Front. Neurosci.Frontiers in NeuroscienceFront. Neurosci.1662-453XFrontiers Media S.A.10.3389/fnins.2021.740799NeuroscienceCorrectionCorrigendum: Circadian Chimeric Mice Reveal an Interplay Between the Suprachiasmatic Nucleus and Local Brain Clocks in the Control of Sleep and MemoryMaywoodElizabeth Susan1*CheshamJohanna Elizabeth1Winsky-SommererRaphaelle2SmyllieNicola Jane1HastingsMichael Harvey1*1Division of Neurobiology, MRC Laboratory of Molecular Biology, Cambridge, United Kingdom2Surrey Sleep Research Centre, Faculty of Health and Medical Sciences, University of Surrey, Guildford, United Kingdom
Edited and reviewed by: Natsuko Tsujino, University of Tsukuba, Japan
*Correspondence: Elizabeth Susan Maywood emaywood@mrc-lmb.cam.ac.ukMichael Harvey Hastings mha@mrc-lmb.cam.ac.uk
This article was submitted to Sleep and Circadian Rhythms, a section of the journal Frontiers in Neuroscience
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A Corrigendum on Circadian Chimeric Mice Reveal an Interplay Between the Suprachiasmatic Nucleus and Local Brain Clocks in the Control of Sleep and Memory by Maywood, E. S., Chesham, J. E., Winsky-Sommerer, R., Smyllie, N. J., and Hastings, M. H. (2021). Front. Neurosci. 15:639281. doi: 10.3389/fnins.2021.639281REM sleepNREM sleepelectroencephalogramcircadian misalignmentsuprachiasmatic nucleus
In the original article, there was an error in assignment of mouse strain identity.
A correction has been made to **Materials and Methods**, **Animals and housing**, **Paragraph number 1**:
All experiments were conducted in accordance with the UK Animals (Scientific Procedures) Act of 1986, with local ethical approval (MRC LMB, AWERB). Drd1a-Cre mice (Tg(Drd1-cre)EY266Gsat/Mmucd, RRID:MMRRC_030779-UCD) were purchased from the GENSAT project (Rockefeller University, New York, United States), through the Mutant Mouse Regional Resource Centers (MMRRC, United States). ROSA-YFP mice were provided by Dr. A. McKenzie (MRC LMB). Temporally chimeric mice were created by crossing Drd1a-Cre, ROSA26-EYFP mice with homozygotes for the floxed CK1ε Tau allele (Smyllie et al., 2016). All mice expressed the PER2::LUC bioluminescent reporter (Yoo et al., 2005) and had a C57/BL/6J background. This generated four genotypes: CRE-negative, CK1εWT/WT; CRE-positive, CK1εWT/WT; CRE-negative, CK1εTau/Tau (Tau controls); CRE-positive, CK1εTau/Tau (chimera). The first two groups were combined as WT, in light of no differences between them. Males aged 4–6 months old were used to avoid the estrous modulation of activity patterns.
The authors apologize for this error and state that this does not change the scientific conclusions of the article in any way. The original article has been updated.
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