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种内群体比较作图揭示了花生 A、B 基因组二倍体种之间高度的大片段共线性。

Comparative mapping in intraspecific populations uncovers a high degree of macrosynteny between A- and B-genome diploid species of peanut.

机构信息

Institute of Plant Breeding, Genetics, and Genomics, The University of Georgia, Athens, 30602, USA.

出版信息

BMC Genomics. 2012 Nov 10;13:608. doi: 10.1186/1471-2164-13-608.

Abstract

BACKGROUND

Cultivated peanut or groundnut (Arachis hypogaea L.) is an important oilseed crop with an allotetraploid genome (AABB, 2n = 4x = 40). Both the low level of genetic variation within the cultivated gene pool and its polyploid nature limit the utilization of molecular markers to explore genome structure and facilitate genetic improvement. Nevertheless, a wealth of genetic diversity exists in diploid Arachis species (2n = 2x = 20), which represent a valuable gene pool for cultivated peanut improvement. Interspecific populations have been used widely for genetic mapping in diploid species of Arachis. However, an intraspecific mapping strategy was essential to detect chromosomal rearrangements among species that could be obscured by mapping in interspecific populations. To develop intraspecific reference linkage maps and gain insights into karyotypic evolution within the genus, we comparatively mapped the A- and B-genome diploid species using intraspecific F2 populations. Exploring genome organization among diploid peanut species by comparative mapping will enhance our understanding of the cultivated tetraploid peanut genome. Moreover, new sources of molecular markers that are highly transferable between species and developed from expressed genes will be required to construct saturated genetic maps for peanut.

RESULTS

A total of 2,138 EST-SSR (expressed sequence tag-simple sequence repeat) markers were developed by mining a tetraploid peanut EST assembly including 101,132 unigenes (37,916 contigs and 63,216 singletons) derived from 70,771 long-read (Sanger) and 270,957 short-read (454) sequences. A set of 97 SSR markers were also developed by mining 9,517 genomic survey sequences of Arachis. An SSR-based intraspecific linkage map was constructed using an F2 population derived from a cross between K 9484 (PI 298639) and GKBSPSc 30081 (PI 468327) in the B-genome species A. batizocoi. A high degree of macrosynteny was observed when comparing the homoeologous linkage groups between A (A. duranensis) and B (A. batizocoi) genomes. Comparison of the A- and B-genome genetic linkage maps also showed a total of five inversions and one major reciprocal translocation between two pairs of chromosomes under our current mapping resolution.

CONCLUSIONS

Our findings will contribute to understanding tetraploid peanut genome origin and evolution and eventually promote its genetic improvement. The newly developed EST-SSR markers will enrich current molecular marker resources in peanut.

摘要

背景

栽培花生或落花生(Arachis hypogaea L.)是一种重要的油料作物,具有异源四倍体基因组(AABB,2n = 4x = 40)。栽培基因库中遗传变异水平低及其多倍体性质限制了分子标记的利用,以探索基因组结构并促进遗传改良。然而,二倍体 Arachis 物种(2n = 2x = 20)中存在丰富的遗传多样性,它们是栽培花生改良的宝贵基因库。种间群体已广泛用于二倍体 Arachis 物种的遗传图谱构建。然而,种内图谱策略对于检测物种间的染色体重排至关重要,因为这些重排可能会被种间群体的图谱掩盖。为了构建二倍体 Arachis 种内参考连锁图谱并深入了解属内的核型进化,我们使用种内 F2 群体比较了 A 基因组和 B 基因组的二倍体物种。通过比较二倍体花生物种的基因组组织,将增强我们对栽培四倍体花生基因组的理解。此外,需要开发来自表达基因的高度可转移到物种间的新的分子标记源,以为花生构建饱和遗传图谱。

结果

通过挖掘包含 70771 条长读(Sanger)和 270957 条短读(454)序列的 101132 个单体(37916 个 contigs 和 63216 个单体)的四倍体花生 EST 组装,共开发了 2138 个 EST-SSR(表达序列标签简单重复序列)标记。通过挖掘 Arachis 的 9517 个基因组普查序列,还开发了一套 97 个 SSR 标记。使用来自 B 基因组物种 A. batizocoi 的 K9484(PI298639)和 GKBSPSc30081(PI468327)之间杂交产生的 F2 群体,构建了基于 SSR 的种内连锁图谱。当比较 A(A. duranensis)和 B(A. batizocoi)基因组的同源连锁群时,观察到高度的宏同线性。A-和 B-基因组遗传连锁图谱的比较还显示,在我们当前的图谱分辨率下,两对染色体之间总共发生了五次倒位和一次主要的相互易位。

结论

我们的研究结果将有助于理解四倍体花生基因组的起源和进化,并最终促进其遗传改良。新开发的 EST-SSR 标记将丰富花生当前的分子标记资源。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/40a9/3532320/d419a5393cdc/1471-2164-13-608-1.jpg

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