School of Life Sciences, College of Medical, Veterinary and Life Sciences, University of Glasgow, Glasgow, UK.
J Cell Sci. 2012 Jun 1;125(Pt 11):2721-31. doi: 10.1242/jcs.100685. Epub 2012 Feb 17.
Rho GTPases are regulated in complex spatiotemporal patterns that might be dependent, in part at least, on the multiplicity of their GTP exchange factors (GEFs). Here, we examine the extent of and basis for functional specialisation of the Rom2 and Tus1 GEFs that activate the yeast Rho1 GTPase, the orthologue of mammalian RhoA. First, we find that these GEFs selectively activate different Rho1-effector branches. Second, the synthetic genetic networks around ROM2 and TUS1 confirm very different global in vivo roles for these GEFs. Third, the GEFs are not functionally interchangeable: Tus1 cannot replace the essential role of Rom2, even when overexpressed. Fourth, we find that Rom2 and Tus1 localise differently: Rom2 to the growing bud surface and to the bud neck at cytokinesis; Tus1 only to the bud neck, but in a distinct pattern. Finally, we find that these GEFs are dependent on different protein co-factors: Rom2 function and localisation is largely dependent on Ack1, a SEL1-domain-containing protein; Tus1 function and localisation is largely dependent on the Tus1-interacting protein Ypl066w (which we name Rgl1). We have revealed a surprising level of diversity among the Rho1 GEFs that contributes another level of complexity to the spatiotemporal control of Rho1.
Rho GTPases 的调控具有复杂的时空模式,这种模式至少部分依赖于它们的 GTP 交换因子 (GEF) 的多样性。在这里,我们研究了激活酵母 Rho1 GTPase(哺乳动物 RhoA 的同源物)的 Rom2 和 Tus1 GEF 的功能特化程度和基础。首先,我们发现这些 GEF 选择性地激活不同的 Rho1 效应分支。其次,ROM2 和 TUS1 的合成遗传网络证实了这些 GEF 在体内具有非常不同的全局作用。第三,GEFs 不能在功能上互换:即使过表达,Tus1 也不能替代 Rom2 的必需作用。第四,我们发现 Rom2 和 Tus1 的定位不同:Rom2 定位于生长的芽表面和有丝分裂时的芽颈;Tus1 仅定位于芽颈,但模式不同。最后,我们发现这些 GEFs 依赖于不同的蛋白共因子:Rom2 的功能和定位在很大程度上依赖于 Ack1,一种包含 SEL1 结构域的蛋白;Tus1 的功能和定位在很大程度上依赖于 Tus1 相互作用蛋白 Ypl066w(我们将其命名为 Rgl1)。我们揭示了 Rho1 GEF 之间令人惊讶的多样性,这为 Rho1 的时空调控增加了另一个层次的复杂性。