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Identification of potentially pathogenic variants for autism spectrum disorders using gene-burden analysis
ID Rihar, Nika (Author), ID Krgović, Danijela (Author), ID Kokalj-Vokač, Nadja (Author), ID Stangler Herodež, Špela (Author), ID Zorc, Minja (Author), ID Dovč, Peter (Author)

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Abstract
Gene-burden analyses have lately become a very successful way for the identification of genes carrying risk variants underlying the analysed disease. This approach is also suitable for complex disorders like autism spectrum disorder (ASD). The gene-burden analysis using Testing Rare Variants with Public Data (TRAPD) software was conducted on whole exome sequencing data of Slovenian patients with ASD to determine potentially novel disease risk variants in known ASD-associated genes as well as in others. To choose the right control group for testing, principal component analysis based on the 1000 Genomes and ASD cohort samples was conducted. The subsequent protein structure and ligand binding analysis using I-TASSER package were performed to detect changes in protein structure and ligand binding to determine a potential pathogenic consequence of observed mutation. The obtained results demonstrate an association of two variants–p.Glu198Lys (PPP2R5D:c.592G>A) and p.Arg253Gln (PPP2R5D:c.758G>A) with the ASD. Substitution p.Glu198Lys (PPP2R5D:c.592G>A) is a variant, previously described as pathogenic in association with ASD combined with intellectual disability, whereas p.Arg253Gln (PPP2R5D:c.758G>A) has not been described as an ASD-associated pathogenic variant yet. The results indicate that the filtering process was suitable and could be used in the future for detection of novel pathogenic variants when analysing groups of ASD patients.

Language:English
Keywords:medicine, genetics, genetic tests, autism, autism spectrum disorder, protein structure, protein structure prediction, Slovenian people, computer software, polymerase chain reaction, pathogenesis, mutation
Work type:Article
Typology:1.01 - Original Scientific Article
Organization:BF - Biotechnical Faculty
Publication status:Published
Publication version:Version of Record
Year:2023
Number of pages:17 str.
Numbering:Vol. 18, iss. 5, art. e0273957
PID:20.500.12556/RUL-147014 This link opens in a new window
UDC:575:61
ISSN on article:1932-6203
DOI:10.1371/journal.pone.0273957 This link opens in a new window
COBISS.SI-ID:152010499 This link opens in a new window
Publication date in RUL:20.06.2023
Views:470
Downloads:102
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Record is a part of a journal

Title:PloS one
Publisher:PLOS
ISSN:1932-6203
COBISS.SI-ID:2005896 This link opens in a new window

Licences

License:CC BY 4.0, Creative Commons Attribution 4.0 International
Link:http://creativecommons.org/licenses/by/4.0/
Description:This is the standard Creative Commons license that gives others maximum freedom to do what they want with the work as long as they credit the author.

Secondary language

Language:Slovenian
Keywords:medicina, genetika, genetski testi, avtizem

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