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Tn1a 启动子的自然变异调控水稻分蘖。

Natural variation in the Tn1a promoter regulates tillering in rice.

机构信息

Frontiers Science Center for Molecular Design Breeding, Key Laboratory of Crop Heterosis and Utilization (MOE), Beijing Key Laboratory of Crop Genetic Improvement, College of Agronomy and Biotechnology, China Agricultural University, Beijing, China.

College of Agriculture, Henan University of Science and Technology, Luoyang, China.

出版信息

Plant Biotechnol J. 2024 Dec;22(12):3345-3360. doi: 10.1111/pbi.14453. Epub 2024 Aug 27.

Abstract

Rice tillering is an important agronomic trait that influences plant architecture and ultimately affects yield. This can be genetically improved by mining favourable variations in genes associated with tillering. Based on a previous study on dynamic tiller number, we cloned the gene Tiller number 1a (Tn1a), which encodes a membrane-localised protein containing the C2 domain that negatively regulates tillering in rice. A 272 bp insertion/deletion at 387 bp upstream of the start codon in the Tn1a promoter confers a differential transcriptional response and results in a change in tiller number. Moreover, the TCP family transcription factors Tb2 and TCP21 repress the Tn1a promoter activity by binding to the TCP recognition site within the 272 bp indel. In addition, we identified that Tn1a may affect the intracellular K content by interacting with a cation-chloride cotransporter (OsCCC1), thereby affecting the expression of downstream tillering-related genes. The Tn1a allele, associated with high tillering, might have been preferably preserved in rice varieties in potassium-poor regions during domestication. The discovery of Tn1a is of great significance for further elucidating the genetic basis of tillering characteristics in rice and provides a new and favourable allele for promoting the geographic adaptation of rice to soil potassium.

摘要

水稻分蘖是一个重要的农艺性状,影响植物的结构,最终影响产量。通过挖掘与分蘖相关的基因中的有利变异,可以在遗传上对其进行改良。基于之前对动态分蘖数的研究,我们克隆了分蘖数 1a(Tn1a)基因,该基因编码一种定位于膜上的蛋白,含有 C2 结构域,负调控水稻的分蘖。在 Tn1a 启动子起始密码子上游的 387bp 处有一个 272bp 的插入/缺失,导致转录反应的差异,从而导致分蘖数的变化。此外,TCP 家族转录因子 Tb2 和 TCP21 通过结合 272bp 缺失内的 TCP 识别位点来抑制 Tn1a 启动子的活性。此外,我们发现 Tn1a 可能通过与阳离子-氯离子共转运蛋白(OsCCC1)相互作用来影响细胞内的 K 含量,从而影响下游与分蘖相关的基因的表达。与高分蘖相关的 Tn1a 等位基因,可能在驯化过程中在钾缺乏地区的水稻品种中被优先保留。Tn1a 的发现对进一步阐明水稻分蘖特性的遗传基础具有重要意义,并为促进水稻对土壤钾的地理适应性提供了一个新的有利等位基因。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/26bc/11606419/fdb79619e1be/PBI-22-3345-g002.jpg

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