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利用 bulked RILs 的 QTL 作图和转录组分析鉴定水稻耐盐基因的功能多态性。

Combining QTL mapping and transcriptome profiling of bulked RILs for identification of functional polymorphism for salt tolerance genes in rice (Oryza sativa L.).

机构信息

Rice Genome Laboratory, National Research Centre on Plant Biotechnology, New Delhi 110012, India.

出版信息

Mol Genet Genomics. 2010 Aug;284(2):121-36. doi: 10.1007/s00438-010-0551-6. Epub 2010 Jul 3.

Abstract

Identification of genes for quantitative traits is difficult using any single approach due to complex inheritance of the traits and limited resolving power of the individual techniques. Here a combination of genetic mapping and bulked transcriptome profiling was used to narrow down the number of differentially expressed salt-responsive genes in rice in order to identify functional polymorphism of genes underlying the quantitative trait loci (QTL). A population of recombinant inbred lines (RILs) derived from cross between salt-tolerant variety CSR 27 and salt-sensitive variety MI 48 was used to map QTL for salt ion concentrations in different tissues and salt stress susceptibility index (SSI) for spikelet fertility, grain weight, and grain yield. Eight significant QTL intervals were mapped on chromosomes 1, 8, and 12 for the salt ion concentrations and a QTL controlling SSI for spikelet fertility was co-located in one of these intervals on chromosome 8. However, there were total 2,681 genes in these QTL intervals, making it difficult to pinpoint the genes responsible for the functional differences for the traits. Similarly, transcriptome profiling of the seedlings of tolerant and sensitive parents grown under control and salt-stress conditions showed 798 and 2,407 differentially expressed gene probes, respectively. By analyzing pools of RNA extracted from ten each of extremely tolerant and extremely sensitive RILs to normalize the background noise, the number of differentially expressed genes under salt stress was drastically reduced to 30 only. Two of these genes, an integral transmembrane protein DUF6 and a cation chloride cotransporter, were not only co-located in the QTL intervals but also showed the expected distortion of allele frequencies in the extreme tolerant and sensitive RILs, and therefore are suitable for future validation studies and development of functional markers for salt tolerance in rice to facilitate marker-assisted breeding.

摘要

由于性状的复杂遗传和个别技术的分辨率有限,使用任何单一方法都难以鉴定数量性状基因。在这里,我们结合遗传图谱和大量转录组分析,缩小了水稻中差异表达的盐响应基因的数量,以鉴定数量性状基因座(QTL)下的功能多态性。利用耐盐品种 CSR 27 和盐敏感品种 MI 48 杂交衍生的重组自交系(RIL)群体,对不同组织中的盐离子浓度和小穗育性、粒重和产量的盐胁迫敏感性指数(SSI)进行 QTL 作图。在染色体 1、8 和 12 上共定位到 8 个显著的盐离子浓度 QTL 区间,控制小穗育性 SSI 的 QTL 也位于其中一个染色体 8 的区间内。然而,这些 QTL 区间中总共有 2681 个基因,很难确定负责这些性状功能差异的基因。同样,在对照和盐胁迫条件下生长的耐盐和敏感亲本的幼苗转录组分析分别显示了 798 个和 2407 个差异表达的基因探针。通过分析从每个极端耐盐和敏感 RIL 中提取的 10 个 RNA 池来归一化背景噪声,盐胁迫下差异表达的基因数量急剧减少到仅 30 个。其中两个基因,一个完整的跨膜蛋白 DUF6 和一个阳离子氯离子共转运蛋白,不仅位于 QTL 区间内,而且在极端耐盐和敏感 RIL 中也显示出预期的等位基因频率扭曲,因此非常适合未来的验证研究和水稻耐盐性的功能标记开发,以促进标记辅助育种。

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