水稻品质与产量性状亲本多态性及等位基因变异研究利用SSR标记

S. Rathi, S. Upadhyay, P. Singh, Rajesh Kumar, P. ., P. Bisen, Bapsila Loitongbam, Sanchika Snehi
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引用次数: 1

摘要

目的:多态性标记的鉴定是进行QTL定位实验的先决条件,因为如果亲本对感兴趣的性状具有多态性,那么在后代中进一步选择植物就变得容易。因此,本研究的目的是鉴定亲本改良桑巴马苏里和巴德沙布格的籽粒品质和产量性状的多态性标记。研究地点和时间:研究于2019年在巴纳拉斯印度教大学农业科学研究所遗传与植物育种系分子育种实验室进行,瓦拉纳西- 221 005,印度。方法:本研究采用改良的Samba Mahsuri和Badshabhog两种亲本。DNA提取是按照Murray和Thompson建议的CTAB方法进行的。采用标准PCR方案。结果:利用随机选择的576个SSR标记进行亲本多态性调查,其中26个与水稻香气、煮食品质、籽粒尺寸和产量相关性状相关的基因特异性标记分布在12条染色体上。共有96个标记存在多态性,其中4个为基因特异性标记,多态性率为16.67%。多态性率最高的是6号染色体(26.67%),其次是4号染色体(21.43%),最低的是10号染色体(8.93%)。基因特异性标记nksbad2、ARO7、BADEX7_5和SSI存在多态性。结论:基于本研究,所鉴定的多态性标记可进一步用于F2:3群体的基因分型、连锁分析以及籽粒品质和产量性状的QTL定位。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Study of Parental Polymorphism and Allelic Variation for Grain Quality and Yield Traits in Rice (Oryza sativa L.) Using SSR Markers
Aim: Identification of polymorphic markers is prerequisite for conducting any QTL mapping experiment because if the parents are polymorphic for the traits of interest, then further selection of plants in the progenies becomes easy. Hence, the objective of the present study was to identify polymorphic markers for grain quality and yield traits among the parental lines Improved Samba Mahsuri and Badshabhog. Place and Duration of Study: It was carried out at Molecular Breeding Lab, Department of Genetics and Plant Breeding, Institute of Agricultural Sciences, Banaras Hindu University, Varanasi - 221 005, India, during 2019. Methodology: Two parents Improved Samba Mahsuri and Badshabhog were used for the present study. The DNA extraction was done as per the CTAB method suggested by Murray and Thompson. Standard PCR protocol was followed. Results: For parental polymorphism survey, a total of 576 randomly selected SSR markers including 26 gene specific markers related to aroma, cooking and eating quality, grain dimension and yield related traits distributed across the 12 chromosomes of rice were used. Overall, 96 markers including 4 gene specific markers were found to be polymorphic between the two genotypes indicating a total polymorphism percentage of 16.67%. The highest polymorphism percentage was recorded on chromosome 6 (26.67%) followed by chromosome 4 (21.43%) and the lowest polymorphism percentage was observed on chromosome 10 (8.93%). The gene specific markers nksbad2, ARO7, BADEX7_5 and SSI were found to be polymorphic. Conclusion: Based on the present study it may be concluded that the polymorphic markers identified will further be utilized in genotyping of F2:3 population, linkage analysis and mapping QTL’s for grain quality and yield traits.
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