Developmental Transcriptome of Aplysia Californica'

Developmental Transcriptome of Aplysia Californica'

RESEARCH ARTICLE Developmental Transcriptome of Aplysia californica ANDREAS HEYLAND1Ã, ZER VUE2, CHRISTIAN R. VOOLSTRA2,3, 2 4,5Ã MO´ NICA MEDINA , AND LEONID L. MOROZ 1Integrative Biology, University of Guelph, Ontario, Canada 2University of California, Merced, School of Natural Sciences, Merced, California 3Red Sea Research Center, King Abdullah University of Science and Technology (KAUST), Thuwal, Saudi Arabia 4The Whitney Laboratory for Marine Bioscience, University of Florida, Florida 5Department of Neuroscience, University of Florida, Florida ABSTRACT Genome-wide transcriptional changes in development provide important insight into mechanisms underlying growth, differentiation, and patterning. However, such large-scale developmental studies have been limited to a few representatives of Ecdysozoans and Chordates. Here, we characterize transcriptomes of embryonic, larval, and metamorphic development in the marine mollusc Aplysia californica and reveal novel molecular components associated with life history transitions. Specifically, we identify more than 20 signal peptides, putative hormones, and transcription factors in association with early development and metamorphic stages—many of which seem to be evolutionarily conserved elements of signal transduction pathways. We also characterize genes related to biomineralization—a critical process of molluscan development. In summary, our experiment provides the first large-scale survey of gene expression in mollusc development, and complements previous studies on the regulatory mechanisms underlying body plan patterning and the formation of larval and juvenile structures. This study serves as a resource for further functional annotation of transcripts and genes in Aplysia, specifically and molluscs in general. A comparison of the Aplysia developmental transcriptome with similar studies in the zebra fish Danio rerio, the fruit fly Drosophila melanogaster, the nematode Caenorhabditis elegans,and other studies on molluscs suggests an overall highly divergent pattern of gene regulatory mechanisms that are likely a consequence of the different developmental modes of these organisms. J. Exp. Zool. (Mol. Dev. Evol.) 316:113–134, 2011. & 2010 Wiley-Liss, Inc. How to cite this article: Heyland A, Vue Z, Voolstra CR, Medina M, Moroz LL. 2011. J. Exp. Zool. (Mol. Dev. Evol.) Developmental transcriptome of Aplysia californica.J.Exp.Zool.(Mol.Dev.Evol.) 316:113–134, 2011 316:113–134. Grant Sponsors: Swiss National Science Foundation Stipendium fuer Identification of spatial and temporal dynamics of patterns of Angehende Forscher, Brain Research Foundation; NSERC; Grant number: gene expression during development provides important insights C400230; Grant Sponsor: CFI; Grant number: 460175; Grant Sponsor: NIH; Grant numbers: P50HG002806; RO1NS06076; RR025699; Grant Sponsor: into mechanisms linking phenotypes with genotypes. A detailed NSF; Grant numbers: 0744649; DEB-0542330. understanding of the regulatory machinery underlying gene Additional Supporting Information may be found in the online version of expression (i.e. cis and trans regulation) is essential to address this article. fundamental questions about the genomic basis of complex ÃCorrespondence to: Andreas Heyland, Integrative Biology, University of developmental programs (e.g. see Davidson, 2001; Wilkins, 2001; Guelph, ON, N1G-2L6, Canada. E-mail: aheyland@ufl.edu and Leonid L. Rifkin et al., 2003). Major insights into these mechanisms Moroz, University of Florida, 9505 Ocean Shore Blvd, St. Augustine, FL 32080. E-mail: [email protected]fl.edu originate primarily from representatives of the Deuterostomata Received 3 March 2010; Revised 8 September 2010; Accepted 12 October and Ecdysozoa, and limited information exists on genome-wide 2010 changes in gene expression patterns for the Lophotrochozoa (but Published online 6 December 2010 in Wiley Online Library (wileyonline see Williams et al., 2009; Fiedler et al., 2010). Still, the library.com). DOI: 10.1002/jez.b.21383 & 2010 WILEY-LISS, INC. 114 HEYLAND ET AL. sequencing of several molluscan and annelid genomes and a from each nonredundant sequence in the Aplysia EST database. growing number of large-scale transcriptome projects has We refer to the two arrays as: Aplysia Annotated Array (AAA) recently been accomplished. These include the genome of the (GEO platform accession GPL3635) and Aplysia Discovery Array limpet Lottia gigantea (JGI), the snail Biomphalaria glabrata (DAA) (GEO platform accession GPL3636). All array files have (Washington University, NCBI Project ID: 12879), the clam been deposited on GEO (project accession: GSE14941). Additional Spisula solidissima (Marine Biological Laboratory, NCBI Project details about the protocols used, including