| 释义 |
- References
- Further reading
{{Infobox_gene}}Neuroligin-3 is a protein that in humans is encoded by the NLGN3 gene.[1][2][3]This gene encodes a member of the neuroligin family of neuronal cell surface proteins. Neuroligins may act as splice site-specific ligands for beta-neurexins and may be involved in the formation and remodeling of central nervous system synapses. Mutations in this gene may be associated with autism spectrum disorders (ASDs). Multiple transcript variants encoding distinct isoforms have been identified for this gene, but their full length sequences have not been determined.[4] References1. ^{{cite journal | vauthors = Philibert RA, Winfield SL, Sandhu HK, Martin BM, Ginns EI | title = The structure and expression of the human neuroligin-3 gene | journal = Gene | volume = 246 | issue = 1–2 | pages = 303–10 |date=May 2000 | pmid = 10767552 | pmc = | doi =10.1016/S0378-1119(00)00049-4 }}
2. ^{{cite journal | vauthors = Nagase T, Kikuno R, Ishikawa K, Hirosawa M, Ohara O | title = Prediction of the coding sequences of unidentified human genes. XVII. The complete sequences of 100 new cDNA clones from brain which code for large proteins in vitro | journal = DNA Res | volume = 7 | issue = 2 | pages = 143–50 |date=Sep 2000 | pmid = 10819331 | pmc = | doi =10.1093/dnares/7.2.143 }}
3. ^{{cite web | title = Entrez Gene: NLGN3 neuroligin 3| url = https://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=54413| accessdate = }}
4. ^{{cite web | title = Entrez Gene: NLGN3 neuroligin 3| url = https://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=54413| accessdate = }}
Further reading{{refbegin | 2}}- {{cite journal | vauthors=Missler M, Fernandez-Chacon R, Südhof TC |title=The making of neurexins |journal=J. Neurochem. |volume=71 |issue= 4 |pages= 1339–47 |year= 1998 |pmid= 9751164 |doi=10.1046/j.1471-4159.1998.71041339.x }}
- {{cite journal | vauthors=Cantallops I, Cline HT |title=Synapse formation: if it looks like a duck and quacks like a duck ... |journal=Curr. Biol. |volume=10 |issue= 17 |pages= R620–3 |year= 2000 |pmid= 10996085 |doi=10.1016/S0960-9822(00)00663-1 }}
- {{cite journal | vauthors=Ichtchenko K, Nguyen T, Südhof TC |title=Structures, alternative splicing, and neurexin binding of multiple neuroligins |journal=J. Biol. Chem. |volume=271 |issue= 5 |pages= 2676–82 |year= 1996 |pmid= 8576240 |doi=10.1074/jbc.271.5.2676 }}
- {{cite journal |vauthors=Irie M, Hata Y, Takeuchi M, etal |title=Binding of neuroligins to PSD-95 |journal=Science |volume=277 |issue= 5331 |pages= 1511–5 |year= 1997 |pmid= 9278515 |doi=10.1126/science.277.5331.1511 }}
- {{cite journal | vauthors=Nguyen T, Südhof TC |title=Binding properties of neuroligin 1 and neurexin 1beta reveal function as heterophilic cell adhesion molecules |journal=J. Biol. Chem. |volume=272 |issue= 41 |pages= 26032–9 |year= 1997 |pmid= 9325340 |doi=10.1074/jbc.272.41.26032 }}
- {{cite journal | vauthors=Gilbert M, Smith J, Roskams AJ, Auld VJ |title=Neuroligin 3 is a vertebrate gliotactin expressed in the olfactory ensheathing glia, a growth-promoting class of macroglia |journal=Glia |volume=34 |issue= 3 |pages= 151–64 |year= 2001 |pmid= 11329178 |doi=10.1002/glia.1050 }}
- {{cite journal |vauthors=Strausberg RL, Feingold EA, Grouse LH, etal |title=Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=99 |issue= 26 |pages= 16899–903 |year= 2003 |pmid= 12477932 |doi= 10.1073/pnas.242603899 | pmc=139241 }}
- {{cite journal |vauthors=Jamain S, Quach H, Betancur C, etal |title=Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism |journal=Nat. Genet. |volume=34 |issue= 1 |pages= 27–9 |year= 2003 |pmid= 12669065 |doi= 10.1038/ng1136 | pmc=1925054 }}
- {{cite journal |vauthors=Ota T, Suzuki Y, Nishikawa T, etal |title=Complete sequencing and characterization of 21,243 full-length human cDNAs |journal=Nat. Genet. |volume=36 |issue= 1 |pages= 40–5 |year= 2004 |pmid= 14702039 |doi= 10.1038/ng1285 }}
- {{cite journal |vauthors=Vincent JB, Kolozsvari D, Roberts WS, etal |title=Mutation screening of X-chromosomal neuroligin genes: no mutations in 196 autism probands |journal=Am. J. Med. Genet. B Neuropsychiatr. Genet. |volume=129 |issue= 1 |pages= 82–4 |year= 2005 |pmid= 15274046 |doi= 10.1002/ajmg.b.30069 }}
- {{cite journal |vauthors=Gauthier J, Bonnel A, St-Onge J, etal |title=NLGN3/NLGN4 gene mutations are not responsible for autism in the Quebec population |journal=Am. J. Med. Genet. B Neuropsychiatr. Genet. |volume=132 |issue= 1 |pages= 74–5 |year= 2005 |pmid= 15389766 |doi= 10.1002/ajmg.b.30066 }}
- {{cite journal |vauthors=Yan J, Oliveira G, Coutinho A, etal |title=Analysis of the neuroligin 3 and 4 genes in autism and other neuropsychiatric patients |journal=Mol. Psychiatry |volume=10 |issue= 4 |pages= 329–32 |year= 2005 |pmid= 15622415 |doi= 10.1038/sj.mp.4001629 }}
- {{cite journal |vauthors=Otsuki T, Ota T, Nishikawa T, etal |title=Signal sequence and keyword trap in silico for selection of full-length human cDNAs encoding secretion or membrane proteins from oligo-capped cDNA libraries |journal=DNA Res. |volume=12 |issue= 2 |pages= 117–26 |year= 2007 |pmid= 16303743 |doi= 10.1093/dnares/12.2.117 }}
- {{cite journal |vauthors=Blasi F, Bacchelli E, Pesaresi G, etal |title=Absence of coding mutations in the X-linked genes neuroligin 3 and neuroligin 4 in individuals with autism from the IMGSAC collection |journal=Am. J. Med. Genet. B Neuropsychiatr. Genet. |volume=141 |issue= 3 |pages= 220–1 |year= 2006 |pmid= 16508939 |doi= 10.1002/ajmg.b.30287 }}
- {{cite journal |vauthors=Talebizadeh Z, Lam DY, Theodoro MF, etal |title=Novel splice isoforms for NLGN3 and NLGN4 with possible implications in autism |journal=J. Med. Genet. |volume=43 |issue= 5 |pages= e21 |year= 2006 |pmid= 16648374 |doi= 10.1136/jmg.2005.036897 | pmc=2564526 }}
- {{cite journal |vauthors=Yamakawa H, Oyama S, Mitsuhashi H, etal |title=Neuroligins 3 and 4X interact with syntrophin-gamma2, and the interactions are affected by autism-related mutations |journal=Biochem. Biophys. Res. Commun. |volume=355 |issue= 1 |pages= 41–6 |year= 2007 |pmid= 17292328 |doi= 10.1016/j.bbrc.2007.01.127 }}
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