4.8 Article

Structure of the C9orf72 ARF GAP complex that is haploinsufficient in ALS and FTD

Journal

NATURE
Volume 585, Issue 7824, Pages 251-+

Publisher

NATURE PORTFOLIO
DOI: 10.1038/s41586-020-2633-x

Keywords

-

Funding

  1. NIH [R01GM111730, R01GM130995]
  2. Department of Defense Peer Reviewed Medical Research Program Discovery Award [W81XWH2010086]
  3. Bakar Fellows program
  4. Pew-Stewart Scholarship for Cancer Research
  5. Association for Frontotemporal Degeneration
  6. EMBO Long-Term Fellowship
  7. Damon Runyon-Rachleff Innovation Award
  8. U.S. Department of Defense (DOD) [W81XWH2010086] Funding Source: U.S. Department of Defense (DOD)

Ask authors/readers for more resources

Mutation ofC9orf72is the most prevalent defect associated with amyotrophic lateral sclerosis and frontotemporal degeneration(1). Together with hexanucleotide-repeat expansion(2,3), haploinsufficiency ofC9orf72contributes to neuronal dysfunction(4-6). Here we determine the structure of the C9orf72-SMCR8-WDR41 complex by cryo-electron microscopy. C9orf72 and SMCR8 both contain longin and DENN (differentially expressed in normal and neoplastic cells) domains(7), and WDR41 is a beta-propeller protein that binds to SMCR8 such that the whole structure resembles an eye slip hook. Contacts between WDR41 and the DENN domain of SMCR8 drive the lysosomal localization of the complex in conditions of amino acid starvation. The structure suggested that C9orf72-SMCR8 is a GTPase-activating protein (GAP), and we found that C9orf72-SMCR8-WDR41 acts as a GAP for the ARF family of small GTPases. These data shed light on the function of C9orf72 in normal physiology, and in amyotrophic lateral sclerosis and frontotemporal degeneration. The cryo-electron microscopy structure of C9orf72-SMCR8-WDR41 suggests that this complex is a GTPase-activating protein for ARF-family small GTPases, which sheds light on the role ofC9orf72mutations in neuronal dysfunction.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.8
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available