Differential expression of neurexin genes in the mouse brain.

RRID AB_514500 RRID AB_840257 RRIDs: RRID SCR_003070 brain in situ hybridization mice neurexin synapse trans-synaptic adhesion

Journal

The Journal of comparative neurology
ISSN: 1096-9861
Titre abrégé: J Comp Neurol
Pays: United States
ID NLM: 0406041

Informations de publication

Date de publication:
15 08 2019
Historique:
received: 14 09 2018
revised: 04 01 2019
accepted: 01 02 2019
pubmed: 15 2 2019
medline: 15 9 2020
entrez: 15 2 2019
Statut: ppublish

Résumé

Synapses, highly specialized membrane junctions between neurons, connect presynaptic neurotransmitter release sites and postsynaptic ligand-gated channels. Neurexins (Nrxns), a family of presynaptic adhesion molecules, have been characterized as major regulators of synapse development and function. Via their extracellular domains, Nrxns bind to different postsynaptic proteins, generating highly diverse functional readouts through their postsynaptic binding partners. Not surprisingly given these versatile protein interactions, mutations and deletions of Nrxn genes have been identified in patients with autism spectrum disorders, intellectual disabilities, and schizophrenia. Therefore, elucidating the expression profiles of Nrxns in the brain is of high significance. Here, using chromogenic and fluorescent in situ hybridization, we characterize the expression patterns of Nrxn isoforms throughout the brain. We found that each Nrxn isoform displays a unique expression profile in a region-, cell type-, and sensory system-specific manner. Interestingly, we also found that αNrxn1 and αNrxn2 mRNAs are expressed in non-neuronal cells, including astrocytes and oligodendrocytes. Lastly, we found diverse expression patterns of genes that encode Nrxn binding proteins, such as Neuroligins (Nlgns), Leucine-rich repeat transmembrane neuronal protein (Lrrtms) and Latrophilins (Adgrls), suggesting that Nrxn proteins can mediate numerous combinations of trans-synaptic interactions. Together, our anatomical profiling of Nrxn gene expression reflects the diverse roles of Nrxn molecules.

Identifiants

pubmed: 30761534
doi: 10.1002/cne.24664
pmc: PMC6592846
mid: NIHMS1521319
doi:

Substances chimiques

Neural Cell Adhesion Molecules 0
Protein Isoforms 0

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1940-1965

Subventions

Organisme : NINDS NIH HHS
ID : R01 NS085215
Pays : United States

Informations de copyright

© 2019 Wiley Periodicals, Inc.

