z-logo
open-access-imgOpen Access
Roles of old players in the suppression of a new player: networks for the transcriptional control of angiogenesis
Author(s) -
Tetsuro Watabe
Publication year - 2010
Publication title -
the journal of biochemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.28
H-Index - 115
eISSN - 1756-2651
pISSN - 0021-924X
DOI - 10.1093/jb/mvq146
Subject(s) - angiogenesis , transcription factor , microbiology and biotechnology , basic helix loop helix , transcription (linguistics) , vascular endothelial growth factor , in vitro , in vivo , biology , cancer research , chemistry , vegf receptors , dna binding protein , genetics , gene , linguistics , philosophy
During the formation of blood vessels, Id1, a member of the helix-loop-helix (HLH) family, and TAL1/SCL, a basic HLH (bHLH) transcription factor, play important roles in the activation of endothelial cells. Recent reports revealed that E2-2, another bHLH transcription factor, inhibits angiogenesis in vitro and in vivo by suppressing the expression of vascular endothelial growth factor receptor 2 (VEGFR2). Id1 and TAL1/SCL dimerize with E2-2 and relieve the E2-2-mediated down-regulation of VEGFR2 expression, leading to the activation of endothelial cells. These findings reveal a novel interplay between HLH transcription factors that regulate angiogenesis.

The content you want is available to Zendy users.

Already have an account? Click here to sign in.
Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom