Notch signaling is a critical initiator of roof plate formation as revealed by the use of RNA profiling of the dorsal neural tube.

BMP Dorsal interneurons Fate segregation Mib1 Mouse embryos Neural crest Notch Quail embryos delta1

Journal

BMC biology
ISSN: 1741-7007
Titre abrégé: BMC Biol
Pays: England
ID NLM: 101190720

Informations de publication

Date de publication:
23 04 2021
Historique:
received: 21 12 2020
accepted: 25 03 2021
entrez: 24 4 2021
pubmed: 25 4 2021
medline: 15 12 2021
Statut: epublish

Résumé

The dorsal domain of the neural tube is an excellent model to investigate the generation of complexity during embryonic development. It is a highly dynamic and multifaceted region being first transiently populated by prospective neural crest (NC) cells that sequentially emigrate to generate most of the peripheral nervous system. Subsequently, it becomes the definitive roof plate (RP) of the central nervous system. The RP, in turn, constitutes a patterning center for dorsal interneuron development. The factors underlying establishment of the definitive RP and its segregation from NC and dorsal interneurons are currently unknown. We performed a transcriptome analysis at trunk levels of quail embryos comparing the dorsal neural tube at premigratory NC and RP stages. This unraveled molecular heterogeneity between NC and RP stages, and within the RP itself. By implementing these genes, we asked whether Notch signaling is involved in RP development. First, we observed that Notch is active at the RP-interneuron interface. Furthermore, gain and loss of Notch function in quail and mouse embryos, respectively, revealed no effect on early NC behavior. Constitutive Notch activation caused a local downregulation of RP markers with a concomitant development of dI1 interneurons, as well as an ectopic upregulation of RP markers in the interneuron domain. Reciprocally, in mice lacking Notch activity, both the RP and dI1 interneurons failed to form and this was associated with expansion of the dI2 population. Collectively, our results offer a new resource for defining specific cell types, and provide evidence that Notch is required to establish the definitive RP, and to determine the choice between RP and interneuron fates, but not the segregation of RP from NC.

Sections du résumé

BACKGROUND
The dorsal domain of the neural tube is an excellent model to investigate the generation of complexity during embryonic development. It is a highly dynamic and multifaceted region being first transiently populated by prospective neural crest (NC) cells that sequentially emigrate to generate most of the peripheral nervous system. Subsequently, it becomes the definitive roof plate (RP) of the central nervous system. The RP, in turn, constitutes a patterning center for dorsal interneuron development. The factors underlying establishment of the definitive RP and its segregation from NC and dorsal interneurons are currently unknown.
RESULTS
We performed a transcriptome analysis at trunk levels of quail embryos comparing the dorsal neural tube at premigratory NC and RP stages. This unraveled molecular heterogeneity between NC and RP stages, and within the RP itself. By implementing these genes, we asked whether Notch signaling is involved in RP development. First, we observed that Notch is active at the RP-interneuron interface. Furthermore, gain and loss of Notch function in quail and mouse embryos, respectively, revealed no effect on early NC behavior. Constitutive Notch activation caused a local downregulation of RP markers with a concomitant development of dI1 interneurons, as well as an ectopic upregulation of RP markers in the interneuron domain. Reciprocally, in mice lacking Notch activity, both the RP and dI1 interneurons failed to form and this was associated with expansion of the dI2 population.
CONCLUSIONS
Collectively, our results offer a new resource for defining specific cell types, and provide evidence that Notch is required to establish the definitive RP, and to determine the choice between RP and interneuron fates, but not the segregation of RP from NC.

Identifiants

pubmed: 33892704
doi: 10.1186/s12915-021-01014-3
pii: 10.1186/s12915-021-01014-3
pmc: PMC8063321
doi:

Substances chimiques

RNA 63231-63-0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

84

Subventions

Organisme : Israel Science Foundation
ID : 209/18
Organisme : National Health and Medical Research Council
ID : APP1144004

