Interaction of ETS-1 and ERGB/FLI-1 proteins with DNA is modulated by spacing between multiple binding sites as well as phosphorylation

被引:0
|
作者
Hodge, DR
Robinson, L
Watson, D
Lautenberger, J
Zhang, XK
Venanzoni, M
Seth, A
机构
[1] UNIV TORONTO, DEPT PATHOL, TORONTO, ON M5S 1B2, CANADA
[2] UNIV TORONTO, MRC, PERIODONTAL PHYSIOL GRP, TORONTO, ON M5S 1B2, CANADA
[3] WOMENS COLL HOSP, MOLEC PATHOL LAB, TORONTO, ON M5S 1B2, CANADA
[4] NCI, MOLEC ONCOL LAB, FREDERICK, MD 21702 USA
[5] PROGRAM RESOURCES INC DYNCORP, FREDERICK, MD 21702 USA
[6] MED UNIV S CAROLINA, CTR MOLEC & STRUCT BIOL, CHARLESTON, SC 29425 USA
关键词
ETS-1; ERGB FL1-1; transcription factors; HIV-1; enhancer; transactivation; EBS palindrome; Cam-KII phosphorylation site; TRANSCRIPTION; COMPLEX; FAMILY; GENE; IDENTIFICATION; PROTOONCOGENE; ACTIVATION; MECHANISM; SEQUENCES; ONCOGENE;
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
ETS is a family of transcription factors that contain a highly conserved ETS DNA binding domain. Various members of the ETS family are expressed in cells of hematopoietic lineage. ETS-1, ETS-2 and ERGB/FLI-1 are expressed at high levels in T-lymphocytes. HIV-1 infects T-cells and it has been shown that its LTR contains binding sites for various transcription factors. In this study we show that the HIV-1 core enhancer is directly regulated by ERGB/FLI-1 protein positively, as well as, negatively, depending upon the presence or absence of accessory factors in different cell types. In addition, we show that the ETS-1 transactivation activity is enhanced upon dephosphorylation of the Calmodulin-dependant Protein Kinase II phosphorylation site located in exon VII. Finally, we demonstrate that the spacing two EBS cores in palindromic or direct play a crucial role in binding of ETS proteins to DNA.
引用
收藏
页码:11 / 18
页数:8
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