Activation of FoxM1 during G2 requires cyclin A/Cdk-dependent relief of autorepression by the FoxM1 N-terminal domain.

The Forkhead transcription factor FoxM1 is an important regulator of gene expression during the G(2) phase. Here, we show that FoxM1 transcriptional activity is kept low during G(1)/S through the action of its N-terminal autoinhibitory domain. We found that cyclin A/cdk complexes are required to pho...

Full description

Bibliographic Details
Main Authors: Laoukili, J, Alvarez, M, Meijer, L, Stahl, M, Mohammed, S, Kleij, L, Heck, A, Medema, R
Format: Journal article
Language:English
Published: 2008
_version_ 1797106143674236928
author Laoukili, J
Alvarez, M
Meijer, L
Stahl, M
Mohammed, S
Kleij, L
Heck, A
Medema, R
author_facet Laoukili, J
Alvarez, M
Meijer, L
Stahl, M
Mohammed, S
Kleij, L
Heck, A
Medema, R
author_sort Laoukili, J
collection OXFORD
description The Forkhead transcription factor FoxM1 is an important regulator of gene expression during the G(2) phase. Here, we show that FoxM1 transcriptional activity is kept low during G(1)/S through the action of its N-terminal autoinhibitory domain. We found that cyclin A/cdk complexes are required to phosphorylate and activate FoxM1 during G(2) phase. Deletion of the N-terminal autoinhibitory region of FoxM1 generates a mutant of FoxM1 (DeltaN-FoxM1) that is active throughout the cell cycle and no longer depends on cyclin A for its activation. Mutation of two cyclin A/cdk sites in the C-terminal transactivation domain leads to inactivation of full-length FoxM1 but does not affect the transcriptional activity of the DeltaN-FoxM1 mutant. We show that the intramolecular interaction of the N- and C-terminal domains depends on two RXL/LXL motifs in the C terminus of FoxM1. Mutation of these domains leads to a similar gain of function as deletion of the N-terminal repressor domain. Based on these observations we propose a model in which FoxM1 is kept inactive during the G(1)/S transition through the action of the N-terminal autorepressor domain, while phosphorylation by cyclin A/cdk complexes during G(2) results in relief of inhibition by the N terminus, allowing activation of FoxM1-mediated gene transcription.
first_indexed 2024-03-07T06:57:32Z
format Journal article
id oxford-uuid:fea0d45e-dbc5-49c1-a182-acea2f2e6fd3
institution University of Oxford
language English
last_indexed 2024-03-07T06:57:32Z
publishDate 2008
record_format dspace
spelling oxford-uuid:fea0d45e-dbc5-49c1-a182-acea2f2e6fd32022-03-27T13:38:10ZActivation of FoxM1 during G2 requires cyclin A/Cdk-dependent relief of autorepression by the FoxM1 N-terminal domain.Journal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:fea0d45e-dbc5-49c1-a182-acea2f2e6fd3EnglishSymplectic Elements at Oxford2008Laoukili, JAlvarez, MMeijer, LStahl, MMohammed, SKleij, LHeck, AMedema, RThe Forkhead transcription factor FoxM1 is an important regulator of gene expression during the G(2) phase. Here, we show that FoxM1 transcriptional activity is kept low during G(1)/S through the action of its N-terminal autoinhibitory domain. We found that cyclin A/cdk complexes are required to phosphorylate and activate FoxM1 during G(2) phase. Deletion of the N-terminal autoinhibitory region of FoxM1 generates a mutant of FoxM1 (DeltaN-FoxM1) that is active throughout the cell cycle and no longer depends on cyclin A for its activation. Mutation of two cyclin A/cdk sites in the C-terminal transactivation domain leads to inactivation of full-length FoxM1 but does not affect the transcriptional activity of the DeltaN-FoxM1 mutant. We show that the intramolecular interaction of the N- and C-terminal domains depends on two RXL/LXL motifs in the C terminus of FoxM1. Mutation of these domains leads to a similar gain of function as deletion of the N-terminal repressor domain. Based on these observations we propose a model in which FoxM1 is kept inactive during the G(1)/S transition through the action of the N-terminal autorepressor domain, while phosphorylation by cyclin A/cdk complexes during G(2) results in relief of inhibition by the N terminus, allowing activation of FoxM1-mediated gene transcription.
spellingShingle Laoukili, J
Alvarez, M
Meijer, L
Stahl, M
Mohammed, S
Kleij, L
Heck, A
Medema, R
Activation of FoxM1 during G2 requires cyclin A/Cdk-dependent relief of autorepression by the FoxM1 N-terminal domain.
title Activation of FoxM1 during G2 requires cyclin A/Cdk-dependent relief of autorepression by the FoxM1 N-terminal domain.
title_full Activation of FoxM1 during G2 requires cyclin A/Cdk-dependent relief of autorepression by the FoxM1 N-terminal domain.
title_fullStr Activation of FoxM1 during G2 requires cyclin A/Cdk-dependent relief of autorepression by the FoxM1 N-terminal domain.
title_full_unstemmed Activation of FoxM1 during G2 requires cyclin A/Cdk-dependent relief of autorepression by the FoxM1 N-terminal domain.
title_short Activation of FoxM1 during G2 requires cyclin A/Cdk-dependent relief of autorepression by the FoxM1 N-terminal domain.
title_sort activation of foxm1 during g2 requires cyclin a cdk dependent relief of autorepression by the foxm1 n terminal domain
work_keys_str_mv AT laoukilij activationoffoxm1duringg2requirescyclinacdkdependentreliefofautorepressionbythefoxm1nterminaldomain
AT alvarezm activationoffoxm1duringg2requirescyclinacdkdependentreliefofautorepressionbythefoxm1nterminaldomain
AT meijerl activationoffoxm1duringg2requirescyclinacdkdependentreliefofautorepressionbythefoxm1nterminaldomain
AT stahlm activationoffoxm1duringg2requirescyclinacdkdependentreliefofautorepressionbythefoxm1nterminaldomain
AT mohammeds activationoffoxm1duringg2requirescyclinacdkdependentreliefofautorepressionbythefoxm1nterminaldomain
AT kleijl activationoffoxm1duringg2requirescyclinacdkdependentreliefofautorepressionbythefoxm1nterminaldomain
AT hecka activationoffoxm1duringg2requirescyclinacdkdependentreliefofautorepressionbythefoxm1nterminaldomain
AT medemar activationoffoxm1duringg2requirescyclinacdkdependentreliefofautorepressionbythefoxm1nterminaldomain