Phylointeractomics reconstructs functional evolution of protein binding

Molecular phylogenomics investigates evolutionary relationships based on genomic data. However, despite genomic sequence conservation, changes in protein interactions can occur relatively rapidly and may cause strong functional diversification. To investigate such functional evolution, we here combi...

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Bibliographic Details
Main Authors: Kappei, Dennis (Author) , Buchholz, Frank (Author)
Format: Article (Journal)
Language:English
Published: 2017
In: Nature Communications
Year: 2017, Volume: 8
ISSN:2041-1723
DOI:10.1038/ncomms14334
Online Access:Verlag, kostenfrei, Volltext: http://dx.doi.org/10.1038/ncomms14334
Verlag, kostenfrei, Volltext: https://www.nature.com/articles/ncomms14334
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Author Notes:Dennis Kappei, Marion Scheibe, Maciej Paszkowski-Rogacz, Alina Bluhm, Toni Ingolf Gossmann, Sabrina Dietz, Mario Dejung, Holger Herlyn, Frank Buchholz, Matthias Mann, Falk Butter
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Summary:Molecular phylogenomics investigates evolutionary relationships based on genomic data. However, despite genomic sequence conservation, changes in protein interactions can occur relatively rapidly and may cause strong functional diversification. To investigate such functional evolution, we here combine phylogenomics with interaction proteomics. We develop this concept by investigating the molecular evolution of the shelterin complex, which protects telomeres, across 16 vertebrate species from zebrafish to humans covering 450 million years of evolution. Our phylointeractomics screen discovers previously unknown telomere-associated proteins and reveals how homologous proteins undergo functional evolution. For instance, we show that TERF1 evolved as a telomere-binding protein in the common stem lineage of marsupial and placental mammals. Phylointeractomics is a versatile and scalable approach to investigate evolutionary changes in protein function and thus can provide experimental evidence for phylogenomic relationships.
Item Description:Published 8 Feb 2017
Gesehen am 25.06.2018
Physical Description:Online Resource
ISSN:2041-1723
DOI:10.1038/ncomms14334