Volckaert G, Van de Voorde A, Fiers W
Eur J Biochem. 1980 May;106(1):169-77. doi: 10.1111/j.1432-1033.1980.tb06008.x.
The nucleotide sequence of the second part of the simian virus 40 DNA HindII + III restriction fragment A is presented. The sequence extends from map position 0.533 to 0.424 and together with the first part of Hind-A [Volckaert et al. Proc. Natl Acad. Sci. U.S.A. 75, 2160--2164 (1978)] completes the total hind-A sequence, comprising 1169 base pairs. The second half of Hind-A includes the region corresponding to the second splicing boundary common to small tumor antigen (small-t) and large tumor antigen (large-T) mRNA and it contains coding information for an internal portion of large-T antigen. Two similar secondary structures of reasonable thermodynamic stability can be proposed for the nucleotide sequence of the pre-mRNA corresponding to the region reported here. Their possible relevance to the splicing of the SV40 early mRNAs is discussed. The deduced amino acid sequence is 188 residues long and contains a Lys-Lys-Lys-Arg-Lys-stretch which may be involved in the DNA binding capacity of large-T. A presumptive phosphorylation site is also present.
本文给出了猿猴病毒40(SV40)DNA HindII + III限制片段A第二部分的核苷酸序列。该序列从图谱位置0.533延伸至0.424,并与Hind - A的第一部分[沃尔卡特等人。美国国家科学院院刊75, 2160 - 2164 (1978)]共同构成了完整的Hind - A序列,共计1169个碱基对。Hind - A的后半部分包含了与小肿瘤抗原(small - t)和大肿瘤抗原(large - T)mRNA共有的第二个剪接边界相对应的区域,并且含有大T抗原内部区域的编码信息。对于此处报道区域对应的前体mRNA的核苷酸序列,可以提出两种具有合理热力学稳定性的相似二级结构。讨论了它们与SV40早期mRNA剪接的可能相关性。推导的氨基酸序列长度为188个残基,包含一个可能与大T的DNA结合能力有关的赖氨酸 - 赖氨酸 - 赖氨酸 - 精氨酸 - 赖氨酸延伸序列。还存在一个推测的磷酸化位点。