izpis_h1_title_alt

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

.pdfPDF - Predstavitvena datoteka, prenos (2,68 MB)
MD5: 3749BE1E14691219E34616E39C7F5265
URLURL - Izvorni URL, za dostop obiščite https://journals.plos.org/plosone/article?id=10.1371/journal.pone.0273957 Povezava se odpre v novem oknu

Izvleček
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.

Jezik:Angleški jezik
Ključne besede:medicine, genetics, genetic tests, autism, autism spectrum disorder, protein structure, protein structure prediction, Slovenian people, computer software, polymerase chain reaction, pathogenesis, mutation
Vrsta gradiva:Članek v reviji
Tipologija:1.01 - Izvirni znanstveni članek
Organizacija:BF - Biotehniška fakulteta
Status publikacije:Objavljeno
Različica publikacije:Objavljena publikacija
Leto izida:2023
Št. strani:17 str.
Številčenje:Vol. 18, iss. 5, art. e0273957
PID:20.500.12556/RUL-147014 Povezava se odpre v novem oknu
UDK:575:61
ISSN pri članku:1932-6203
DOI:10.1371/journal.pone.0273957 Povezava se odpre v novem oknu
COBISS.SI-ID:152010499 Povezava se odpre v novem oknu
Datum objave v RUL:20.06.2023
Število ogledov:467
Število prenosov:102
Metapodatki:XML DC-XML DC-RDF
:
Kopiraj citat
Objavi na:Bookmark and Share

Gradivo je del revije

Naslov:PloS one
Založnik:PLOS
ISSN:1932-6203
COBISS.SI-ID:2005896 Povezava se odpre v novem oknu

Licence

Licenca:CC BY 4.0, Creative Commons Priznanje avtorstva 4.0 Mednarodna
Povezava:http://creativecommons.org/licenses/by/4.0/deed.sl
Opis:To je standardna licenca Creative Commons, ki daje uporabnikom največ možnosti za nadaljnjo uporabo dela, pri čemer morajo navesti avtorja.

Sekundarni jezik

Jezik:Slovenski jezik
Ključne besede:medicina, genetika, genetski testi, avtizem

Podobna dela

Podobna dela v RUL:
Podobna dela v drugih slovenskih zbirkah:

Nazaj