RGD Reference Report - HIF-KDM3A-MMP12 regulatory circuit ensures trophoblast plasticity and placental adaptations to hypoxia. - Rat Genome Database

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HIF-KDM3A-MMP12 regulatory circuit ensures trophoblast plasticity and placental adaptations to hypoxia.

Authors: Chakraborty, Damayanti  Cui, Wei  Rosario, Gracy X  Scott, Regan L  Dhakal, Pramod  Renaud, Stephen J  Tachibana, Makoto  Rumi, M A Karim  Mason, Clifford W  Krieg, Adam J  Soares, Michael J 
Citation: Chakraborty D, etal., Proc Natl Acad Sci U S A. 2016 Nov 15;113(46):E7212-E7221. Epub 2016 Nov 2.
RGD ID: 12910498
Pubmed: PMID:27807143   (View Abstract at PubMed)
PMCID: PMC5135375   (View Article at PubMed Central)
DOI: DOI:10.1073/pnas.1612626113   (Journal Full-text)

The hemochorial placenta develops from the coordinated multilineage differentiation of trophoblast stem (TS) cells. An invasive trophoblast cell lineage remodels uterine spiral arteries, facilitating nutrient flow, failure of which is associated with pathological conditions such as preeclampsia, intrauterine growth restriction, and preterm birth. Hypoxia plays an instructive role in influencing trophoblast cell differentiation and regulating placental organization. Key downstream hypoxia-activated events were delineated using rat TS cells and tested in vivo, using trophoblast-specific lentiviral gene delivery and genome editing. DNA microarray analyses performed on rat TS cells exposed to ambient or low oxygen and pregnant rats exposed to ambient or hypoxic conditions showed up-regulation of genes characteristic of an invasive/vascular remodeling/inflammatory phenotype. Among the shared up-regulated genes was matrix metallopeptidase 12 (MMP12). To explore the functional importance of MMP12 in trophoblast cell-directed spiral artery remodeling, we generated an Mmp12 mutant rat model using transcription activator-like nucleases-mediated genome editing. Homozygous mutant placentation sites showed decreased hypoxia-dependent endovascular trophoblast invasion and impaired trophoblast-directed spiral artery remodeling. A link was established between hypoxia/HIF and MMP12; however, evidence did not support Mmp12 as a direct target of HIF action. Lysine demethylase 3A (KDM3A) was identified as mediator of hypoxia/HIF regulation of Mmp12 Knockdown of KDM3A in rat TS cells inhibited the expression of a subset of the hypoxia-hypoxia inducible factor (HIF)-dependent transcripts, including Mmp12, altered H3K9 methylation status, and decreased hypoxia-induced trophoblast cell invasion in vitro and in vivo. The hypoxia-HIF-KDM3A-MMP12 regulatory circuit is conserved and facilitates placental adaptations to environmental challenges.

Gene Ontology Annotations    Click to see Annotation Detail View

Biological Process
TermQualifierEvidenceWithReferenceNotesSourceOriginal Reference(s)
regulation of trophoblast cell migration  IMP 12910498 RGD 
response to hypoxia  IEP 12910498 RGD 

Phenotype Annotations    Click to see Annotation Detail View

Mammalian Phenotype

TermQualifierEvidenceWithReferenceNotesSourceOriginal Reference(s)
abnormal uterine spiral artery remodeling  IMP 12910498 RGD 
decreased fetal weight  IMP 12910498; 12910498; 12910498; 12910498; 12910498 RGD 
decreased litter size  IMP 12910498; 12910498; 12910498 RGD 
Objects Annotated

Genes (Rattus norvegicus)
Mmp12  (matrix metallopeptidase 12)
Mmp12em1Soar  (matrix metallopeptidase 12; TALEN induced mutant 1,Soar)
Mmp12em2Soar  (matrix metallopeptidase 12; TALEN induced mutant 2,Soar)

SD-Mmp12em1Soar  (NA)
SD-Mmp12em2Soar  (NA)

Additional Information