首页> 外文期刊>Gene: An International Journal Focusing on Gene Cloning and Gene Structure and Function >Molecular characterization of a novel ovary-specific gene fem-1 homolog from the oriental river prawn, Macrobrachium nipponense
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Molecular characterization of a novel ovary-specific gene fem-1 homolog from the oriental river prawn, Macrobrachium nipponense

机译:来自东方河虾的新型卵巢特异性基因FEM-1同源物的分子表征,Macrobrachium Nippoonense

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摘要

The feminization-1 (fem-1) gene is characterized by one of the most common protein-protein interaction motifs, ankyrin repeat motifs, displays many expression patterns in vertebrates and invertebrates, and plays an essential role in the sex-determination/differentiation pathway in Caenorhabditis elegans. In this study, a fem-1 homolog, designated as Mnfem-1, was first cloned from the oriental river prawn Macrobrachium nipponense. The prawn Mnfem-1 gene consists of six exons and five introns. The full-length cDNA (2603 bp) of Mnfem-1 contains an open reading frame (ORF) encoding a protein of 622 amino acids. The Mnfem-1 RNA and protein are exclusively expressed in the ovary in adult prawns as revealed by RT-PCR and immunofluorescence analysis, respectively. In situ hybridization results showed that strong positive signals were concentrated at the edge of the previtellogenic and vitellogenic oocyte. During embryogenesis, Mnfem-1 is highly expressed in both unfertilized eggs and embryos at cleavage stage and thereafter dropped to a low level from blastula to zoea, indicating that the Mnfem-1 in early embryos is maternal. After hatching, the Mnfem-1 expression significantly increased in the larvae at length of 2 cm, an important stage of sex differentiation. Yeast two hybridization results showed that the Mnfem-1 protein can be potentially interactive with cathepsin L and proteins containing the domains of insulinase, ankyrin or ubiquitin. Our results suggested that Mnfem-1 could have roles in prawn ovarian development and sex determination/differentiation. (C) 2015 Elsevier B.V. All rights reserved.
机译:女性化-1(FEM-1)基因的特征在于最常见的蛋白质 - 蛋白质相互作用基序之一,Ankyrin重复基序,在脊椎动物和无脊椎动物中显示出许多表达模式,并在性测定/分化途径中起重要作用在Caenorhabditis elegans。在这项研究中,首先从东方河虾Macrobrachium Nipponense克隆了一名FEM-1同源物。虾Mnfem-1基因由六个外显子和五个内含子组成。 MNFEM-1的全长cDNA(2603bp)包含编码622个氨基酸蛋白质的开放阅读框架(ORF)。 MNFEM-1 RNA和蛋白质分别在成人虾中分别在卵巢中表达,分别通过RT-PCR和免疫荧光分析揭示。原位杂交结果表明,浓缩的正信号浓缩在最终恒生和培体卵母细胞的边缘。在胚胎发生期间,MNFEM-1在裂解阶段的未受精的卵和胚胎中高度表达,然后从Blastula降至Zoea的低水平,表明早期胚胎中的MnFem-1是母体。在孵化后,幼虫的MNFEM-1表达在幼虫中显着增加,长度为2cm,性别分化的一个重要阶段。酵母两种杂交结果表明,MNFEM-1蛋白可能与含有胰岛素酶,胰蛋白酶域,Ankyrin或泛素的域的蛋白质相互作用。我们的结果表明,MNFEM-1可能在虾卵巢发育和性别测定/分化中具有作用。 (c)2015 Elsevier B.v.保留所有权利。

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