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水稻 TRIANGULAR HULL1 蛋白作为转录抑制子在调控小穗横向发育中起作用。

The rice TRIANGULAR HULL1 protein acts as a transcriptional repressor in regulating lateral development of spikelet.

机构信息

National Key Facility for Crop Gene Resources and Genetic Improvement, Institute of Crop Science, Chinese Academy of Agricultural Sciences, Beijing, 100081, China.

Shandong Rice Research Institute, Jinan, 250100, China.

出版信息

Sci Rep. 2017 Oct 20;7(1):13712. doi: 10.1038/s41598-017-14146-w.

Abstract

As a basic unit of rice inflorescence, spikelet has profound influence on grain size, weight and yield. The molecular mechanism underlying spikelet development has not been fully elucidated. Here, we identified four allelic rice mutants, s2-89, xd151, xd281 and xd425, which exhibited reduced width of spikelet, especially in the apical region. Map-based cloning revealed that all these mutants had missense mutation in the TRIANGULAR HULL1 (TH1) gene, encoding an ALOG family protein. TH1 has been shown to regulate the lateral development of spikelet, but its mode of action remains unclear. Microscopic analysis revealed that the reduction in spikelet width was caused by decreased cell size rather than cell division. The TH1 protein was shown to localize in the nucleus and possess transcriptional repression activity. TH1 could form a homodimer and point mutation in the s2-89, xd281 and xd425 mutant inhibited homodimerization. The transcriptional repression activity of TH1 was partially relieved by the His129Tyr substitution in the s2-89 mutant. Fusion of an exogenous EAR transcription suppression domain to the mutant protein TH1 could largely complemented the narrow spikelet phenotype. These results indicate that TH1 functions as a transcription repressor and regulates cell expansion during the lateral development of spikelet.

摘要

作为水稻花序的基本单位,小穗对粒大小、重量和产量有深远的影响。小穗发育的分子机制尚未完全阐明。在这里,我们鉴定了四个等位基因水稻突变体,s2-89、xd151、xd281 和 xd425,它们表现出小穗变窄,特别是在顶端区域。基于图谱的克隆表明,这些突变体在编码ALOG 家族蛋白的三角形 hull1(TH1)基因中都有错义突变。TH1 已被证明调节小穗的侧向发育,但作用模式尚不清楚。显微镜分析表明,小穗宽度的减小是由于细胞大小减小而不是细胞分裂引起的。TH1 蛋白被证明定位于细胞核中,并具有转录抑制活性。TH1 可以形成同源二聚体,s2-89、xd281 和 xd425 突变体中的点突变抑制了同源二聚体的形成。s2-89 突变体中 His129Tyr 的取代部分缓解了 TH1 的转录抑制活性。将一个外源性 EAR 转录抑制结构域融合到突变蛋白 TH1 上,可以很大程度上互补小穗变窄的表型。这些结果表明,TH1 作为转录抑制因子发挥作用,调节小穗侧向发育过程中的细胞扩张。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0c3c/5651839/15ca51d525d4/41598_2017_14146_Fig1_HTML.jpg

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