Liu Chunxiao, Zhang Tianzhen
National Key Laboratory of Crop Genetics & Germplasm Enhancement, Cotton Research Institute, Nanjing Agricultural University, Nanjing, 210095, Jiangsu Province, People's Republic of China.
BMC Genomics. 2017 Jan 31;18(1):118. doi: 10.1186/s12864-017-3517-9.
The allotetraploid cotton originated from one hybridization event between an extant progenitor of Gosssypium herbaceum (A) or G. arboreum (A) and another progenitor, G. raimondii Ulbrich (D) 1-1.5 million years ago (Mya). The APETALA2/ethylene-responsive element binding protein (AP2/EREBP) transcription factors constitute one of the largest and most conserved gene families in plants. They are characterized by their AP2 domain, which comprises 60-70 amino acids, and are classified into four main subfamilies: the APETALA2 (AP2), Related to ABI3/VP1 (RAV), Dehydration-Responsive Element Binding protein (DREB) and Ethylene-Responsive Factor (ERF) subfamilies. The AP2/EREBP genes play crucial roles in plant growth, development and biotic and abiotic stress responses. Hence, understanding the molecular characteristics of cotton stress tolerance and gene family expansion would undoubtedly facilitate cotton resistance breeding and evolution research.
A total of 269 AP2/EREBP genes were identified in the G. raimondii (D5) cotton genome. The protein domain architecture and intron/exon structure are simple and relatively conserved within each subfamily. They are distributed throughout all chromosomes but are clustered on various chromosomes due to genomic tandem duplication. We identified 73 tandem duplicated genes and 221 segmental duplicated gene pairs which contributed to the expansion of AP2/EREBP superfamily. Of them, tandem duplication was the most important force of the expansion of the B3 group. Transcriptome analysis showed that 504 AP2/EREBP genes were expressed in at least one tested G. hirsutum TM-1 tissues. In G. hirsutum, 151 non-repeated genes of the DREB and ERF subfamily genes were responsive to different stresses: 132 genes were induced by cold, 63 genes by drought and 94 genes by heat. qRT-PCR confirmed that 13 GhDREB and 15 GhERF genes were induced by cold and/or drought. No transcripts detected for 53 of the 111 tandem duplicated genes in TM-1. In addition, some homoeologous genes showed biased expression toward either A-or D-subgenome.
The AP2/EREBP genes were obviously expanded in Gossypium. The GhDREB and GhERF genes play crucial roles in cotton stress responses. Our genome-wide analysis of AP2/EREBP genes in cotton provides valuable information for characterizing the molecular functions of AP2/EREBP genes and reveals insights into their evolution in polyploid plants.
异源四倍体棉花起源于100万至150万年前(百万年前)陆地棉(A)或亚洲棉(A)的现存祖先与另一个祖先雷蒙德氏棉(D)之间的一次杂交事件。APETALA2/乙烯响应元件结合蛋白(AP2/EREBP)转录因子是植物中最大且最保守的基因家族之一。它们的特征在于其AP2结构域,该结构域由60 - 70个氨基酸组成,并被分为四个主要亚家族:APETALA2(AP2)、与ABI3/VP1相关(RAV)、脱水响应元件结合蛋白(DREB)和乙烯响应因子(ERF)亚家族。AP2/EREBP基因在植物生长、发育以及生物和非生物胁迫响应中发挥着关键作用。因此,了解棉花抗逆性的分子特征和基因家族扩张无疑将有助于棉花抗性育种和进化研究。
在雷蒙德氏棉(D5)棉花基因组中总共鉴定出269个AP2/EREBP基因。每个亚家族内的蛋白质结构域架构和内含子/外显子结构简单且相对保守。它们分布于所有染色体上,但由于基因组串联重复而在不同染色体上成簇分布。我们鉴定出73个串联重复基因和221个片段重复基因对,它们促成了AP2/EREBP超家族的扩张。其中,串联重复是B3组扩张的最重要力量。转录组分析表明,504个AP2/EREBP基因在至少一种测试的陆地棉TM - 1组织中表达。在陆地棉中,DREB和ERF亚家族基因的151个非重复基因对不同胁迫有响应:132个基因受冷诱导,63个基因受干旱诱导,94个基因受热诱导。qRT - PCR证实13个GhDREB和15个GhERF基因受冷和/或干旱诱导。在TM - 1的111个串联重复基因中有53个未检测到转录本。此外,一些同源基因表现出对A或D亚基因组的偏向性表达。
AP2/EREBP基因在棉属中明显扩张。GhDREB和GhERF基因在棉花胁迫响应中发挥关键作用。我们对棉花AP2/EREBP基因的全基因组分析为表征AP2/EREBP基因的分子功能提供了有价值的信息,并揭示了它们在多倍体植物中的进化见解。