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Emergence and Evolution of Hominidae-Specific Coding and Noncoding Genomic Sequences
Family Hominidae, which includes humans and great apes, is recognized for unique complex social behavior and intellectual abilities. Despite the increasing genome data, however, the genomic origin of its phenotypic uniqueness has remained elusive. Clade-specific genes and highly conserved noncoding...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4987104/ https://www.ncbi.nlm.nih.gov/pubmed/27289096 http://dx.doi.org/10.1093/gbe/evw132 |
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author | Saber, Morteza Mahmoudi Adeyemi Babarinde, Isaac Hettiarachchi, Nilmini Saitou, Naruya |
author_facet | Saber, Morteza Mahmoudi Adeyemi Babarinde, Isaac Hettiarachchi, Nilmini Saitou, Naruya |
author_sort | Saber, Morteza Mahmoudi |
collection | PubMed |
description | Family Hominidae, which includes humans and great apes, is recognized for unique complex social behavior and intellectual abilities. Despite the increasing genome data, however, the genomic origin of its phenotypic uniqueness has remained elusive. Clade-specific genes and highly conserved noncoding sequences (HCNSs) are among the high-potential evolutionary candidates involved in driving clade-specific characters and phenotypes. On this premise, we analyzed whole genome sequences along with gene orthology data retrieved from major DNA databases to find Hominidae-specific (HS) genes and HCNSs. We discovered that Down syndrome critical region 4 (DSCR4) is the only experimentally verified gene uniquely present in Hominidae. DSCR4 has no structural homology to any known protein and was inferred to have emerged in several steps through LTR/ERV1, LTR/ERVL retrotransposition, and transversion. Using the genomic distance as neutral evolution threshold, we identified 1,658 HS HCNSs. Polymorphism coverage and derived allele frequency analysis of HS HCNSs showed that these HCNSs are under purifying selection, indicating that they may harbor important functions. They are overrepresented in promoters/untranslated regions, in close proximity of genes involved in sensory perception of sound and developmental process, and also showed a significantly lower nucleosome occupancy probability. Interestingly, many ancestral sequences of the HS HCNSs showed very high evolutionary rates. This suggests that new functions emerged through some kind of positive selection, and then purifying selection started to operate to keep these functions. |
format | Online Article Text |
id | pubmed-4987104 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-49871042016-08-22 Emergence and Evolution of Hominidae-Specific Coding and Noncoding Genomic Sequences Saber, Morteza Mahmoudi Adeyemi Babarinde, Isaac Hettiarachchi, Nilmini Saitou, Naruya Genome Biol Evol Research Article Family Hominidae, which includes humans and great apes, is recognized for unique complex social behavior and intellectual abilities. Despite the increasing genome data, however, the genomic origin of its phenotypic uniqueness has remained elusive. Clade-specific genes and highly conserved noncoding sequences (HCNSs) are among the high-potential evolutionary candidates involved in driving clade-specific characters and phenotypes. On this premise, we analyzed whole genome sequences along with gene orthology data retrieved from major DNA databases to find Hominidae-specific (HS) genes and HCNSs. We discovered that Down syndrome critical region 4 (DSCR4) is the only experimentally verified gene uniquely present in Hominidae. DSCR4 has no structural homology to any known protein and was inferred to have emerged in several steps through LTR/ERV1, LTR/ERVL retrotransposition, and transversion. Using the genomic distance as neutral evolution threshold, we identified 1,658 HS HCNSs. Polymorphism coverage and derived allele frequency analysis of HS HCNSs showed that these HCNSs are under purifying selection, indicating that they may harbor important functions. They are overrepresented in promoters/untranslated regions, in close proximity of genes involved in sensory perception of sound and developmental process, and also showed a significantly lower nucleosome occupancy probability. Interestingly, many ancestral sequences of the HS HCNSs showed very high evolutionary rates. This suggests that new functions emerged through some kind of positive selection, and then purifying selection started to operate to keep these functions. Oxford University Press 2016-06-11 /pmc/articles/PMC4987104/ /pubmed/27289096 http://dx.doi.org/10.1093/gbe/evw132 Text en © The Author(s) 2016. Published by Oxford University Press on behalf of the Society for Molecular Biology and Evolution. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Saber, Morteza Mahmoudi Adeyemi Babarinde, Isaac Hettiarachchi, Nilmini Saitou, Naruya Emergence and Evolution of Hominidae-Specific Coding and Noncoding Genomic Sequences |
title | Emergence and Evolution of Hominidae-Specific Coding and Noncoding Genomic Sequences |
title_full | Emergence and Evolution of Hominidae-Specific Coding and Noncoding Genomic Sequences |
title_fullStr | Emergence and Evolution of Hominidae-Specific Coding and Noncoding Genomic Sequences |
title_full_unstemmed | Emergence and Evolution of Hominidae-Specific Coding and Noncoding Genomic Sequences |
title_short | Emergence and Evolution of Hominidae-Specific Coding and Noncoding Genomic Sequences |
title_sort | emergence and evolution of hominidae-specific coding and noncoding genomic sequences |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4987104/ https://www.ncbi.nlm.nih.gov/pubmed/27289096 http://dx.doi.org/10.1093/gbe/evw132 |
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