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开发一种经济高效的高通量中密度5K基因分型检测方法用于花生种质鉴定和育种。

Development of a cost-effective high-throughput mid-density 5K genotyping assay for germplasm characterization and breeding in groundnut.

作者信息

Pandey Manish K, Sharma Vinay, Khan Aamir W, Joshi Pushpesh, Gangurde Sunil S, Bajaj Prasad, Janila Pasupuleti, Chitikineni Annapurna, Bhat Ramesh, Motagi Babu N, Sangh Chandramohan, Radhakrishnan Thankappan, Bera Sandip K, Gorjanc Gregor, Gujjula Krishna Reddy, Hall Nathan, Carrasco Claudio D, Arjun Kandalam, Chandram Srinivas, Varshney Rajeev K

机构信息

Center for Excellence in Genomics and Systems Biology (CEGSB) and Center for Pre -Breeding Research (CPBR), International Crops Research Institute for the Semi-Arid Tropics (ICRISAT), Hyderabad, India.

WA State Agricultural Biotechnology Centre, Centre for Crop and Food Innovation, Murdoch University, Murdoch, WA, Australia.

出版信息

Plant Genome. 2025 Jun;18(2):e70019. doi: 10.1002/tpg2.70019.

Abstract

Groundnut (Arachis hypogaea L.), also known as peanut, is an allotetraploid legume crop composed of two different progenitor sub-genomes. This crop is an important source for food, feed, and confectioneries. Leveraging translational genomics research has expedited the precision and speed in making selections of progenies in several crops through either marker-assisted selection or genomic selection, including groundnut. The availability of foundational genomic resources such as reference genomes for diploid progenitors and cultivated tetraploids, offered substantial opportunities for genomic interventions, including the development of genotyping assays. Here, a cost-effective and high-throughput genotyping assay has been developed with 5,081 single nucleotide polymorphisms (SNPs) referred to as "mid-density assay." This multi-purpose assay includes 5,000 highly informative SNPs selected based on higher polymorphism information content (PIC) from our previously developed high-density "Axiom_Arachis" array containing 58,233 SNPs. Additionally 82 SNPs associated with five resilience and quality traits were included for marker-assisted selection. To test the utility of the mid-density genotyping (MDG) assay, 2,573 genotypes from distinct sets of breeding populations were genotyped with the 5,081 SNPs. PIC of the SNPs in the MDG ranged from 0.34 to 0.37 among diverse sets. The first three principal components collectively explained 82.08% of the variance among these genotypes. The mid-density assay demonstrated a proficient ability to distinguish between the genotypes, offering a high level of genome-wide nucleotide diversity. This assay holds promise for possible deployment in the identification of varietal seed mixtures, genetic purity within gene bank germplasms and seed systems, foreground and background selection in backcross breeding programs, genomic selection, and sparse trait mapping studies in groundnut.

摘要

花生(Arachis hypogaea L.),也被称为花生米,是一种由两个不同的祖先亚基因组组成的异源四倍体豆科作物。这种作物是食品、饲料和糖果的重要来源。利用转化基因组学研究加快了通过标记辅助选择或基因组选择在几种作物(包括花生)中选择后代的精度和速度。基础基因组资源的可用性,如二倍体祖先和栽培四倍体的参考基因组,为基因组干预提供了大量机会,包括基因分型检测的开发。在此,开发了一种具有成本效益的高通量基因分型检测方法,该方法使用了5081个单核苷酸多态性(SNP),称为“中密度检测”。这种多功能检测包括从我们之前开发的包含58233个SNP的高密度“Axiom_Arachis”阵列中基于更高的多态性信息含量(PIC)选择的5000个高信息量SNP。此外,还纳入了与五个抗逆性和品质性状相关的82个SNP用于标记辅助选择。为了测试中密度基因分型(MDG)检测的实用性,使用这5081个SNP对来自不同育种群体的2573个基因型进行了基因分型。在不同组中,MDG中SNP的PIC范围为0.34至0.37。前三个主成分共同解释了这些基因型间82.08%的变异。中密度检测显示出区分基因型的出色能力,提供了高水平的全基因组核苷酸多样性。该检测有望用于花生品种种子混合物的鉴定、基因库种质和种子系统内的遗传纯度鉴定、回交育种计划中的前景和背景选择、基因组选择以及稀疏性状定位研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d2e3/11958872/a776a611fba1/TPG2-18-e70019-g003.jpg

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