Liu Shi, Gao Zhongqi, Wang Xuezheng, Luan Feishi, Dai Zuyun, Yang Zhongzhou, Zhang Qian
Key Laboratory of Biology and Genetic Improvement of Horticulture Crops (Northeast Region), Ministry of Agriculture and Rural Affairs, Northeast Agricultural University, Harbin, 150030, China.
Horticulture and Landscape Architecture College, Northeast Agricultural University, Harbin, 150030, China.
Theor Appl Genet. 2022 Jan;135(1):185-200. doi: 10.1007/s00122-021-03958-0. Epub 2021 Oct 11.
A gene controlling golden flesh trait in watermelon was discovered and fine mapped to a 39.08 Kb region on chromosome 1 through a forward genetic strategy, and Cla97C01G008760 (annotated as phytoene synthase protein, ClPsy1 ) was recognized as the most likely candidate gene. Vitamin A deficiency is a worldwide public nutrition problem, and β-carotene is the precursor for vitamin A synthesis. Watermelon with golden flesh (gf, which occurs due to an accumulated abundance of β-carotene) is an important germplasm resource. In this study, a genetic analysis of segregated gf gene populations indicated that gf was controlled by a single recessive gene. BSA-seq (Bulked segregation analysis) and an initial linkage analysis placed the gf locus in a 290-Kb region on watermelon chromosome 1. Further fine mapping in a large population including over 1000 F plants narrowed this region to 39.08 Kb harboring two genes, Cla97C01G008760 and Cla97C01G008770, which encode phytoene synthase (ClPsy1) and GATA zinc finger domain-containing protein, respectively. Gene sequence alignment and expression analysis between parental lines revealed Cla97C01G008760 as the best possible candidate gene for the gf trait. Nonsynonymous SNP mutations in the first exon of ClPsy1 between parental lines co-segregated with the gf trait only among individuals in the genetic population and were not related to flesh color in natural watermelon panels. Promoter sequence analysis of 26 watermelon accessions revealed two SNPs in the cis-acting element sequences corresponding to MYB and MYC2 transcription factors. RNA-seq data and qRT-PCR verification showed that two MYBs exhibited expression trends similar to that of ClPsy1 in the parental lines and may regulate the ClPsy1 expression. Further research findings indicate that the gf trait is determined not only by ClPsy1 but also by ClLCYB, ClCRTISO and ClNCED7, which play important roles in watermelon β-carotene accumulation.
通过正向遗传学策略,在西瓜中发现了一个控制金黄色果肉性状的基因,并将其精细定位到1号染色体上一个39.08 Kb的区域,Cla97C01G008760(注释为八氢番茄红素合成酶蛋白,ClPsy1)被认为是最有可能的候选基因。维生素A缺乏是一个全球性的公共营养问题,而β-胡萝卜素是维生素A合成的前体。果肉为金黄色的西瓜(gf,由于β-胡萝卜素大量积累而出现)是一种重要的种质资源。在本研究中,对分离的gf基因群体进行遗传分析表明,gf由单个隐性基因控制。BSA-seq(混合分组分析法)和初步连锁分析将gf基因座定位在西瓜1号染色体上一个290-Kb的区域。在包括1000多株F植株的大群体中进一步精细定位,将该区域缩小到39.08 Kb,该区域包含两个基因Cla97C01G008760和Cla97C01G008770,它们分别编码八氢番茄红素合成酶(ClPsy1)和含GATA锌指结构域的蛋白。亲本系之间的基因序列比对和表达分析表明,Cla97C01G008760是gf性状最有可能的候选基因。亲本系之间ClPsy1第一个外显子中的非同义SNP突变仅在遗传群体中的个体间与gf性状共分离,与自然西瓜群体的果肉颜色无关。对26份西瓜种质的启动子序列分析揭示了与MYB和MYC2转录因子相对应的顺式作用元件序列中的两个SNP。RNA-seq数据和qRT-PCR验证表明,两个MYB在亲本系中的表达趋势与ClPsy1相似,并可能调控ClPsy1的表达。进一步的研究结果表明,gf性状不仅由ClPsy1决定,还由ClLCYB、ClCRTISO和ClNCED7决定,它们在西瓜β-胡萝卜素积累中起重要作用。