Literature DB >> 12055102

TIMAP, a novel CAAX box protein regulated by TGF-beta1 and expressed in endothelial cells.

Wangsen Cao1, Subhendra N Mattagajasingh, Hangxue Xu, Kwanghee Kim, Wolfgang Fierlbeck, Jie Deng, Charles J Lowenstein, Barbara J Ballermann.   

Abstract

Representational difference analysis of the glomerular endothelial cell response to transforming growth factor-beta1 (TGF-beta1) revealed a novel gene, TIMAP (TGF-beta-inhibited membrane-associated protein), which contains 10 exons and maps to human chromosome 20.q11.22. By Northern blot, TIMAP mRNA is highly expressed in all cultured endothelial and hematopoietic cells. The frequency of the TIMAP SAGE tag is much greater in endothelial cell SAGE databases than in nonendothelial cells. Immunofluorescence studies of rat tissues show that anti-TIMAP antibodies localize to vascular endothelium. TGF-beta1 represses TIMAP through a protein synthesis- and histone deacetylase-dependent process. The TIMAP protein contains five ankyrin repeats, a protein phosphatase-1 (PP1)-interacting domain, a COOH-terminal CAAX box, a domain arrangement similar to that of MYPT3, and a PP1 inhibitor. A green fluorescent protein-TIMAP fusion protein localized to the plasma membrane in a CAAX box-dependent fashion. Hence, TIMAP is a novel gene highly expressed in endothelial and hematopoietic cells and regulated by TGF-beta1. On the basis of its domain structure, TIMAP may serve a signaling function, potentially through interaction with PP1.

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Year:  2002        PMID: 12055102     DOI: 10.1152/ajpcell.00442.2001

Source DB:  PubMed          Journal:  Am J Physiol Cell Physiol        ISSN: 0363-6143            Impact factor:   4.249


  14 in total

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Review 3.  Role of myosin light chain phosphatase in cardiac physiology and pathophysiology.

Authors:  Audrey N Chang; Kristine E Kamm; James T Stull
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5.  TIMAP protects endothelial barrier from LPS-induced vascular leakage and is down-regulated by LPS.

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Review 8.  Myosin phosphatase: structure, regulation and function.

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Review 10.  Histone deacetylase 3 (HDAC3) as an important epigenetic regulator of kidney diseases.

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Journal:  J Mol Med (Berl)       Date:  2021-10-26       Impact factor: 4.599

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