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IDENTIFICATION OF THE TAX INTERACTION REGION OF SERUM RESPONSE FACTOR THAT MEDIATES THE ABERRANT INDUCTION OF IMMEDIATE-EARLY GENES THROUGH CARG BOXES BY HTLV-I TAX
被引:0
|作者:
FUJII, M
CHUHJO, T
MINAMINO, T
MASAAKI, N
MIYAMOTO, K
SEIKI, M
机构:
[1] KANAZAWA UNIV,CANC RES INST,DEPT MOLEC ONCOL & VIROL,KANAZAWA,ISHIKAWA 920,JAPAN
[2] KANAZAWA UNIV,DEPT INTERNAL MED 3,KANAZAWA,ISHIKAWA 920,JAPAN
[3] HOKURIKU UNIV,SCH PHARM,DEV MED RES LAB,KANAZAWA,ISHIKAWA 920,JAPAN
来源:
关键词:
HTLV-I;
TAX;
SRF;
TRANSCRIPTION;
D O I:
暂无
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:
Tax of human T-cell leukemia virus type I (HTLV-I) activates transcription at a CArG box of various immediate early genes such as the proto-oncogene c-fos. To do this, Tax does not directly bind to the CArG box, but instead binds to the CArG binding factor SRF. In this study, we investigated the domain of SRF required for the activation by Tax and studied the role of this domain on transcriptional regulation at the CArG box. Using a fusion protein of SRF with a yeast transcription factor GAL4, the 14 amino acid (aa) portion (aa 422-435) of SRF was identified as the domain required for Tax activation [Tax-responsive region of SRF (TRRS)]. By means of a two hybrid system, we showed that TRRS was essential for the interaction of SRF with Tax in vivo. The over-expression of SRF with a deletion of TRRS inhibited the Tax activation at the CArG box. Thus, TRRS is the domain of SRF that is essential for Tax activation at the CArG box. Unlike to Tax activation, TRRS was not required for TPA (12-o-tetradecanoylphobol-13-acetate) induction at the CArG box, but a TRRS deletion enhanced the basal activity at the CArG box both under serum-starved and TPA-stimulated conditions. These results suggest that TRRS negatively regulates the transcriptional activation function of SRF, and consequently contributes to the low basal activity at the CArG box before TPA induction.
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页码:7 / 14
页数:8
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