INDEPENDENT EXPRESSION OF THE TRANSFORMING AMINO-TERMINAL DOMAIN OF SV40 LARGE T-ANTIGEN FROM AN ALTERNATIVELY SPLICED 3RD SV40 EARLY MESSENGER-RNA

被引:81
作者
ZERRAHN, J [1 ]
KNIPPSCHILD, U [1 ]
WINKLER, T [1 ]
DEPPERT, W [1 ]
机构
[1] UNIV HAMBURG,HEINRICH PETTE INST EXPTL VIROL & IMMUNOL,MARTINISTR 52,D-20251 HAMBURG,GERMANY
关键词
ALTERNATIVE SPLICING; DIFFERENTIAL PHOSPHORYLATION; SV40 LARGE T-ANTIGEN; TRANSFORMING DOMAINS;
D O I
10.1002/j.1460-2075.1993.tb06162.x
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We found that simian virus 40 (SV40), in addition to the SV40 early proteins large T antigen (large T) and small t antigen (small t), codes for a third early protein with a molecular weight of 17 kDa. This protein (17kT) is expressed from an alternatively spliced third SV40 early mRNA, using a splice donor site at position 4425 and a splice acceptor site at position 3679 of the SV40 genome. The 17kT protein consists of 135 amino acids. Of these, 131 correspond to the amino-terminus of large T, while the four carboxy-terminal amino acids are unique and encoded by a different reading frame 17kT mRNA, and the corresponding protein, were found in all SV40 transformed cells analyzed, as well as in SV40 infected cells. Transfection of a cDNA expression vector encoding the 17kT protein into rat F111 fibroblasts induced phenotypic transformation of these cells. The expression of the transforming amino-terminal domain of large T as an independent 17kT protein might provide a means for individually regulating the various functions associated with this domain.
引用
收藏
页码:4739 / 4746
页数:8
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