Ho A K, Raczniak G A, Ives E B, Wente S R
Department of Cell Biology and Physiology, Washington University School of Medicine, St. Louis, Missouri 63110, USA.
Mol Biol Cell. 1998 Feb;9(2):355-73. doi: 10.1091/mbc.9.2.355.
Integral membrane proteins are predicted to play key roles in the biogenesis and function of nuclear pore complexes (NPCs). Revealing how the transport apparatus is assembled will be critical for understanding the mechanism of nucleocytoplasmic transport. We observed that expression of the carboxyl-terminal 200 amino acids of the nucleoporin Nup116p had no effect on wild-type yeast cells, but it rendered the nup116 null strain inviable at all temperatures and coincidentally resulted in the formation of nuclear membrane herniations at 23 degrees C. To identify factors related to NPC function, a genetic screen for high-copy suppressors of this lethal nup116-C phenotype was conducted. One gene (designated SNL1 for suppressor of nup116-C lethal) was identified whose expression was necessary and sufficient for rescuing growth. Snl1p has a predicted molecular mass of 18.3 kDa, a putative transmembrane domain, and limited sequence similarity to Pom152p, the only previously identified yeast NPC-associated integral membrane protein. By both indirect immunofluorescence microscopy and subcellular fractionation studies, Snl1p was localized to both the nuclear envelope and the endoplasmic reticulum. Membrane extraction and topology assays suggested that Snl1p was an integral membrane protein, with its carboxyl-terminal region exposed to the cytosol. With regard to genetic specificity, the nup116-C lethality was also suppressed by high-copy GLE2 and NIC96. Moreover, high-copy SNL1 suppressed the temperature sensitivity of gle2-1 and nic96-G3 mutant cells. The nic96-G3 allele was identified in a synthetic lethal genetic screen with a null allele of the closely related nucleoporin nup100. Gle2p physically associated with Nup116p in vitro, and the interaction required the N-terminal region of Nup116p. Therefore, genetic links between the role of Snl1p and at least three NPC-associated proteins were established. We suggest that Snl1p plays a stabilizing role in NPC structure and function.
预测整合膜蛋白在核孔复合体(NPC)的生物发生和功能中起关键作用。揭示转运装置如何组装对于理解核质运输机制至关重要。我们观察到核孔蛋白Nup116p的羧基末端200个氨基酸的表达对野生型酵母细胞没有影响,但它使nup116缺失菌株在所有温度下都无法存活,并且巧合的是在23摄氏度时导致核膜疝的形成。为了鉴定与NPC功能相关的因子,对这种致死性nup116-C表型的高拷贝抑制子进行了遗传筛选。鉴定出一个基因(命名为SNL1,即nup116-C致死性的抑制子),其表达对于挽救生长是必要且充分的。Snl1p的预测分子量为18.3 kDa,有一个假定的跨膜结构域,并且与Pom152p有有限的序列相似性,Pom152p是之前唯一鉴定出的与酵母NPC相关的整合膜蛋白。通过间接免疫荧光显微镜和亚细胞分级分离研究,Snl1p定位于核膜和内质网。膜提取和拓扑分析表明Snl1p是一种整合膜蛋白,其羧基末端区域暴露于细胞质中。关于遗传特异性,高拷贝的GLE2和NIC96也抑制了nup116-C的致死性。此外,高拷贝的SNL1抑制了gle2-1和nic96-G3突变细胞的温度敏感性。nic96-G3等位基因是在与密切相关的核孔蛋白nup100的缺失等位基因进行的合成致死遗传筛选中鉴定出来的。Gle2p在体外与Nup116p物理结合,并且这种相互作用需要Nup116p的N末端区域。因此,建立了Snl1p的作用与至少三种与NPC相关的蛋白质之间的遗传联系。我们认为Snl1p在NPC的结构和功能中起稳定作用。