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水稻(Oryza sativa L.)高分蘖矮化突变基因的鉴定与精细定位

Characterizations and fine mapping of a mutant gene for high tillering and dwarf in rice (Oryza sativa L.).

作者信息

Zou Junhuang, Chen Zengxiang, Zhang Shuying, Zhang Weiping, Jiang Guanghuai, Zhao Xianfeng, Zhai Wenxue, Pan Xuebiao, Zhu Lihuang

机构信息

National Plant Gene Research Centre (Beijing), Institute of Genetics and Developmental Biology, Chinese Academy of Science, Beijing, 100101, China.

出版信息

Planta. 2005 Nov;222(4):604-12. doi: 10.1007/s00425-005-0007-0. Epub 2005 Nov 4.

Abstract

A rice htd-1 mutant, related to tillering and dwarfing, was characterized. We show that the htd-1 mutant increases its tiller number by releasing axillary buds from dormant stage rather than by initiating more axillary buds. The dwarf is caused by averagely reducing each internode and panicle. Based on this dwarfing pattern, the htd-1 mutant could be grouped into dn-type dwarf defined by Takeda (Gamma Field Symp 16:1, 1977). In addition, the dwarfing of the htd-1 mutant was found independent of GA based on the analyses of two GA-mediated processes. Based on the quantitative determination of IAA and ABA and application of the two hormones exogenously to the seedlings, we inferred that the high tillering capacity of the htd-1 mutant should not be attributed to a defect in the synthesis of IAA or ABA. The genetic analysis of the htd-1 mutant indicated that the phenotypes of high tillering and dwarf were controlled by a recessive gene, termed htd1. By map-based cloning, the htd1 gene was fine mapped in a 30-kb DNA region on chromosome 4. Sequencing the target DNA region and comparing the counterpart DNA sequences between the htd-1 mutant and other rice varieties revealed a nucleotide substitution corresponding to an amino acid substitution from prolin to leucine in a predicted rice gene, OsCCD7, the rice orthologous gene of AtMAX3/CCD7. With the evidence of the association between the presence of one amino acid change in OsCCD7 and the abnormal phenotypes of the htd-1 mutant, OsCCD7 was identified as the candidate of the HTD1 gene.

摘要

对一个与分蘖和矮化相关的水稻htd - 1突变体进行了表征。我们发现,htd - 1突变体通过使腋芽从休眠阶段释放来增加分蘖数,而非通过起始更多腋芽。矮化是由平均缩短每个节间和穗部导致的。基于这种矮化模式,htd - 1突变体可归类为武田所定义的dn型矮化(《伽马田研讨会论文集》第16卷:第1页,1977年)。此外,基于对两个赤霉素介导过程的分析,发现htd - 1突变体的矮化与赤霉素无关。通过对吲哚 - 3 - 乙酸(IAA)和脱落酸(ABA)的定量测定以及将这两种激素外源施加到幼苗上,我们推断htd - 1突变体的高分蘖能力不应归因于IAA或ABA合成缺陷。htd - 1突变体的遗传分析表明,高分蘖和矮化表型由一个隐性基因控制,命名为htd1。通过图位克隆,htd1基因被精细定位在第4号染色体上一个30 kb的DNA区域。对目标DNA区域进行测序,并比较htd - 1突变体与其他水稻品种的对应DNA序列,发现在一个预测的水稻基因OsCCD7(拟南芥MAX3/CCD7的水稻直系同源基因)中有一个核苷酸替换,对应一个氨基酸从脯氨酸替换为亮氨酸。鉴于OsCCD7中一个氨基酸变化与htd - 1突变体异常表型之间存在关联的证据,OsCCD7被鉴定为HTD1基因的候选基因。

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