Cargando…

Genetic aetiologies for childhood speech disorder: novel pathways co-expressed during brain development

Childhood apraxia of speech (CAS), the prototypic severe childhood speech disorder, is characterized by motor programming and planning deficits. Genetic factors make substantive contributions to CAS aetiology, with a monogenic pathogenic variant identified in a third of cases, implicating around 20...

Descripción completa

Detalles Bibliográficos
Autores principales: Kaspi, Antony, Hildebrand, Michael S., Jackson, Victoria E., Braden, Ruth, van Reyk, Olivia, Howell, Tegan, Debono, Simone, Lauretta, Mariana, Morison, Lottie, Coleman, Matthew J., Webster, Richard, Coman, David, Goel, Himanshu, Wallis, Mathew, Dabscheck, Gabriel, Downie, Lilian, Baker, Emma K., Parry-Fielder, Bronwyn, Ballard, Kirrie, Harrold, Eva, Ziegenfusz, Shaun, Bennett, Mark F., Robertson, Erandee, Wang, Longfei, Boys, Amber, Fisher, Simon E., Amor, David J., Scheffer, Ingrid E., Bahlo, Melanie, Morgan, Angela T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10208970/
https://www.ncbi.nlm.nih.gov/pubmed/36117209
http://dx.doi.org/10.1038/s41380-022-01764-8
_version_ 1785046782951030784
author Kaspi, Antony
Hildebrand, Michael S.
Jackson, Victoria E.
Braden, Ruth
van Reyk, Olivia
Howell, Tegan
Debono, Simone
Lauretta, Mariana
Morison, Lottie
Coleman, Matthew J.
Webster, Richard
Coman, David
Goel, Himanshu
Wallis, Mathew
Dabscheck, Gabriel
Downie, Lilian
Baker, Emma K.
Parry-Fielder, Bronwyn
Ballard, Kirrie
Harrold, Eva
Ziegenfusz, Shaun
Bennett, Mark F.
Robertson, Erandee
Wang, Longfei
Boys, Amber
Fisher, Simon E.
Amor, David J.
Scheffer, Ingrid E.
Bahlo, Melanie
Morgan, Angela T.
author_facet Kaspi, Antony
Hildebrand, Michael S.
Jackson, Victoria E.
Braden, Ruth
van Reyk, Olivia
Howell, Tegan
Debono, Simone
Lauretta, Mariana
Morison, Lottie
Coleman, Matthew J.
Webster, Richard
Coman, David
Goel, Himanshu
Wallis, Mathew
Dabscheck, Gabriel
Downie, Lilian
Baker, Emma K.
Parry-Fielder, Bronwyn
Ballard, Kirrie
Harrold, Eva
Ziegenfusz, Shaun
Bennett, Mark F.
Robertson, Erandee
Wang, Longfei
Boys, Amber
Fisher, Simon E.
Amor, David J.
Scheffer, Ingrid E.
Bahlo, Melanie
Morgan, Angela T.
author_sort Kaspi, Antony
collection PubMed
description Childhood apraxia of speech (CAS), the prototypic severe childhood speech disorder, is characterized by motor programming and planning deficits. Genetic factors make substantive contributions to CAS aetiology, with a monogenic pathogenic variant identified in a third of cases, implicating around 20 single genes to date. Here we aimed to identify molecular causation in 70 unrelated probands ascertained with CAS. We performed trio genome sequencing. Our bioinformatic analysis examined single nucleotide, indel, copy number, structural and short tandem repeat variants. We prioritised appropriate variants arising de novo or inherited that were expected to be damaging based on in silico predictions. We identified high confidence variants in 18/70 (26%) probands, almost doubling the current number of candidate genes for CAS. Three of the 18 variants affected SETBP1, SETD1A and DDX3X, thus confirming their roles in CAS, while the remaining 15 occurred in genes not previously associated with this disorder. Fifteen variants arose de novo and three were inherited. We provide further novel insights into the biology of child speech disorder, highlighting the roles of chromatin organization and gene regulation in CAS, and confirm that genes involved in CAS are co-expressed during brain development. Our findings confirm a diagnostic yield comparable to, or even higher, than other neurodevelopmental disorders with substantial de novo variant burden. Data also support the increasingly recognised overlaps between genes conferring risk for a range of neurodevelopmental disorders. Understanding the aetiological basis of CAS is critical to end the diagnostic odyssey and ensure affected individuals are poised for precision medicine trials.
