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TRIM32 and Malin in Neurological and Neuromuscular Rare Diseases.

Lorena KumarasingheLu XiongMaria Adelaida Garcia-GimenoElisa LazzariPascual SanzGermana Meroni
Published in: Cells (2021)
Tripartite motif (TRIM) proteins are RING E3 ubiquitin ligases defined by a shared domain structure. Several of them are implicated in rare genetic diseases, and mutations in TRIM32 and TRIM-like malin are associated with Limb-Girdle Muscular Dystrophy R8 and Lafora disease, respectively. These two proteins are evolutionary related, share a common ancestor, and both display NHL repeats at their C-terminus. Here, we revmniew the function of these two related E3 ubiquitin ligases discussing their intrinsic and possible common pathophysiological pathways.
Keyphrases
  • muscular dystrophy
  • genome wide
  • small molecule
  • duchenne muscular dystrophy
  • cerebral ischemia