Cargando…

Genome-wide detection of human intronic AG-gain variants located between splicing branchpoints and canonical splice acceptor sites

Human genetic variants that introduce an AG into the intronic region between the branchpoint (BP) and the canonical splice acceptor site (ACC) of protein-coding genes can disrupt pre-mRNA splicing. Using our genome-wide BP database, we delineated the BP-ACC segments of all human introns and found ex...

Descripción completa

Detalles Bibliográficos
Autores principales: Zhang, Peng, Chaldebas, Matthieu, Ogishi, Masato, Al Qureshah, Fahd, Ponsin, Khoren, Feng, Yi, Rinchai, Darawan, Milisavljevic, Baptiste, Han, Ji Eun, Moncada-Vélez, Marcela, Keles, Sevgi, Schröder, Bernd, Stenson, Peter D., Cooper, David N., Cobat, Aurélie, Boisson, Bertrand, Zhang, Qian, Boisson-Dupuis, Stéphanie, Abel, Laurent, Casanova, Jean-Laurent
Formato: Online Artículo Texto
Lenguaje:English
Publicado: National Academy of Sciences 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10655562/
https://www.ncbi.nlm.nih.gov/pubmed/37931111
http://dx.doi.org/10.1073/pnas.2314225120
_version_ 1785136849372577792
author Zhang, Peng
Chaldebas, Matthieu
Ogishi, Masato
Al Qureshah, Fahd
Ponsin, Khoren
Feng, Yi
Rinchai, Darawan
Milisavljevic, Baptiste
Han, Ji Eun
Moncada-Vélez, Marcela
Keles, Sevgi
Schröder, Bernd
Stenson, Peter D.
Cooper, David N.
Cobat, Aurélie
Boisson, Bertrand
Zhang, Qian
Boisson-Dupuis, Stéphanie
Abel, Laurent
Casanova, Jean-Laurent
author_facet Zhang, Peng
Chaldebas, Matthieu
Ogishi, Masato
Al Qureshah, Fahd
Ponsin, Khoren
Feng, Yi
Rinchai, Darawan
Milisavljevic, Baptiste
Han, Ji Eun
Moncada-Vélez, Marcela
Keles, Sevgi
Schröder, Bernd
Stenson, Peter D.
Cooper, David N.
Cobat, Aurélie
Boisson, Bertrand
Zhang, Qian
Boisson-Dupuis, Stéphanie
Abel, Laurent
Casanova, Jean-Laurent
author_sort Zhang, Peng
collection PubMed
description Human genetic variants that introduce an AG into the intronic region between the branchpoint (BP) and the canonical splice acceptor site (ACC) of protein-coding genes can disrupt pre-mRNA splicing. Using our genome-wide BP database, we delineated the BP-ACC segments of all human introns and found extreme depletion of AG/YAG in the [BP+8, ACC-4] high-risk region. We developed AGAIN as a genome-wide computational approach to systematically and precisely pinpoint intronic AG-gain variants within the BP-ACC regions. AGAIN identified 350 AG-gain variants from the Human Gene Mutation Database, all of which alter splicing and cause disease. Among them, 74% created new acceptor sites, whereas 31% resulted in complete exon skipping. AGAIN also predicts the protein-level products resulting from these two consequences. We performed AGAIN on our exome/genomes database of patients with severe infectious diseases but without known genetic etiology and identified a private homozygous intronic AG-gain variant in the antimycobacterial gene SPPL2A in a patient with mycobacterial disease. AGAIN also predicts a retention of six intronic nucleotides that encode an in-frame stop codon, turning AG-gain into stop-gain. This allele was then confirmed experimentally to lead to loss of function by disrupting splicing. We further showed that AG-gain variants inside the high-risk region led to misspliced products, while those outside the region did not, by two case studies in genes STAT1 and IRF7. We finally evaluated AGAIN on our 14 paired exome-RNAseq samples and found that 82% of AG-gain variants in high-risk regions showed evidence of missplicing. AGAIN is publicly available from https://hgidsoft.rockefeller.edu/AGAIN and https://github.com/casanova-lab/AGAIN.
format Online
Article
Text
id pubmed-10655562
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher National Academy of Sciences
record_format MEDLINE/PubMed
spelling pubmed-106555622023-11-06 Genome-wide detection of human intronic AG-gain variants located between splicing branchpoints and canonical splice acceptor sites Zhang, Peng Chaldebas, Matthieu Ogishi, Masato Al Qureshah, Fahd Ponsin, Khoren Feng, Yi Rinchai, Darawan Milisavljevic, Baptiste Han, Ji Eun Moncada-Vélez, Marcela Keles, Sevgi Schröder, Bernd Stenson, Peter D. Cooper, David N. Cobat, Aurélie Boisson, Bertrand Zhang, Qian Boisson-Dupuis, Stéphanie Abel, Laurent Casanova, Jean-Laurent Proc Natl Acad Sci U S A Biological Sciences Human genetic variants that introduce an AG into the intronic region between the branchpoint (BP) and the canonical splice acceptor site (ACC) of protein-coding genes can disrupt pre-mRNA splicing. Using our genome-wide BP database, we delineated the BP-ACC segments of all human introns and found extreme depletion of AG/YAG in the [BP+8, ACC-4] high-risk region. We developed AGAIN as a genome-wide computational approach to systematically and precisely pinpoint intronic AG-gain variants within the BP-ACC regions. AGAIN identified 350 AG-gain variants from the Human Gene Mutation Database, all of which alter splicing and cause disease. Among them, 74% created new acceptor sites, whereas 31% resulted in complete exon skipping. AGAIN also predicts the protein-level products resulting from these two consequences. We performed AGAIN on our exome/genomes database of patients with severe infectious diseases but without known genetic etiology and identified a private homozygous intronic AG-gain variant in the antimycobacterial gene SPPL2A in a patient with mycobacterial disease. AGAIN also predicts a retention of six intronic nucleotides that encode an in-frame stop codon, turning AG-gain into stop-gain. This allele was then confirmed experimentally to lead to loss of function by disrupting splicing. We further showed that AG-gain variants inside the high-risk region led to misspliced products, while those outside the region did not, by two case studies in genes STAT1 and IRF7. We finally evaluated AGAIN on our 14 paired exome-RNAseq samples and found that 82% of AG-gain variants in high-risk regions showed evidence of missplicing. AGAIN is publicly available from https://hgidsoft.rockefeller.edu/AGAIN and https://github.com/casanova-lab/AGAIN. National Academy of Sciences 2023-11-06 2023-11-14 /pmc/articles/PMC10655562/ /pubmed/37931111 http://dx.doi.org/10.1073/pnas.2314225120 Text en Copyright © 2023 the Author(s). Published by PNAS. https://creativecommons.org/licenses/by/4.0/This open access article is distributed under Creative Commons Attribution License 4.0 (CC BY) (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Biological Sciences
Zhang, Peng
Chaldebas, Matthieu
Ogishi, Masato
Al Qureshah, Fahd
Ponsin, Khoren
Feng, Yi
Rinchai, Darawan
Milisavljevic, Baptiste
Han, Ji Eun
Moncada-Vélez, Marcela
Keles, Sevgi
Schröder, Bernd
Stenson, Peter D.
Cooper, David N.
Cobat, Aurélie
Boisson, Bertrand
Zhang, Qian
Boisson-Dupuis, Stéphanie
Abel, Laurent
Casanova, Jean-Laurent
Genome-wide detection of human intronic AG-gain variants located between splicing branchpoints and canonical splice acceptor sites
title Genome-wide detection of human intronic AG-gain variants located between splicing branchpoints and canonical splice acceptor sites
title_full Genome-wide detection of human intronic AG-gain variants located between splicing branchpoints and canonical splice acceptor sites
title_fullStr Genome-wide detection of human intronic AG-gain variants located between splicing branchpoints and canonical splice acceptor sites
title_full_unstemmed Genome-wide detection of human intronic AG-gain variants located between splicing branchpoints and canonical splice acceptor sites
title_short Genome-wide detection of human intronic AG-gain variants located between splicing branchpoints and canonical splice acceptor sites
title_sort genome-wide detection of human intronic ag-gain variants located between splicing branchpoints and canonical splice acceptor sites
topic Biological Sciences
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10655562/
https://www.ncbi.nlm.nih.gov/pubmed/37931111
http://dx.doi.org/10.1073/pnas.2314225120
work_keys_str_mv AT zhangpeng genomewidedetectionofhumanintronicaggainvariantslocatedbetweensplicingbranchpointsandcanonicalspliceacceptorsites
AT chaldebasmatthieu genomewidedetectionofhumanintronicaggainvariantslocatedbetweensplicingbranchpointsandcanonicalspliceacceptorsites
AT ogishimasato genomewidedetectionofhumanintronicaggainvariantslocatedbetweensplicingbranchpointsandcanonicalspliceacceptorsites
AT alqureshahfahd genomewidedetectionofhumanintronicaggainvariantslocatedbetweensplicingbranchpointsandcanonicalspliceacceptorsites
AT ponsinkhoren genomewidedetectionofhumanintronicaggainvariantslocatedbetweensplicingbranchpointsandcanonicalspliceacceptorsites
AT fengyi genomewidedetectionofhumanintronicaggainvariantslocatedbetweensplicingbranchpointsandcanonicalspliceacceptorsites
AT rinchaidarawan genomewidedetectionofhumanintronicaggainvariantslocatedbetweensplicingbranchpointsandcanonicalspliceacceptorsites
AT milisavljevicbaptiste genomewidedetectionofhumanintronicaggainvariantslocatedbetweensplicingbranchpointsandcanonicalspliceacceptorsites
AT hanjieun genomewidedetectionofhumanintronicaggainvariantslocatedbetweensplicingbranchpointsandcanonicalspliceacceptorsites
AT moncadavelezmarcela genomewidedetectionofhumanintronicaggainvariantslocatedbetweensplicingbranchpointsandcanonicalspliceacceptorsites
AT kelessevgi genomewidedetectionofhumanintronicaggainvariantslocatedbetweensplicingbranchpointsandcanonicalspliceacceptorsites
AT schroderbernd genomewidedetectionofhumanintronicaggainvariantslocatedbetweensplicingbranchpointsandcanonicalspliceacceptorsites
AT stensonpeterd genomewidedetectionofhumanintronicaggainvariantslocatedbetweensplicingbranchpointsandcanonicalspliceacceptorsites
AT cooperdavidn genomewidedetectionofhumanintronicaggainvariantslocatedbetweensplicingbranchpointsandcanonicalspliceacceptorsites
AT cobataurelie genomewidedetectionofhumanintronicaggainvariantslocatedbetweensplicingbranchpointsandcanonicalspliceacceptorsites
AT boissonbertrand genomewidedetectionofhumanintronicaggainvariantslocatedbetweensplicingbranchpointsandcanonicalspliceacceptorsites
AT zhangqian genomewidedetectionofhumanintronicaggainvariantslocatedbetweensplicingbranchpointsandcanonicalspliceacceptorsites
AT boissondupuisstephanie genomewidedetectionofhumanintronicaggainvariantslocatedbetweensplicingbranchpointsandcanonicalspliceacceptorsites
AT abellaurent genomewidedetectionofhumanintronicaggainvariantslocatedbetweensplicingbranchpointsandcanonicalspliceacceptorsites
AT casanovajeanlaurent genomewidedetectionofhumanintronicaggainvariantslocatedbetweensplicingbranchpointsandcanonicalspliceacceptorsites