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  Phylointeractomics reconstructs functional evolution of protein binding.

Kappei, D., Scheibe, M., Paszkowski-Rogacz, M., Bluhm, A., Gossmann, T. I., Dietz, S., et al. (2017). Phylointeractomics reconstructs functional evolution of protein binding. Nature communications, 8: 14334. doi:10.1038/ncomms14334.

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Kappei, Dennis1, Author           
Scheibe, Marion, Author
Paszkowski-Rogacz, Maciej1, Author           
Bluhm, Alina, Author
Gossmann, Toni Ingolf, Author
Dietz, Sabrina, Author
Dejung, Mario, Author
Herlyn, Holger, Author
Buchholz, Frank1, Author           
Mann, Matthias, Author
Butter, Falk, Author
Affiliations:
1Max Planck Institute for Molecular Cell Biology and Genetics, ou_2340692              

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 Abstract: 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.

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 Dates: 2017-02-08
 Publication Status: Issued
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 Identifiers: DOI: 10.1038/ncomms14334
Other: cbg-6787
PMID: 28176777
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Title: Nature communications
  Other : Nat Commun
Source Genre: Journal
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Pages: - Volume / Issue: 8 Sequence Number: 14334 Start / End Page: - Identifier: -