TY - JOUR
T1 - The selector gene Pax7 dictates alternate pituitary cell fates through its pioneer action on chromatin remodeling
AU - Budry, L.
AU - Balsalobre, A.
AU - Gauthier, Y.
AU - Khetchoumian, K.
AU - L'Honore, A.
AU - Vallette-Kasic, S.
AU - Brue, T
AU - Figarella-Branger, D.
AU - Meij, B.P.
AU - Drouin, J.
PY - 2012
Y1 - 2012
N2 - Genes Dev. 2012 Oct 15;26(20):2299-310. doi: 10.1101/gad.200436.112.
The selector gene Pax7 dictates alternate pituitary cell fates through its pioneer action on chromatin remodeling.
Budry L, Balsalobre A, Gauthier Y, Khetchoumian K, L'honoré A, Vallette S, Brue T, Figarella-Branger D, Meij B, Drouin J.
Source
Laboratoire de Génétique Moléculaire, Institut de Recherches Cliniques de Montréal (IRCM), Montréal, Quebec H2W 1R7, Canada;
Abstract
The anterior and intermediate lobes of the pituitary gland derive from the surface ectoderm. They provide a simple system to assess mechanisms of developmental identity established by tissue determinants. Each lobe contains a lineage expressing the hormone precursor pro-opiomelanocortin (POMC): the corticotropes and melanotropes. The T-box transcription factor Tpit controls terminal differentiation of both lineages. We now report on the unique role of Pax7 as a selector of intermediate lobe and melanotrope identity. Inactivation of the Pax7 gene results in loss of melanotrope gene expression and derepression of corticotrope genes. Pax7 acts by remodeling chromatin and allowing Tpit binding to a new subset of enhancers for activation of melanotrope-specific genes. Thus, the selector function of Pax7 is exerted through pioneer transcription factor activity. Genome-wide, the Pax7 pioneer activity is preferentially associated with composite binding sites that include paired and homeodomain motifs. Pax7 expression is conserved in human and dog melanotropes and defines two subtypes of pituitary adenomas causing Cushing's disease. In summary, expression of Pax7 provides a unique tissue identity to the pituitary intermediate lobe that alters Tpit-driven differentiation through pioneer and classical transcription factor activities.
PMID:
23070814
[PubMed - in process]
PMCID:
PMC3475802
[Available on 2013/4/15]
AB - Genes Dev. 2012 Oct 15;26(20):2299-310. doi: 10.1101/gad.200436.112.
The selector gene Pax7 dictates alternate pituitary cell fates through its pioneer action on chromatin remodeling.
Budry L, Balsalobre A, Gauthier Y, Khetchoumian K, L'honoré A, Vallette S, Brue T, Figarella-Branger D, Meij B, Drouin J.
Source
Laboratoire de Génétique Moléculaire, Institut de Recherches Cliniques de Montréal (IRCM), Montréal, Quebec H2W 1R7, Canada;
Abstract
The anterior and intermediate lobes of the pituitary gland derive from the surface ectoderm. They provide a simple system to assess mechanisms of developmental identity established by tissue determinants. Each lobe contains a lineage expressing the hormone precursor pro-opiomelanocortin (POMC): the corticotropes and melanotropes. The T-box transcription factor Tpit controls terminal differentiation of both lineages. We now report on the unique role of Pax7 as a selector of intermediate lobe and melanotrope identity. Inactivation of the Pax7 gene results in loss of melanotrope gene expression and derepression of corticotrope genes. Pax7 acts by remodeling chromatin and allowing Tpit binding to a new subset of enhancers for activation of melanotrope-specific genes. Thus, the selector function of Pax7 is exerted through pioneer transcription factor activity. Genome-wide, the Pax7 pioneer activity is preferentially associated with composite binding sites that include paired and homeodomain motifs. Pax7 expression is conserved in human and dog melanotropes and defines two subtypes of pituitary adenomas causing Cushing's disease. In summary, expression of Pax7 provides a unique tissue identity to the pituitary intermediate lobe that alters Tpit-driven differentiation through pioneer and classical transcription factor activities.
PMID:
23070814
[PubMed - in process]
PMCID:
PMC3475802
[Available on 2013/4/15]
U2 - 10.1101/gad.200436.112
DO - 10.1101/gad.200436.112
M3 - Article
SN - 0890-9369
VL - 26
SP - 2299
EP - 2310
JO - Genes and Development
JF - Genes and Development
IS - 20
ER -