A Genetic Interaction Map of Insulin Production Identifies Mfi as an Inhibitor of Mitochondrial Fission

Endocrinology. 2018 Sep 1;159(9):3321-3330. doi: 10.1210/en.2018-00426.

Abstract

Insulin production by the pancreatic β cell is critical for the glucose homeostasis of the whole organism. Although the transcription factors required for insulin production are known, the upstream pathways that control insulin production are less clear. To further elucidate this regulatory network, we created a genetic interaction map of insulin production by performing ∼20,000 pairwise RNA interference knockdowns of insulin promoter regulators. Our map correctly predicted known physical complexes in the electron transport chain and a role for Spry2 in the unfolded protein response. To further validate our map, we used it to predict the function of an unannotated gene encoding a 37-kDa protein with no identifiable domains we have termed mitochondrial fission factor interactor (Mfi). We have shown that Mfi is a binding partner of the mitochondrial fission factor and that Mfi inhibits dynamin-like protein 1 recruitment to mitochondria. Our data provide a resource to understand the regulatory network of insulin promoter activity.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Line
  • Dynamins
  • GTP Phosphohydrolases
  • Gene Regulatory Networks
  • Humans
  • Insulin / biosynthesis*
  • Insulin / genetics
  • Insulin-Secreting Cells / metabolism*
  • Intracellular Signaling Peptides and Proteins
  • Membrane Proteins / metabolism
  • Mice
  • Microtubule-Associated Proteins
  • Mitochondria / metabolism*
  • Mitochondrial Dynamics / genetics*
  • Mitochondrial Proteins / metabolism
  • Promoter Regions, Genetic / genetics
  • Unfolded Protein Response

Substances

  • Insulin
  • Intracellular Signaling Peptides and Proteins
  • Membrane Proteins
  • Mff protein, human
  • Microtubule-Associated Proteins
  • Mitochondrial Proteins
  • SPRY2 protein, human
  • GTP Phosphohydrolases
  • DNM1L protein, human
  • Dynamins