a list of features on ID: 12960), the planarian Schmidtea mediteranea (Robb et al., eacharray,canbefoundontheGEOwebsiteandaredescribedin 2008), the leech Helobdella robusta (JGI), the polychate worm Moroz et al. (2006). We assembled all original contigs into 39,352 Capitella teleta (JGI), the transcriptomes of the mussel Mytilus unique contigs. These contigs were used for all analyses presented californianus (JGI), the oyster Crassostrea gigas (JGI), the in this article. A complete list of these contigs, annotation, and neuronal transcriptome of the sea hare Aplysia californica expression values can be found in Appendix 2. (Moroz et al., 2006) and the Aplysia genome project (Broad Experimental Designs. We extracted RNA from eight develop- Institute, A. californica genome project). The availability of these mental samples (Fig. 1), using an RNAaquousTM micro kit resources represents a unique opportunity to perform compara- (Ambion, Austin, TX). mRNA was quantified using a Nanodrop tive and genome-wide analyses of development on a transcrip- ND1000 (Thermo Scientific), and quality was assessed using a tional level. BioanalyzerTM 2100 (Agilent). We then added equal amounts of The sea hare A. californica (Mollusca: Gastropoda: Opistho- mRNA from each sample to a pooled sample, which was used for branchia: Anaspidae) has been used extensively for physiological each hybridization. Appendix 7 summarizes details on biological and cellular studies of behavior (Kandel, ’79; Glanzman, ’95; samples used in the experiment as well as the names of original Leonard and Edstrom, 2004). Still, studies describing embryogen- files submitted to GEO. All hybridizations were performed by esis and larval development in this and related species are limited Mogene Lc (St. Louis, MO). (but see Kriegstein et al., ’74; Kriegstein, ’77; Kandel, ’79; Kandel et al., ’80; Capo et al., 2009). Here, we analyze temporal and Data Analysis. Methodologies for assessment of dye bias and spatial gene expression changes during embryogenesis, larval normalization of this array are described in Moroz et al. (2006). development, and metamorphic stages using microarrays Microarray files were filtered using ControlType (0). We then and in situ hybridization (ISH). Specifically, we monitor more assembled all contigs from AAA and ADA into one master file than 39,000 unique transcripts from the recently sequenced and averaged expression levels of 60 mers belonging to the same A. californica neuronal transcriptome (Moroz et al., 2006) during nonredundant contigs (see above). Because we were primarily development. By correlating relative gene expression levels with interested in gene expression profiling through all developmental life history transitions, changes in body plan during develop- stages, we did not perform any additional filtering at this stage. ment, as well as changes on the level of the larval, juvenile and Cluster Analysis. We performed k-cluster and hierarchical cluster adult nervous system, we provide novel insights into the analysis for the entire dataset (Appendix 3) and various subsets development and neurogenesis of Aplysia.Specifically,we using SPSS v. 16. Parameters for hierarchical cluster analysis on analyze transcriptional changes related to biomineralization the entire dataset were set using average linkages between groups and metamorphic stages as well as neurotransmitter and with Pearson correlation. In addition to the final dendrogram, we hormonal signaling mechanisms, and identify novel genes also plotted the proximity matrix. K-means clustering was associated with these processes. Furthermore, we validate performed using 999 iterations and a convergence criterion of developmental changes in expression of selected transcripts 0.02. The same criteria were used for k-cluster analyses on using fluorescent and nonfluorescent ISH and RT-PCR. This is the peptides and biomineralization-related genes. first time that such an analysis was performed at the present scale in any lophotrochozoan species (but see Williams et al., 2009; GO Annotation and Enrichment Analysis. We were able to Fiedler et al., 2010). This study, therefore, provides the annotate 25% of all contigs (i.e. 9,879) using BLAST (NCBI and foundation for future research on mechanisms underlying Swissprot), and from this dataset 3% (i.e. 1,108) could be annotated development, neurogenesis, and metamorphosis in Aplysia and using automated GO annotation algorithms implemented in other molluscs. Blast2Go [36]. We then tested enrichment of specific GO categories within all the three developmental categories for all 1,108 contigs. All raw data from the analysis can be found in Appendix 4. MATERIAL AND METHODS We used Fisher’s exact test to compare GO categories for Microarray embryogenesis, larval development, and

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