Cargando…

A genome alignment of 120 mammals highlights ultraconserved element variability and placenta-associated enhancers

BACKGROUND: Multiple alignments of mammalian genomes have been the basis of many comparative genomic studies aiming at annotating genes, detecting regions under evolutionary constraint, and studying genome evolution. A key factor that affects the power of comparative analyses is the number of specie...

Descripción completa

Detalles Bibliográficos
Autores principales: Hecker, Nikolai, Hiller, Michael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6941714/
https://www.ncbi.nlm.nih.gov/pubmed/31899510
http://dx.doi.org/10.1093/gigascience/giz159
_version_ 1783484588192956416
author Hecker, Nikolai
Hiller, Michael
author_facet Hecker, Nikolai
Hiller, Michael
author_sort Hecker, Nikolai
collection PubMed
description BACKGROUND: Multiple alignments of mammalian genomes have been the basis of many comparative genomic studies aiming at annotating genes, detecting regions under evolutionary constraint, and studying genome evolution. A key factor that affects the power of comparative analyses is the number of species included in a genome alignment. RESULTS: To utilize the increased number of sequenced genomes and to provide an accessible resource for genomic studies, we generated a mammalian genome alignment comprising 120 species. We used this alignment and the CESAR method to provide protein-coding gene annotations for 119 non-human mammals. Furthermore, we illustrate the utility of this alignment by 2 exemplary analyses. First, we quantified how variable ultraconserved elements (UCEs) are among placental mammals. Leveraging the high taxonomic coverage in our alignment, we estimate that UCEs contain on average 4.7%–15.6% variable alignment columns. Furthermore, we show that the center regions of UCEs are generally most constrained. Second, we identified enhancer sequences that are only conserved in placental mammals. We found that these enhancers are significantly associated with placenta-related genes, suggesting that some of these enhancers may be involved in the evolution of placental mammal-specific aspects of the placenta. CONCLUSION: The 120-mammal alignment and all other data are available for analysis and visualization in a genome browser at https://genome-public.pks.mpg.de/and for download at https://bds.mpi-cbg.de/hillerlab/120MammalAlignment/.
format Online
Article
Text
id pubmed-6941714
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Oxford University Press
record_format MEDLINE/PubMed
spelling pubmed-69417142020-01-07 A genome alignment of 120 mammals highlights ultraconserved element variability and placenta-associated enhancers Hecker, Nikolai Hiller, Michael Gigascience Data Note BACKGROUND: Multiple alignments of mammalian genomes have been the basis of many comparative genomic studies aiming at annotating genes, detecting regions under evolutionary constraint, and studying genome evolution. A key factor that affects the power of comparative analyses is the number of species included in a genome alignment. RESULTS: To utilize the increased number of sequenced genomes and to provide an accessible resource for genomic studies, we generated a mammalian genome alignment comprising 120 species. We used this alignment and the CESAR method to provide protein-coding gene annotations for 119 non-human mammals. Furthermore, we illustrate the utility of this alignment by 2 exemplary analyses. First, we quantified how variable ultraconserved elements (UCEs) are among placental mammals. Leveraging the high taxonomic coverage in our alignment, we estimate that UCEs contain on average 4.7%–15.6% variable alignment columns. Furthermore, we show that the center regions of UCEs are generally most constrained. Second, we identified enhancer sequences that are only conserved in placental mammals. We found that these enhancers are significantly associated with placenta-related genes, suggesting that some of these enhancers may be involved in the evolution of placental mammal-specific aspects of the placenta. CONCLUSION: The 120-mammal alignment and all other data are available for analysis and visualization in a genome browser at https://genome-public.pks.mpg.de/and for download at https://bds.mpi-cbg.de/hillerlab/120MammalAlignment/. Oxford University Press 2020-01-03 /pmc/articles/PMC6941714/ /pubmed/31899510 http://dx.doi.org/10.1093/gigascience/giz159 Text en © The Author(s) 2020. Published by Oxford University Press. 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 Data Note
Hecker, Nikolai
Hiller, Michael
A genome alignment of 120 mammals highlights ultraconserved element variability and placenta-associated enhancers
title A genome alignment of 120 mammals highlights ultraconserved element variability and placenta-associated enhancers
title_full A genome alignment of 120 mammals highlights ultraconserved element variability and placenta-associated enhancers
title_fullStr A genome alignment of 120 mammals highlights ultraconserved element variability and placenta-associated enhancers
title_full_unstemmed A genome alignment of 120 mammals highlights ultraconserved element variability and placenta-associated enhancers
title_short A genome alignment of 120 mammals highlights ultraconserved element variability and placenta-associated enhancers
title_sort genome alignment of 120 mammals highlights ultraconserved element variability and placenta-associated enhancers
topic Data Note
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6941714/
https://www.ncbi.nlm.nih.gov/pubmed/31899510
http://dx.doi.org/10.1093/gigascience/giz159
work_keys_str_mv AT heckernikolai agenomealignmentof120mammalshighlightsultraconservedelementvariabilityandplacentaassociatedenhancers
AT hillermichael agenomealignmentof120mammalshighlightsultraconservedelementvariabilityandplacentaassociatedenhancers
AT heckernikolai genomealignmentof120mammalshighlightsultraconservedelementvariabilityandplacentaassociatedenhancers
AT hillermichael genomealignmentof120mammalshighlightsultraconservedelementvariabilityandplacentaassociatedenhancers