Document Detail


The c-Myc-regulated microRNA-17~92 (miR-17~92) and miR-106a~363 clusters target hCYP19A1 and hGCM1 to inhibit human trophoblast differentiation.
MedLine Citation:
PMID:  23438603     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Mononuclear cytotrophoblasts of the human placenta proliferate rapidly, subsequently fuse, and differentiate to form multinucleated syncytiotrophoblast with induction of aromatase (hCYP19A1) and chorionic gonadotropin (hCGβ) expression. Using microarray analysis, we identified members of the miR-17~92 cluster and its paralogs, miR-106a~363 and miR-106b~25, that are significantly downregulated upon syncytiotrophoblast differentiation. Interestingly, miR-19b and miR-106a directly targeted hCYP19A1 expression, while miR-19b also targeted human GCM1 (hGCM1), a transcription factor critical for mouse labyrinthine trophoblast development. Overexpression of these microRNAs (miRNAs) impaired syncytiotrophoblast differentiation. hGCM1 knockdown decreased hCYP19A1 and hCGβ expression, substantiating its important role in human trophoblast differentiation. Expression of the c-Myc proto-oncogene was increased in proliferating cytotrophoblasts compared to that in differentiated syncytiotrophoblast. Moreover, c-Myc overexpression upregulated miR-17~92 and inhibited hCYP19A1 and hCGβ expression. Binding of endogenous c-Myc to genomic regions upstream of the miR-17~92 and miR-106a~363 clusters in cytotrophoblasts dramatically decreased upon syncytiotrophoblast differentiation. Intriguingly, we observed higher levels of miR-106a and -19b and lower aromatase and hGCM1 expression in placentas from preeclamptic women than in placentas from gestation-matched normotensive women. Our findings reveal that c-Myc-regulated members of the miR-17~92 and miR-106a~363 clusters inhibit trophoblast differentiation by repressing hGCM1 and hCYP19A1 and suggest that aberrant regulation of these miRNAs may contribute to the pathogenesis of preeclampsia.
Authors:
Premlata Kumar; Yanmin Luo; Carmen Tudela; James M Alexander; Carole R Mendelson
Related Documents :
7942283 - The mammalian uv response: mechanism of dna damage induced gene expression.
17588603 - Dimer composition and promoter context contribute to functional cooperation between ap-...
19185603 - Mcp-1 involvement in glial differentiation of neuroprogenitor cells through app signaling.
Publication Detail:
Type:  Journal Article; Research Support, N.I.H., Extramural     Date:  2013-02-25
Journal Detail:
Title:  Molecular and cellular biology     Volume:  33     ISSN:  1098-5549     ISO Abbreviation:  Mol. Cell. Biol.     Publication Date:  2013 May 
Date Detail:
Created Date:  2013-04-08     Completed Date:  2013-05-29     Revised Date:  2014-03-19    
Medline Journal Info:
Nlm Unique ID:  8109087     Medline TA:  Mol Cell Biol     Country:  United States    
Other Details:
Languages:  eng     Pagination:  1782-96     Citation Subset:  IM    
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Descriptor/Qualifier:
Aromatase / genetics*,  metabolism
Base Sequence
Cell Differentiation
Cells, Cultured
Female
Gene Expression Regulation, Developmental
Humans
MicroRNAs / genetics*,  metabolism
Nuclear Proteins / genetics*,  metabolism
Placenta / metabolism
Pre-Eclampsia / genetics
Pregnancy
Proto-Oncogene Proteins c-myc / metabolism*
Transcription Factors / genetics*,  metabolism
Trophoblasts / cytology*,  metabolism
Grant Support
ID/Acronym/Agency:
R01 DK031206/DK/NIDDK NIH HHS; R01 DK031206/DK/NIDDK NIH HHS
Chemical
Reg. No./Substance:
0/GCM1 protein, human; 0/MIRN106 microRNA, human; 0/MIRN17-92 microRNA, human; 0/MIRN19 microRNA, human; 0/MIRN363 microRNA, human; 0/MicroRNAs; 0/Nuclear Proteins; 0/Proto-Oncogene Proteins c-myc; 0/Transcription Factors; EC 1.14.14.1/Aromatase; EC 1.14.14.1/CYP19A1 protein, human
Comments/Corrections

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


Previous Document:  ATM- and ATR-mediated phosphorylation of XRCC3 regulates DNA double-strand break-induced checkpoint ...
Next Document:  BRG1 is required for formation of senescence-associated heterochromatin foci induced by oncogenic RA...