Lee W C, Mélèse T
Department of Biological Sciences, Columbia University, New York, NY 10027.
Proc Natl Acad Sci U S A. 1989 Nov;86(22):8808-12. doi: 10.1073/pnas.86.22.8808.
Nuclear proteins contain specific regions that are required for entry into the nucleus. Using ligand blotting, we have shown that a 67-kDa yeast nuclear envelope protein (p67) recognizes synthetic peptides containing the yeast histone H2B or simian virus 40 large tumor antigen nuclear localization sequence. Both free peptide and peptide conjugated to human serum albumin are recognized. The interaction between p67 and the nuclear localization sequences is specific; neither a mutant peptide that is incompetent for nuclear transport in vivo nor HSA can interact with p67 on blots. Moreover, although the wild-type peptide competes for binding to p67, the mutant peptides do not. p67 appears to be located at the nuclear envelope and is not present in other subcellular fractions. The nuclear localization sequence-binding protein is not extracted from the nuclear envelope with nonionic detergents and only partially extracted with high-salt buffer or 8 M urea, suggestive of a tight association with the nuclear envelope. Together our results are consistent with a role for p67 in nuclear transport.
核蛋白含有进入细胞核所需的特定区域。通过配体印迹法,我们发现一种67 kDa的酵母核膜蛋白(p67)能够识别含有酵母组蛋白H2B或猿猴病毒40大T抗原核定位序列的合成肽。游离肽和与人血清白蛋白偶联的肽均可被识别。p67与核定位序列之间的相互作用具有特异性;在体内不能进行核转运的突变肽和人血清白蛋白在印迹上均不能与p67相互作用。此外,虽然野生型肽能竞争与p67的结合,但突变肽则不能。p67似乎位于核膜上,不存在于其他亚细胞组分中。核定位序列结合蛋白不能用非离子去污剂从核膜中提取出来,用高盐缓冲液或8 M尿素只能部分提取,这表明它与核膜紧密结合。我们的结果共同表明p67在核转运中发挥作用。