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CpG island turnover events predict evolutionary changes in enhancer activity
by
Baumgartner, Marybeth
, Yim, Kristina M.
, Uebbing, Severin
, Dutrow, Emily V.
, Nottoli, Timothy
, Rosales Larios, María F.
, Kocher, Acadia A.
, Noonan, James P.
in
Animal Genetics and Genomics
/ animal models
/ Animals
/ Biodiversity
/ Bioinformatics
/ Biomedical and Life Sciences
/ Blacklisting
/ Brain
/ Comparative genomics
/ CpG Islands
/ Diencephalon
/ DNA methylation
/ Embryogenesis
/ Enhancer Elements, Genetic
/ Enhancers
/ Evolution
/ Evolution, Molecular
/ Evolutionary Biology
/ Evolutionary genetics
/ Gene mapping
/ Gene regulation
/ Genes
/ Genetic diversity
/ Genomes
/ genomic islands
/ Histone Code
/ Histones
/ Human Genetics
/ Humans
/ Life Sciences
/ Mice
/ Microbial Genetics and Genomics
/ Orphan CpG islands
/ Plant Genetics and Genomics
/ Species
/ Species Specificity
/ transcription (genetics)
/ Transcription factors
/ Transcriptional enhancer evolution
/ Transposition
2024
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CpG island turnover events predict evolutionary changes in enhancer activity
by
Baumgartner, Marybeth
, Yim, Kristina M.
, Uebbing, Severin
, Dutrow, Emily V.
, Nottoli, Timothy
, Rosales Larios, María F.
, Kocher, Acadia A.
, Noonan, James P.
in
Animal Genetics and Genomics
/ animal models
/ Animals
/ Biodiversity
/ Bioinformatics
/ Biomedical and Life Sciences
/ Blacklisting
/ Brain
/ Comparative genomics
/ CpG Islands
/ Diencephalon
/ DNA methylation
/ Embryogenesis
/ Enhancer Elements, Genetic
/ Enhancers
/ Evolution
/ Evolution, Molecular
/ Evolutionary Biology
/ Evolutionary genetics
/ Gene mapping
/ Gene regulation
/ Genes
/ Genetic diversity
/ Genomes
/ genomic islands
/ Histone Code
/ Histones
/ Human Genetics
/ Humans
/ Life Sciences
/ Mice
/ Microbial Genetics and Genomics
/ Orphan CpG islands
/ Plant Genetics and Genomics
/ Species
/ Species Specificity
/ transcription (genetics)
/ Transcription factors
/ Transcriptional enhancer evolution
/ Transposition
2024
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CpG island turnover events predict evolutionary changes in enhancer activity
by
Baumgartner, Marybeth
, Yim, Kristina M.
, Uebbing, Severin
, Dutrow, Emily V.
, Nottoli, Timothy
, Rosales Larios, María F.
, Kocher, Acadia A.
, Noonan, James P.
in
Animal Genetics and Genomics
/ animal models
/ Animals
/ Biodiversity
/ Bioinformatics
/ Biomedical and Life Sciences
/ Blacklisting
/ Brain
/ Comparative genomics
/ CpG Islands
/ Diencephalon
/ DNA methylation
/ Embryogenesis
/ Enhancer Elements, Genetic
/ Enhancers
/ Evolution
/ Evolution, Molecular
/ Evolutionary Biology
/ Evolutionary genetics
/ Gene mapping
/ Gene regulation
/ Genes
/ Genetic diversity
/ Genomes
/ genomic islands
/ Histone Code
/ Histones
/ Human Genetics
/ Humans
/ Life Sciences
/ Mice
/ Microbial Genetics and Genomics
/ Orphan CpG islands
/ Plant Genetics and Genomics
/ Species
/ Species Specificity
/ transcription (genetics)
/ Transcription factors
/ Transcriptional enhancer evolution
/ Transposition
2024
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CpG island turnover events predict evolutionary changes in enhancer activity
Journal Article
CpG island turnover events predict evolutionary changes in enhancer activity
2024
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Overview
Background
Genetic changes that modify the function of transcriptional enhancers have been linked to the evolution of biological diversity across species. Multiple studies have focused on the role of nucleotide substitutions, transposition, and insertions and deletions in altering enhancer function. CpG islands (CGIs) have recently been shown to influence enhancer activity, and here we test how their turnover across species contributes to enhancer evolution.
Results
We integrate maps of CGIs and enhancer activity-associated histone modifications obtained from multiple tissues in nine mammalian species and find that CGI content in enhancers is strongly associated with increased histone modification levels. CGIs show widespread turnover across species and species-specific CGIs are strongly enriched for enhancers exhibiting species-specific activity across all tissues and species. Genes associated with enhancers with species-specific CGIs show concordant biases in their expression, supporting that CGI turnover contributes to gene regulatory innovation. Our results also implicate CGI turnover in the evolution of Human Gain Enhancers (HGEs), which show increased activity in human embryonic development and may have contributed to the evolution of uniquely human traits. Using a humanized mouse model, we show that a highly conserved HGE with a large CGI absent from the mouse ortholog shows increased activity at the human CGI in the humanized mouse diencephalon.
Conclusions
Collectively, our results point to CGI turnover as a mechanism driving gene regulatory changes potentially underlying trait evolution in mammals.
Publisher
BioMed Central,Springer Nature B.V,BMC
Subject
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