Zhang Kaijing, Li Ying, Zhu Wenwei, Wei Yifan, Njogu Martin Kagiki, Lou Qunfeng, Li Ji, Chen Jinfeng
National Key Laboratory of Crop Genetics and Germplasm Enhancement, College of Horticulture, Nanjing Agricultural University, Nanjing, China.
College of Agriculture, Anhui Science and Technology University, Fengyang, China.
Front Plant Sci. 2020 Sep 25;11:570817. doi: 10.3389/fpls.2020.570817. eCollection 2020.
Leaf color mutants are the ideal materials to explore the pathways of chlorophyll metabolism, chloroplast development and photosynthesis system. In this study, a new virescent leaf mutant 104Y was identified by spontaneous mutation, whose cotyledon and upper five true leaves were yellow color. The yellow true leaves gradually turned green from top to bottom with increased chlorophyll contents. Genetic analysis indicated that the virescent leaf was controlled by one single recessive gene , which was accurately mapped into 36.0-39.7 Mb interval on chromosome 3 by using BSA-seq and linkage analysis. Fine mapping analysis further narrowed into 73-kb genomic region including eight genes with BC and F populations. Through BSA-seq and cDNA sequencing analysis, only one nonsynonymous mutation existed in the gene encoding auxin F-box protein was identified, which was predicted as the candidate gene controlling virescent leaf. Comparative transcriptome analysis and quantitative real-time PCR analysis revealed that the expression level of was not changed between EC1 and 104Y. However, RNA-seq analysis identified that the key genes involved in chlorophyll biosynthesis and auxin signaling transduction network were mainly down-regulated in 104Y compared with EC1, which indicated that the regulatory functions of could be performed at post-transcriptional level rather than transcriptional level. This is the first report to map-based clone an auxin F-box protein gene related to virescent leaf in cucumber. The results will exhibit a new insight into the chlorophyll biosynthesis regulated by auxin signaling transduction network.
叶色突变体是探索叶绿素代谢、叶绿体发育和光合作用系统途径的理想材料。本研究通过自发突变鉴定出一个新的黄化叶突变体104Y,其幼苗子叶和上部五片真叶呈黄色。随着叶绿素含量增加,黄色真叶从顶部到底部逐渐变绿。遗传分析表明,黄化叶由一对隐性基因控制,利用混合分组分析法(BSA-seq)和连锁分析将其精确定位到3号染色体上36.0-39.7 Mb区间。精细定位分析利用回交(BC)和F群体进一步将其缩小到73 kb的基因组区域,该区域包含8个基因。通过BSA-seq和cDNA测序分析,在编码生长素F-box蛋白的基因中仅鉴定到一个非同义突变,该基因被预测为控制黄化叶的候选基因。比较转录组分析和实时定量PCR分析表明,该基因在黄瓜绿叶自交系EC1和突变体104Y之间的表达水平没有变化。然而,RNA测序分析表明,与EC1相比,104Y中参与叶绿素生物合成和生长素信号转导网络的关键基因主要下调,这表明该基因的调控功能可能在转录后水平而非转录水平发挥作用。这是首次基于图位克隆黄瓜中一个与黄化叶相关的生长素F-box蛋白基因的报道。这些结果将为生长素信号转导网络调控叶绿素生物合成提供新的见解。