Farnesylation-defective rheb increases axonal length independently of mTORC1 activity in embryonic primary neurons

Seunghyuk Choi, Ali Sadra, Jieun Kang, Jae Ryun Ryu, June Hoan Kim, Woong Sun, Sung Oh Huh

Research output: Contribution to journalArticle

Abstract

Rheb (Ras homolog enriched in the brain) is a small GTPase protein that plays an important role in cell signaling for development of the neocortex through modulation of mTORC1 (mammalian-target-of-rapamycin-complex-1) activity. mTORC1 is known to control various biological processes including axonal growth in forming complexes at the lysosomal membrane compartment. As such, anchoring of Rheb on the lysosomal membrane via the farnesylation of Rheb at its cysteine residue (C180) is required for its promotion of mTOR activity. To test the significance of Rheb farnesylation, we overexpressed a farnesylation mutant form of Rheb, Rheb C180S, in primary rat hippocampal neurons and also in mouse embryonic neurons using in utero electroporation. Interestingly, we found that Rheb C180S maintained promotional effect of axonal elongation similar to the wild-type Rheb in both test systems. On the other hand, Rheb C180S failed to exhibit the multiple axon-promoting effect which is found in wild-type Rheb. The levels of phospho-4EBP1, a downstream target of mTORC1, were surprisingly increased in Rheb C180S transfected neurons, despite the levels of phosphorylated mTOR being significantly decreased compared to control vector transfectants. A specific mTORC1 inhibitor, rapamycin, also could not completely abolish axon elongation characteristics of Rheb C180S in transfected cells. Our data suggests that Rheb in a non-membrane compartment can promote the axonal elongation via phosphorylation of 4EBP1 and through an mTORC1-independent pathway.

Original languageEnglish
Pages (from-to)172-182
Number of pages11
JournalExperimental Neurobiology
Volume28
Issue number2
DOIs
Publication statusPublished - 2019 Apr 1

Fingerprint

Prenylation
Neurons
Brain
mechanistic target of rapamycin complex 1
Axons
Biological Phenomena
Electroporation
Membranes
Monomeric GTP-Binding Proteins
Neocortex
Sirolimus
Cysteine

Keywords

  • Axons
  • MTOR protein
  • Protein farnesylation
  • Rheb protein

ASJC Scopus subject areas

  • Clinical Neurology
  • Cellular and Molecular Neuroscience

Cite this

Farnesylation-defective rheb increases axonal length independently of mTORC1 activity in embryonic primary neurons. / Choi, Seunghyuk; Sadra, Ali; Kang, Jieun; Ryu, Jae Ryun; Kim, June Hoan; Sun, Woong; Huh, Sung Oh.

In: Experimental Neurobiology, Vol. 28, No. 2, 01.04.2019, p. 172-182.

Research output: Contribution to journalArticle

Choi, Seunghyuk ; Sadra, Ali ; Kang, Jieun ; Ryu, Jae Ryun ; Kim, June Hoan ; Sun, Woong ; Huh, Sung Oh. / Farnesylation-defective rheb increases axonal length independently of mTORC1 activity in embryonic primary neurons. In: Experimental Neurobiology. 2019 ; Vol. 28, No. 2. pp. 172-182.
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