生物
基因家族
基因
基因组
遗传学
基因复制
芸苔属
转录组
油菜
植物
基因表达
作者
Yufei Xue,Jiayi Jiang,Xia Yang,Huanhuan Jiang,Youjie Du,Xiaodan Liu,Ruifang Xie,Yourong Chai
出处
期刊:Gene
[Elsevier BV]
日期:2020-04-15
卷期号:747: 144674-144674
被引量:23
标识
DOI:10.1016/j.gene.2020.144674
摘要
• FAE gene family was identified in Brassica napus and its parental species. • The whole-genome and segmental duplication contributed to FAE gene famlily expansion. • FAE genes were expressed in various organs and tissues with different levels. • The Leptosphaeria maculans -responsive FAE genes were identified in B. napus . • BnKCS22 and BnELO04 both responded to phytohormone treatments and abiotic stress. Very long chain fatty acids (VLCFAs) that are structural components of cell membrane lipid, cuticular waxes and seed oil, play crucial roles in plant growth, development and stress response. Fatty acid elongases (FAEs) comprising KCS and ELO, are key enzymes for VLCFA biosynthesis in plants. Although reference genomes of Brassica napus and its parental speices both have been sequenced, whole-genome analysis of FAE gene family in these Brassica speices is not reported. Here, 58, 33 and 30 KCS genes were identified in B. napus , B. rapa and B. oleracea genomes, respectively, whereas 14, 6 and 8 members were obtained for ELO genes. These KCS genes were unevenly located in 37 chromosomes and 3 scaffolds of 3 Brassica species, while these ELO genes were mapped to 19 chromosomes. The KCS and ELO proteins were divided into 8 and 4 subclasses, respectively. Gene structure and protein motifs remained highly conserved in each KCS or ELO subclass. Most promoters of KCS and ELO genes harbored various plant growth-, phytohormone-, and stress response-related cis -acting elements. 20 SSR loci existed in the KCS and ELO genes/promoters. The whole-genome duplication and segmental duplication mainly contributed to expansion of KCS and ELO genes in these genomes. Transcriptome analysis showed that KCS and ELO genes in 3 Brassica species were expressed in various tissues/organs with different levels, whereas 1 BnELO gene and 6 BnKCS genes might be pathogen-responsive genes. The qRT-PCR assay showed that BnKCS22 and BnELO04 responded to various phytohormone treatments and abiotic stresses. This work lays the foundation for further function identification of KCS and ELO genes in B. napus and its progenitors.
科研通智能强力驱动
Strongly Powered by AbleSci AI