Putting human Tid-1 in context: an insight into its role in the cell and in different disease states

Cell Commun Signal. 2022 Jul 19;20(1):109. doi: 10.1186/s12964-022-00912-5.

Abstract

Background: Tumorous imaginal disc 1 (hTid-1) or DnaJ homolog subfamily A member 3 (DNAJA3), is a part of the heat shock protein (Hsp) 40 family and is predominantly found to reside in the mitochondria. hTid-1 has two mRNA splicing variants, hTid-1S and hTid-1L of 40 and 43 kDa respectively in the cytosol which are later processed upon import into the mitochondrial matrix. hTid-1 protein is a part of the DnaJ family of proteins which are co-chaperones and specificity factors for DnaK proteins of the Hsp70 family, and bind to Hsp70, thereby activating its ATPase activity. hTid-1 has been found to be critical for a lot of important cellular processes such as proliferation, differentiation, growth, survival, senescence, apoptosis, and movement and plays key roles in the embryo and skeletal muscle development.

Main body: hTid-1 participates in several protein-protein interactions in the cell, which mediate different processes such as proteasomal degradation and autophagy of the interacting protein partners. hTid-1 also functions as a co-chaperone and participates in interactions with several different viral oncoproteins. hTid-1 also plays a critical role in different human diseases such as different cancers, cardiomyopathies, and neurodegenerative disorders.

Conclusion: This review article is the first of its kind presenting consolidated information on the research findings of hTid-1 to date. This review suggests that the current knowledge of the role of hTid-1 in disorders like cancers, cardiomyopathies, and neurodegenerative diseases can be correlated with the findings of its protein-protein interactions that can provide a deep insight into the pathways by which hTid-1 affects disease pathogenesis and it can be stated that hTid-1 may serve as an important therapeutic target for these disorders. Video Abstract.

Keywords: Alzheimer’s disease; Apoptosis; Cancer; Cardiac myopathies; Mitochondria; Parkinson’s disease; Tumorigenesis; hTid-1.

Publication types

  • Review
  • Video-Audio Media
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Apoptosis / genetics
  • HSP40 Heat-Shock Proteins* / genetics
  • HSP40 Heat-Shock Proteins* / metabolism
  • HSP70 Heat-Shock Proteins / metabolism
  • Heat-Shock Proteins* / metabolism
  • Humans
  • Molecular Chaperones / genetics

Substances

  • DNAJA3 protein, human
  • HSP40 Heat-Shock Proteins
  • HSP70 Heat-Shock Proteins
  • Heat-Shock Proteins
  • Molecular Chaperones