Forward genetics identifies a novel sleep mutant with sleep state inertia and REM sleep deficits

Author:

Banks Gareth T.1ORCID,Guillaumin Mathilde C. C.2ORCID,Heise Ines1ORCID,Lau Petrina1ORCID,Yin Minghui1ORCID,Bourbia Nora1ORCID,Aguilar Carlos1,Bowl Michael R.1ORCID,Esapa Chris1,Brown Laurence A.2ORCID,Hasan Sibah2,Tagliatti Erica3ORCID,Nicholson Elizabeth3ORCID,Bains Rasneer Sonia4ORCID,Wells Sara4ORCID,Vyazovskiy Vladyslav V.25ORCID,Volynski Kirill3ORCID,Peirson Stuart N.2ORCID,Nolan Patrick M.1ORCID

Affiliation:

1. Mammalian Genetics Unit, MRC Harwell Institute, Harwell Science and Innovation Campus, Oxfordshire, UK.

2. Sleep and Circadian Neuroscience Institute (SCNi), Nuffield Department of Clinical Neurosciences, University of Oxford, Oxford, UK.

3. UCL Queen Square Institute of Neurology, University College London, London, UK.

4. Mary Lyon Centre, MRC Harwell Institute, Harwell Science and Innovation Campus, Oxfordshire, UK.

5. Department of Physiology, Anatomy and Genetics, University of Oxford, Oxford, UK.

Abstract

A noninvasive sleep screen uncovers a Vamp2 mouse mutation with synaptic deficits underlying substantial sleep disturbances.

Funder

Medical Research Council

Biotechnology and Biological Sciences Research Council

John Fell Fund, University of Oxford

Wellcome Trust Centre for Mitochondrial Research

ERUK

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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