
Michael Granato
VerifiedUniversity of Pennsylvania · Rehabilitation Medicine
Active 1994–2024
Research topics
- Genetics
- Biology
- Neuroscience
Selected publications
PLoS ONE · 2022 · 25 citations
- Biology
- Neuroscience
- Genetics
BACKGROUND: The ability to filter sensory information into relevant versus irrelevant stimuli is a fundamental, conserved property of the central nervous system and is accomplished in part through habituation learning. Synaptic plasticity that underlies habituation learning has been described at the cellular level, yet the genetic regulators of this plasticity remain poorly understood, as do circuits that mediate sensory filtering. METHODS: To identify genes critical for plasticity, a forward genetic screen for zebrafish genes that mediate habituation learning was performed, which identified a mutant allele, doryp177, that caused reduced habituation of the acoustic startle response. In this study, we combine whole-genome sequencing with behavioral analyses to characterize and identify the gene affected in doryp177 mutants. RESULTS: Whole-genome sequencing identified the calcium voltage-gated channel auxiliary subunit alpha-2/delta-3 (cacna2d3) as a candidate gene affected in doryp177 mutants. Behavioral characterization of larvae homozygous for two additional, independently derived mutant alleles of cacna2d3, together with failure of these alleles to complement doryp177, confirmed a critical role for cacna2d3 in habituation learning. Notably, detailed analyses of the acoustic response in mutant larvae also revealed increased startle sensitivity to acoustic stimuli, suggesting a broader role for cacna2d3 in controlling innate response thresholds to acoustic stimuli. CONCLUSIONS: Taken together, our data demonstrate a critical role for cacna2d3 in sensory filtering, a process that is disrupted in human CNS disorders, e.g. ADHD, schizophrenia, and autism.
Recent grants
The role of the zebrafish diwanka gene in motor axon guidance
NSF · $400k · 2005–2009
NIH · $4.8M · 2016
Cellular and molecular analysis of startle modulation
NIH · $2.6M · 2021–2027
NIH · $160k · 2015
NIH · $926k · 2006
Frequent coauthors
- 48 shared
Christiane Nüsslein–Volhard
Max Planck Institute for Biology
- 42 shared
Pascal Haffter
Max Planck Institute for Developmental Biology
- 42 shared
Mary C. Mullins
University of Pennsylvania
- 40 shared
Carl‐Philipp Heisenberg
- 39 shared
Yun‐Jin Jiang
National Health Research Institutes
- 38 shared
Michael Brand
TU Dresden
- 38 shared
Jörg Odenthal
- 37 shared
Robert N. Kelsh
University of Bath
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