Identification of SV40 large T-antigen-associated proteins in cardiomyocytes from transgenic mice

1993 ◽  
Vol 264 (5) ◽  
pp. H1693-H1700 ◽  
Author(s):  
A. I. Daud ◽  
N. A. Lanson ◽  
W. C. Claycomb ◽  
L. J. Field

A cell line derived from transgenic mice expressing the SV40 large T-antigen oncogene in the heart was used to identify cardiomyocyte targets for T-antigen binding. A novel protein of molecular mass of 193 kDa was identified as an associated protein by virtue of its ability to be co-immunoprecipitated with multiple anti-T-antigen antibodies. Two previously described proteins, p120 and p53, were also observed to complex with T-antigen in transformed cardiomyocytes. In addition, several proteins that cross-reacted with either anti-T-antigen or anti-p53 antibodies were identified. Two of these proteins, of apparent molecular masses of 250 and 110 kDa, were only observed in cardiomyocytes. Expression of a third cross-reacting protein of a molecular mass of 180 kDa appeared to be dependent on the growth status of the cells. These proteins may be important constituents of the cardiomyocyte cell cycle, as well as potential cellular targets for myocardial regeneration.

1991 ◽  
Vol 173 (2) ◽  
pp. 383-393 ◽  
Author(s):  
R S Wildin ◽  
A M Garvin ◽  
S Pawar ◽  
D B Lewis ◽  
K M Abraham ◽  
...  

In the mouse and human, mRNA transcripts encoding the lymphocyte-specific protein tyrosine kinase p56lck are derived from two separate promoters resulting in heterogeneity in the 5' untranslated region sequence. The proximal promoter lies just 5' to the coding region for the gene and is active only in thymocytes. In contrast, the distal promoter lies 34 kilobases (kb) 5' in the human, and is active both in thymocytes and mature peripheral T cells. As previously reported, transgenic mice bearing functional proximal promoter sequence juxtaposed with the SV40 large T antigen gene invariably develop lymphoid tumors confined to the thymus. In the current work, transgenic mice bearing a 2.6-kb fragment of the human distal promoter fused to the SV40 large T antigen gene express large T antigen in thymocytes and in peripheral lymphoid cells, and develop tumors of both the thymus and the peripheral lymphoid organs. The ability of the human distal promoter to function appropriately in transgenic mice is consistent with the strong similarity observed between the mouse and human distal promoter sequences. With the exception of a single short interval that serves as a target for binding of nuclear factors, significant sequence similarity is not seen when the distal and proximal promoter sequences are compared. Hence, developmentally regulated, lineage-specific transcription of the lck gene is mediated by distinct promoter sequences that appear to be capable of functioning independently.


2006 ◽  
Vol 140 (2) ◽  
pp. 211-220 ◽  
Author(s):  
Masahiko Kanehira ◽  
Tomonori Kaifu ◽  
Kozue Maya ◽  
Mitsuji Kaji ◽  
Akira Nakamura ◽  
...  

1991 ◽  
Vol 12 (11) ◽  
pp. 2059-2062 ◽  
Author(s):  
Kimi Araki ◽  
Okio Hino ◽  
Jun-ichi Miyazaki ◽  
Ken-ichi Yamamura

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