Su Weihua, Ren Yongjuan, Wang Dongjiao, Huang Long, Fu Xueqin, Ling Hui, Su Yachun, Huang Ning, Tang Hanchen, Xu Liping, Que Youxiong
Key Laboratory of Sugarcane Biology and Genetic Breeding, Ministry of Agriculture, Fujian Agriculture and Forestry University, Fuzhou, 350002, China.
Key Laboratory of Genetics, Breeding and Multiple Utilization of Crops, Ministry of Education, Fujian Agriculture and Forestry University, Fuzhou, 350002, China.
BMC Genomics. 2020 Dec 7;21(1):868. doi: 10.1186/s12864-020-07264-9.
Calcineurin B-like protein (CBL)-interacting protein kinases (CIPKs) are the primary components of calcium sensors, and play crucial roles in plant developmental processes, hormone signaling transduction, and in the response to exogenous stresses.
In this study, 48 CIPK genes (SsCIPKs) were identified from the genome of Saccharum spontaneum. Phylogenetic reconstruction suggested that the SsCIPK gene family may have undergone six gene duplication events from the last common ancestor (LCA) of SsCIPKs. Whole-genome duplications (WGDs) served as the driving force for the amplification of SsCIPKs. The Nonsynonymous to synonymous substitution ratio (Ka/Ks) analysis showed that the duplicated genes were possibly under strong purifying selection pressure. The divergence time of these duplicated genes had an average duplication time of approximately 35.66 Mya, suggesting that these duplication events occurred after the divergence of the monocots and eudicots (165 Mya). The evolution of gene structure analysis showed that the SsCIPK family genes may involve intron losses. Ten ScCIPK genes were amplified from sugarcane (Saccharum spp. hybrids). The results of real-time quantitative polymerase chain reaction (qRT-PCR) demonstrated that these ten ScCIPK genes had different expression patterns under abscisic acid (ABA), polyethylene glycol (PEG), and sodium chloride (NaCl) stresses. Prokaryotic expression implied that the recombinant proteins of ScCIPK3, - 15 and - 17 could only slightly enhance growth under salinity stress conditions, but the ScCIPK21 did not. Transient N. benthamiana plants overexpressing ScCIPKs demonstrated that the ScCIPK genes were involved in responding to external stressors through the ethylene synthesis pathway as well as to bacterial infections.
In generally, a comprehensive genome-wide analysis of evolutionary relationship, gene structure, motif composition, and gene duplications of SsCIPK family genes were performed in S. spontaneum. The functional study of expression patterns in sugarcane and allogenic expressions in E. coli and N. benthamiana showed that ScCIPKs played various roles in response to different stresses. Thus, these results improve our understanding of the evolution of the CIPK gene family in sugarcane as well as provide a basis for in-depth functional studies of CIPK genes in sugarcane.
类钙调神经磷酸酶B蛋白(CBL)相互作用蛋白激酶(CIPK)是钙传感器的主要成分,在植物发育过程、激素信号转导以及对外源胁迫的响应中发挥关键作用。
在本研究中,从割手密基因组中鉴定出48个CIPK基因(SsCIPKs)。系统发育重建表明,SsCIPK基因家族可能从SsCIPKs的最后一个共同祖先(LCA)经历了6次基因复制事件。全基因组复制(WGDs)是SsCIPKs扩增的驱动力。非同义替换与同义替换比率(Ka/Ks)分析表明,复制基因可能处于强烈的纯化选择压力之下。这些复制基因的分歧时间平均复制时间约为3566万年前,表明这些复制事件发生在单子叶植物和双子叶植物分化(1.65亿年前)之后。基因结构进化分析表明,SsCIPK家族基因可能涉及内含子丢失。从甘蔗(甘蔗属杂交种)中扩增出10个ScCIPK基因。实时定量聚合酶链反应(qRT-PCR)结果表明,这10个ScCIPK基因在脱落酸(ABA)、聚乙二醇(PEG)和氯化钠(NaCl)胁迫下具有不同的表达模式。原核表达表明,ScCIPK3、-15和-17的重组蛋白在盐胁迫条件下只能略微促进生长,但ScCIPK21则不能。过表达ScCIPKs的本氏烟草瞬时植株表明,ScCIPK基因通过乙烯合成途径以及对细菌感染参与对外界应激源的响应。
总体而言,对割手密中SsCIPK家族基因的进化关系、基因结构、基序组成和基因复制进行了全面的全基因组分析。甘蔗中表达模式和大肠杆菌及本氏烟草中异源表达的功能研究表明,ScCIPKs在应对不同胁迫中发挥着多种作用。因此,这些结果增进了我们对甘蔗中CIPK基因家族进化的理解,并为深入研究甘蔗中CIPK基因的功能提供了基础。