MCM Proteins Are Negative Regulators of Hypoxia-Inducible Factor 1

Maimon E. Hubbi, Weibo Luo, Jin H. Baek, Gregg L. Semenza

Research output: Contribution to journalArticle

50 Citations (Scopus)

Abstract

MCM proteins are components of a DNA helicase that plays an essential role in DNA replication and cell proliferation. However, MCM proteins are present in excess relative to origins of replication, suggesting they may serve other functions. Decreased proliferation is a fundamental physiological response to hypoxia in many cell types, and hypoxia-inducible factor 1 (HIF-1) has been implicated in this process. Here, we demonstrate that multiple MCM proteins bind directly to the HIF-1α subunit and synergistically inhibit HIF-1 transcriptional activity via distinct O2-dependent mechanisms. MCM3 inhibits transactivation domain function, whereas MCM7 enhances HIF-1α ubiquitination and proteasomal degradation. HIF-1 activity decreases when quiescent cells re-enter the cell cycle, and this effect is MCM dependent. Exposure to hypoxia leads to MCM2-7 downregulation in diverse cell types. These studies reveal a function of MCM proteins apart from their DNA helicase activity and establish a direct link between HIF-1 and the cell-cycle machinery.

Original languageEnglish (US)
Pages (from-to)700-712
Number of pages13
JournalMolecular Cell
Volume42
Issue number5
DOIs
StatePublished - Jun 10 2011

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Hypoxia-Inducible Factor 1
DNA Helicases
Proteins
Cell Cycle
Cell Hypoxia
Replication Origin
Ubiquitination
DNA Replication
Transcriptional Activation
Down-Regulation
Cell Proliferation

ASJC Scopus subject areas

  • Molecular Biology
  • Cell Biology

Cite this

MCM Proteins Are Negative Regulators of Hypoxia-Inducible Factor 1. / Hubbi, Maimon E.; Luo, Weibo; Baek, Jin H.; Semenza, Gregg L.

In: Molecular Cell, Vol. 42, No. 5, 10.06.2011, p. 700-712.

Research output: Contribution to journalArticle

Hubbi, Maimon E. ; Luo, Weibo ; Baek, Jin H. ; Semenza, Gregg L. / MCM Proteins Are Negative Regulators of Hypoxia-Inducible Factor 1. In: Molecular Cell. 2011 ; Vol. 42, No. 5. pp. 700-712.
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