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以鹰嘴豆干旱产量指数(DYI)为例的全基因组顺式调控特征对农艺性状的调控。

Genome-wide cis-regulatory signatures for modulation of agronomic traits as exemplified by drought yield index (DYI) in chickpea.

机构信息

Genomics-Assisted Breeding and Crop Improvement Laboratory, National Institute of Plant Genome Research (NIPGR), Aruna Asaf Ali Marg, New Delhi, 110067, India.

Division of Genetics, Indian Agricultural Research Institute (IARI), New Delhi, 110012, India.

出版信息

Funct Integr Genomics. 2019 Nov;19(6):973-992. doi: 10.1007/s10142-019-00691-2. Epub 2019 Jun 8.

Abstract

Developing functional molecular tags from the cis-regulatory sequence components of genes is vital for their deployment in efficient genetic dissection of complex quantitative traits in crop plants including chickpea. The current study identified 431,194 conserved non-coding SNP (CNSNP) from the cis-regulatory element regions of genes which were annotated on a chickpea genome. These genome-wide CNSNP marker resources are made publicly accessible through a user-friendly web-database ( http://www.cnsnpcicarbase.com ). The CNSNP-based quantitative trait loci (QTL) and expression QTL (eQTL) mapping and genome-wide association study (GWAS) were further integrated with global gene expression landscapes, molecular haplotyping, and DNA-protein interaction study in the association panel and recombinant inbred lines (RIL) mapping population to decode complex genetic architecture of one of the vital seed yield trait under drought stress, drought yield index (DYI), in chickpea. This delineated two constituted natural haplotypes and alleles from a histone H3 protein-coding gene and its transcriptional regulator NAC transcription factor (TF) harboring the major QTLs and trans-acting eQTL governing DYI in chickpea. The effect of CNSNPs in TF-binding cis-element of a histone H3 gene in altering the binding affinity and transcriptional activity of NAC TF based on chromatin immunoprecipitation-quantitative PCR (ChIP-qPCR) assay was evident. The CNSNP-led promising molecular tags scanned will essentially have functional significance to decode transcriptional gene regulatory function and thus can drive translational genomic analysis in chickpea.

摘要

从基因的顺式调控序列元件中开发功能分子标记对于在包括鹰嘴豆在内的作物植物中高效遗传解析复杂数量性状至关重要。本研究从鹰嘴豆基因组中基因的顺式调控元件区域鉴定出 431,194 个保守非编码 SNP(CNSNP)。这些全基因组 CNSNP 标记资源可通过用户友好的网络数据库(http://www.cnsnpcicarbase.com)公开获取。基于 CNSNP 的数量性状基因座(QTL)和表达 QTL(eQTL)作图以及全基因组关联研究(GWAS)与全局基因表达图谱、分子单倍型和 DNA-蛋白质相互作用研究进一步整合,在关联面板和重组自交系(RIL)作图群体中对鹰嘴豆干旱胁迫下一个重要种子产量性状干旱产量指数(DYI)的复杂遗传结构进行解码。这从一个组蛋白 H3 蛋白编码基因及其转录调节剂 NAC 转录因子(TF)中划定了两个构成的自然单倍型和等位基因,它们含有控制鹰嘴豆 DYI 的主要 QTL 和反式作用 eQTL。基于染色质免疫沉淀定量 PCR(ChIP-qPCR)实验,CNSNP 改变 TF 结合组蛋白 H3 基因顺式元件的结合亲和力和转录活性的效应在 TF 结合顺式元件中显而易见。基于 CNSNP 的有前途的分子标记扫描将具有功能意义,可用于解码转录基因调控功能,从而可以推动鹰嘴豆的转化基因组分析。

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