Huang P, Miao S, Fan H, Sheng Q, Yan Y, Wang L, Koide S S
National Laboratory of Medical Molecular Biology, Institute of Basic Medical Sciences, Chinese Academy of Medical Sciences, Faculty of Basic Medicine, Peking Union Medical College, 5 Dong Dan 3 Tiao, Beijing 100005.
Mol Hum Reprod. 2000 Dec;6(12):1069-78. doi: 10.1093/molehr/6.12.1069.
The YWK-II cDNA, RSD-2, encoding a sperm membrane protein was isolated from a rat testis cDNA expression library. Using the RSD-2 insert in combination with rapid amplification of cDNA ends (RACE), the corresponding human gene was isolated from a human testis cDNA expression library. The human testis cDNA, HSD-2, is 3654 bp in length and contains an open reading frame of 763 codons. Hydropathicity analysis showed that the deduced polypeptide is a single strand transmembrane protein. The deduced polypeptide has partial homology with the amyloid precursor protein (APP) and high homology with the amyloid precursor homologue, APLP2/APPH. The YWK-II gene was mapped and assigned to human chromosome locus: 11q24-25. Northern blotting of various human tissue RNAs using the HSD-2 cDNA as a probe showed that the gene is transcribed ubiquitously. The cytoplasmic domain of HSD-2 was expressed in Escherichia coli. In-vitro studies showed that the recombinant polypeptide bound to a GTP-binding protein (G(o)) and was phosphorylated by protein kinase C and cdc2 kinase. In mammalian F11 cells, the recombinant polypeptide was found to be coupled to G(o). Thus, the YWK-II component has the characteristics of a G(o)-coupled receptor and may be involved in G(o)-mediated signal transduction pathway. Protein kinase C and cdc2 kinase may regulate this pathway in spermatozoa by phosphorylating the cytoplasmic domain of the YWK-II component.
从大鼠睾丸cDNA表达文库中分离出编码精子膜蛋白的YWK-II cDNA,即RSD-2。利用RSD-2插入片段结合cDNA末端快速扩增技术(RACE),从人睾丸cDNA表达文库中分离出相应的人类基因。人睾丸cDNA,即HSD-2,长度为3654 bp,包含一个763个密码子的开放阅读框。亲水性分析表明,推导的多肽是一种单链跨膜蛋白。推导的多肽与淀粉样前体蛋白(APP)有部分同源性,与淀粉样前体同源物APLP2/APPH有高度同源性。YWK-II基因被定位并指定到人类染色体位点:11q24 - 25。用HSD-2 cDNA作为探针,对各种人类组织RNA进行Northern印迹分析表明,该基因在各处均有转录。HSD-2的胞质结构域在大肠杆菌中表达。体外研究表明,重组多肽与一种GTP结合蛋白(G(o))结合,并被蛋白激酶C和cdc2激酶磷酸化。在哺乳动物F11细胞中,发现重组多肽与G(o)偶联。因此,YWK-II成分具有G(o)偶联受体的特征,可能参与G(o)介导的信号转导途径。蛋白激酶C和cdc2激酶可能通过磷酸化YWK-II成分的胞质结构域来调节精子中的这一途径。