Yan Liuling, von Zitzewitz Jarislav, Skinner Jeffrey S, Hayes Patrick M, Dubcovsky Jorge
Department of Plant Sciences, University of California Davis 95616, USA.
Genome. 2005 Oct;48(5):905-12. doi: 10.1139/g05-035.
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.
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。