We are interested in how the brain changes with experience to alter behaviour – or how circuits in the brain learn and remember.
NeurobiologyZebrafishMemoryHabituationO-BendNf1
Team
- Owen RANDLETT
CR, INSERM - Dominique BAAS
MCU, UCBL - Isabelle DARVAUX-HUBERT
AI, INSERM - Laurie-Anne LAMIRÉ
Post-Doc, INSERM - Romane DORADO DONCEL
MASTER STUDENT
PROJETS
We work with larval zebrafish, which are a very small and transparent model vertebrate. Despite being less than a week old, zebrafish larvae can be trained to form long-term memories. We have developed paradigms to train larvae to ignore repeated stimuli. This simple form of learning is known as habituation, and offers a tractable paradigm to study the general phenomenon of learning and memory. Despite the apparent triviality of habituation (simply learning to ignore a given stimulus), how the brain actually accomplishes this selective filtration of specific stimuli is still largely mysterious. Indeed, we have shown that habituation is a complex phenomenon that involves multiple independent plasticity events that each tune individual components of behaviour. We hope to gain insights into this process at the molecular, cellular and circuit levels.
To study the mechanisms of habituation we exploit the advantages of the larval zebrafish, including:
1) Optical transparency for imaging neuronal activity in intact and behaving animals. This allows us to measure how neurons and circuits adapt in real-time during habituation.
2) The small size of the brain allows for whole-brain imaging on standard microscopes, allowing us to routinely quantify neural activity and anatomy in the whole-circuit context (see www.zbra.in).
3) High-throughput quantitative behavioural analyses. This gives us precise measures of the outputs of plasticity at the behavioural level.
4) Amenability to genetic and transgenic manipulation. This allows us to study the role of specific genes and pathways in plasticity processes.
SELECTED PUBLICATIONS
- Distributed Plasticity Drives Visual Habituation Learning in Larval Zebrafish.
Randlett O, Haesemeyer M, Forkin G, Shoenhard H, Schier AF, Engert F, Granato M.Current Biology (2019) 29(8):1337-1345 - Whole-brain activity mapping onto a zebrafish brain atlas.
Randlett O, Wee CL, Naumann EA, Onyeka N, David S, Fitzgerald JE, Ruben P, Lacoste AMB, Clemens R, Florian E, Schier AF.Nature Methods (2015) 12(11):1039–1046. - Phenotypic Landscape of Schizophrenia-Associated Genes Defines Candidates and Their Shared Functions.
Thyme SB, Pieper LM, Li EH, Pandey S, Wang Y, Morris NS, Sha C, Choi JW, Herrera KJ, Soucy ER, Zimmerman S, Randlett O, Greenwood J, McCarroll SA, Schier AF.Cell (2019) 177(2):478-491.e20. - Zebrafish oxytocin neurons drive nocifensive behavior via brainstem premotor targets.
Wee CL, Nikitchenko M, Wang WC, Luks-Morgan SJ, Song E, Gagnon JA, Randlett O, Bianco IH, Lacoste AMB, Glushenkova E, Barrios JP, Schier AF, Kunes S, Engert F, Douglass AD.Nature Neuroscience (2019) 22(9):1477-1492. - Brain-wide Organization of Neuronal Activity and Convergent Sensorimotor Transformations in Larval Zebrafish.
Chen X, Mu Y, Hu Y, Kuan AT, Nikitchenko M, Randlett O, Chen AB, Gavornik JP, Sompolinsky H, Engert F, Ahrens MB. Neuron (2018) 100(4):876-890.e5. - Expansion microscopy of zebrafish for neuroscience and developmental biology studies.
Freifeld L, Odstrcil I, Förster D, Ramirez A, Gagnon JA, Randlett O, Costa EK, Asano S, Celiker OT, Gao R, Martin-Alarcon DA, Reginato P, Dick C, Chen L, Schoppik D, Engert F, Baier H, Boyden ES. PNAS (2017) 114(50):E10799-E10808. - Whole-brain serial-section electron microscopy in larval zebrafish.
Hildebrand DGC, Cicconet M, Torres RM, Choi W, Quan TM, Moon J, Wetzel AW, Scott Champion A, Graham BJ, Randlett O, Plummer GS, Portugues R, Bianco IH, Saalfeld S, Baden AD, Lillaney K, Burns R, Vogelstein JT, Schier AF, Lee WA, Jeong WK, Lichtman JW, Engert F. Nature (2017) 545(7654):345-349. - Brain-wide mapping of neural activity controlling zebrafish exploratory locomotion.
Dunn TW, Mu Y, Narayan S, Randlett O, Naumann EA, Yang CT, Schier AF, Freeman J, Engert F, Ahrens MB. Elife (2016) 5:e12741. - The Oriented Emergence of Axons from Retinal Ganglion Cells Is Directed by Laminin Contact In Vivo.
Randlett O, Lucia P, Zolessi FR, Harris WA. Neuron (2011) 70(2):266–280. - Cellular Requirements for Building a Retinal Neuropil.
Randlett O*, MacDonald RB*, Takeshi Y, Almeida AD, Suzuki SC, Wong RO, Harris WA. Cell Reports (2013) 3(2):282–290.
OPEN POSITIONS :
We are always seeking motivated students or postdoc.
Please contact owen.randlett@univ-lyon1.fr
FUNDING
