TY - JOUR
T1 - Hypoxia. cross talk between oxygen sensing and the cell cycle machinery
AU - Semenza, Gregg L.
PY - 2011/9
Y1 - 2011/9
N2 - A fundamental physiological property of mammalian cells is the regulation of proliferation according to O 2 availability. Progression through the cell cycle is inhibited under hypoxic conditions in many, but not all, cell types, and this G1 arrest is dependent on hypoxia-inducible factor (HIF) 1α. Components of the hexameric MCM helicase, which binds to replication origins before the onset of DNA synthesis, are present in large excess in mammalian cells relative to origins, suggesting that they may have additional functions. Screens for (HIF) 1α interacting proteins revealed that MCM7 binds to the amino-terminal PER-SIMARNT (PAS) domain of (HIF) 1α and stimulates prolyl hydroxylationdependent ubiquitination and degradation of (HIF) 1α, whereas MCM3 binds to the carboxyl terminus of (HIF) 1α and enhances asparaginyl hydroxylation-dependent inhibition of (HIF) 1α transactivation domain function. Thus MCM proteins inhibit HIF activity via two distinct O 2-dependent mechanisms. Under prolonged hypoxic conditions, MCM mRNA expression is inhibited in a (HIF) 1α -dependent manner. Thus HIF and MCM proteins act in a mutually antagonistic manner, providing a novel molecular mechanism for homeostatic regulation of cell proliferation based on the relative levels of these proteins.
AB - A fundamental physiological property of mammalian cells is the regulation of proliferation according to O 2 availability. Progression through the cell cycle is inhibited under hypoxic conditions in many, but not all, cell types, and this G1 arrest is dependent on hypoxia-inducible factor (HIF) 1α. Components of the hexameric MCM helicase, which binds to replication origins before the onset of DNA synthesis, are present in large excess in mammalian cells relative to origins, suggesting that they may have additional functions. Screens for (HIF) 1α interacting proteins revealed that MCM7 binds to the amino-terminal PER-SIMARNT (PAS) domain of (HIF) 1α and stimulates prolyl hydroxylationdependent ubiquitination and degradation of (HIF) 1α, whereas MCM3 binds to the carboxyl terminus of (HIF) 1α and enhances asparaginyl hydroxylation-dependent inhibition of (HIF) 1α transactivation domain function. Thus MCM proteins inhibit HIF activity via two distinct O 2-dependent mechanisms. Under prolonged hypoxic conditions, MCM mRNA expression is inhibited in a (HIF) 1α -dependent manner. Thus HIF and MCM proteins act in a mutually antagonistic manner, providing a novel molecular mechanism for homeostatic regulation of cell proliferation based on the relative levels of these proteins.
KW - Hypoxia-inducible factor
KW - MCM proteins
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U2 - 10.1152/ajpcell.00176.2011
DO - 10.1152/ajpcell.00176.2011
M3 - Article
C2 - 21677261
AN - SCOPUS:80052200933
SN - 0363-6143
VL - 301
SP - C550-C552
JO - American Journal of Physiology - Cell Physiology
JF - American Journal of Physiology - Cell Physiology
IS - 3
ER -