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Pathogenicity and selective constraint on variation near splice sites

Title: Pathogenicity and selective constraint on variation near splice sites
Authors: Lord, Jenny; Gallone, Giuseppe; Short, Patrick J.; McRae, Jeremy F.; Ironfield, Holly; Wynn, Elizabeth H.; Gerety, Sebastian S.; He, Liu; Kerr, Bronwyn; Johnson, Diana S.; McCann, Emma; Kinning, Esther; Flinter, Frances; Temple, I. Karen; Clayton-Smith, Jill; McEntagart, Meriel; Lynch, Sally Ann; Joss, Shelagh; Douzgou, Sofia; Dabir, Tabib; Clowes, Virginia; McConnell, Vivienne P.M.; Lam, Wayne; Wright, Caroline F.; FitzPatrick, David R.; Firth, Helen V.; Barrett, Jeffrey C.; Hurles, Matthew E.; on behalf of the Deciphering Developmental Disorders study
Publisher Information: Cold Spring Harbor Laboratory Press
Publication Year: 2019
Collection: HighWire Press (Stanford University)
Subject Terms: RESEARCH
Description: Mutations that perturb normal pre-mRNA splicing are significant contributors to human disease. We used exome sequencing data from 7833 probands with developmental disorders (DDs) and their unaffected parents, as well as more than 60,000 aggregated exomes from the Exome Aggregation Consortium, to investigate selection around the splice sites and quantify the contribution of splicing mutations to DDs. Patterns of purifying selection, a deficit of variants in highly constrained genes in healthy subjects, and excess de novo mutations in patients highlighted particular positions within and around the consensus splice site of greater functional relevance. By using mutational burden analyses in this large cohort of proband–parent trios, we could estimate in an unbiased manner the relative contributions of mutations at canonical dinucleotides (73%) and flanking noncanonical positions (27%), and calculate the positive predictive value of pathogenicity for different classes of mutations. We identified 18 patients with likely diagnostic de novo mutations in dominant DD-associated genes at noncanonical positions in splice sites. We estimate 35%–40% of pathogenic variants in noncanonical splice site positions are missing from public databases.
Document Type: text
File Description: text/html
Language: English
Relation: http://genome.cshlp.org/cgi/content/short/29/2/159; http://dx.doi.org/10.1101/gr.238444.118
DOI: 10.1101/gr.238444.118
Availability: http://genome.cshlp.org/cgi/content/short/29/2/159; https://doi.org/10.1101/gr.238444.118
Rights: Copyright (C) 2019, Cold Spring Harbor Laboratory Press
Accession Number: edsbas.8C6EE4A2
Database: BASE