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ClaCSLH1基因的敲除导致西瓜植株矮化。

The knockout of ClaCSLH1 induced dwarfing in watermelon.

作者信息

Bao Jiancheng, Shi Jiale, Qin Yuanyuan, Hua Shengqi, Wu Yanhong, Yang Congji, Gu Yige, Dong Wei

机构信息

School of Life Science, Henan University, Kaifeng, 475004, Henan, People's Republic of China.

出版信息

Theor Appl Genet. 2025 May 19;138(6):120. doi: 10.1007/s00122-025-04909-9.

Abstract

In agriculture, selecting ideal plant types with desirable traits, such as dwarfing and upright stem structures, significantly enhances crop yield and quality by optimizing light absorption, spatial efficiency, and nutrient utilization. Developing new varieties of dwarf watermelon is a crucial objective in watermelon breeding. In this study, we constructed an F population using the wild-type V063 as the paternal parent and the dwarf variety dw-n as the maternal parent. The dwarfing trait was found to be governed by a pair of recessive alleles. Through bulk segregant analysis sequencing (BSA-seq) and RNA sequencing (RNA-seq), we identified the gene Cla97C02G035450, which encodes cellulose synthase-like H1 (CSLH1), as a candidate gene associated with the dwarfing phenotype. ClaCLSH1 belongs to the ClaCESA/CSLs family, which is involved in the cell wall formation by regulating the synthesis of cellulose and hemicellulose. Microscopic analyses revealed that dw-n exhibited shorter internode cells, thicker cell walls, and elevated hemicellulose content compared to V063. Subcellular localization studies demonstrated that the CLACSLH1 protein is primarily localized in the nucleus and the cell membrane/wall. Notably, the overexpression of CLACSLH1 in the dw-n background rescued its dwarf phenotype. Furthermore, experiments indicated that knockdown of CLACSLH1 resulted in excessive hemicellulose synthesis, inhibited internode cell elongation, and ultimately led to the stunted phenotype observed in dw-n. This research provides innovative insights into the development of superior dwarf watermelon varieties and advances our understanding of the molecular mechanisms underlying watermelon dwarfism.

摘要

在农业中,选择具有理想性状的理想植物类型,如矮化和直立茎结构,通过优化光吸收、空间效率和养分利用,可显著提高作物产量和品质。培育矮化西瓜新品种是西瓜育种的一个关键目标。在本研究中,我们以野生型V063为父本、矮化品种dw-n为母本构建了一个F群体。发现矮化性状由一对隐性等位基因控制。通过混合分组分析法测序(BSA-seq)和RNA测序(RNA-seq),我们鉴定出编码类纤维素合酶H1(CSLH1)的基因Cla97C02G035450为与矮化表型相关的候选基因。ClaCLSH1属于ClaCESA/CSLs家族,该家族通过调节纤维素和半纤维素的合成参与细胞壁形成。显微镜分析显示,与V063相比,dw-n的节间细胞较短、细胞壁较厚且半纤维素含量升高。亚细胞定位研究表明,CLACSLH1蛋白主要定位于细胞核和细胞膜/细胞壁。值得注意的是,在dw-n背景下过表达CLACSLH1可挽救其矮化表型。此外,实验表明,敲低CLACSLH1会导致半纤维素过度合成,抑制节间细胞伸长,并最终导致dw-n中观察到的发育不良表型。本研究为优质矮化西瓜品种的培育提供了创新性见解,并增进了我们对西瓜矮化分子机制的理解。

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