miR-93 regulates Msk2-mediated chromatin remodelling in diabetic nephropathy
Shawn S. Badal,
Yin Wang,
Jianyin Long,
David L. Corcoran,
Benny H. Chang,
Luan D. Truong,
Yashpal S. Kanwar,
Paul A. Overbeek and
Farhad R. Danesh ()
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Shawn S. Badal: Section of Nephrology, The University of Texas MD Anderson Cancer Center
Yin Wang: Section of Nephrology, The University of Texas MD Anderson Cancer Center
Jianyin Long: Section of Nephrology, The University of Texas MD Anderson Cancer Center
David L. Corcoran: Center for Genomic and Computational Biology, Duke University
Benny H. Chang: Baylor College of Medicine
Luan D. Truong: Houston Methodist Hospital
Yashpal S. Kanwar: Feinberg School of Medicine, Northwestern University
Paul A. Overbeek: Baylor College of Medicine
Farhad R. Danesh: Section of Nephrology, The University of Texas MD Anderson Cancer Center
Nature Communications, 2016, vol. 7, issue 1, 1-15
Abstract:
Abstract How the kidney responds to the metabolic cues from the environment remains a central question in kidney research. This question is particularly relevant to the pathogenesis of diabetic nephropathy (DN) in which evidence suggests that metabolic events in podocytes regulate chromatin structure. Here, we show that miR-93 is a critical metabolic/epigenetic switch in the diabetic milieu linking the metabolic state to chromatin remodelling. Mice with inducible overexpression of a miR-93 transgene exclusively in podocytes exhibit significant improvements in key features of DN. We identify miR-93 as a regulator of nucleosomal dynamics in podocytes. miR-93 has a critical role in chromatin reorganization and progression of DN by modulating its target Msk2, a histone kinase, and its substrate H3S10. These findings implicate a central role for miR-93 in high glucose-induced chromatin remodelling in the kidney, and provide evidence for a previously unrecognized role for Msk2 as a target for DN therapy.
Date: 2016
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Persistent link: https://EconPapers.repec.org/RePEc:nat:natcom:v:7:y:2016:i:1:d:10.1038_ncomms12076
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DOI: 10.1038/ncomms12076
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