Environmental Responsiveness of Tubulin Glutamylation in Sensory Cilia Is Regulated by the P38 MAPK Pathway

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Date

2018

Journal Title

Journal ISSN

Volume Title

Publisher

Nature Portfolio

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GOLD

Green Open Access

Yes

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69

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164

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Yes
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Abstract

Glutamylation is a post-translational modification found on tubulin that can alter the interaction between microtubules (MTs) and associated proteins. The molecular mechanisms regulating tubulin glutamylation in response to the environment are not well understood. Here, we show that in the sensory cilia of Caenorhabditis elegans, tubulin glutamylation is upregulated in response to various signals such as temperature, osmolality, and dietary conditions. Similarly, tubulin glutamylation is modified in mammalian photoreceptor cells following light adaptation. A tubulin glutamate ligase gene ttll-4, which is essential for tubulin glutamylation of axonemal MTs in sensory cilia, is activated by p38 MAPK. Amino acid substitution of TTLL-4 has revealed that a Thr residue (a putative MAPKphosphorylation site) is required for enhancement of tubulin glutamylation. Intraflagellar transport (IFT), a bidirectional trafficking system specifically observed along axonemal MTs, is required for the formation, maintenance, and function of sensory cilia. Measurement of the velocity of IFT particles revealed that starvation accelerates IFT, which was also dependent on the Thr residue of TTLL-4. Similarly, starvation-induced attenuation of avoidance behaviour from high osmolality conditions was also dependent on ttll-4. Our data suggest that a novel evolutionarily conserved regulatory system exists for tubulin glutamylation in sensory cilia in response to the environment.

Description

Kaplan, Oktay Ismail/0000-0002-8733-0920; Blacque, Oliver/0000-0003-1598-2695; Hameed, Saira/0000-0001-6115-9646; Tsutsumi, Koji/0000-0002-4260-2101; Teramoto, Takayuki/0000-0001-7060-7148

Keywords

C. ELEGANS, MECHANISM, Threonine, MAP Kinase Signaling System, PROTEIN, Glutamic Acid, POLYGLUTAMYLATION, Environment, p38 Mitogen-Activated Protein Kinases, Article, Olfactory Receptor Neurons, Tubulin, Animals, Peptide Synthases, Phosphorylation, VERTEBRATE PHOTORECEPTORS, Caenorhabditis elegans, Caenorhabditis elegans Proteins, NEURONS, NEMATODE CAENORHABDITIS-ELEGANS, IDENTIFICATION, INTRAFLAGELLAR TRANSPORT MOTORS, ENZYMES, Protein Processing, Post-Translational

Fields of Science

0301 basic medicine, 03 medical and health sciences, 0303 health sciences

Citation

WoS Q

Q1

Scopus Q

Q1
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OpenCitations Citation Count
21

Source

Scientific Reports

Volume

8

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CrossRef : 14

Scopus : 21

PubMed : 15

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21

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23

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4

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2

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