Spatiotemporal transcriptomics reveals the evolutionary history of the endoderm germ layer

The concept of germ layers has been one of the foremost organizing principles in developmental biology, classification, systematics and evolution for 150 years (refs 1, 2, 3). Of the three germ layers, the mesoderm is found in bilaterian animals but is absent in species in the phyla Cnidaria and Ctenophora, which has been taken as evidence that the mesoderm was the final germ layer to evolve. The origin of the ectoderm and endoderm germ layers, however, remains unclear, with models supporting the antecedence of each as well as a simultaneous origin. Here we determine the temporal and spatial components of gene expression spanning embryonic development for all Caenorhabditis elegans genes and use it to determine the evolutionary ages of the germ layers. The gene expression program of the mesoderm is induced after those of the ectoderm and endoderm, thus making it the last germ layer both to evolve and to develop. Strikingly, the C. elegans endoderm and ectoderm expression programs do not co-induce; rather the endoderm activates earlier, and this is also observed in the expression of endoderm orthologues during the embryology of the frog Xenopus tropicalis, the sea anemone Nematostella vectensis and the sponge Amphimedon queenslandica. Querying the phylogenetic ages of specifically expressed genes reveals that the endoderm comprises older genes. Taken together, we propose that the endoderm program dates back to the origin of multicellularity, whereas the ectoderm originated as a secondary germ layer freed from ancestral feeding functions.

[1]  A. Minelli Animal Evolution: Interrelationships of the Living Phyla , 2007 .

[2]  Richard Durbin,et al.  Sequence analysis Fast and accurate short read alignment with Burrows – Wheeler transform , 2009 .

[3]  E. Shapiro,et al.  Single-cell sequencing-based technologies will revolutionize whole-organism science , 2013, Nature Reviews Genetics.

[4]  R. J. Hill,et al.  The T-box transcription factors TBX-37 and TBX-38 link GLP-1/Notch signaling to mesoderm induction in C. elegans embryos , 2004, Development.

[5]  F. Schram Animal evolution: Interrelationships of living Phyla , 1995 .

[6]  Lewis Wolpert,et al.  Principles of Development , 1997 .

[7]  Thomas J. Nicholas,et al.  Automated analysis of embryonic gene expression with cellular resolution in C. elegans , 2008, Nature Methods.

[8]  B. Degnan,et al.  Evolutionary origin of gastrulation: insights from sponge development , 2014, BMC Biology.

[9]  B. Schierwater,et al.  Concatenated Analysis Sheds Light on Early Metazoan Evolution and Fuels a Modern “Urmetazoon” Hypothesis , 2009, PLoS biology.

[10]  Kathleen F. Kerr,et al.  The External RNA Controls Consortium: a progress report , 2005, Nature Methods.

[11]  Dave T. Gerrard,et al.  Gene expression divergence recapitulates the developmental hourglass model , 2010, Nature.

[12]  Itai Yanai,et al.  Developmental milestones punctuate gene expression in the Caenorhabditis embryo. , 2012, Developmental cell.

[13]  R. Waterston,et al.  Multidimensional regulation of gene expression in the C. elegans embryo , 2012, Genome research.

[14]  Leon Anavy,et al.  BLIND ordering of large-scale transcriptomic developmental timecourses , 2014, Development.

[15]  Leonid Peshkin,et al.  Mapping gene expression in two Xenopus species: evolutionary constraints and developmental flexibility. , 2011, Developmental cell.

[16]  U. Technau,et al.  Origin and evolution of endoderm and mesoderm. , 2003, The International journal of developmental biology.

[17]  William B. Wood,et al.  Segregation of developmental potential in early embryos of caenorhabditis elegans , 1980, Cell.

[18]  T. Hashimshony,et al.  CEL-Seq: single-cell RNA-Seq by multiplexed linear amplification. , 2012, Cell reports.

[19]  Xin Gao,et al.  Using OrthoMCL to assign proteins to OrthoMCL-DB groups or to cluster proteomes into new ortholog groups. , 2011, Current protocols in bioinformatics.

