High-throughput functional analysis of autism genes in zebrafish identifies convergence in dopaminergic and neuroimmune pathways

Hellen Weinschutz Mendes(Yale University), Uma Neelakantan(Yale University), Yunqing Liu(Yale University), Sarah E. Fitzpatrick(Yale University), Tianying Chen(Yale University), Weimiao Wu(Yale University), April Pruitt(Yale University), David Jin(Yale University), Priyanka Jamadagni(Yale University), Marina Carlson(Yale University), Cheryl Lacadie(Yale University), Kristen Enriquez(Yale University), Ningshan Li(Cancer Research And Biostatistics), Dejian Zhao(Yale University), Sundas Ijaz(Yale University), Catalina Sakai(Yale University), Christina Szi(Yale University), Brendan Rooney(Yale University), Marcus Ghosh(University College London), Ijeoma Nwabudike(Yale University), Andrea Gorodezky(Yale University), Sumedha Chowdhury(Yale University), Meeraal Zaheer(Yale University), Sarah McLaughlin(Yale University), Joseph M. Fernandez(Yale University), Jia Qian Wu(Yale University), Jeffrey Eilbott(Yale University), Brent Vander Wyk(Yale University), Jason Rihel(University College London), Xenophon Papademetris(Yale University), Zuoheng Wang(Yale University), Ellen J. Hoffman(Yale University)
Cell Reports
March 1, 2023
Cited by 83Open Access
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Abstract

Advancing from gene discovery in autism spectrum disorders (ASDs) to the identification of biologically relevant mechanisms remains a central challenge. Here, we perform parallel in vivo functional analysis of 10 ASD genes at the behavioral, structural, and circuit levels in zebrafish mutants, revealing both unique and overlapping effects of gene loss of function. Whole-brain mapping identifies the forebrain and cerebellum as the most significant contributors to brain size differences, while regions involved in sensory-motor control, particularly dopaminergic regions, are associated with altered baseline brain activity. Finally, we show a global increase in microglia resulting from ASD gene loss of function in select mutants, implicating neuroimmune dysfunction as a key pathway relevant to ASD biology.


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