The human CD6 gene is transcriptionally regulated by RUNX and Ets transcription factors in T cells

被引:18
作者
Arman, Monica [1 ]
Aguilera-Montilla, Noemi [2 ]
Mas, Virginia [1 ]
Puig-Kroeger, Amaya [2 ]
Pignatelli, Miguel [3 ]
Guigo, Roderic [4 ]
Corbi, Angel-Luis [2 ]
Lozano, Francisco [1 ]
机构
[1] Univ Barcelona, Fac Med, Inst Invest Biomed August Pi & Sunyer, Hosp Clin,Serv Immunol, Barcelona 08036, Spain
[2] CSIC, Ctr Invest Biol, Dept Fisiopatol Mol & Celular, E-28040 Madrid, Spain
[3] Univ Barcelona, Fac Biol, Dept Genet, E-08028 Barcelona, Spain
[4] Univ Pompeu Fabra, Inst Municipal Invest Med, Res Grp Biomed Informat, Barcelona 08003, Spain
关键词
Human CD6; T cells; Gene regulation; Transcription factors; RUNX; Ets; CORE-BINDING-FACTOR; COLONY-STIMULATING FACTOR; ANTI-CD6; MONOCLONAL-ANTIBODY; PROMOTER ACTIVITY; AUTO-INHIBITION; FUSION PROTEIN; DNA-BINDING; GM-CSF; EXPRESSION; ACTIVATION;
D O I
10.1016/j.molimm.2009.04.018
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
CD6 is a lymphocyte surface receptor involved in lymphocyte activation and differentiation processes that is constitutively expressed on developing and mature T cells and on the B1a cells. To define the molecular basis for the tissue-specific expression of CD6 we have identified the transcription factors that control the activity of the proximal regulatory region of the human CD6 gene. The TATA-less CD6 promoter contains multiple transcriptional start sites, and its preferential activity in human T lymphocytes is dependent on RUNX- and Ets-binding sites located within a highly conserved region. RUNX and Ets-1 factors transactivated the CD6 promoter through recognition of the -215 and -230 binding sites, respectively. Chromatin immunoprecipitation assays revealed that RUNX1 constitutively occupies the CD6 promoter in vivo, and knockdown experiments demonstrated that the steady-state level of CD6 mRNA is dependent on the expression of RUNX1, RUNX3 and Ets-1 transcription factors. Therefore, RUNX1/3 and Ets1 control the expression of CD6 in human T lymphocytes, thus expanding the range of T-cell specific and developmentally regulated lymphocyte gene targets involved in T-cell activation and differentiation. (C) 2009 Elsevier Ltd. All rights reserved.
引用
收藏
页码:2226 / 2235
页数:10
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