Références

Mol Cell Neurosci. 1999 Mar;13(3):218-27
pubmed: 10408888
J Cell Biol. 2001 Jul 23;154(2):435-45
pubmed: 11470830
J Neurosci. 2001 Oct 1;21(19):7691-704
pubmed: 11567059
Genomics. 2002 Jun;79(6):849-59
pubmed: 12036300
Cell. 2004 Dec 29;119(7):1013-26
pubmed: 15620359
Proc Natl Acad Sci U S A. 2005 Apr 26;102(17):6137-42
pubmed: 15837930
Science. 1992 Jul 3;257(5066):50-6
pubmed: 1621094
Neuron. 2005 Oct 20;48(2):229-36
pubmed: 16242404
Neuroscience. 2006;138(2):433-46
pubmed: 16406382
Neuron. 2006 Jul 20;51(2):171-8
pubmed: 16846852
Nat Neurosci. 2007 Feb;10(2):186-95
pubmed: 17237775
Nat Genet. 2007 Mar;39(3):319-28
pubmed: 17322880
Science. 2007 Apr 20;316(5823):445-9
pubmed: 17363630
Science. 2007 Oct 5;318(5847):71-6
pubmed: 17823315
J Biol Chem. 2008 Jan 25;283(4):2323-34
pubmed: 18006501
J Med Genet. 2008 Apr;45(4):239-43
pubmed: 18057082
Am J Hum Genet. 2008 Jan;82(1):199-207
pubmed: 18179900
Neurosci Lett. 2008 Jun 27;438(3):368-70
pubmed: 18490107
Proc Natl Acad Sci U S A. 2008 Sep 30;105(39):15124-9
pubmed: 18812509
Brain Res Rev. 2010 May;63(1-2):83-92
pubmed: 19948188
Neuron. 2009 Dec 24;64(6):791-8
pubmed: 20064387
Neuron. 2009 Dec 24;64(6):799-806
pubmed: 20064388
Biol Psychiatry. 2010 Apr 15;67(8):770-3
pubmed: 20163789
J Neurosci. 2010 Mar 24;30(12):4408-18
pubmed: 20335477
Am J Med Genet B Neuropsychiatr Genet. 2010 Jun 5;153B(4):937-47
pubmed: 20468056
Neuron. 2010 May 13;66(3):403-16
pubmed: 20471353
Cell. 2010 Jun 11;141(6):1068-79
pubmed: 20537373
Neuron. 2010 Jul 15;67(1):61-74
pubmed: 20624592
EMBO J. 2011 Jun 03;30(14):2908-19
pubmed: 21642956
Am J Hum Genet. 2012 Jan 13;90(1):133-41
pubmed: 22209245
J Biol Chem. 2012 Mar 16;287(12):9399-413
pubmed: 22262843
Front Neural Circuits. 2012 Apr 19;6:18
pubmed: 22529781
Transl Psychiatry. 2012 Sep 04;2:e158
pubmed: 22948383
J Neurosci. 2012 Dec 12;32(50):18035-46
pubmed: 23238719
J Neurosci. 2013 Feb 20;33(8):3612-23
pubmed: 23426688
Perception. 2013;42(3):341-55
pubmed: 23837210
PLoS One. 2013 Jun 28;8(6):e67114
pubmed: 23840597
Proc Natl Acad Sci U S A. 2014 Apr 1;111(13):E1291-9
pubmed: 24639501
Neuron. 2014 Oct 22;84(2):386-98
pubmed: 25284007
Dev Neurobiol. 2015 Jul;75(7):738-56
pubmed: 25369517
Transl Psychiatry. 2014 Nov 25;4:e484
pubmed: 25423136
Mol Genet Genomic Med. 2014 Nov;2(6):512-21
pubmed: 25614873
Elife. 2015 May 18;4:e07794
pubmed: 25985086
Nat Neurosci. 2015 Jul;18(7):997-1007
pubmed: 26030848
Glia. 2015 Nov;63(11):2023-2039
pubmed: 26119281
Neuron. 2015 Jul 15;87(2):326-40
pubmed: 26182417
Cell. 2016 Jan 14;164(1-2):183-196
pubmed: 26771491
Proc Natl Acad Sci U S A. 2016 Apr 12;113(15):4206-11
pubmed: 27035941
Neuron. 2016 May 18;90(4):752-67
pubmed: 27133466
Sci Rep. 2016 Oct 17;6:35456
pubmed: 27748445
Elife. 2016 Dec 13;5:
pubmed: 27960072
Cereb Cortex. 2017 Jan 1;27(1):216-232
pubmed: 28013231
Proc Natl Acad Sci U S A. 2017 Feb 14;114(7):E1253-E1262
pubmed: 28154140
Nat Neurosci. 2017 Apr;20(4):602-611
pubmed: 28263302
Neuron. 2017 May 3;94(3):611-625.e4
pubmed: 28472659
Mol Autism. 2017 May 22;8:21
pubmed: 28540026
Nat Commun. 2017 Sep 1;8(1):408
pubmed: 28864826
Cell. 2017 Nov 2;171(4):745-769
pubmed: 29100073
Nature. 2017 Nov 8;551(7679):192-197
pubmed: 29120426
Neuron. 1995 Mar;14(3):497-507
pubmed: 7695896
J Neurosci. 1995 Apr;15(4):2849-56
pubmed: 7722633
Cell. 1995 May 5;81(3):435-43
pubmed: 7736595
J Comp Neurol. 1978 Sep 15;181(2):375-95
pubmed: 80412
J Biol Chem. 1996 Feb 2;271(5):2676-82
pubmed: 8576240
J Biol Chem. 1998 Dec 25;273(52):34716-23
pubmed: 9856994

Auteurs

Motokazu Uchigashima (M)

Department of Neurobiology, Brudnick Neuropsychiatric Research Institute, University of Massachusetts Medical School, Worcester, Massachusetts.
Department of Anatomy, Hokkaido University Graduate School of Medicine, Sapporo, Hokkaido, Japan.

Amy Cheung (A)

Department of Neurobiology, Brudnick Neuropsychiatric Research Institute, University of Massachusetts Medical School, Worcester, Massachusetts.

Julie Suh (J)

Department of Neurobiology, Brudnick Neuropsychiatric Research Institute, University of Massachusetts Medical School, Worcester, Massachusetts.

Masahiko Watanabe (M)

Department of Anatomy, Hokkaido University Graduate School of Medicine, Sapporo, Hokkaido, Japan.

Kensuke Futai (K)

Department of Neurobiology, Brudnick Neuropsychiatric Research Institute, University of Massachusetts Medical School, Worcester, Massachusetts.

Articles similaires

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male
Humans Meals Time Factors Female Adult

Classifications MeSH