Cloning, expression promoter analysis of vasa gene in Japanese flounder (Paralichthys olivaceus)

被引:27
|
作者
Wu, Xiaomeng
Wang, Zhongkai
Jiang, Jiajun
Gao, Jinning
Wang, Jing
Zhou, Xiaosu
Zhang, Quanqi [1 ]
机构
[1] Ocean Univ China, Coll Marine Life Sci, Qingdao 266003, Peoples R China
基金
美国国家科学基金会;
关键词
Alternative splicing; Expression profile; Genomic organization; Promoter analysis; Vasa; GREEN FLUORESCENT PROTEIN; DIFFERENTIAL EXPRESSION; GERM-CELLS; DROSOPHILA-VASA; ZEBRAFISH VASA; MURINE HOMOLOG; TELEOST FISH; RNA; SPERMATOGENESIS; ENCODES;
D O I
10.1016/j.cbpb.2013.06.004
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Vasa is a DEAD box helicase and has shown essential functions during gametogenesis and embryogenesis. In most species, research revealed a specific expression of vasa gene in the germ cells. Thus, vasa has become the candidate gene in identifying germ cells. In this study, the vasa gene was isolated from gonads of Japanese flounder (Paralichthys olivaceus). In the 11.4 kb genomic sequence, 23 exons were identified besides 5' and 3' flanking regions. The promoter region contained several putative TF binding sites which may have the function of regulating vasa expression. Quantitative real-time PCR analysis showed that vasa gene expression was restricted to adult gonads, with a higher level in the ovary. Development expression profiling revealed a maternal deposit and constant embryonic expression at early stages, but the relative mRNA amount decreased after gastrula. Nine other PoVasa transcripts were detected and their expression in gonads and during early development was not all the same, implying potential different functions during gametogenesis or early embryonic development. These results together confirmed the feasibility of using vasa as a marker of germ cells and that vasa gene had an important role in spermatogenesis and oogenesis. Furthermore, our study laid the groundwork for identifying fish primordial germ cells (PGCs) and investigating germ cell biology. (C) 2013 Elsevier Inc. All rights reserved.
引用
收藏
页码:41 / 50
页数:10
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