Touré A, Dorseuil O, Morin L, Timmons P, Jégou B, Reibel L, Gacon G
Institut Cochin de Génétique Moléculaire, INSERM Unité 257, 24 Rue du faubourg Saint Jacques, 75014 Paris, France.
J Biol Chem. 1998 Mar 13;273(11):6019-23. doi: 10.1074/jbc.273.11.6019.
In a search for new partners of the activated form of Rac GTPase, we have isolated through a two-hybrid cloning procedure a human cDNA encoding a new GTPase-activating protein (GAP) for Rho family GTPases. A specific mRNA of 3.2 kilobases was detected in low abundance in many cell types and found highly expressed in testis. A protein of the predicted size 58 kDa, which we call MgcRacGAP, was detected in human testis as well as in germ cell tumor extracts by immunoblotting with antibodies specific to recombinant protein. In vitro, the GAP domain of MgcRacGAP strongly stimulates Rac1 and Cdc42 GTPase activity but is almost inactive on RhoA. N-terminal to its GAP domain, MgcRacGAP contains a cysteine-rich zinc finger-like motif characteristic of the Chimaerin family of RhoGAPs. The closest homolog of MgcRacGAP is RotundRacGAP, a product of the Drosophila rotund locus. In situ hybridization experiments in human testis demonstrate a specific expression of mgcRacGAP mRNA in spermatocytes similar to that of rotundRacGAP in Drosophila testis. Therefore, protein sequence similarity and analogous developmental and tissue specificities of gene expression support the hypothesis that RotundRacGAP and MgcRacGAP have equivalent functions in insect and mammalian germ cells. Since rotundRacGAP deletion leads to male sterility in the fruit fly, the mgcRacGAP gene may prove likewise to play a key role in mammalian male fertility.
为了寻找Rac GTP酶激活形式的新伙伴,我们通过双杂交克隆程序分离出一种人类cDNA,它编码一种针对Rho家族GTP酶的新型GTP酶激活蛋白(GAP)。在许多细胞类型中检测到一种3.2千碱基的特异性mRNA,其丰度较低,在睾丸中高度表达。通过用重组蛋白特异性抗体进行免疫印迹,在人类睾丸以及生殖细胞肿瘤提取物中检测到一种预测大小为58 kDa的蛋白,我们将其称为MgcRacGAP。在体外,MgcRacGAP的GAP结构域强烈刺激Rac1和Cdc42 GTP酶活性,但对RhoA几乎无活性。在其GAP结构域的N端,MgcRacGAP含有一个富含半胱氨酸的锌指样基序,这是RhoGAPs的Chimaerin家族所特有的。MgcRacGAP最接近的同源物是RotundRacGAP,它是果蝇rotund基因座的产物。人类睾丸的原位杂交实验表明,mgcRacGAP mRNA在精母细胞中的特异性表达与果蝇睾丸中rotundRacGAP的表达相似。因此,蛋白质序列相似性以及基因表达的类似发育和组织特异性支持了这样的假设,即RotundRacGAP和MgcRacGAP在昆虫和哺乳动物生殖细胞中具有等效功能。由于rotundRacGAP缺失会导致果蝇雄性不育,mgcRacGAP基因可能同样在哺乳动物雄性生育中起关键作用。