Northeast Institute of Geography and Agroecology, Chinese Academy of Sciences, Harbin 150081, China.
Proc Natl Acad Sci U S A. 2012 Aug 7;109(32):E2155-64. doi: 10.1073/pnas.1117982109. Epub 2012 May 22.
The complex and coordinated regulation of flowering has high ecological and agricultural significance. The maturity locus E1 has a large impact on flowering time in soybean, but the molecular basis for the E1 locus is largely unknown. Through positional cloning, we delimited the E1 locus to a 17.4-kb region containing an intron-free gene (E1). The E1 protein contains a putative bipartite nuclear localization signal and a region distantly related to B3 domain. In the recessive allele, a nonsynonymous substitution occurred in the putative nuclear localization signal, leading to the loss of localization specificity of the E1 protein and earlier flowering. The early-flowering phenotype was consistently observed in three ethylmethanesulfonate-induced mutants and two natural mutations that harbored a premature stop codon or a deletion of the entire E1 gene. E1 expression was significantly suppressed under short-day conditions and showed a bimodal diurnal pattern under long-day conditions, suggesting its response to photoperiod and its dominant effect induced by long day length. When a functional E1 gene was transformed into the early-flowering cultivar Kariyutaka with low E1 expression, transgenic plants carrying exogenous E1 displayed late flowering. Furthermore, the transcript abundance of E1 was negatively correlated with that of GmFT2a and GmFT5a, homologues of FLOWERING LOCUS T that promote flowering. These findings demonstrated the key role of E1 in repressing flowering and delaying maturity in soybean. The molecular identification of the maturity locus E1 will contribute to our understanding of the molecular mechanisms by which a short-day plant regulates flowering time and maturity.
开花的复杂和协调调控具有重要的生态和农业意义。成熟 locus E1 对大豆的开花时间有很大影响,但 E1 基因座的分子基础在很大程度上是未知的。通过定位克隆,我们将 E1 基因座限定在一个包含无内含子基因(E1)的 17.4kb 区域内。E1 蛋白包含一个假定的二部分核定位信号和一个与 B3 结构域远相关的区域。在隐性等位基因中,假定的核定位信号中发生了非同义替换,导致 E1 蛋白的定位特异性丧失,从而导致开花提前。在三个乙磺酸诱导的突变体和两个含有提前终止密码子或整个 E1 基因缺失的自然突变体中,均观察到早花表型。E1 表达在短日照条件下显著受到抑制,并在长日照条件下表现出双峰昼夜节律模式,表明其对光周期的反应及其在长日照长度下的显性作用。当一个功能性 E1 基因被转化到开花早的低 E1 表达品种 Kariyutaka 中时,携带外源 E1 的转基因植株表现出晚花。此外,E1 的转录丰度与促进开花的同源物 GmFT2a 和 GmFT5a 的转录丰度呈负相关。这些发现表明 E1 在抑制大豆开花和延迟成熟方面起着关键作用。成熟 locus E1 的分子鉴定将有助于我们理解短日照植物调节开花时间和成熟的分子机制。