A miR‐372/let‐7 Axis Regulates Human Germ Versus Somatic Cell Fates. (17th May 2016)

• Record Type: Journal Article
• Authors: Tran, Nam D.; Kissner, Michael; Subramanyam, Deepa; Parchem, Ronald J.; Laird, Diana J.; Blelloch, Robert H.
• Is Part Of: Stem cells. Volume 34:Number 7(2016:Jul.)
• Page Start: 1985
• Page End: 1991
• Publication Date: 2016-05-17
• Subjects: Embryonic stem cells -- Primordial germ cells -- microRNA -- mir‐372 -- let‐7; Cloning -- Periodicals; Clone cells -- Periodicals; Stem cells -- Periodicals; Cell Differentiation -- Periodicals; Cell Division -- Periodicals; Clone Cells -- Periodicals; Hematopoietic Stem Cells -- Periodicals; Stem Cells -- Periodicals; 571.84
• DOI: 10.1002/stem.2378
• Languages: English
• ISSNs: 1066-5099

Abstract

Abstract: The embryonic stem cell cycle (ESCC) and let‐7 families of miRNAs function antagonistically in the switch between mouse embryonic stem cell self‐renewal and somatic differentiation. Here, we report that the human ESCC miRNA miR‐372 and let‐7 act antagonistically in germline differentiation from human embryonic stem cells (hESCs) and human induced pluripotent stem cells (iPSCs). hESC and iPSC‐derived primordial germ cell‐like cells (PGCLCs) expressed high levels of miR‐372 and conversely, somatic cells expressed high levels of let‐7. Manipulation of miRNA levels by introduction of miRNA mimics or knockdown with miRNA sponges demonstrated that miR‐372 promotes whereas let‐7 antagonizes PGCLC differentiation. Knockdown of the individual miR‐372 targets SMARCC1, MECP2, CDKN1, RBL2, RHOC, and TGFBR2 increased PGCLC production, whereas knockdown of the let‐7 targets CMYC and NMYC suppressed PGCLC differentiation. These findings uncover a miR‐372/let‐7 axis regulating human primordial germ cell (PGC) specification. Stem Cells 2016;34:1985–1991 Abstract : Let‐7 and miR‐294 antagonistically regulate somatic versus germline fates through their influence on multiple cellular pathways.