Ontology highlight
ABSTRACT:
SUBMITTER: Perez Millan MI
PROVIDER: S-EPMC4940164 | biostudies-literature | 2016 Jun
REPOSITORIES: biostudies-literature
Pérez Millán María Inés MI Brinkmeier Michelle L ML Mortensen Amanda H AH Camper Sally A SA
eLife 20160628
Mutations in PROP1 are the most common cause of hypopituitarism in humans; therefore, unraveling its mechanism of action is highly relevant from a therapeutic perspective. Our current understanding of the role of PROP1 in the pituitary gland is limited to the repression and activation of the pituitary transcription factor genes Hesx1 and Pou1f1, respectively. To elucidate the comprehensive PROP1-dependent gene regulatory network, we conducted genome-wide analysis of PROP1 DNA binding and effects ...[more]