4.3 Article

Neurofibromin Loss of Function Drives Excessive Grooming in Drosophila

Journal

G3-GENES GENOMES GENETICS
Volume 6, Issue 4, Pages 1083-1093

Publisher

GENETICS SOCIETY AMERICA
DOI: 10.1534/g3.115.026484

Keywords

Drosophila; grooming; neurofibromatosis; Nf1

Funding

  1. National Institutes of Health (NIH) [R00 MH092294]
  2. NIH [R01 AG045036]
  3. Fonds Wetenschappelijk Onderzoek-FWO postdoctoral fellowship [1288814N]
  4. Elise Besthoff Charitable Foundation
  5. NSF [1359369]
  6. Div Of Biological Infrastructure
  7. Direct For Biological Sciences [1359369] Funding Source: National Science Foundation

Ask authors/readers for more resources

Neurofibromatosis I is a common genetic disorder that results in tumor formation, and predisposes individuals to a range of cognitive/behavioral symptoms, including deficits in attention, visuospatial skills, learning, language development, and sleep, and autism spectrum disorder-like traits. The nf1-encoded neurofibromin protein (Nf1) exhibits high conservation, from the common fruit fly, Drosophila melanogaster, to humans. Drosophila provides a powerful platform to investigate the signaling cascades upstream and downstream of Nf1, and the fly model exhibits similar behavioral phenotypes to mammalian models. In order to understand how loss of Nf1 affects motor behavior in flies, we combined traditional activity monitoring with video analysis of grooming behavior. In nf1 mutants, spontaneous grooming was increased up to 7x. This increase in activity was distinct from previously described dopamine-dependent hyperactivity, as dopamine transporter mutants exhibited slightly decreased grooming. Finally, we found that relative grooming frequencies can be compared in standard activity monitors that measure infrared beam breaks, enabling the use of activity monitors as an automated method to screen for grooming phenotypes. Overall, these data suggest that loss of nf1 produces excessive activity that is manifested as increased grooming, providing a platform to dissect the molecular genetics of neurofibromin signaling across neuronal circuits.

Authors

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

Reviews

Primary Rating

4.3
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available