Tubulin polyglutamylation, a regulator of microtubule functions, can cause neurodegeneration

Neurosci Lett. 2021 Feb 16:746:135656. doi: 10.1016/j.neulet.2021.135656. Epub 2021 Jan 19.

Abstract

Neurodegenerative diseases lead to a progressive demise of neuronal functions that ultimately results in neuronal death. Besides a large variety of molecular pathways that have been linked to the degeneration of neurons, dysfunctions of the microtubule cytoskeleton are common features of many human neurodegenerative disorders. Yet, it is unclear whether microtubule dysfunctions are causative, or mere bystanders in the disease progression. A so-far little explored regulatory mechanism of the microtubule cytoskeleton, the posttranslational modifications of tubulin, emerge as candidate mechanisms involved in neuronal dysfunction, and thus, degeneration. Here we review the role of tubulin polyglutamylation, a prominent modification of neuronal microtubules. We discuss the current understanding of how polyglutamylation controls microtubule functions in healthy neurons, and how deregulation of this modification leads to neurodegeneration in mice and humans.

Keywords: AGTPBP1; Axonal transport; CCP; Human disease; MAP; Microtubule; Microtubule severing; Microtubule-Associated Proteins; Mouse models; NNA1; Neurodegeneration; Polyglutamylation; Posttranslational modifications; TTLL; Tubulin code; pcd mouse.

Publication types

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

MeSH terms

  • Animals
  • Humans
  • Microtubules / metabolism*
  • Microtubules / pathology
  • Neurodegenerative Diseases / metabolism*
  • Neurodegenerative Diseases / pathology
  • Polyglutamic Acid / metabolism*
  • Protein Processing, Post-Translational / physiology
  • Tubulin / metabolism*

Substances

  • Tubulin
  • Polyglutamic Acid