Intraflagellar transport 20: New target for the treatment of ciliopathies

Biochim Biophys Acta Mol Cell Res. 2020 Jul;1867(7):118641. doi: 10.1016/j.bbamcr.2019.118641. Epub 2019 Dec 30.

Abstract

Cilia are ubiquitous in mammalian cells. The formation and assembly of cilia depend on the normal functioning of the ciliary transport system. In recent years, various proteins involved in the intracellular transport of the cilium have attracted attention, as many diseases are caused by disorders in cilia formation. Intraflagellar transport 20 (IFT20) is a subunit of IFT complex B, which contains approximately 20 protein particles. Studies have shown that defects in IFT20 are associated with numerous system -related diseases, such as those of the urinary system, cardiovascular system, skeletal system, nervous system, immune system, reproductive system, and respiratory system. This review summarizes current research on IFT20.We describe studies related to the role of IFT20 in cilia formation and discuss new targets for treating diseases associated with ciliary dysplasia.

Keywords: Cilia; Ciliopathies; Intraflagellar transport; Intraflagellar transport 20.

Publication types

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

MeSH terms

  • Biological Transport / genetics*
  • Carrier Proteins / antagonists & inhibitors
  • Carrier Proteins / genetics*
  • Cilia / genetics*
  • Cilia / metabolism
  • Ciliopathies / drug therapy
  • Ciliopathies / genetics*
  • Ciliopathies / pathology
  • Humans

Substances

  • Carrier Proteins
  • IFT20 protein, human