Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
3
pubmed:dateCreated
2010-9-9
pubmed:abstractText
The role of de novo mutations (DNMs) in common diseases remains largely unknown. Nonetheless, the rate of de novo deleterious mutations and the strength of selection against de novo mutations are critical to understanding the genetic architecture of a disease. Discovery of high-impact DNMs requires substantial high-resolution interrogation of partial or complete genomes of families via resequencing. We hypothesized that deleterious DNMs may play a role in cases of autism spectrum disorders (ASD) and schizophrenia (SCZ), two etiologically heterogeneous disorders with significantly reduced reproductive fitness. We present a direct measure of the de novo mutation rate (?) and selective constraints from DNMs estimated from a deep resequencing data set generated from a large cohort of ASD and SCZ cases (n = 285) and population control individuals (n = 285) with available parental DNA. A survey of ?430 Mb of DNA from 401 synapse-expressed genes across all cases and 25 Mb of DNA in controls found 28 candidate DNMs, 13 of which were cell line artifacts. Our calculated direct neutral mutation rate (1.36 × 10(-8)) is similar to previous indirect estimates, but we observed a significant excess of potentially deleterious DNMs in ASD and SCZ individuals. Our results emphasize the importance of DNMs as genetic mechanisms in ASD and SCZ and the limitations of using DNA from archived cell lines to identify functional variants.
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/20797689-10625077, http://linkedlifedata.com/resource/pubmed/commentcorrection/20797689-10978293, http://linkedlifedata.com/resource/pubmed/commentcorrection/20797689-11371586, http://linkedlifedata.com/resource/pubmed/commentcorrection/20797689-11738536, http://linkedlifedata.com/resource/pubmed/commentcorrection/20797689-11986135, http://linkedlifedata.com/resource/pubmed/commentcorrection/20797689-12202775, http://linkedlifedata.com/resource/pubmed/commentcorrection/20797689-12497628, http://linkedlifedata.com/resource/pubmed/commentcorrection/20797689-12520017, http://linkedlifedata.com/resource/pubmed/commentcorrection/20797689-12824425, http://linkedlifedata.com/resource/pubmed/commentcorrection/20797689-12892872, http://linkedlifedata.com/resource/pubmed/commentcorrection/20797689-15254446, http://linkedlifedata.com/resource/pubmed/commentcorrection/20797689-15374571, http://linkedlifedata.com/resource/pubmed/commentcorrection/20797689-15389766, http://linkedlifedata.com/resource/pubmed/commentcorrection/20797689-15572359, http://linkedlifedata.com/resource/pubmed/commentcorrection/20797689-15858952, http://linkedlifedata.com/resource/pubmed/commentcorrection/20797689-15916472, http://linkedlifedata.com/resource/pubmed/commentcorrection/20797689-15965030, http://linkedlifedata.com/resource/pubmed/commentcorrection/20797689-16432200, http://linkedlifedata.com/resource/pubmed/commentcorrection/20797689-16452087, http://linkedlifedata.com/resource/pubmed/commentcorrection/20797689-17098931, http://linkedlifedata.com/resource/pubmed/commentcorrection/20797689-17236127, http://linkedlifedata.com/resource/pubmed/commentcorrection/20797689-17357078, http://linkedlifedata.com/resource/pubmed/commentcorrection/20797689-17404129, http://linkedlifedata.com/resource/pubmed/commentcorrection/20797689-17594490, http://linkedlifedata.com/resource/pubmed/commentcorrection/20797689-17988326, http://linkedlifedata.com/resource/pubmed/commentcorrection/20797689-17999366, http://linkedlifedata.com/resource/pubmed/commentcorrection/20797689-18511947, http://linkedlifedata.com/resource/pubmed/commentcorrection/20797689-18668039, http://linkedlifedata.com/resource/pubmed/commentcorrection/20797689-18801879, http://linkedlifedata.com/resource/pubmed/commentcorrection/20797689-18984621, http://linkedlifedata.com/resource/pubmed/commentcorrection/20797689-19224114, http://linkedlifedata.com/resource/pubmed/commentcorrection/20797689-20220176, http://linkedlifedata.com/resource/pubmed/commentcorrection/20797689-20360734, http://linkedlifedata.com/resource/pubmed/commentcorrection/20797689-20385823, http://linkedlifedata.com/resource/pubmed/commentcorrection/20797689-8885043, http://linkedlifedata.com/resource/pubmed/commentcorrection/20797689-9847410, http://linkedlifedata.com/resource/pubmed/commentcorrection/20797689-9950425
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:status
MEDLINE
pubmed:month
Sep
pubmed:issn
1537-6605
pubmed:author
pubmed-author:AddingtonAnjené MAM, pubmed-author:AwadallaPhilipP, pubmed-author:BoykoAdamA, pubmed-author:BustamanteCarlosC, pubmed-author:CôtéMélanieM, pubmed-author:CasalsFerranF, pubmed-author:DaoudHusseinH, pubmed-author:DeLisiJ Lynn EJL, pubmed-author:DrapeauPierreP, pubmed-author:DubéMarie-PierreMP, pubmed-author:Eyre-WalkerAdamA, pubmed-author:FombonneEricE, pubmed-author:GauthierJulieJ, pubmed-author:GriffingAlexander RAR, pubmed-author:HamdanFadi FFF, pubmed-author:HenrionEdouardE, pubmed-author:JooberRidhaR, pubmed-author:KeeblerJonJ, pubmed-author:KrebsMarie-OdileMO, pubmed-author:LafrenièreRonald GRG, pubmed-author:MarineauClaudeC, pubmed-author:MilletBrunoB, pubmed-author:MottronLaurentL, pubmed-author:MyersRachel ARA, pubmed-author:PitonAmélieA, pubmed-author:RapoportJudith LJL, pubmed-author:RouleauGuy AGA, pubmed-author:Roy-GagnonMarie-HélèneMH, pubmed-author:SpiegelmanDanD, pubmed-author:StoneEric AEA, pubmed-author:TarabeuxJulienJ, pubmed-author:XiongLanL, pubmed-author:YangYanY, pubmed-author:ZilversmitMartineM
pubmed:copyrightInfo
2010 The American Society of Human Genetics. Published by Elsevier Inc. All rights reserved.
pubmed:issnType
Electronic
pubmed:day
10
pubmed:volume
87
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
316-24
pubmed:dateRevised
2011-7-26
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