Roles of miR-204 in retinal development and maintenance

Exp Cell Res. 2021 Sep 1;406(1):112737. doi: 10.1016/j.yexcr.2021.112737. Epub 2021 Jul 26.

Abstract

The retina is the innermost part of the eye of most vertebrates and it is essential for vision. The development, maintenance, and function of this laminated structure is tightly regulated by numerous genes. Deficiencies in the expression of these genes as well as deregulation of various molecular mechanisms can cause retinopathies and blindness. MicroRNAs (miRNAs) are one of the most important and effective molecular regulatory mechanisms that underlie the biology of the retina. miRNAs have specific functional roles in the development and maintenance of different retinal layers and retinal cell types. While previous studies have reported a large number of miRNAs linked to development, maintenance and diseases of the retina, no comprehensive study has properly discussed and integrated data from these studies. Given the particular importance of miR-204 in retinal biology, we intend to critically discuss the expression and functional significance of this miRNA in the development, maintenance, and pathologies of the retina. Moreover, we explore biological processes through which miR-204 influences retinal pathophysiology. This review highlights the crucial functions of miR-204 in the retina and suggests the putative mechanism of miR-204 action in retinal biology.

Keywords: Development; Maintenance; Retina; Retinopathy; miR-204.

Publication types

  • Review

MeSH terms

  • Animals
  • Base Sequence
  • Conserved Sequence
  • Diabetic Retinopathy / genetics*
  • Diabetic Retinopathy / metabolism
  • Diabetic Retinopathy / pathology
  • Discs Large Homolog 1 Protein / genetics
  • Discs Large Homolog 1 Protein / metabolism
  • Disease Models, Animal
  • Gene Expression Regulation
  • Glaucoma / genetics*
  • Glaucoma / metabolism
  • Glaucoma / pathology
  • Humans
  • Macular Degeneration / genetics*
  • Macular Degeneration / metabolism
  • Macular Degeneration / pathology
  • Membrane Proteins / genetics
  • Membrane Proteins / metabolism
  • MicroRNAs / genetics*
  • MicroRNAs / metabolism
  • Optic Nerve Injuries / genetics*
  • Optic Nerve Injuries / metabolism
  • Optic Nerve Injuries / pathology
  • Rapamycin-Insensitive Companion of mTOR Protein / genetics
  • Rapamycin-Insensitive Companion of mTOR Protein / metabolism
  • Retina / metabolism
  • Retina / pathology
  • Retinoblastoma / genetics*
  • Retinoblastoma / metabolism
  • Retinoblastoma / pathology
  • Signal Transduction

Substances

  • DLG1 protein, human
  • Discs Large Homolog 1 Protein
  • MIRN204 microRNA, human
  • Membrane Proteins
  • MicroRNAs
  • RICTOR protein, human
  • Rapamycin-Insensitive Companion of mTOR Protein
  • SYNJ2BP protein, human