Regional effect on the molecular clock rate of protein evolution in Eutherian and Metatherian genomes.

Eutheria GC content Landscapes Metatheria Molecular clock Neutral evolution Protein evolution Substitution rate

Journal

BMC ecology and evolution
ISSN: 2730-7182
Titre abrégé: BMC Ecol Evol
Pays: England
ID NLM: 101775613

Informations de publication

Date de publication:
04 08 2021
Historique:
received: 08 11 2019
accepted: 22 07 2021
entrez: 5 8 2021
pubmed: 6 8 2021
medline: 10 8 2021
Statut: epublish

Résumé

Different types of proteins diverge at vastly different rates. Moreover, the same type of protein has been observed to evolve with different rates in different phylogenetic lineages. In the present study we measured the rates of protein evolution in Eutheria (placental mammals) and Metatheria (marsupials) on a genome-wide basis and we propose that the gene position in the genome landscape has an important influence on the rate of protein divergence. We analyzed a protein-encoding gene set (n = 15,727) common to 16 mammals (12 Eutheria and 4 Metatheria). Using sliding windows that averaged regional effects of protein divergence we constructed landscapes in which strong and lineage-specific regional effects were seen on the molecular clock rate of protein divergence. Within each lineage, the relatively high rates were preferentially found in subtelomeric chromosomal regions. Such regions were observed to contain important and well-studied loci for fetal growth, uterine function and the generation of diversity in the adaptive repertoire of immunoglobulins. A genome landscape approach visualizes lineage-specific regional differences between Eutherian and Metatherian rates of protein evolution. This phenomenon of chromosomal position is a new element that explains at least part of the lineage-specific effects and differences between proteins on the molecular clock rates.

Sections du résumé

BACKGROUND
Different types of proteins diverge at vastly different rates. Moreover, the same type of protein has been observed to evolve with different rates in different phylogenetic lineages. In the present study we measured the rates of protein evolution in Eutheria (placental mammals) and Metatheria (marsupials) on a genome-wide basis and we propose that the gene position in the genome landscape has an important influence on the rate of protein divergence.
RESULTS
We analyzed a protein-encoding gene set (n = 15,727) common to 16 mammals (12 Eutheria and 4 Metatheria). Using sliding windows that averaged regional effects of protein divergence we constructed landscapes in which strong and lineage-specific regional effects were seen on the molecular clock rate of protein divergence. Within each lineage, the relatively high rates were preferentially found in subtelomeric chromosomal regions. Such regions were observed to contain important and well-studied loci for fetal growth, uterine function and the generation of diversity in the adaptive repertoire of immunoglobulins.
CONCLUSIONS
A genome landscape approach visualizes lineage-specific regional differences between Eutherian and Metatherian rates of protein evolution. This phenomenon of chromosomal position is a new element that explains at least part of the lineage-specific effects and differences between proteins on the molecular clock rates.

Identifiants

pubmed: 34348656
doi: 10.1186/s12862-021-01882-x
pii: 10.1186/s12862-021-01882-x
pmc: PMC8336415
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

153

Subventions

Organisme : Fonds Wetenschappelijk Onderzoek
ID : G078814N
Organisme : Fonds Wetenschappelijk Onderzoek
ID : SBO151086
Organisme : onderzoeksraad, ku leuven
ID : C14/18/094
Organisme : fonds wetenschappelijk onderzoek
ID : G0E1420N, G098321N

Informations de copyright

© 2021. The Author(s).

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Auteurs

Raf Huttener (R)

Gene Expression Unit, Dept. of Cellular and Molecular Medicine, KU Leuven, Herestraat 49, O&N1, Bus 901, 3000, Leuven, Belgium.

Lieven Thorrez (L)

Tissue Engineering Laboratory, Department of Development and Regeneration, KU Leuven, Kortrijk, Belgium.

Thomas In't Veld (TI)

Gene Expression Unit, Dept. of Cellular and Molecular Medicine, KU Leuven, Herestraat 49, O&N1, Bus 901, 3000, Leuven, Belgium.

Barney Potter (B)

Department of Microbiology, Immunology and Transplantation, Rega Institute, KU Leuven, Leuven, Belgium.

Guy Baele (G)

Department of Microbiology, Immunology and Transplantation, Rega Institute, KU Leuven, Leuven, Belgium.

Mikaela Granvik (M)

Gene Expression Unit, Dept. of Cellular and Molecular Medicine, KU Leuven, Herestraat 49, O&N1, Bus 901, 3000, Leuven, Belgium.

Leentje Van Lommel (L)

Gene Expression Unit, Dept. of Cellular and Molecular Medicine, KU Leuven, Herestraat 49, O&N1, Bus 901, 3000, Leuven, Belgium.

Frans Schuit (F)

Gene Expression Unit, Dept. of Cellular and Molecular Medicine, KU Leuven, Herestraat 49, O&N1, Bus 901, 3000, Leuven, Belgium. frans.schuit@kuleuven.be.

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