西瓜条纹色关键候选基因ClAPRR2的鉴定与特性研究

IF 4.2 2区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
Shuang Liang , Miaomiao Yang , Linlin Zhang , Xufeng Fang , Xian Zhang , Chunhua Wei , Zuyun Dai , Zhongzhou Yang , Chaonan Wang , Bin Liu , Feishi Luan , Shi Liu
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引用次数: 0

摘要

西瓜的条纹颜色是一种重要的商业性状,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不完全清楚。在初步定位研究的基础上,以浅绿色条纹的ZXG1555和绿色条纹的Saskatchewan (COS)西瓜品系为亲本,构建了大容量F2代群体(710株)进行精细定位。控制条纹颜色的基因位于第9染色体的85.284kb区域,包含5个候选基因。结合亲本表型,测定果皮和条纹的叶绿素含量。亲本序列比对和转录水平分析预测cl97c09g175170(编码双组分响应调控因子样蛋白APRR2)是条纹色性状的最佳候选基因。ClAPRR2编码区的两个snp导致了氨基酸替换,但并不位于保守结构域,而一个12bp的插入导致了翻译的过早终止和保守结构域35个氨基酸的缺失,这可能影响了ZXG1555的ClAPRR2功能。亚细胞定位分析表明,ClAPRR2在ZXG1555细胞膜中表达,而位于COS的细胞核和细胞膜中。在亲本系之间的启动子区域也检测到核苷酸多态性和缺失,并导致顺式作用元件的变异。荧光素酶活性提示启动子变异可能不是调控ClAPRR2表达的主要因素。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Identification and characterization of ClAPRR2, a key candidate gene controlling watermelon stripe color
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 F2 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.
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来源期刊
Plant Science
Plant Science 生物-生化与分子生物学
CiteScore
9.10
自引率
1.90%
发文量
322
审稿时长
33 days
期刊介绍: Plant Science will publish in the minimum of time, research manuscripts as well as commissioned reviews and commentaries recommended by its referees in all areas of experimental plant biology with emphasis in the broad areas of genomics, proteomics, biochemistry (including enzymology), physiology, cell biology, development, genetics, functional plant breeding, systems biology and the interaction of plants with the environment. Manuscripts for full consideration should be written concisely and essentially as a final report. The main criterion for publication is that the manuscript must contain original and significant insights that lead to a better understanding of fundamental plant biology. Papers centering on plant cell culture should be of interest to a wide audience and methods employed result in a substantial improvement over existing established techniques and approaches. Methods papers are welcome only when the technique(s) described is novel or provides a major advancement of established protocols.
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