Lisa Goodrich

Lisa Goodrich, PhD

Professor of Neurobiology
Department Vice Chair

Assembly and Function of Auditory Circuitry

Our auditory system allows us to hear the rich sounds of everyday life—music, the voices of friends and family, birdsongs—as well as sounds that cause alarm or signal danger. Crucial to the sense of hearing is the accurate wiring and function of the intricate neural circuitry within and between the ear and the brain. While much has been learned about the cellular and molecular building blocks underlying developmental processes from cell fate specification to synapse formation and refinement, we still do not fully understand how the specialized circuitry of the auditory system arises during development, matures and functions, and exhibits resiliency in the face of stressors or aging.

To learn how auditory neural networks acquire their unique properties and function across the lifespan, the Goodrich lab employs mouse genetics, single cell sequencing, and sensitive anatomical analyses, together with timelapse imaging and physiological approaches. We investigate circuit assembly, maintenance, and function in the auditory system both in the ear and the auditory brainstem. Peripherally and centrally, specific classes of neurons acquire unique genetic identities, physiological properties, and elaborate morphologies and connectivity patterns that are appropriate for their role in the circuit. We are studying how these features develop, from the genetic and epigenetic programs underlying acquisition of spiral ganglion neuron subtype identity, to the development, maintenance, and degeneration of their specialized synapses that ensure rapid and reliable transmission from the inner ear to the brain. Within the brain, we are examining the molecular, genetic, and physiological properties of neurons that receive auditory information from the ear, as well as those that send signals to the ear and shape auditory function and responses to stressors, in part by interactions with the immune system.

Publications View
In vivo analysis of Lrig genes reveals redundant and independent functions in the inner ear.
Authors: Authors: Del Rio T, Nishitani AM, Yu WM, Goodrich LV.
PLoS Genet
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Functional interactions between Fat family cadherins in tissue morphogenesis and planar polarity.
Authors: Authors: Saburi S, Hester I, Goodrich L, McNeill H.
Development
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Comparison of phenotypes between different vangl2 mutants demonstrates dominant effects of the Looptail mutation during hair cell development.
Authors: Authors: Yin H, Copley CO, Goodrich LV, Deans MR.
PLoS One
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Mutation of Rubie, a novel long non-coding RNA located upstream of Bmp4, causes vestibular malformation in mice.
Authors: Authors: Roberts KA, Abraira VE, Tucker AF, Goodrich LV, Andrews NC.
PLoS One
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Control of neuronal morphology by the atypical cadherin Fat3.
Authors: Authors: Deans MR, Krol A, Abraira VE, Copley CO, Tucker AF, Goodrich LV.
Neuron
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Developmental profiling of spiral ganglion neurons reveals insights into auditory circuit assembly.
Authors: Authors: Lu CC, Appler JM, Houseman EA, Goodrich LV.
J Neurosci
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Principles of planar polarity in animal development.
Authors: Authors: Goodrich LV, Strutt D.
Development
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Spatiotemporal fate map of neurogenin1 (Neurog1) lineages in the mouse central nervous system.
Authors: Authors: Kim EJ, Hori K, Wyckoff A, Dickel LK, Koundakjian EJ, Goodrich LV, Johnson JE.
J Comp Neurol
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Connecting the ear to the brain: Molecular mechanisms of auditory circuit assembly.
Authors: Authors: Appler JM, Goodrich LV.
Prog Neurobiol
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Vertebrate Lrig3-ErbB interactions occur in vitro but are unlikely to play a role in Lrig3-dependent inner ear morphogenesis.
Authors: Authors: Abraira VE, Satoh T, Fekete DM, Goodrich LV.
PLoS One
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