Conserved autism-associated genes tune social feeding behavior in C. elegans

Animal foraging is an essential and evolutionarily conserved behavior that occurs in social and solitary contexts, but the underlying molecular pathways are not well defined. We discover that conserved autism-associated genes (NRXN1(nrx-1), NLGN3(nlg-1), GRIA1,2,3(glr-1), GRIA2(glr-2), and GLRA2,GABRA3(avr-15)) regulate aggregate feeding in C. elegans, a simple social behavior. NRX-1 functions in chemosensory neurons (ADL and ASH) independently of its postsynaptic partner NLG-1 to regulate social feeding. Glutamate from these neurons is also crucial for aggregate feeding, acting independently of NRX-1 and NLG-1. Compared to solitary counterparts, social animals show faster presynaptic release and more presynaptic release sites in ASH neurons, with only the latter requiring nrx-1. Disruption of these distinct signaling components additively converts behavior from social to solitary. Collectively, we find that aggregate feeding is tuned by conserved autism-associated genes through complementary synaptic mechanisms, revealing molecular principles driving social feeding.

Authors

Institutions

Publication Details

Journal
Nature Communications
Published
2024-10-28
DOI
https://doi.org/10.1038/s41467-024-53590-x
Citations
16
Primary Topic
Genetics, Aging, and Longevity in Model Organisms
Type
article
Field-Weighted Citation Impact
3.64

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Conserved autism-associated genes tune social feeding behavior in C. elegans

Sreekanth H. Chalasani, Dustin Haskell, Kristi Zoga, Kirthi C. Reddy et al.
16 citations
Nature Communications
Genetics, Aging, and Longevity in Model Organisms
3.64
article

Conserved autism-associated genes tune social feeding behavior in C. elegans

Sreekanth H. Chalasani, Dustin Haskell, Kristi Zoga, Kirthi C. Reddy, Mara H. Cowen, Michael P. Hart
article en
16 citations

Abstract

Animal foraging is an essential and evolutionarily conserved behavior that occurs in social and solitary contexts, but the underlying molecular pathways are not well defined. We discover that conserved autism-associated genes (NRXN1(nrx-1), NLGN3(nlg-1), GRIA1,2,3(glr-1), GRIA2(glr-2), and GLRA2,GABRA3(avr-15)) regulate aggregate feeding in C. elegans, a simple social behavior. NRX-1 functions in chemosensory neurons (ADL and ASH) independently of its postsynaptic partner NLG-1 to regulate social feeding. Glutamate from these neurons is also crucial for aggregate feeding, acting independently of NRX-1 and NLG-1. Compared to solitary counterparts, social animals show faster presynaptic release and more presynaptic release sites in ASH neurons, with only the latter requiring nrx-1. Disruption of these distinct signaling components additively converts behavior from social to solitary. Collectively, we find that aggregate feeding is tuned by conserved autism-associated genes through complementary synaptic mechanisms, revealing molecular principles driving social feeding.

Nature CommunicationsVol. 15(1)
Salk Institute for Biological Studies (US), University of Pennsylvania (US), Center for Autism and Related Disorders (US)
National Science Foundation, National Institutes of Health, Perelman School of Medicine, University of Pennsylvania, National Institute of Mental Health, National Institute of General Medical Sciences
Zero hunger
Openalex Percentile: Top 6%
Genetics, Aging, and Longevity in Model Organisms
3.64
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.

Conserved autism-associated genes tune social feeding behavior in C. elegans — Sreekanth H. Chalasani, Dustin Haskell, et al. · Nature Communications (2024) | TGRS Research Map | TGRS