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Motifome comparison between modern human, Neanderthal and Denisovan

BACKGROUND: The availability of the genomes of two archaic humans, Neanderthal and Denisovan, and that of modern humans provides researchers an opportunity to investigate genetic differences between these three subspecies on a genome-wide scale. Here we describe an algorithm that predicts statistica...

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Autores principales: Cserhati, Matyas F., Mooter, Mary-Ellen, Peterson, Lauren, Wicks, Benjamin, Xiao, Peng, Pauley, Mark, Guda, Chittibabu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6006668/
https://www.ncbi.nlm.nih.gov/pubmed/29914355
http://dx.doi.org/10.1186/s12864-018-4710-1
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author Cserhati, Matyas F.
Mooter, Mary-Ellen
Peterson, Lauren
Wicks, Benjamin
Xiao, Peng
Pauley, Mark
Guda, Chittibabu
author_facet Cserhati, Matyas F.
Mooter, Mary-Ellen
Peterson, Lauren
Wicks, Benjamin
Xiao, Peng
Pauley, Mark
Guda, Chittibabu
author_sort Cserhati, Matyas F.
collection PubMed
description BACKGROUND: The availability of the genomes of two archaic humans, Neanderthal and Denisovan, and that of modern humans provides researchers an opportunity to investigate genetic differences between these three subspecies on a genome-wide scale. Here we describe an algorithm that predicts statistically significant motifs based on the difference between a given motif’s actual and expected distributions. The algorithm was previously applied to plants but was modified for this work. RESULTS: The result of applying the algorithm to the human, Neanderthal, and Denisovan genomes is a catalog of potential regulatory motifs in these three human subspecies. We examined the distributions of these motifs in genetic elements including human retroviruses, human accelerated regions, and human accelerated conserved noncoding sequences regions. Differences in these distributions could be the origin of differences in phenotype between the three subspecies. Twenty significant motifs common to all three genomes were found; thirty-three were found in endogenous retroviruses in Neanderthal and Denisovan. Ten of these motifs mapped to the 22 bp core of MiR-1304. The core of this genetic element regulates the ENAM and AMTN genes, which take part in odontogenesis and whose 3’ UTRs contained significant motifs. The introns of 20 genes were found to contain a large number of significant motifs, which were also overrepresented in 49 human accelerated regions. These genes include NAV2, SorCS2, TRAPPC9, GRID1, PRDM16, CAMTA1, and ASIC which are all involved in neuroregulation. Further analysis of these genes using the GO database indicates that many are associated with neurodevelopment. Also, varying numbers of significant motifs were found to occur in regions of the Neanderthal and Denisovan genomes that are missing from the human genome, suggesting further functional differences between modern and archaic humans. CONCLUSION: Although Neanderthal and Denisovan are now extinct, detailed examination of elements from their genomes can shed light on possible phenotypic and cognitive differences between these two archaic human subspecies and modern humans. Genetic similarities and differences between these three subspecies and other fossil hominids would also be of interest. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12864-018-4710-1) contains supplementary material, which is available to authorized users.
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spelling pubmed-60066682018-06-26 Motifome comparison between modern human, Neanderthal and Denisovan Cserhati, Matyas F. Mooter, Mary-Ellen Peterson, Lauren Wicks, Benjamin Xiao, Peng Pauley, Mark Guda, Chittibabu BMC Genomics Research Article BACKGROUND: The availability of the genomes of two archaic humans, Neanderthal and Denisovan, and that of modern humans provides researchers an opportunity to investigate genetic differences between these three subspecies on a genome-wide scale. Here we describe an algorithm that predicts statistically significant motifs based on the difference between a given motif’s actual and expected distributions. The algorithm was previously applied to plants but was modified for this work. RESULTS: The result of applying the algorithm to the human, Neanderthal, and Denisovan genomes is a catalog of potential regulatory motifs in these three human subspecies. We examined the distributions of these motifs in genetic elements including human retroviruses, human accelerated regions, and human accelerated conserved noncoding sequences regions. Differences in these distributions could be the origin of differences in phenotype between the three subspecies. Twenty significant motifs common to all three genomes were found; thirty-three were found in endogenous retroviruses in Neanderthal and Denisovan. Ten of these motifs mapped to the 22 bp core of MiR-1304. The core of this genetic element regulates the ENAM and AMTN genes, which take part in odontogenesis and whose 3’ UTRs contained significant motifs. The introns of 20 genes were found to contain a large number of significant motifs, which were also overrepresented in 49 human accelerated regions. These genes include NAV2, SorCS2, TRAPPC9, GRID1, PRDM16, CAMTA1, and ASIC which are all involved in neuroregulation. Further analysis of these genes using the GO database indicates that many are associated with neurodevelopment. Also, varying numbers of significant motifs were found to occur in regions of the Neanderthal and Denisovan genomes that are missing from the human genome, suggesting further functional differences between modern and archaic humans. CONCLUSION: Although Neanderthal and Denisovan are now extinct, detailed examination of elements from their genomes can shed light on possible phenotypic and cognitive differences between these two archaic human subspecies and modern humans. Genetic similarities and differences between these three subspecies and other fossil hominids would also be of interest. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12864-018-4710-1) contains supplementary material, which is available to authorized users. BioMed Central 2018-06-18 /pmc/articles/PMC6006668/ /pubmed/29914355 http://dx.doi.org/10.1186/s12864-018-4710-1 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Cserhati, Matyas F.
Mooter, Mary-Ellen
Peterson, Lauren
Wicks, Benjamin
Xiao, Peng
Pauley, Mark
Guda, Chittibabu
Motifome comparison between modern human, Neanderthal and Denisovan
title Motifome comparison between modern human, Neanderthal and Denisovan
title_full Motifome comparison between modern human, Neanderthal and Denisovan
title_fullStr Motifome comparison between modern human, Neanderthal and Denisovan
title_full_unstemmed Motifome comparison between modern human, Neanderthal and Denisovan
title_short Motifome comparison between modern human, Neanderthal and Denisovan
title_sort motifome comparison between modern human, neanderthal and denisovan
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6006668/
https://www.ncbi.nlm.nih.gov/pubmed/29914355
http://dx.doi.org/10.1186/s12864-018-4710-1
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