McCourt Paula C, Morgan Jeanelle M, Nickels Joseph T
Pharmacogenomics Division, Medical Diagnostics Laboratories, LLC, Hamilton, New Jersey 08690, USA.
J Biol Chem. 2009 May 1;284(18):11930-41. doi: 10.1074/jbc.M900857200. Epub 2009 Mar 2.
Saccharomyces cerevisiae cells lacking the amphiphysin-like orthologs, Rvs161 or Rvs167, are unable to thrive under many stress conditions. Here we show cells lacking Rvs161 require Cdc55, the B subunit of the yeast ceramide-activated protein phosphatase, for viability under heat stress. By using specific rvs mutant alleles, we linked this lethal genetic interaction to loss of Rvs161 endocytic domain function. Recessive mutations in the sphingolipid pathway, such as deletion of the very long-chain fatty acid elongase, Sur4, suppress the osmotic growth defect of rvs161 cells. We demonstrate that Cdc55 is required for sur4-dependent suppressor activity and that protein phosphatase activation, through overexpression of CDC55 alone, can also remediate this defect. Loss of SUR4 in rvs161 cells reinitiates Ste3 a-factor receptor endocytosis and requires Cdc55 function to do so. Moreover, overexpression of CDC55 reinitiates Ste3 endocytic-dependent degradation and restores fluid phase endocytosis in rvs161 cells. In contrast, loss of SUR4 or CDC55 overexpression does not remediate the actin polarization defects of osmotic stressed rvs161 cells. Importantly, remediation of rvs161 defects by protein phosphatase activation requires the ceramide-activated protein phosphatase catalytic subunit, Sit4, and the protein phosphatase 2A catalytic subunits, Pph21/Pph22. Finally, genetic analyses reveal a synthetic lethal interaction between loss of CDC55 and gene deletions lethal with rvs161, all of which function in endocytosis.
缺乏类发动蛋白直系同源物Rvs161或Rvs167的酿酒酵母细胞在许多应激条件下无法存活。在此我们表明,缺乏Rvs161的细胞在热应激下的存活需要酵母神经酰胺激活蛋白磷酸酶的B亚基Cdc55。通过使用特定的rvs突变等位基因,我们将这种致死性遗传相互作用与Rvs161内吞结构域功能的丧失联系起来。鞘脂途径中的隐性突变,如超长链脂肪酸延长酶Sur4的缺失,可抑制rvs161细胞的渗透生长缺陷。我们证明Cdc55是sur4依赖性抑制活性所必需的,并且仅通过过表达CDC55激活蛋白磷酸酶也可以补救这一缺陷。rvs161细胞中Sur4的缺失重新启动了Ste3 a因子受体的内吞作用,并且需要Cdc55的功能才能实现。此外,CDC55的过表达重新启动了Ste3内吞依赖性降解,并恢复了rvs161细胞中的液相内吞作用。相比之下,Sur4的缺失或CDC55的过表达并不能补救渗透应激的rvs161细胞的肌动蛋白极化缺陷。重要的是,通过蛋白磷酸酶激活补救rvs161缺陷需要神经酰胺激活蛋白磷酸酶催化亚基Sit4和蛋白磷酸酶2A催化亚基Pph21/Pph22。最后,遗传分析揭示了Cdc55缺失与对rvs161致死的基因缺失之间的合成致死相互作用,所有这些基因都在内吞作用中发挥作用。