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m6A mRNA Methylation Regulates Human β-Cell Biology in Physiological States and in Type 2 Diabetes.

Nature metabolism | 2019

The regulation of islet cell biology is critical for glucose homeostasis1.N6 -methyladenosine (m6A) is the most abundant internal messenger RNA (mRNA) modification in mammals2. Here we report that the m6A landscape segregates human type 2 diabetes (T2D) islets from controls significantly better than the transcriptome and that m6A is vital for β-cell biology. m6A-sequencing in human T2D islets reveals several hypomethylated transcripts involved in cell-cycle progression, insulin secretion, and the Insulin/IGF1-AKT-PDX1 pathway. Depletion of m6A levels in EndoC-βH1 induces cell-cycle arrest and impairs insulin secretion by decreasing AKT phosphorylation and PDX1 protein levels. β-cell specific Mettl14 knock-out mice, which display reduced m6A levels, mimic the islet phenotype in human T2D with early diabetes onset and mortality due to decreased β-cell proliferation and insulin degranulation. Our data underscore the significance of RNA methylation in regulating human β-cell biology, and provide a rationale for potential therapeutic targeting of m6A modulators to preserve β-cell survival and function in diabetes.

Pubmed ID: 31867565 RIS Download

Associated grants

  • Agency: NHGRI NIH HHS, United States
    Id: RM1 HG008935
  • Agency: NIDDK NIH HHS, United States
    Id: P30 DK036836
  • Agency: NIDDK NIH HHS, United States
    Id: UC4 DK116278
  • Agency: NIDDK NIH HHS, United States
    Id: R01 DK067536
  • Agency: Howard Hughes Medical Institute, United States
  • Agency: NIDDK NIH HHS, United States
    Id: R01 DK117639
  • Agency: NIDDK NIH HHS, United States
    Id: R01 DK103215

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