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Efficient Identification of Causal Mutations through Sequencing of Bulked F2 from Two Allelic Bloomless Mutants of Sorghum bicolor

机译:通过测序从两个高粱双色等位基因无花突变体中的散装F2序列有效鉴定因果突变

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摘要

Sorghum (Sorghum bicolor Moench, L.) plant accumulates copious layers of epi-cuticular wax (EW) on its aerial surfaces, to a greater extent than most other crops. EW provides a vapor barrier that reduces water loss, and is therefore considered to be a major determinant of sorghum's drought tolerance. However, little is known about the genes responsible for wax accumulation in sorghum. We isolated two allelic mutants, bloomless40-1 (bm40-1) and bm40-2, from a mutant library constructed from ethyl methane sulfonate (EMS) treated seeds of an inbred, BTx623. Both mutants were nearly devoid of the EW layer. Each bm mutant was crossed to the un-mutated BTx623 to generated F2 populations that segregated for the bm phenotype. Genomic DNA from 20 bm F2 plants from each population was bulked for whole genome sequencing. A single gene, Sobic.001G228100, encoding a GDSL-like lipase/acylhydrolase, had unique homozygous mutations in each bulked F2 population. Mutant bm40-1 harbored a missense mutation in the gene, whereas bm40-2 had a splice donor site mutation. Our findings thus provide strong evidence that mutation in this GDSL-like lipase gene causes the bm phenotype, and further demonstrate that this approach of sequencing two independent allelic mutant populations is an efficient method for identifying causal mutations. Combined with allelic mutants, MutMap provides powerful method to identify all causal genes for the large collection of bm mutants in sorghum, which will provide insight into how sorghum plants accumulate such abundant EW on their aerial surface. This knowledge may facilitate the development of tools for engineering drought-tolerant crops with reduced water loss.
机译:高粱(Sorghum bicolor Moench,L.)植物在其表皮上积累了大量表皮蜡(EW),其程度比大多数其他农作物更大。 EW提供了减少水分流失的防潮层,因此被认为是高粱抗旱性的主要决定因素。然而,对于导致高粱中蜡积累的基因知之甚少。我们从由自交系BTx623的甲烷磺酸乙酯(EMS)处理的种子构建的突变体文库中分离了两个等位基因突变体,Bloomless40-1(bm40-1)和bm40-2。两个突变体几乎都没有EW层。每个bm突变体与未突变的BTx623杂交,产生针对bm表型分离的F2群体。扩增来自每个种群的20 bm F2植物的基因组DNA,进行全基因组测序。编码GDSL样脂肪酶/酰基水解酶的单一基因Sobic.001G228100在每个庞大的F2群体中均具有独特的纯合突变。突变体bm40-1在该基因中包含一个错义突变,而bm40-2具有一个剪接供体位点突变。因此,我们的发现提供了有力的证据,表明该GDSL样脂肪酶基因中的突变会导致bm表型,并进一步证明,对两个独立的等位基因突变群体进行测序的这种方法是鉴定因果突变的有效方法。与等位基因突变体结合,MutMap提供了一种强大的方法来鉴定高粱中bm突变体的大量收集的所有病因基因,这将提供有关高粱植物如何在其地表上积累如此丰富的EW的见识。这些知识可能有助于开发用于工程化耐旱作物并减少水分流失的工具。

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