Return to search

The making of a branching annelid: an analysis of complete mitochondrial genome and ribosomal data of Ramisyllis multicaudata

Ramisyllis multicaudata is a member of Syllidae (Annelida, Errantia, Phyllodocida) with a remarkable branching body plan. Using a next-generation sequencing approach, the complete mitochondrial
genomes of R. multicaudata and Trypanobia sp. are sequenced and analysed, representing the first ones from Syllidae. The gene order in these two syllids does not follow the order proposed as the putative ground pattern in Errantia. The phylogenetic relationships of R. multicaudata are discerned using a phylogenetic approach with the nuclear 18S and the mitochondrial 16S and cox1 genes. Ramisyllis multicaudata is the sister group of a clade containing Trypanobia species. Both genera, Ramisyllis and Trypanobia, together with Parahaplosyllis, Trypanosyllis, Eurysyllis, and Xenosyllis are located in a long branched clade. The long branches are explained by an accelerated mutational rate in the 18S rRNA gene. Using a phylogenetic backbone, we propose a scenario in which the
postembryonic addition of segments that occurs in most syllids, their huge diversity of reproductive modes, and their ability to regenerate lost parts, in combination, have provided an evolutionary basis to develop a new branching body pattern as realised in Ramisyllis.

Identiferoai:union.ndltd.org:DRESDEN/oai:qucosa:de:qucosa:13415
Date January 2015
CreatorsAguado, M. Teresa, Glasby, Christopher J., Schroeder, Paul C., Weigert, Anne, Bleidorn, Christoph
ContributorsUniversidad Autónoma de Madrid, Museum and Art Gallery of the Northern Territory,, Washington State University, Universität Leipzig, Max-Planck-Institut für Evolutionäre Anthropologie
PublisherNature Publishing Group
Source SetsHochschulschriftenserver (HSSS) der SLUB Dresden
LanguageEnglish
Detected LanguageEnglish
Typedoc-type:article, info:eu-repo/semantics/article, doc-type:Text
SourceScientific reports 2015, 5:1038
Rightsinfo:eu-repo/semantics/openAccess

Page generated in 0.0019 seconds