Références

Genes Dev. 2002 Mar 1;16(5):548-53
pubmed: 11877374
Development. 2000 Jul;127(13):2811-21
pubmed: 10851127
J Biol Chem. 2013 Jan 25;288(4):2580-92
pubmed: 23223237
Science. 1999 Apr 30;284(5415):770-6
pubmed: 10221902
Stem Cell Reports. 2019 May 14;12(5):1159-1177
pubmed: 31031189
Dev Biol. 2005 Jan 15;277(2):287-95
pubmed: 15617675
Development. 2012 Jan;139(2):259-68
pubmed: 22159578
Trends Genet. 2017 Oct;33(10):715-727
pubmed: 28851604
Development. 2019 Mar 27;146(12):
pubmed: 30846445
Development. 2006 Jul;133(13):2467-76
pubmed: 16728479
Curr Top Dev Biol. 2019;132:417-450
pubmed: 30797516
Development. 2007 Feb;134(3):491-501
pubmed: 17185320
Development. 2001 Apr;128(8):1467-79
pubmed: 11262245
Development. 2012 Nov;139(22):4261-70
pubmed: 23052907
Science. 1994 May 6;264(5160):835-9
pubmed: 7513443
J Comp Neurol. 2009 Dec 20;517(6):751-64
pubmed: 19842206
Dev Cell. 2004 Apr;6(4):539-50
pubmed: 15068793
Dev Biol. 2007 Mar 1;303(1):181-90
pubmed: 17150208
BMC Neurosci. 2019 Apr 29;20(1):21
pubmed: 31036074
Genes Dev. 2002 Oct 15;16(20):2699-712
pubmed: 12381668
Genes Dev. 1998 Nov 1;12(21):3394-407
pubmed: 9808626
Development. 2002 Feb;129(4):863-73
pubmed: 11861470
BMC Biol. 2016 Mar 24;14:23
pubmed: 27012662
J Cell Sci. 2013 May 1;126(Pt 9):2060-8
pubmed: 23444378
Nat Rev Neurosci. 2004 Oct;5(10):808-12
pubmed: 15378040
Development. 2004 Nov;131(21):5327-39
pubmed: 15456730
Development. 2010 Feb;137(4):585-95
pubmed: 20110324
Neuron. 1999 May;23(1):71-81
pubmed: 10402194
Dev Biol. 2004 Jun 15;270(2):382-92
pubmed: 15183721
Development. 2002 May;129(10):2459-72
pubmed: 11973277
Dev Dyn. 2008 May;237(5):1500-8
pubmed: 18386821
Development. 2019 Jan 16;146(2):
pubmed: 30651295
Development. 2007 Oct;134(19):3449-60
pubmed: 17728348
Nat Neurosci. 2001 Jul;4(7):683-4
pubmed: 11426219
Cell Tissue Res. 1998 Nov;294(2):297-307
pubmed: 9799446
Mol Cell Biol. 2009 Jul;29(13):3633-43
pubmed: 19398580
Development. 2005 Aug;132(15):3459-70
pubmed: 16000382
EMBO J. 2002 Feb 1;21(3):294-302
pubmed: 11823422
Cell Rep. 2018 Jun 5;23(10):2928-2941
pubmed: 29874580
Biochim Biophys Acta. 2004 Jan 5;1676(1):51-62
pubmed: 14732490
Genes Dev. 2004 Nov 15;18(22):2822-34
pubmed: 15545635
Elife. 2017 Sep 19;6:
pubmed: 28925352
Dev Neurobiol. 2012 Dec;72(12):1471-81
pubmed: 22821665
Dev Biol. 2007 May 15;305(2):616-24
pubmed: 17362912
Adv Anat Embryol Cell Biol. 1984;85:1-164
pubmed: 6741688
J Anat. 1988 Aug;159:37-47
pubmed: 3248971
BMC Evol Biol. 2014 Aug 06;14:157
pubmed: 25099342
Development. 2004 Mar;131(5):1017-28
pubmed: 14973289
Int J Dev Biol. 2017;61(3-4-5):195-203
pubmed: 28621417
Development. 2004 Mar;131(5):965-73
pubmed: 14973298
Histochem Cell Biol. 2012 Aug;138(2):179-86
pubmed: 22820859
Mol Biol Cell. 2008 Jun;19(6):2588-96
pubmed: 18400942
Proc Natl Acad Sci U S A. 2018 Jun 26;115(26):E5954-E5962
pubmed: 29891676
Dis Model Mech. 2019 Nov 14;12(11):
pubmed: 31628096
Dev Neurobiol. 2010 Oct;70(12):796-812
pubmed: 20683859
Dev Biol. 1989 Sep;135(1):124-32
pubmed: 2548906
BMC Biol. 2014 Jul 12;12:53
pubmed: 25015411
Development. 2019 Jul 25;146(14):
pubmed: 31239243
J Anat. 2020 Feb;236(2):334-350
pubmed: 31670387
Development. 2019 Feb 1;146(3):
pubmed: 30709911
Development. 2014 Apr;141(8):1726-36
pubmed: 24715462
Genome Biol. 2016 Apr 28;17:77
pubmed: 27121950
Proc Natl Acad Sci U S A. 2007 Sep 11;104(37):14700-5
pubmed: 17804805
Nature. 2000 Feb 17;403(6771):734-40
pubmed: 10693795
Development. 1999 Nov;126(21):4749-62
pubmed: 10518492
Development. 1996 Nov;122(11):3607-16
pubmed: 8951076
Genes Dev. 2014 Feb 15;28(4):305-16
pubmed: 24532711
Development. 1997 Apr;124(8):1611-21
pubmed: 9108377
J Cell Biol. 2008 Feb 11;180(3):607-18
pubmed: 18268106
Development. 2004 Nov;131(21):5393-403
pubmed: 15469980
Development. 2013 Jun;140(11):2269-79
pubmed: 23615280
Development. 2001 Nov;128(21):4127-38
pubmed: 11684651

Auteurs

Shai Ofek (S)

Department of Medical Neurobiology, Institute of Medical Research Israel-Canada (IMRIC) and the Edmond and Lily Safra Center for Brain Sciences (ELSC), Hebrew University of Jerusalem-Hadassah Medical School, P.O.Box 12272, 9112102, Jerusalem, Israel.

Sophie Wiszniak (S)

Centre for Cancer Biology, University of South Australia and SA Pathology, North Terrace, Adelaide, SA, 5001, Australia.

Sarah Kagan (S)

Department of Medical Neurobiology, Institute of Medical Research Israel-Canada (IMRIC) and the Edmond and Lily Safra Center for Brain Sciences (ELSC), Hebrew University of Jerusalem-Hadassah Medical School, P.O.Box 12272, 9112102, Jerusalem, Israel.

Markus Tondl (M)

Centre for Cancer Biology, University of South Australia and SA Pathology, North Terrace, Adelaide, SA, 5001, Australia.

Quenten Schwarz (Q)

Centre for Cancer Biology, University of South Australia and SA Pathology, North Terrace, Adelaide, SA, 5001, Australia. Quenten.Schwarz@unisa.edu.au.

Chaya Kalcheim (C)

Department of Medical Neurobiology, Institute of Medical Research Israel-Canada (IMRIC) and the Edmond and Lily Safra Center for Brain Sciences (ELSC), Hebrew University of Jerusalem-Hadassah Medical School, P.O.Box 12272, 9112102, Jerusalem, Israel. kalcheim@cc.huji.ac.il.

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