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RNA Exosome Complex-Mediated Control of Redox Status in Pluripotent Stem Cells
Author(s) -
Maria Skamagki,
Cheng Zhang,
Christian Roß,
Aparna Ananthanarayanan,
Zhong Liu,
Quanhua Mu,
Uttiya Basu,
Jiguang Wang,
Rui Zhao,
Hu Li,
Kitai Kim
Publication year - 2017
Publication title -
stem cell reports
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.207
H-Index - 76
ISSN - 2213-6711
DOI - 10.1016/j.stemcr.2017.08.024
Subject(s) - biology , exosome complex , induced pluripotent stem cell , microbiology and biotechnology , exosome , gene expression , rna , dna damage , stem cell , microrna , gene , dna , microvesicles , non coding rna , biochemistry , embryonic stem cell
The RNA exosome complex targets AU-rich element (ARE)-containing mRNAs in eukaryotic cells. We identified a transcription factor, ZSCAN10, which binds to the promoters of multiple RNA exosome complex subunits in pluripotent stem cells to maintain subunit gene expression. We discovered that induced pluripotent stem cell clones generated from aged tissue donors (A-iPSC) show poor expression of ZSCAN10, leading to poor RNA exosome complex expression, and a subsequent elevation in ARE-containing RNAs, including glutathione peroxidase 2 (Gpx2). Excess GPX2 leads to excess glutathione-mediated reactive oxygen species scavenging activity that blunts the DNA damage response and apoptosis. Expression of ZSCAN10 in A-iPSC recovers RNA exosome gene expression, the DNA damage response, and apoptosis. These findings reveal the central role of ZSCAN10 and the RNA exosome complex in maintaining pluripotent stem cell redox status to support a normal DNA damage response.

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