was used as biomarker of genotoxicity. Blood samples were collected from 30 paint workers and 30 control subjects matched with respect to age and other confounding factors except for exposure to toluene. SCE frequency was found to be significantly higher in paint workers (4.81 ± 0.92) as compared to control individuals (1.73 ± 0.54) (p < 0.05). We also investigated influence of polymorphisms of CYP2E1 and CYP1A1m2 genes on SCE frequency. Our results showed that there was significant increase in frequencies of SCE among the mutant genotypes of CYP2E1 and CYP1A1m2 as compared to wild genotypes. Our study indicated that long term exposure of toluene can increase genotoxic risk in paint workers.
本研究调查了主要暴露于甲苯的油漆工人的遗传损伤,因为甲苯是油漆稀释剂中使用的主要溶剂。采用姐妹染色单体交换(SCE)试验作为遗传毒性的生物标志物。采集了30名油漆工人和30名对照对象的血液样本,这些样本在年龄和其他混杂因素方面相匹配,除了接触甲苯。油漆工人的SCE频率(4.81±0.92)明显高于对照组(1.73±0.54)(p < 0.05)。我们还研究了CYP2E1和CYP1A1m2基因多态性对SCE频率的影响。我们的研究结果表明,与野生基因型相比,CYP2E1和CYP1A1m2突变基因型的SCE频率显著增加。我们的研究表明,长期接触甲苯会增加油漆工人的遗传毒性风险。
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引用次数: 5
Identification of Proximal and Distal 22q11.2 Microduplications among Patients with Cleft Lip and/or Palate: A Novel Inherited Atypical 0.6 Mb Duplication 唇裂和/或腭裂患者近端和远端22q11.2微重复的鉴定:一种新的遗传非典型0.6 Mb重复
Q3 Biochemistry, Genetics and Molecular Biology Pub Date : 2015-11-12 DOI: 10.1155/2015/398063
M. Sedghi, H. Abdali, M. Memarzadeh, Mansoor Salehi, N. Nouri, M. Hosseinzadeh, N. Nouri
Misalignments of low-copy repeats (LCRs) located in chromosome 22, particularly band 22q11.2, predispose to rearrangements. A variety of phenotypic features are associated with 22q11.2 microduplication syndrome which makes it challenging for the genetic counselors to recommend appropriate genetic assessment and counseling for the patients. In this study, multiplex ligation probe dependent amplification (MLPA) analysis was performed on 378 patients with cleft lip and/or palate to characterize rearrangements in patients suspected of 22q11.2 microduplication and microdeletion syndromes. Of 378 cases, 15 were diagnosed with a microdeletion with various sizes and 3 with duplications. For the first time in this study an atypical 0.6 Mb duplication is reported. Illustration of the phenotypes associated with the microduplications increases the knowledge of phenotypes reported in the literature.
位于22号染色体上的低拷贝重复序列(lcr),特别是22q11.2带,易发生重排。22q11.2微重复综合征与多种表型特征相关,这使得遗传咨询师为患者推荐适当的遗传评估和咨询具有挑战性。本研究对378例唇裂和/或腭裂患者进行多重结扎探针依赖扩增(MLPA)分析,以表征疑似22q11.2微重复和微缺失综合征患者的重排。在378例中,15例被诊断为不同大小的微缺失,3例被诊断为重复。本研究首次报道了非典型的0.6 Mb重复。与微复制相关的表型插图增加了文献中报道的表型知识。
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引用次数: 4
Importance of genetic diversity assessment in crop plants and its recent advances: an overview of its analytical perspectives. 作物遗传多样性评估的重要性及其最新进展:分析视角概述。
Q3 Biochemistry, Genetics and Molecular Biology Pub Date : 2015-01-01 Epub Date: 2015-03-19 DOI: 10.1155/2015/431487
M Govindaraj, M Vetriventhan, M Srinivasan

The importance of plant genetic diversity (PGD) is now being recognized as a specific area since exploding population with urbanization and decreasing cultivable lands are the critical factors contributing to food insecurity in developing world. Agricultural scientists realized that PGD can be captured and stored in the form of plant genetic resources (PGR) such as gene bank, DNA library, and so forth, in the biorepository which preserve genetic material for long period. However, conserved PGR must be utilized for crop improvement in order to meet future global challenges in relation to food and nutritional security. This paper comprehensively reviews four important areas; (i) the significance of plant genetic diversity (PGD) and PGR especially on agriculturally important crops (mostly field crops); (ii) risk associated with narrowing the genetic base of current commercial cultivars and climate change; (iii) analysis of existing PGD analytical methods in pregenomic and genomic era; and (iv) modern tools available for PGD analysis in postgenomic era. This discussion benefits the plant scientist community in order to use the new methods and technology for better and rapid assessment, for utilization of germplasm from gene banks to their applied breeding programs. With the advent of new biotechnological techniques, this process of genetic manipulation is now being accelerated and carried out with more precision (neglecting environmental effects) and fast-track manner than the classical breeding techniques. It is also to note that gene banks look into several issues in order to improve levels of germplasm distribution and its utilization, duplication of plant identity, and access to database, for prebreeding activities. Since plant breeding research and cultivar development are integral components of improving food production, therefore, availability of and access to diverse genetic sources will ensure that the global food production network becomes more sustainable. The pros and cons of the basic and advanced statistical tools available for measuring genetic diversity are briefly discussed and their source links (mostly) were provided to get easy access; thus, it improves the understanding of tools and its practical applicability to the researchers.

植物遗传多样性(PGD)的重要性现已被公认为一个特殊领域,因为人口爆炸和城市化以及可耕地减少是导致发展中国家粮食不安全的关键因素。农业科学家意识到,植物遗传多样性可以通过基因库、DNA 库等植物遗传资源(PGR)的形式获取并储存在生物库中,从而长期保存遗传物质。然而,保存的植物遗传资源必须用于作物改良,以应对未来与粮食和营养安全有关的全球性挑战。本文全面回顾了四个重要领域:(i) 植物遗传多样性(PGD)和 PGR 的意义,尤其是对重要农作物(主要是大田作物)的意义;(ii) 当前商业栽培品种遗传基础缩小和气候变化带来的风险;(iii) 前基因组和基因组时代现有 PGD 分析方法的分析;(iv) 后基因组时代可用于 PGD 分析的现代工具。这些讨论有利于植物科学家利用新方法和新技术进行更好、更快的评估,以便将基因库中的种质资源用于应用育种计划。随着新生物技术的出现,与传统育种技术相比,基因操作的进程正在加快,并以更加精确(忽略环境影响)和快速的方式进行。此外,基因库还研究了几个问题,以提高种质资源的分布和利用水平、植物特征的复制以及数据库的访问,促进育种前活动。由于植物育种研究和栽培品种开发是提高粮食产量不可或缺的组成部分,因此,提供和获取多种基因资源将确保全球粮食生产网络更具可持续性。本文简要讨论了可用于衡量遗传多样性的基本和先进统计工具的利弊,并提供了这些工具的源链接(大部分),以便于访问;从而提高了研究人员对工具及其实际应用性的理解。
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引用次数: 0
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