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六行穗3(VRS3)是一种控制大麦侧小穗发育的组蛋白去甲基化酶。

Six-Rowed Spike3 (VRS3) Is a Histone Demethylase That Controls Lateral Spikelet Development in Barley.

作者信息

van Esse G Wilma, Walla Agatha, Finke Andreas, Koornneef Maarten, Pecinka Ales, von Korff Maria

机构信息

Department of Plant Breeding and Genetics, Max Planck Institute for Plant Breeding Research, 50829 Köln, Germany.

Institute for Plant Genetics, Heinrich-Heine-Universität Düsseldorf, 40225 Düsseldorf, Germany.

出版信息

Plant Physiol. 2017 Aug;174(4):2397-2408. doi: 10.1104/pp.17.00108. Epub 2017 Jun 27.

Abstract

The complex nature of crop genomes has long prohibited the efficient isolation of agronomically relevant genes. However, recent advances in next-generation sequencing technologies provide new ways to accelerate fine-mapping and gene isolation in crops. We used RNA sequencing of allelic () mutants with altered spikelet development for gene identification and functional analysis in barley (). Variant calling in two allelic mutants revealed that encodes a putative histone Lys demethylase with a conserved zinc finger and Jumonji C and N domain. Sanger sequencing of this candidate gene in independent allelic mutants revealed a series of mutations in conserved domains, thus confirming our candidate as the gene and suggesting that the row type in barley is determined epigenetically. Global transcriptional profiling in developing shoot apical meristems of suggested that VRS3 acts as a transcriptional activator of the row-type genes () and (; ). Comparative transcriptome analysis of the row-type mutants , (), and confirmed that all three genes act as transcriptional activators of and quantitative variation in the expression levels of in these mutants correlated with differences in the number of developed lateral spikelets. The identification of genes and pathways affecting seed number in small grain cereals will enable to further unravel the transcriptional networks controlling this important yield component.

摘要

作物基因组的复杂特性长期以来一直阻碍着与农艺相关基因的有效分离。然而,新一代测序技术的最新进展为加速作物精细定位和基因分离提供了新方法。我们利用小穗发育改变的等位基因()突变体的RNA测序在大麦()中进行基因鉴定和功能分析。对两个等位基因突变体进行变异检测发现,编码一个具有保守锌指结构以及Jumonji C和N结构域的假定组蛋白赖氨酸去甲基化酶。对独立等位基因突变体中的该候选基因进行桑格测序,发现在保守结构域存在一系列突变,从而证实我们的候选基因即为基因,并表明大麦中的行型是由表观遗传决定的。对发育中的茎尖分生组织进行全局转录谱分析表明,VRS3作为行型基因()和(;)的转录激活因子发挥作用。对行型突变体、()和进行比较转录组分析证实,这三个基因均作为的转录激活因子发挥作用,并且这些突变体中表达水平的定量变化与发育的侧生小穗数量差异相关。鉴定影响小粒谷物种子数量的基因和途径将有助于进一步揭示控制这一重要产量构成要素的转录网络。

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