Inhibition of the TEF/TEAD transcription factor activity by nuclear calcium and distinct kinase pathways

被引:25
作者
Thompson, M
Andrade, VA
Andrade, SJ
Pusl, T
Ortega, JM
Goes, AM
Leite, MF [1 ]
机构
[1] Univ Fed Minas Gerais, Dept Physiol & Biophys, BR-31270901 Belo Horizonte, MG, Brazil
[2] Univ Fed Minas Gerais, Dept Biochem & Immunol, BR-31270901 Belo Horizonte, MG, Brazil
[3] Univ Munich, Dept Med 2, Grosshadern Clin, D-81377 Munich, Germany
关键词
TEAD; nuclear calcium; cytosolic calcium; kinases;
D O I
10.1016/S0006-291X(02)03024-3
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
Transcription enhancer factor (TEF/TEAD) is a family of four transcription factors that share a common TEA-DNA binding domain and are involved in similar cellular functions, such as cell differentiation and proliferation. All adult tissues express at least one of the four TEAD genes, so this family of transcription factors may be of widespread importance, yet little is known about their regulation. Here we examine the factors that regulate TEAD activity in CHO cells. RT-PCR indicated the presence of TEAD-1, TEAD-3, and both isoforms of TEAD-4, but not TEAD-2. Quantitative measurements showed that TEAD-4 is most abundant, followed by TEAD-3, then TEAD-1. We examined the relative effects of nuclear and cytosolic Ca2+ on TEAD activity, since TEAD proteins are localized to the nucleus and since free Ca2+ within the nucleus selectively regulates transcription in some systems. Chelation of nuclear but not cytosolic Ca2+ increased TEAD activity two times above control. Inhibition of mitogen-activated protein kinase (MAPK) also increased TEAD activity, while cAMP decreased TEAD activity, and protein kinase C had no effect. Together, these results show that nuclear Ca2+, MAPK, and cAMP each negatively regulate the activity of the TEAD transcription factor. (C) 2003 Elsevier Science (USA). All rights reserved.
引用
收藏
页码:267 / 274
页数:8
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