format Online
Article
Text
id pubmed-10208970
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-102089702023-05-26 Genetic aetiologies for childhood speech disorder: novel pathways co-expressed during brain development Kaspi, Antony Hildebrand, Michael S. Jackson, Victoria E. Braden, Ruth van Reyk, Olivia Howell, Tegan Debono, Simone Lauretta, Mariana Morison, Lottie Coleman, Matthew J. Webster, Richard Coman, David Goel, Himanshu Wallis, Mathew Dabscheck, Gabriel Downie, Lilian Baker, Emma K. Parry-Fielder, Bronwyn Ballard, Kirrie Harrold, Eva Ziegenfusz, Shaun Bennett, Mark F. Robertson, Erandee Wang, Longfei Boys, Amber Fisher, Simon E. Amor, David J. Scheffer, Ingrid E. Bahlo, Melanie Morgan, Angela T. Mol Psychiatry Article Childhood apraxia of speech (CAS), the prototypic severe childhood speech disorder, is characterized by motor programming and planning deficits. Genetic factors make substantive contributions to CAS aetiology, with a monogenic pathogenic variant identified in a third of cases, implicating around 20 single genes to date. Here we aimed to identify molecular causation in 70 unrelated probands ascertained with CAS. We performed trio genome sequencing. Our bioinformatic analysis examined single nucleotide, indel, copy number, structural and short tandem repeat variants. We prioritised appropriate variants arising de novo or inherited that were expected to be damaging based on in silico predictions. We identified high confidence variants in 18/70 (26%) probands, almost doubling the current number of candidate genes for CAS. Three of the 18 variants affected SETBP1, SETD1A and DDX3X, thus confirming their roles in CAS, while the remaining 15 occurred in genes not previously associated with this disorder. Fifteen variants arose de novo and three were inherited. We provide further novel insights into the biology of child speech disorder, highlighting the roles of chromatin organization and gene regulation in CAS, and confirm that genes involved in CAS are co-expressed during brain development. Our findings confirm a diagnostic yield comparable to, or even higher, than other neurodevelopmental disorders with substantial de novo variant burden. Data also support the increasingly recognised overlaps between genes conferring risk for a range of neurodevelopmental disorders. Understanding the aetiological basis of CAS is critical to end the diagnostic odyssey and ensure affected individuals are poised for precision medicine trials. Nature Publishing Group UK 2022-09-18 2023 /pmc/articles/PMC10208970/ /pubmed/36117209 http://dx.doi.org/10.1038/s41380-022-01764-8 Text en © The Author(s) 2022, corrected publication 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Kaspi, Antony
Hildebrand, Michael S.
Jackson, Victoria E.
Braden, Ruth
van Reyk, Olivia
Howell, Tegan
Debono, Simone
Lauretta, Mariana
Morison, Lottie
Coleman, Matthew J.
Webster, Richard
Coman, David
Goel, Himanshu
Wallis, Mathew
Dabscheck, Gabriel
Downie, Lilian
Baker, Emma K.
Parry-Fielder, Bronwyn
Ballard, Kirrie
Harrold, Eva
Ziegenfusz, Shaun
Bennett, Mark F.
Robertson, Erandee
Wang, Longfei
Boys, Amber
Fisher, Simon E.
Amor, David J.
Scheffer, Ingrid E.
Bahlo, Melanie
Morgan, Angela T.
