Fine Mapping and Cloning of the Grain Number Per-Panicle Gene (Gnp4) on Chromosome 4 in Rice (Oryza sativa L.)

Zhan-ying ZHANG , Jin-jie LI , Guo-xin YAO , Hong-liang ZHANG, Hui-jing DOU, Hong-li SHI, Xing-ming SUN, Zi-chao LI
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引用次数: 20

Abstract

Grain number per-panicle is one of the most important components for rice yield. Spikelets on the primary and secondary branches determine the grain number per-panicle in rice. In this study, we identified a natural mutant, gnp4, lack of lateral spikelet on the secondary branches in the field condition. In addition, the Gnp4 and Lax1-1 double mutant showed dramatically reduced secondary branches and spikelets in panicle at reproductive stage, and tillers at vegetative stage. By map-based cloning approach, and using four F2 segregating populations, the Gnp4 gene was finally mapped to a 10.7-kb region on the long arm of chromosome 4 in rice. In this region, only one gene was predicted, and genomic DNA sequencing of the 10.7-kb region showed no nucleotide differences between the mutant and wild type. Interestingly, we found that the methylation level of several cytosines in the promoter CpG islands region of the predicted gene in gnp4 were different from the wild type. Thus, we propose that the DNA methylation changes at these sites may induce to decrease expression level of Gnp4, consequently, resulting in phenotypic variation.

水稻4号染色体每穗粒数基因(Gnp4)的精细定位与克隆
摘要每穗粒数是水稻产量的重要组成部分之一。水稻一次枝和二次枝上的小穗决定每穗粒数。在本研究中,我们鉴定了一个自然突变体gnp4,该突变体在田间条件下次级枝上缺乏侧穗。此外,Gnp4和Lax1-1双突变体在生殖期次枝和穗部小穗显著减少,营养期分蘖显著减少。通过定位克隆方法,利用4个F2分离群体,最终将Gnp4基因定位在水稻4号染色体长臂上10.7 kb的区域。在这个区域,只有一个基因被预测到,10.7 kb区域的基因组DNA测序显示突变型和野生型之间没有核苷酸差异。有趣的是,我们发现gnp4中预测基因的启动子CpG岛区域的几个胞嘧啶的甲基化水平与野生型不同。因此,我们认为这些位点的DNA甲基化变化可能导致Gnp4表达水平降低,从而导致表型变异。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Agricultural Sciences in China
Agricultural Sciences in China AGRICULTURE, MULTIDISCIPLINARY-
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3.2 months
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