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大麦中重复的分生组织特性基因HvAP1a和HvAP1b的分子特征分析

Molecular characterization of the duplicated meristem identity genes HvAP1a and HvAP1b in barley.

作者信息

Yan Liuling, von Zitzewitz Jarislav, Skinner Jeffrey S, Hayes Patrick M, Dubcovsky Jorge

机构信息

Department of Plant Sciences, University of California Davis 95616, USA.

出版信息

Genome. 2005 Oct;48(5):905-12. doi: 10.1139/g05-035.

Abstract

The vernalization gene VRN-1 has been identified as a MADS-box transcription factor orthologous to the meristem identity gene APETALA1 (AP1). A single copy of this gene was found in diploid wheat, but 2 copies were reported in barley. In this study, we present a detailed characterization of these 2 copies to understand their respective roles in the vernalization response. We identified 2 groups of barley bacterial artificial chromosomes (BACs), each containing 1 AP1 copy designated hereafter as HvAP1a and HvAP1b. A physical map of the VRN-H1 region showed that the HvAP1a BACs were part of the VRN-H1 region but that the HvAP1b BACs were not. Numerous structural changes were observed between the barley and wheat VRN-1 physical maps. In a population segregating for VRN-H1, the HvAP1a gene cosegregated with growth habit, suggesting that HvAP1a is the barley vernalization gene VRN-H1. The other copy, HvAP1b, was mapped on the centromeric region of chromosome 1H, the chromosome where vernalization gene VRN-H3 was previously mapped. We developed a mapping population segregating for VRN-H3 and showed that 2 molecular makers flanking HvAP1b locus were not linked to growth habit. The HvAP1b copy has a complete deletion of the first 2 exons, suggesting that it is a truncated pseudogene and not a candidate for VRN-H3. In summary, this study contributed a detailed physical map of the barley VRN-H1 region, showed several structural differences with the orthologous wheat region, and clarified the identity of the barley VRN-H1 gene.

摘要

春化基因VRN-1已被鉴定为与分生组织特性基因APETALA1(AP1)直系同源的MADS盒转录因子。在二倍体小麦中发现了该基因的一个拷贝,但在大麦中报道有两个拷贝。在本研究中,我们对这两个拷贝进行了详细表征,以了解它们在春化反应中的各自作用。我们鉴定出两组大麦细菌人工染色体(BAC),每组都包含一个AP1拷贝,以下分别命名为HvAP1a和HvAP1b。VRN-H1区域的物理图谱显示,HvAP1a BAC是VRN-H1区域的一部分,但HvAP1b BAC不是。在大麦和小麦的VRN-1物理图谱之间观察到许多结构变化。在一个对VRN-H1进行分离的群体中,HvAP1a基因与生长习性共分离,这表明HvAP1a是大麦春化基因VRN-H1。另一个拷贝HvAP1b被定位在1H染色体的着丝粒区域,之前春化基因VRN-H3也被定位在该染色体上。我们构建了一个对VRN-H3进行分离的定位群体,并表明位于HvAP1b基因座两侧的两个分子标记与生长习性不连锁。HvAP1b拷贝的前两个外显子完全缺失,这表明它是一个截短的假基因,而不是VRN-H3的候选基因。总之,本研究提供了大麦VRN-H1区域的详细物理图谱,显示了与直系同源小麦区域的几个结构差异,并阐明了大麦VRN-H1基因的身份。

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