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虹鳟鱼中一个类瓦萨基因的克隆、特征分析及其在生殖细胞谱系中的表达

Cloning and characterization of a vasa-like gene in rainbow trout and its expression in the germ cell lineage.

作者信息

Yoshizaki G, Sakatani S, Tominaga H, Takeuchi T

机构信息

Department of Aquatic Biosciences, Tokyo University of Fisheries, Tokyo, Japan.

出版信息

Mol Reprod Dev. 2000 Apr;55(4):364-71. doi: 10.1002/(SICI)1098-2795(200004)55:4<364::AID-MRD2>3.0.CO;2-8.

Abstract

The origin of germ cells and the molecular mechanisms of primordial germ cell (PGC) determination in teleosts are unclear. Vasa is a member of the DEAD protein family and plays an indispensable role in germ cell determination in Drosophila and Xenopus species. In this study, we isolated and characterized a rainbow trout vasa cDNA as a first step towards understanding the molecular mechanisms of PGC determination and development and to develop a molecular marker to identify the PGCs in rainbow trout. Cloning of vasa cDNA was performed by degenerate- and RACE-PCR. The predicted amino acid sequence of rainbow trout Vasa contained eight consensus sequences for the DEAD protein family and five arginine-glycine-glycine repeats, a common character of known Vasa homologues. Overall amino acid similarity to the Vasa of Drosophila was 79.2%. Whole-mount in situ hybridization of eyed stage embryos (eighty somite stage) revealed that signals were localized to the putative PGCs. In adult rainbow trout tissues, both ovaries and testes contained large amounts of vasa gene transcripts. A reverse transcription-polymerase chain reaction analysis of unfertilized eggs proved that trout vasa is a maternal factor. Although we have not determined whether rainbow trout vasa functions as a germ cell determinant, its limited expression in the germ cell lineage proved that rainbow trout vasa can be used as a marker molecule for PGCs. This marker will make it possible to identify the PGCs or presumptive PGCs in early trout embryos whose germ cells can not be distinguished by morphological characteristics.

摘要

硬骨鱼类生殖细胞的起源以及原始生殖细胞(PGC)决定的分子机制尚不清楚。Vasa是DEAD蛋白家族的成员,在果蝇和非洲爪蟾属物种的生殖细胞决定过程中发挥着不可或缺的作用。在本研究中,我们分离并鉴定了虹鳟鱼的vasa cDNA,这是朝着了解PGC决定和发育的分子机制以及开发用于鉴定虹鳟鱼中PGC的分子标记迈出的第一步。vasa cDNA的克隆通过简并PCR和RACE-PCR进行。虹鳟鱼Vasa的预测氨基酸序列包含DEAD蛋白家族的八个共有序列和五个精氨酸-甘氨酸-甘氨酸重复序列,这是已知Vasa同源物的共同特征。与果蝇Vasa的总体氨基酸相似性为79.2%。对眼期胚胎(80体节期)进行的全胚胎原位杂交显示,信号定位于假定的PGC。在成年虹鳟鱼组织中,卵巢和睾丸都含有大量的vasa基因转录本。对未受精卵的逆转录-聚合酶链反应分析证明,虹鳟鱼vasa是一种母体因子。尽管我们尚未确定虹鳟鱼vasa是否作为生殖细胞决定因子发挥作用,但其在生殖细胞谱系中的有限表达证明虹鳟鱼vasa可作为PGC的标记分子。该标记将使鉴定早期虹鳟鱼胚胎中的PGC或假定的PGC成为可能,这些胚胎的生殖细胞无法通过形态特征加以区分。

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