human T-cell leukemia virus-1;
Tax;
ATF-4;
transactivation;
D O I:
10.1038/sj.onc.1201119
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:
The Tax protein of the Human T-cell Leukemia Virus (HTLV) activates the expression of viral mRNA through a three 21 bp repeat enhancer located within the HTLV-1 LTR, Since Tax does not bind to the 21bp DNA repeats directly, it has been speculated that Tax interacts with cellular protein(s) which mediate binding to the enhancer, We employed the yeast two hybrid system to identify host proteins that are potentially relevant to Tax transactivation. We identified a Tax binding protein encoded from a cDNA expression library derived from peripheral blood lymphocytes. The corresponding cDNA has sequence identity with a known transcription factor, activating factor-4 (ATF-4). ATF-4 also binds to GST-Tax fusion protein in vitro. Tax mutants that did not transactivate the HTLV-1 LTR also failed to bind ATF-4. The critical domain for Tax binding resides in a 85 amino acid stretch in the C-terminus of ATF-4, which contains the basic domain and leucine zipper, We further demonstrated that both full length and N-terminal truncated ATF-4 were able to enhance Tax transactivation, Thus, ATF-4 may act as an adapter between Tax and the TRE (Tax responsive element), and play an important role in Tax-mediated transactivation.
机构:
DUKE UNIV, MED CTR,HOWARD HUGHES MED INST,DEPT MED, GENET SECT, DURHAM, NC 27710 USADUKE UNIV, MED CTR,HOWARD HUGHES MED INST,DEPT MED, GENET SECT, DURHAM, NC 27710 USA
机构:
DUKE UNIV, MED CTR,HOWARD HUGHES MED INST,DEPT MED, GENET SECT, DURHAM, NC 27710 USADUKE UNIV, MED CTR,HOWARD HUGHES MED INST,DEPT MED, GENET SECT, DURHAM, NC 27710 USA