Cui Shuliang, Nikolovski Sonia, Nanayakkara Kamani, Selwood Lynne
Department of Zoology, The University of Melbourne, Royal Parade, Parkville, Victoria, Australia.
Mol Reprod Dev. 2005 May;71(1):19-28. doi: 10.1002/mrd.20175.
In the brushtail possum oocyte, vesicles accumulate in a polarized fashion at the vegetal pole and cytoplasm rich in mitochondria and containing the germinal vesicle comprise the animal pole. During cleavage to early blastocyst stages, animal pole cytoplasm locates to the cells of the embryonic hemisphere (pluriblast) and vegetal pole vesicular cytoplasm to cells of the abembryonic hemisphere (trophoblast). Previously identified 16 amino acid residues, associated with the vesicle-rich cytoplasm were used for molecular cloning and characterization of a vesicle associated protein, VAP1. The degenerate primer was used in a 3'RACE for vap1 gene cloning. The cDNA encoding VAP1 was 516 bp in length with no significant homologies and coded for 172 amino acid residues for the mature protein. The N-terminal domain of VAP1 showed a structural homology to the cysteine protease inhibitor, Cystatin. Gene expression studies during oogenesis revealed that vap1 had an ovary-specific, possibly oocyte-specific expression, which occurs during follicle formation and growth and in adult ovaries. Recombinant VAP1 fusion protein generated polyclonal antibodies in the mouse and in the brushtail possum.
在帚尾袋貂卵母细胞中,囊泡以极化方式在植物极积累,富含线粒体且包含生发泡的细胞质构成动物极。在卵裂至早期囊胚阶段,动物极细胞质定位于胚胎半球(多细胞胚层)的细胞,而植物极囊泡状细胞质定位于反胚胎半球(滋养层)的细胞。先前鉴定出的与富含囊泡的细胞质相关的16个氨基酸残基被用于囊泡相关蛋白VAP1的分子克隆和特性分析。简并引物用于vap1基因克隆的3'RACE。编码VAP1的cDNA长度为516 bp,无明显同源性,编码成熟蛋白的172个氨基酸残基。VAP1的N端结构域与半胱氨酸蛋白酶抑制剂胱抑素具有结构同源性。卵子发生过程中的基因表达研究表明,vap1具有卵巢特异性,可能是卵母细胞特异性表达,发生在卵泡形成和生长过程以及成年卵巢中。重组VAP1融合蛋白在小鼠和帚尾袋貂中产生多克隆抗体。