Mohl M, Winkler S, Wieland T, Lutz S
Institut für Experimentelle und Klinische Pharmakologie und Toxikologie, Universität Heidelberg, Maybachstr 14, D-68169 Mannheim, Germany.
Naunyn Schmiedebergs Arch Pharmacol. 2006 Aug;373(5):333-41. doi: 10.1007/s00210-006-0083-0. Epub 2006 Jul 29.
According to cDNA sequence homologies, Gef10 is related to the Rho-specific guanine nucleotide exchange factors GrinchGEF and p164-RhoGEF. Like these GEFs, Gef10 exhibits only weak homology to known pleckstrin homology domains, but contains a putative WD40-like domain. As detected by RT-PCR, Gef10 is transcribed in at least two splice variants in different human tissues. Although the Gef10 sequence contains two putative transmembrane segments, recombinantly expressed Gef10 displays a cytosolic localisation. As detected by guanine nucleotide exchange activity assay, precipitation assay of GTP-bound Rho proteins and serum response element dependent gene transcription Gef10 activates RhoA-C, but not Rac1 or Cdc42. In the reporter gene assay, Gef10 preferentially activated RhoB. When expressed in NIH3T3 cells, Gef10 induced actin stress fibre, but not lamellipodia or filopodia formation. We conclude that Gef10 is the third member of a Rho-specific GEF family with unusual protein architecture.
根据cDNA序列同源性,Gef10与Rho特异性鸟嘌呤核苷酸交换因子GrinchGEF和p164 - RhoGEF相关。与这些GEF一样,Gef10与已知的普列克底物蛋白同源结构域仅有微弱的同源性,但含有一个假定的WD40样结构域。通过RT - PCR检测发现,Gef10在不同的人体组织中至少以两种剪接变体形式转录。尽管Gef10序列包含两个假定的跨膜片段,但重组表达的Gef10定位于胞质。通过鸟嘌呤核苷酸交换活性测定、结合GTP的Rho蛋白沉淀测定以及血清反应元件依赖性基因转录检测发现,Gef10激活RhoA - C,但不激活Rac1或Cdc42。在报告基因测定中,Gef10优先激活RhoB。当在NIH3T3细胞中表达时,Gef10诱导肌动蛋白应激纤维形成,但不诱导片状伪足或丝状伪足形成。我们得出结论,Gef10是具有异常蛋白质结构的Rho特异性GEF家族的第三个成员。