Kalderon D, Roberts B L, Richardson W D, Smith A E
Cell. 1984 Dec;39(3 Pt 2):499-509. doi: 10.1016/0092-8674(84)90457-4.
A short sequence of amino acids including Lys-128 is required for the normal nuclear accumulation of wild-type and deleted forms of SV40 large T antigen. A cytoplasmic large T mutant that lacks sequences from around Lys-128 localizes to the nucleus if the missing sequence is attached to its amino terminus. The implication that the sequence element around Lys-128 acts as an autonomous signal capable of specifying nuclear location was tested directly by transferring it to the amino termini of beta-galactosidase and of pyruvate kinase, normally a cytoplasmic protein. Sequences that included the putative signal induced each of the fusion proteins to accumulate completely in the nucleus but had no discernible effect when Lys-128 was replaced by Thr. By reducing the size of the transposed sequence we conclude that Pro-Lys-Lys-Lys-Arg-Lys-Val can act as a nuclear location signal. The sequence may represent a prototype of similar sequences in other nuclear proteins.
野生型和缺失形式的SV40大T抗原正常核积累需要一段包括赖氨酸-128的短氨基酸序列。如果缺失序列连接到其氨基末端,缺乏赖氨酸-128周围序列的细胞质大T突变体就会定位于细胞核。通过将赖氨酸-128周围的序列元件转移到β-半乳糖苷酶和丙酮酸激酶(通常是一种细胞质蛋白)的氨基末端,直接测试了该序列元件作为能够指定核定位的自主信号的含义。包含推定信号的序列诱导每种融合蛋白完全在细胞核中积累,但当赖氨酸-128被苏氨酸取代时没有明显影响。通过减小转座序列的大小,我们得出结论,脯氨酸-赖氨酸-赖氨酸-赖氨酸-精氨酸-赖氨酸-缬氨酸可以作为核定位信号。该序列可能代表其他核蛋白中类似序列的原型。