Emtage J L, Bucci M, Watkins J L, Wente S R
Department of Cell Biology and Physiology, Washington University School of Medicine, St Louis, MO 63110, USA.
J Cell Sci. 1997 Apr;110 ( Pt 7):911-25. doi: 10.1242/jcs.110.7.911.
Studies of the essential nucleoporin Nup145p have shown that its depletion is coincident with a block in RNA export and that deletion of its amino-terminal domain results in clustering of nuclear pore complexes. To further define the functional domains of Nup145p, we have characterized a panel of nup145 mutants. Deletions from both the amino terminus and the carboxy terminus resulted in temperature sensitive mutants that accumulated polyadenylated RNA in the nucleus at the non-permissive temperature. In addition, these mutants also displayed constitutive clustering of nuclear pore complexes in localized patches of the nuclear envelope. These results suggested that an internal region of Nup145p consisting of amino acids 593-893 is essential for function. Accordingly, when this region was deleted, growth was not supported at any temperature, whereas the region alone was able to complement a null mutation when expressed on a high copy plasmid. Previous studies have suggested that Nup145p is cleaved into two polypeptides of approximately 65 and 80 kDa. Interestingly, our experiments suggest that cleavage occurs in vivo. However, a small internal deletion of 17 amino acid residues that abolished cleavage had no effect on cell growth. Therefore, cleavage is not necessary for Nup145p function. When a sequence harboring the Nup145p cleavage site required for Nup145p cleavage was inserted in a chimeric protein, it was not sufficient for mediating cleavage. Cleavage likely requires a second region from amino acid residues 247-524 in addition to the cleavage site.
对必需核孔蛋白Nup145p的研究表明,其缺失与RNA输出受阻同时发生,并且其氨基末端结构域的缺失会导致核孔复合体聚集。为了进一步确定Nup145p的功能结构域,我们对一组nup145突变体进行了表征。氨基末端和羧基末端的缺失均产生了温度敏感型突变体,这些突变体在非允许温度下会在细胞核中积累多聚腺苷酸化RNA。此外,这些突变体还在核膜的局部斑块中表现出核孔复合体的组成性聚集。这些结果表明,由氨基酸593 - 893组成的Nup145p内部区域对其功能至关重要。因此,当该区域被删除时,在任何温度下都无法支持生长,而单独该区域在高拷贝质粒上表达时能够弥补无效突变。先前的研究表明,Nup145p被切割成两条分别约为65 kDa和80 kDa的多肽。有趣的是,我们的实验表明切割发生在体内。然而,一个消除切割的17个氨基酸残基的小内部缺失对细胞生长没有影响。因此,切割对于Nup145p的功能不是必需的。当将一个包含Nup145p切割所需切割位点的序列插入嵌合蛋白中时,它不足以介导切割。切割可能除了切割位点外还需要氨基酸残基247 - 524的第二个区域。