O genoma de ctenóforos "forçam" cientistas evolucionistas a hipóteses absurdas

segunda-feira, junho 09, 2014

The ctenophore genome and the evolutionary origins of neural systems

Leonid L. Moroz, Kevin M. Kocot, Mathew R. Citarella, Sohn Dosung, Tigran P. Norekian, Inna S. Povolotskaya, Anastasia P. Grigorenko, Christopher Dailey, Eugene Berezikov, Katherine M. Buckley, Andrey Ptitsyn, Denis Reshetov, Krishanu Mukherjee, Tatiana P. Moroz, Yelena Bobkova, Fahong Yu, Vladimir V. Kapitonov, Jerzy Jurka, Yuri V. Bobkov, Joshua J. Swore, David O. Girardo, Alexander Fodor, Fedor Gusev, Rachel Sanford, Rebecca Bruders et al.

AffiliationsContributionsCorresponding authors

Nature 510, 109–114 (05 June 2014) doi:10.1038/nature13400

Received 15 September 2013 Accepted 23 April 2014 Published online 21 May 2014 Corrected online 04 June 2014

Image/Imagem: UCMP - Berkeley, CA.


Abstract

Abstract• Introduction• Ctenophore phylogeny• Ctenophore innovations• Parallel evolution of neural organization• Discussion• Methods• Accession codes• Change history• References• Acknowledgements• Author information• Extended data figures and tables• Supplementary information

The origins of neural systems remain unresolved. In contrast to other basal metazoans, ctenophores (comb jellies) have both complex nervous and mesoderm-derived muscular systems. These holoplanktonic predators also have sophisticated ciliated locomotion, behaviour and distinct development. Here we present the draft genome of Pleurobrachia bachei, Pacific sea gooseberry, together with ten other ctenophore transcriptomes, and show that they are remarkably distinct from other animal genomes in their content of neurogenic, immune and developmental genes. Our integrative analyses place Ctenophora as the earliest lineage within Metazoa. This hypothesis is supported by comparative analysis of multiple gene families, including the apparent absence of HOX genes, canonical microRNA machinery, and reduced immune complement in ctenophores. Although two distinct nervous systems are well recognized in ctenophores, many bilaterian neuron-specific genes and genes of ‘classical’ neurotransmitter pathways either are absent or, if present, are not expressed in neurons. Our metabolomic and physiological data are consistent with the hypothesis that ctenophore neural systems, and possibly muscle specification, evolved independently from those in other animals.

Subject terms: Phylogeny Phylogenetics Comparative genomics Genetics of the nervous system

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