| Literature DB >> 28944589 |
Jeremy Pasquier1, Ingo Braasch2, Peter Batzel3, Cedric Cabau4, Jérome Montfort1, Thaovi Nguyen1, Elodie Jouanno1, Camille Berthelot5, Christophe Klopp4, Laurent Journot6, John H Postlethwait3, Yann Guiguen1, Julien Bobe1.
Abstract
Whole-genome duplications (WGDs) are important evolutionary events. Our understanding of underlying mechanisms, including the evolution of duplicated genes after WGD, however, remains incomplete. Teleost fish experienced a common WGD (teleost-specific genome duplication, or TGD) followed by a dramatic adaptive radiation leading to more than half of all vertebrate species. The analysis of gene expression patterns following TGD at the genome level has been limited by the lack of suitable genomic resources. The recent concomitant release of the genome sequence of spotted gar (a representative of holosteans, the closest-related lineage of teleosts that lacks the TGD) and the tissue-specific gene expression repertoires of over 20 holostean and teleostean fish species, including spotted gar, zebrafish, and medaka (the PhyloFish project), offers a unique opportunity to study the evolution of gene expression following TGD in teleosts. We show that most TGD duplicates gained their current status (loss of one duplicate gene or retention of both duplicates) relatively rapidly after TGD (i.e., prior to the divergence of medaka and zebrafish lineages). The loss of one duplicate is the most common fate after TGD with a probability of approximately 80%. In addition, the fate of duplicate genes after TGD, including subfunctionalization, neofunctionalization, or retention of two "similar" copies occurred not only before but also after the divergence of species tested, in consistency with a role of the TGD in speciation and/or evolution of gene function. Finally, we report novel cases of TGD ohnolog subfunctionalization and neofunctionalization that further illustrate the importance of these processes.Entities:
Keywords: PhyloFish; medaka; teleost; transcriptome; zebrafish
Mesh:
Year: 2017 PMID: 28944589 PMCID: PMC5679426 DOI: 10.1002/jez.b.22770
Source DB: PubMed Journal: J Exp Zool B Mol Dev Evol ISSN: 1552-5007 Impact factor: 2.656