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控制西瓜条纹颜色的关键候选基因ClAPRR2的鉴定与特性分析

Identification and characterization of ClAPRR2, a key candidate gene controlling watermelon stripe color.

作者信息

Liang Shuang, Yang Miaomiao, Zhang Linlin, Fang Xufeng, Zhang Xian, Wei Chunhua, Dai Zuyun, Yang Zhongzhou, Wang Chaonan, Liu Bin, Luan Feishi, Liu Shi

机构信息

Key Laboratory of Biology and Genetic Improvement of Horticulture Crops (Northeast Region), Ministry of Agriculture and Rural Affairs, College of Horticulture and Landscape Architecture, Northeast Agricultural University, Harbin 150030, China; College of Horticulture and Landscape Architecture, Northeast Agricultural University, Harbin 150030, China.

College of Horticulture, Northwest of A&F University, Yangling 712100, China.

出版信息

Plant Sci. 2025 Mar;352:112383. doi: 10.1016/j.plantsci.2024.112383. Epub 2025 Jan 3.

Abstract

The stripe color of watermelon is a vital commercial trait and is the focus of attention of consumers and researchers. However, the genetic determinants of watermelon stripe color are incompletely understood. Based on the results of preliminary localization studies, we constructed a large-capacity F generation population (710 plants) using light-green striped ZXG1555 and green-striped Cream of Saskatchewan (COS) watermelon strains as parental lines for fine mapping. Genes controlling stripe color were located in an 85.284 kb region on chromosome 9, which contained five candidate genes. Combined with parental phenotypes, chlorophyll contents of rinds and stripes were assayed. Gene sequence alignment and transcriptional level analysis of parental lines predicted Cla97C09G175170 (encoding a two-component response regulator-like protein, APRR2) as the best candidate gene for stripe color trait. Two SNPs in the ClAPRR2 coding region caused amino acid substitutions, but were not located in the conserved domain, while a 12 bp insertion caused premature translation termination and a 35 amino acid deletion in the conserved domain and may have affected ClAPRR2 function in ZXG1555. Subcellular localization analysis showed that ClAPRR2 was expressed in the ZXG1555 cell membrane but was located in the nucleus and cell membrane of COS. Nucleotide polymorphisms and deletions were also detected in the promoter region between parental lines and caused cis-acting element variations. Luciferase activity suggested that promoter variations may not be the main factor in the regulation of ClAPRR2 expression.

摘要

西瓜的条纹颜色是一个重要的商业性状,也是消费者和研究人员关注的焦点。然而,西瓜条纹颜色的遗传决定因素尚未完全明确。基于初步定位研究的结果,我们以浅绿色条纹的ZXG1555和绿色条纹的萨斯喀彻温奶油(COS)西瓜品系为亲本,构建了一个大容量的F代群体(710株植株)用于精细定位。控制条纹颜色的基因位于9号染色体上一个85.284 kb的区域,该区域包含5个候选基因。结合亲本的表型,测定了果皮和条纹的叶绿素含量。对亲本系进行基因序列比对和转录水平分析,预测Cla97C09G175170(编码一种双组分响应调节因子样蛋白,APRR2)是条纹颜色性状的最佳候选基因。ClAPRR2编码区的两个单核苷酸多态性(SNP)导致了氨基酸替换,但不在保守结构域中,而一个12 bp的插入导致了提前翻译终止,并在保守结构域中缺失了35个氨基酸,这可能影响了ZXG1555中ClAPRR2的功能。亚细胞定位分析表明,ClAPRR2在ZXG1555的细胞膜中表达,但在COS的细胞核和细胞膜中定位。在亲本系之间的启动子区域也检测到了核苷酸多态性和缺失,并导致了顺式作用元件的变异。荧光素酶活性表明,启动子变异可能不是调节ClAPRR2表达的主要因素。

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