Genetic aetiologies for childhood speech disorder: novel pathways co-expressed during brain development
title Genetic aetiologies for childhood speech disorder: novel pathways co-expressed during brain development
title_full Genetic aetiologies for childhood speech disorder: novel pathways co-expressed during brain development
title_fullStr Genetic aetiologies for childhood speech disorder: novel pathways co-expressed during brain development
title_full_unstemmed Genetic aetiologies for childhood speech disorder: novel pathways co-expressed during brain development
title_short Genetic aetiologies for childhood speech disorder: novel pathways co-expressed during brain development
title_sort genetic aetiologies for childhood speech disorder: novel pathways co-expressed during brain development
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10208970/
https://www.ncbi.nlm.nih.gov/pubmed/36117209
http://dx.doi.org/10.1038/s41380-022-01764-8
work_keys_str_mv AT kaspiantony geneticaetiologiesforchildhoodspeechdisordernovelpathwayscoexpressedduringbraindevelopment
AT hildebrandmichaels geneticaetiologiesforchildhoodspeechdisordernovelpathwayscoexpressedduringbraindevelopment
AT jacksonvictoriae geneticaetiologiesforchildhoodspeechdisordernovelpathwayscoexpressedduringbraindevelopment
AT bradenruth geneticaetiologiesforchildhoodspeechdisordernovelpathwayscoexpressedduringbraindevelopment
AT vanreykolivia geneticaetiologiesforchildhoodspeechdisordernovelpathwayscoexpressedduringbraindevelopment
AT howelltegan geneticaetiologiesforchildhoodspeechdisordernovelpathwayscoexpressedduringbraindevelopment
AT debonosimone geneticaetiologiesforchildhoodspeechdisordernovelpathwayscoexpressedduringbraindevelopment
AT laurettamariana geneticaetiologiesforchildhoodspeechdisordernovelpathwayscoexpressedduringbraindevelopment
AT morisonlottie geneticaetiologiesforchildhoodspeechdisordernovelpathwayscoexpressedduringbraindevelopment
AT colemanmatthewj geneticaetiologiesforchildhoodspeechdisordernovelpathwayscoexpressedduringbraindevelopment
AT websterrichard geneticaetiologiesforchildhoodspeechdisordernovelpathwayscoexpressedduringbraindevelopment
AT comandavid geneticaetiologiesforchildhoodspeechdisordernovelpathwayscoexpressedduringbraindevelopment
AT goelhimanshu geneticaetiologiesforchildhoodspeechdisordernovelpathwayscoexpressedduringbraindevelopment
AT wallismathew geneticaetiologiesforchildhoodspeechdisordernovelpathwayscoexpressedduringbraindevelopment
AT dabscheckgabriel geneticaetiologiesforchildhoodspeechdisordernovelpathwayscoexpressedduringbraindevelopment
AT downielilian geneticaetiologiesforchildhoodspeechdisordernovelpathwayscoexpressedduringbraindevelopment
AT bakeremmak geneticaetiologiesforchildhoodspeechdisordernovelpathwayscoexpressedduringbraindevelopment
AT parryfielderbronwyn geneticaetiologiesforchildhoodspeechdisordernovelpathwayscoexpressedduringbraindevelopment
AT ballardkirrie geneticaetiologiesforchildhoodspeechdisordernovelpathwayscoexpressedduringbraindevelopment
AT harroldeva geneticaetiologiesforchildhoodspeechdisordernovelpathwayscoexpressedduringbraindevelopment
AT ziegenfuszshaun geneticaetiologiesforchildhoodspeechdisordernovelpathwayscoexpressedduringbraindevelopment
AT bennettmarkf geneticaetiologiesforchildhoodspeechdisordernovelpathwayscoexpressedduringbraindevelopment
AT robertsonerandee geneticaetiologiesforchildhoodspeechdisordernovelpathwayscoexpressedduringbraindevelopment
AT wanglongfei geneticaetiologiesforchildhoodspeechdisordernovelpathwayscoexpressedduringbraindevelopment
AT boysamber geneticaetiologiesforchildhoodspeechdisordernovelpathwayscoexpressedduringbraindevelopment
AT fishersimone geneticaetiologiesforchildhoodspeechdisordernovelpathwayscoexpressedduringbraindevelopment
AT amordavidj geneticaetiologiesforchildhoodspeechdisordernovelpathwayscoexpressedduringbraindevelopment
AT schefferingride geneticaetiologiesforchildhoodspeechdisordernovelpathwayscoexpressedduringbraindevelopment
AT bahlomelanie geneticaetiologiesforchildhoodspeechdisordernovelpathwayscoexpressedduringbraindevelopment
AT morganangelat geneticaetiologiesforchildhoodspeechdisordernovelpathwayscoexpressedduringbraindevelopment