[20]  J. Sulston,et al.  The embryonic cell lineage of the nematode Caenorhabditis elegans. , 1983, Developmental biology.

[21]  B. Goldstein An analysis of the response to gut induction in the C. elegans embryo. , 1995, Development.

[22]  B. Goldstein Establishment of gut fate in the E lineage of C. elegans: the roles of lineage-dependent mechanisms and cell interactions. , 1993, Development.

[23]  S. Leys,et al.  Epithelia, an evolutionary novelty of metazoans. , 2012, Journal of experimental zoology. Part B, Molecular and developmental evolution.

[24]  Rona S. Gertner,et al.  Single-cell transcriptomics reveals bimodality in expression and splicing in immune cells , 2013, Nature.

[25]  D. Lipman,et al.  A genomic perspective on protein families. , 1997, Science.

[26]  J. Finnerty,et al.  Investigating the origins of triploblasty: `mesodermal' gene expression in a diploblastic animal, the sea anemone Nematostella vectensis (phylum, Cnidaria; class, Anthozoa) , 2004, Development.

[27]  Kimberly Van Auken,et al.  WormBase: better software, richer content , 2005, Nucleic Acids Res..

[28]  D. Tautz,et al.  A phylogenetically based transcriptome age index mirrors ontogenetic divergence patterns , 2010, Nature.

[29]  Nicholas H. Putnam,et al.  The Genome of the Ctenophore Mnemiopsis leidyi and Its Implications for Cell Type Evolution , 2013, Science.

[30]  L. Buss,et al.  The evolution of individuality , 1987 .

[31]  Steven J. M. Jones,et al.  ELT-2 is the predominant transcription factor controlling differentiation and function of the C. elegans intestine, from embryo to adult. , 2009, Developmental biology.

[32]  R. Waterston,et al.  Defining the transcriptional redundancy of early bodywall muscle development in C. elegans: evidence for a unified theory of animal muscle development. , 2006, Genes & development.

[33]  J. Priess,et al.  The REF-1 family of bHLH transcription factors pattern C. elegans embryos through Notch-dependent and Notch-independent pathways. , 2005, Developmental cell.

[34]  B. Goldstein,et al.  Culture and manipulation of embryonic cells. , 2012, Methods in cell biology.

[35]  Nicholas H. Putnam,et al.  The genome of the choanoflagellate Monosiga brevicollis and the origin of metazoans , 2008, Nature.

[36]  Kim Jacobsen,et al.  The embryonic cell lineage of the nematode Rhabditophanes sp. , 2008, The International journal of developmental biology.

[37]  B. Hall,et al.  Evolutionary Developmental Biology , 2010, Springer Netherlands.

[38]  B. Goldstein Induction of gut in Caenorhabditis elegans embryos , 1992, Nature.

[39]  J. McIntosh,et al.  Mapping the distribution of differentiation potential for intestine, muscle, and hypodermis during early development in Caenorhabditis elegans , 1985, Cell.

[40]  Damian Smedley,et al.  BioMart Central Portal: an open database network for the biological community , 2011, Database J. Biol. Databases Curation.

[41]  W. Barker Ontogeny and phylogeny. , 1980, Archives of surgery.

[42]  James W. Valentine,et al.  On the Origin of Phyla , 2004 .

[43]  The External Rna Controls Consortium The External RNA Controls Consortium: a progress report , 2005 .

[44]  Leszek P. Pryszcz,et al.  MetaPhOrs: orthology and paralogy predictions from multiple phylogenetic evidence using a consistency-based confidence score , 2010, Nucleic acids research.

[45]  Maja Adamska,et al.  Developmental gene expression provides clues to relationships between sponge and eumetazoan body plans , 2014, Nature Communications.

[46]  Stephen E Von Stetina,et al.  The embryonic muscle transcriptome of Caenorhabditis elegans , 2007, Genome Biology.

[47]  Rebecca R. Helm,et al.  Characterization of differential transcript abundance through time during Nematostella vectensis development , 2013, BMC Genomics.