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DUF1220 Dosage Is Linearly Associated with Increasing Severity of the Three Primary Symptoms of Autism
One of the three most frequently documented copy number variations associated with autism spectrum disorder (ASD) is a 1q21.1 duplication that encompasses sequences encoding DUF1220 protein domains, the dosage of which we previously implicated in increased human brain size. Further, individuals with...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3961203/ https://www.ncbi.nlm.nih.gov/pubmed/24651471 http://dx.doi.org/10.1371/journal.pgen.1004241 |
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author | Davis, Jonathan M. Searles, Veronica B. Anderson, Nathan Keeney, Jonathon Dumas, Laura Sikela, James M. |
author_facet | Davis, Jonathan M. Searles, Veronica B. Anderson, Nathan Keeney, Jonathon Dumas, Laura Sikela, James M. |
author_sort | Davis, Jonathan M. |
collection | PubMed |
description | One of the three most frequently documented copy number variations associated with autism spectrum disorder (ASD) is a 1q21.1 duplication that encompasses sequences encoding DUF1220 protein domains, the dosage of which we previously implicated in increased human brain size. Further, individuals with ASD frequently display accelerated brain growth and a larger brain size that is also associated with increased symptom severity. Given these findings, we investigated the relationship between DUF1220 copy number and ASD severity, and here show that in individuals with ASD (n = 170), the copy number (dosage) of DUF1220 subtype CON1 is highly variable, ranging from 56 to 88 copies following a Gaussian distribution. More remarkably, in individuals with ASD CON1 copy number is also linearly associated, in a dose-response manner, with increased severity of each of the three primary symptoms of ASD: social deficits (p = 0.021), communicative impairments (p = 0.030), and repetitive behaviors (p = 0.047). These data indicate that DUF1220 protein domain (CON1) dosage has an ASD-wide effect and, as such, is likely to be a key component of a major pathway underlying ASD severity. Finally, these findings, by implicating the dosage of a previously unexamined, copy number polymorphic and brain evolution-related gene coding sequence in ASD severity, provide an important new direction for further research into the genetic factors underlying ASD. |
format | Online Article Text |
id | pubmed-3961203 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-39612032014-03-24 DUF1220 Dosage Is Linearly Associated with Increasing Severity of the Three Primary Symptoms of Autism Davis, Jonathan M. Searles, Veronica B. Anderson, Nathan Keeney, Jonathon Dumas, Laura Sikela, James M. PLoS Genet Research Article One of the three most frequently documented copy number variations associated with autism spectrum disorder (ASD) is a 1q21.1 duplication that encompasses sequences encoding DUF1220 protein domains, the dosage of which we previously implicated in increased human brain size. Further, individuals with ASD frequently display accelerated brain growth and a larger brain size that is also associated with increased symptom severity. Given these findings, we investigated the relationship between DUF1220 copy number and ASD severity, and here show that in individuals with ASD (n = 170), the copy number (dosage) of DUF1220 subtype CON1 is highly variable, ranging from 56 to 88 copies following a Gaussian distribution. More remarkably, in individuals with ASD CON1 copy number is also linearly associated, in a dose-response manner, with increased severity of each of the three primary symptoms of ASD: social deficits (p = 0.021), communicative impairments (p = 0.030), and repetitive behaviors (p = 0.047). These data indicate that DUF1220 protein domain (CON1) dosage has an ASD-wide effect and, as such, is likely to be a key component of a major pathway underlying ASD severity. Finally, these findings, by implicating the dosage of a previously unexamined, copy number polymorphic and brain evolution-related gene coding sequence in ASD severity, provide an important new direction for further research into the genetic factors underlying ASD. Public Library of Science 2014-03-20 /pmc/articles/PMC3961203/ /pubmed/24651471 http://dx.doi.org/10.1371/journal.pgen.1004241 Text en © 2014 Davis et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Davis, Jonathan M. Searles, Veronica B. Anderson, Nathan Keeney, Jonathon Dumas, Laura Sikela, James M. DUF1220 Dosage Is Linearly Associated with Increasing Severity of the Three Primary Symptoms of Autism |
title | DUF1220 Dosage Is Linearly Associated with Increasing Severity of the Three Primary Symptoms of Autism |
title_full | DUF1220 Dosage Is Linearly Associated with Increasing Severity of the Three Primary Symptoms of Autism |
title_fullStr | DUF1220 Dosage Is Linearly Associated with Increasing Severity of the Three Primary Symptoms of Autism |
title_full_unstemmed | DUF1220 Dosage Is Linearly Associated with Increasing Severity of the Three Primary Symptoms of Autism |
title_short | DUF1220 Dosage Is Linearly Associated with Increasing Severity of the Three Primary Symptoms of Autism |
title_sort | duf1220 dosage is linearly associated with increasing severity of the three primary symptoms of autism |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3961203/ https://www.ncbi.nlm.nih.gov/pubmed/24651471 http://dx.doi.org/10.1371/journal.pgen.1004241 |
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