Litcius/Paper detail

TRIM32 and Malin in Neurological and Neuromuscular Rare Diseases

Lorena Kumarasinghe, Xiong Lu, Maria Adelaida García-Gimeno, Elisa Lazzari, Pascual Sanz, Germana Meroni

2021Cells16 citationsDOIOpen Access PDF

Abstract

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.

Topics & Concepts

UbiquitinUbiquitin-Protein LigasesUbiquitin ligaseGeneticsBiologyDeubiquitinating enzymeBioinformaticsNeuroscienceMedicineGeneGlycogen Storage Diseases and MyoclonusProtein Tyrosine PhosphatasesGenetics and Neurodevelopmental Disorders
TRIM32 and Malin in Neurological and Neuromuscular Rare Diseases | Litcius