Quaye I K, Toku S, Tanaka T
Department of Biochemistry, School of Medicine, University of the Ryukyus, Nishihara, Okinawa, Japan.
Eur J Cell Biol. 1996 Feb;69(2):151-5.
Nucleolar localization of the fusion protein of rat ribosomal protein L31 and beta-galactosidase was investigated by immunocytochemical means, using the ribosomal protein deletion or substitution mutants that were transiently expressed in COS-1 cells. The signal responsible for nucleolar localization is encoded by the amino acid residues 87 to 92, RLSRKR, located near the C terminus of the ribosomal protein. Mutation of residues 87R and 90R prevented nucleolar localization, whereas mutations including 90R prevented nuclear and nucleolar localization. Further mutations in the sequence revealed that the tetrapeptide RLSR, which was amenable to substitutions at the L and S positions, is critical for nucleolar localization.
通过免疫细胞化学方法,利用在COS-1细胞中瞬时表达的核糖体蛋白缺失或替代突变体,研究了大鼠核糖体蛋白L31与β-半乳糖苷酶融合蛋白的核仁定位。负责核仁定位的信号由位于核糖体蛋白C末端附近的氨基酸残基87至92(RLSRKR)编码。残基87R和90R的突变阻止了核仁定位,而包括90R在内的突变则阻止了细胞核和核仁定位。该序列中的进一步突变表明,四肽RLSR(L和S位置适合替换)对核仁定位至关重要。