Alterations in the balance of tubulin glycylation and glutamylation in photoreceptors leads to retinal degeneration

J Cell Sci. 2017 Mar 1;130(5):938-949. doi: 10.1242/jcs.199091. Epub 2017 Jan 19.

Abstract

Tubulin is subject to a wide variety of posttranslational modifications, which, as part of the tubulin code, are involved in the regulation of microtubule functions. Glycylation has so far predominantly been found in motile cilia and flagella, and absence of this modification leads to ciliary disassembly. Here, we demonstrate that the correct functioning of connecting cilia of photoreceptors, which are non-motile sensory cilia, is also dependent on glycylation. In contrast to many other tissues, only one glycylase, TTLL3, is expressed in retina. Ttll3-/- mice lack glycylation in photoreceptors, which results in shortening of connecting cilia and slow retinal degeneration. Moreover, absence of glycylation results in increased levels of tubulin glutamylation in photoreceptors, and inversely, the hyperglutamylation observed in the Purkinje cell degeneration (pcd) mouse abolishes glycylation. This suggests that both posttranslational modifications compete for modification sites, and that unbalancing the glutamylation-glycylation equilibrium on axonemes of connecting cilia, regardless of the enzymatic mechanism, invariably leads to retinal degeneration.

Keywords: Connecting cilia; Glutamylation; Glycylation; Microtubule; Photoreceptor; Retina; TTLL3; Tubulin.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Apoptosis
  • Cilia / metabolism
  • Glutamic Acid / metabolism*
  • Glycosylation
  • Mice, Inbred C57BL
  • Neuroglia / metabolism
  • Neuroglia / pathology
  • Peptide Synthases / metabolism
  • Phenotype
  • Photoreceptor Cells, Vertebrate / metabolism*
  • Photoreceptor Cells, Vertebrate / pathology*
  • Purkinje Cells / metabolism
  • Purkinje Cells / pathology
  • Retina / metabolism
  • Retina / pathology
  • Retinal Degeneration / metabolism*
  • Retinal Degeneration / pathology*
  • Rhodopsin / metabolism
  • Time Factors
  • Tubulin / metabolism*

Substances

  • Tubulin
  • Glutamic Acid
  • Rhodopsin
  • Peptide Synthases