cDNA cloning, expression and immune function analysis of a novel Rac1 gene (AjRac1) in the sea cucumber Apostichopus japonicus

被引:8
作者
Li, Kaiquan [1 ]
Liu, Lin [1 ]
Shang, Shengnan [1 ]
Wang, Yi [1 ]
Zhan, Yaoyao [1 ]
Song, Jian [1 ]
Zhang, Xiangxiang [1 ]
Chang, Yaqing [1 ]
机构
[1] Dalian Ocean Univ, Minist Agr, Key Lab Mariculture & Stock Enhancement North Chi, Dalian 116023, Liaoning, Peoples R China
基金
中国国家自然科学基金;
关键词
Apostichopus japonicus; Ras-related C3 botulinum toxin substrate 1; Expression analysis; Vibrio splendidus infection; NF-KAPPA-B; IDENTIFICATION; PATHWAY; CELOMOCYTES; REGULATORS; INHIBITOR; GTPASES; GENOME; CDC42;
D O I
10.1016/j.fsi.2017.08.027
中图分类号
S9 [水产、渔业];
学科分类号
0908 ;
摘要
The ras-related C3 botulinum toxin substrate 1 (Rac1) belongs to Ras homolog (Rho) small GTPases subfamily. As an important molecular switch, Rac1 regulates various processes in the cell, especially in cellular immune response. With attempt to clarify characters and functions of Rac1 in sea cucumbers, full length cDNA of a Rac1 homolog in the sea cucumber Apostichopus japonicus (AjRac1) was cloned by transcriptome database mining and rapid amplification of cDNA ends (RACE) techniques. The open reading frame of AjRac1 is 579 bp encoding a protein with a length of 192 aa. Sequence analysis showed that AjRac1 is highly conserved as compared to those from other eukaryotic species. Phylogenetic analysis revealed that amino acid sequence of AjRac1 closely related to those from Strongylocentrotus purpuratus. Results of expression analysis showed that AjRac1 exhibited a relative high expression in blastula stage, adult coelomocytes and respiratory tree in A. japonicus. The transcription of AjRac1 in adult coelomocytes altered significantly at 4 h- and 12 h-after Vibrio splendidus infection, respectively, which indicated that AjRac1 involved in sea cucumber innate immunity. All data presented in this study will deepen our understanding of characterizations and immunological functions of Rac1 in sea cucumbers. (C) 2017 Elsevier Ltd. All rights reserved.
引用
收藏
页码:218 / 226
页数:9
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