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Protein-Coding Genes in Euarchontoglires with Pseudogene Homologs in Humans

An original bioinformatics technique is developed to identify the protein-coding genes in rodents, lagomorphs and nonhuman primates that are pseudogenized in humans. The method is based on per-gene verification of local synteny, similarity of exon-intronic structures and orthology in a set of genome...

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Autores principales: Rubanov, Lev I., Zverkov, Oleg A., Shilovsky, Gregory A., Seliverstov, Alexandr V., Lyubetsky, Vassily A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7555810/
https://www.ncbi.nlm.nih.gov/pubmed/32927891
http://dx.doi.org/10.3390/life10090192
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author Rubanov, Lev I.
Zverkov, Oleg A.
Shilovsky, Gregory A.
Seliverstov, Alexandr V.
Lyubetsky, Vassily A.
author_facet Rubanov, Lev I.
Zverkov, Oleg A.
Shilovsky, Gregory A.
Seliverstov, Alexandr V.
Lyubetsky, Vassily A.
author_sort Rubanov, Lev I.
collection PubMed
description An original bioinformatics technique is developed to identify the protein-coding genes in rodents, lagomorphs and nonhuman primates that are pseudogenized in humans. The method is based on per-gene verification of local synteny, similarity of exon-intronic structures and orthology in a set of genomes. It is applicable to any genome set, even with the number of genomes exceeding 100, and efficiently implemented using fast computer software. Only 50 evolutionary recent human pseudogenes were predicted. Their functional homologs in model species are often associated with the immune system or digestion and mainly express in the testes. According to current evidence, knockout of most of these genes leads to an abnormal phenotype. Some genes were pseudogenized or lost independently in human and nonhuman hominoids.
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spelling pubmed-75558102020-10-19 Protein-Coding Genes in Euarchontoglires with Pseudogene Homologs in Humans Rubanov, Lev I. Zverkov, Oleg A. Shilovsky, Gregory A. Seliverstov, Alexandr V. Lyubetsky, Vassily A. Life (Basel) Communication An original bioinformatics technique is developed to identify the protein-coding genes in rodents, lagomorphs and nonhuman primates that are pseudogenized in humans. The method is based on per-gene verification of local synteny, similarity of exon-intronic structures and orthology in a set of genomes. It is applicable to any genome set, even with the number of genomes exceeding 100, and efficiently implemented using fast computer software. Only 50 evolutionary recent human pseudogenes were predicted. Their functional homologs in model species are often associated with the immune system or digestion and mainly express in the testes. According to current evidence, knockout of most of these genes leads to an abnormal phenotype. Some genes were pseudogenized or lost independently in human and nonhuman hominoids. MDPI 2020-09-10 /pmc/articles/PMC7555810/ /pubmed/32927891 http://dx.doi.org/10.3390/life10090192 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Communication
Rubanov, Lev I.
Zverkov, Oleg A.
Shilovsky, Gregory A.
Seliverstov, Alexandr V.
Lyubetsky, Vassily A.
Protein-Coding Genes in Euarchontoglires with Pseudogene Homologs in Humans
title Protein-Coding Genes in Euarchontoglires with Pseudogene Homologs in Humans
title_full Protein-Coding Genes in Euarchontoglires with Pseudogene Homologs in Humans
title_fullStr Protein-Coding Genes in Euarchontoglires with Pseudogene Homologs in Humans
title_full_unstemmed Protein-Coding Genes in Euarchontoglires with Pseudogene Homologs in Humans
title_short Protein-Coding Genes in Euarchontoglires with Pseudogene Homologs in Humans
title_sort protein-coding genes in euarchontoglires with pseudogene homologs in humans
topic Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7555810/
https://www.ncbi.nlm.nih.gov/pubmed/32927891
http://dx.doi.org/10.3390/life10090192
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