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拟南芥新一代近等基因系库的建立及其在复杂性状解析中的应用。

Development of a next-generation NIL library in Arabidopsis thaliana for dissecting complex traits.

机构信息

Department of Bioagricultural Sciences & Pest Management, Colorado State University, 80523 Fort Collins, CO, USA.

出版信息

BMC Genomics. 2013 Sep 25;14:655. doi: 10.1186/1471-2164-14-655.

Abstract

BACKGROUND

The identification of the loci and specific alleles underlying variation in quantitative traits is an important goal for evolutionary biologists and breeders. Despite major advancements in genomics technology, moving from QTL to causal alleles remains a major challenge in genetics research. Near-isogenic lines are the ideal raw material for QTL validation, refinement of QTL location and, ultimately, gene discovery.

RESULTS

In this study, a population of 75 Arabidopsis thaliana near-isogenic lines was developed from an existing recombinant inbred line (RIL) population derived from a cross between physiologically divergent accessions Kas-1 and Tsu-1. First, a novel algorithm was developed to utilize genome-wide marker data in selecting RILs fully isogenic to Kas-1 for a single chromosome. Seven such RILs were used in 2 generations of crossing to Tsu-1 to create BC1 seed. BC1 plants were genotyped with SSR markers so that lines could be selected that carried Kas-1 introgressions, resulting in a population carrying chromosomal introgressions spanning the genome. BC1 lines were genotyped with 48 genome-wide SSRs to identify lines with a targeted Kas-1 introgression and the fewest genomic introgressions elsewhere. 75 such lines were selected and genotyped at an additional 41 SNP loci and another 930 tags using 2b-RAD genotyping by sequencing. The final population carried an average of 1.35 homozygous and 2.49 heterozygous introgressions per line with average introgression sizes of 5.32 and 5.16 Mb, respectively. In a simple case study, we demonstrate the advantage of maintaining heterozygotes in our library whereby fine-mapping efforts are conducted simply by self-pollination. Crossovers in the heterozygous interval during this single selfing generation break the introgression into smaller, homozygous fragments (sub-NILs). Additionally, we utilize a homozygous NIL for validation of a QTL underlying stomatal conductance, a low heritability trait.

CONCLUSIONS

The present results introduce a new and valuable resource to the Brassicaceae research community that enables rapid fine-mapping of candidate loci in parallel with QTL validation. These attributes along with dense marker coverage and genome-wide chromosomal introgressions make this population an ideal starting point for discovery of genes underlying important complex traits of agricultural and ecological significance.

摘要

背景

鉴定数量性状变异的基因座和特定等位基因是进化生物学家和育种家的重要目标。尽管基因组学技术取得了重大进展,但从 QTL 到因果等位基因的转变仍然是遗传学研究中的一个主要挑战。近等基因系是验证 QTL、细化 QTL 位置以及最终发现基因的理想原始材料。

结果

在这项研究中,从生理上差异较大的 Kas-1 和 Tsu-1 两个品系杂交产生的重组自交系(RIL)群体中,开发了 75 个拟南芥近等基因系。首先,开发了一种新算法,利用全基因组标记数据选择在单个染色体上与 Kas-1 完全同型的 RIL。利用这 7 个 RIL 与 Tsu-1 进行了两代杂交,产生了 BC1 种子。用 SSR 标记对 BC1 植物进行基因型分析,以选择携带 Kas-1 导入片段的系,从而产生了携带全基因组导入片段的群体。用 48 个全基因组 SSR 对 BC1 系进行基因型分析,以鉴定目标 Kas-1 导入片段和其他地方基因组导入片段最少的系。选择了 75 个这样的系,并在另外 41 个 SNP 位点和 930 个标签上进行了 2b-RAD 测序的基因型分析。最终的群体每条系平均携带 1.35 个纯合和 2.49 个杂合导入片段,平均导入片段大小分别为 5.32 和 5.16Mb。在一个简单的案例研究中,我们展示了在我们的文库中保持杂合子的优势,通过自交,精细定位工作可以简单地进行。在这个单一的自交世代中,杂合间隔内的交叉将导入片段打破成更小的纯合片段(亚近等基因系)。此外,我们还利用一个纯合近等基因系验证了气孔导度的一个 QTL,这是一个低遗传力性状。

结论

本研究结果为芸薹科研究社区引入了一个新的、有价值的资源,该资源使候选基因座的快速精细定位能够与 QTL 验证并行进行。这些特性加上密集的标记覆盖和全基因组染色体导入片段,使该群体成为发现对农业和生态具有重要意义的复杂性状的基因的理想起点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5f4a/3849958/3912ab3094b5/1471-2164-14-655-1.jpg

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