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利用重组自交系群体进行全基因组表达数量性状基因座分析,解析花生性状。

Genome-wide expression quantitative trait locus analysis in a recombinant inbred line population for trait dissection in peanut.

机构信息

Key Laboratory of Biology and Genetic Improvement of Oil Crops, Ministry of Agriculture, Oil Crops Research Institute of the Chinese Academy of Agricultural Sciences, Wuhan, China.

National Key Laboratory of Crop Genetic Improvement, Huazhong Agricultural University, Wuhan, China.

出版信息

Plant Biotechnol J. 2020 Mar;18(3):779-790. doi: 10.1111/pbi.13246. Epub 2019 Sep 17.

Abstract

The transcriptome connects genome to the gene function and ultimate phenome in biology. So far, transcriptomic approach was not used in peanut for performing trait mapping in bi-parental populations. In this research, we sequenced the whole transcriptome in immature seeds in a peanut recombinant inbred line (RIL) population and explored thoroughly the landscape of transcriptomic variations and its genetic basis. The comprehensive analysis identified total 49 691 genes in RIL population, of which 92 genes followed a paramutation-like expression pattern. Expression quantitative trait locus (eQTL) analysis identified 1207 local eQTLs and 15 837 distant eQTLs contributing to the whole-genome transcriptomic variation in peanut. There were 94 eQTL hot spot regions detected across the genome with the dominance of distant eQTL. By integrating transcriptomic profile and annotation analyses, we unveiled a putative candidate gene and developed a linked marker InDel02 underlying a major QTL responsible for purple testa colour in peanut. Our result provided a first understanding of genetic basis of whole-genome transcriptomic variation in peanut and illustrates the potential of the transcriptome-aid approach in dissecting important traits in non-model plants.

摘要

转录组将基因组与生物学中的基因功能和最终表型联系起来。迄今为止,在花生中,转录组方法尚未用于在双亲群体中进行性状作图。在这项研究中,我们对花生重组自交系(RIL)群体的未成熟种子进行了全转录组测序,并深入探讨了转录组变异及其遗传基础的全貌。全面的分析鉴定了 RIL 群体中的总共 49691 个基因,其中 92 个基因遵循类似突变的表达模式。表达数量性状基因座(eQTL)分析鉴定了 1207 个局部 eQTL 和 15837 个远程 eQTL,它们共同导致了花生的全基因组转录组变异。在整个基因组中检测到 94 个 eQTL 热点区域,其中以远程 eQTL 为主导。通过整合转录组图谱和注释分析,我们揭示了一个可能的候选基因,并开发了一个与控制花生紫色种皮颜色的主要 QTL 相关的连锁标记 InDel02。我们的研究结果首次阐明了花生全基因组转录组变异的遗传基础,并说明了转录组辅助方法在解析非模式植物重要性状方面的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/716e/11386345/6f80353513d2/PBI-18-779-g002.jpg

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