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Harnessing omics big data in nine vertebrate species by genome-wide prioritization of sequence variants with the highest predicted deleterious effect on protein function
ID Rozman, Vita (Avtor), ID Kunej, Tanja (Avtor)

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Izvleček
Harnessing the genomics big data requires innovation in how we extract and interpret biologically relevant variants. Currently, there is no established catalog of prioritized missense variants associated with deleterious protein function phenotypes. We report in this study, to the best of our knowledge, the first genome-wide prioritization of sequence variants with the most deleterious effect on protein function (potentially deleterious variants [pDelVars]) in nine vertebrate species: human, cattle, horse, sheep, pig, dog, rat, mouse, and zebrafish.The analysis was conducted using the Ensembl/BioMart tool. Genes comprising pDelVars in the highest number of examined species were identified using a Python script. Multiple genomic alignments of the selected genes were built to identify interspecies orthologous potentially deleterious variants, which we defined as the ‘‘ortho-pDelVars.’’ Genome-wide prioritization revealed that in humans, 0.12% of the known variants are predicted to be deleterious. In seven out of nine examined vertebrate species, the genes encoding the multiple PDZ domain crumbs cell polarity complex component (MPDZ) and the transforming acidic coiled-coil containing protein 2 (TACC2) comprise pDelVars. Five interspecies ortho-pDelVars were identified in three genes.These findings offer new ways to harness genomics big data by facilitating the identification of functional polymorphisms in humans and animal models and thus provide a future basis for optimization of protocols for whole genome prioritization of pDelVars and screening of orthologous sequence variants. The approach presented here can inform various postgenomic applications such as personalized medicine and multiomics study of health interventions (iatromics).

Jezik:Angleški jezik
Ključne besede:big data, potentially deleterious variants (pDelVars), orthologous potentially deleterious variants (ortho-pDelVars), PolyPhen (polymorphism phenotyping), SIFT (sorts intolerant from tolerant), single-nucleotide polymorphism (SNP)
Vrsta gradiva:Članek v reviji
Tipologija:1.01 - Izvirni znanstveni članek
Organizacija:BF - Biotehniška fakulteta
Status publikacije:Objavljeno
Različica publikacije:Recenzirani rokopis
Leto izida:2018
Št. strani:Str. 410-421
Številčenje:Vol. 22, no. 6
PID:20.500.12556/RUL-133071 Povezava se odpre v novem oknu
UDK:575
ISSN pri članku:1536-2310
DOI:10.1089/omi.2018.0046 Povezava se odpre v novem oknu
COBISS.SI-ID:4072584 Povezava se odpre v novem oknu
Datum objave v RUL:10.11.2021
Število ogledov:631
Število prenosov:240
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Gradivo je del revije

Naslov:Omics. a ǂjournal of integrative biology
Skrajšan naslov:Omics
Založnik:Mary Ann Liebert
ISSN:1536-2310
COBISS.SI-ID:512299289 Povezava se odpre v novem oknu

Sekundarni jezik

Jezik:Slovenski jezik
Ključne besede:genetika, genomika, bioinformatika, baze podatkov, proteini, vretenčarji

Projekti

Financer:ARRS - Agencija za raziskovalno dejavnost Republike Slovenije
Številka projekta:P4-0220
Naslov:Primerjalna genomika in genomska biodiverziteta

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