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Defining the Gene Repertoire and Spatiotemporal Expression Profiles of Adhesion G Protein-Coupled Receptors in Zebrafish Breanne L

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Defining the Gene Repertoire and Spatiotemporal Expression Profiles of Adhesion G Protein-Coupled Receptors in Zebrafish Breanne L Washington University School of Medicine Digital Commons@Becker Open Access Publications 2015 Defining the gene repertoire and spatiotemporal expression profiles of adhesion G protein-coupled receptors in zebrafish Breanne L. Harty Washington University School of Medicine in St. Louis Arunkumar Krishnan Uppsala Universitet Nicholas E. Sanchez Washington University School of Medicine in St. Louis Helgi B. Schioth Uppsala Universitet Kelly R. Monk Washington University School of Medicine in St. Louis Follow this and additional works at: https://digitalcommons.wustl.edu/open_access_pubs Recommended Citation Harty, Breanne L.; Krishnan, Arunkumar; Sanchez, Nicholas E.; Schioth, Helgi B.; and Monk, Kelly R., ,"Defining the gene repertoire and spatiotemporal expression profiles of adhesion G protein-coupled receptors in zebrafish." BMC Genomics.16,. 62. (2015). https://digitalcommons.wustl.edu/open_access_pubs/3744 This Open Access Publication is brought to you for free and open access by Digital Commons@Becker. It has been accepted for inclusion in Open Access Publications by an authorized administrator of Digital Commons@Becker. For more information, please contact [email protected]. Defining the gene repertoire and spatiotemporal expression profiles of adhesion G protein-coupled receptors in zebrafish Harty et al. Harty et al. BMC Genomics 2015, 16: http://www.biomedcentral.com/1471-2164/16/1/ Harty et al. BMC Genomics (2015) 16:62 DOI 10.1186/s12864-015-1296-8 RESEARCH ARTICLE Open Access Defining the gene repertoire and spatiotemporal expression profiles of adhesion G protein-coupled receptors in zebrafish Breanne L Harty1, Arunkumar Krishnan2, Nicholas E Sanchez1, Helgi B Schiöth2 and Kelly R Monk1,3* Abstract Background: Adhesion G protein-coupled receptors (aGPCRs) are the second largest of the five GPCR families and are essential for a wide variety of physiological processes. Zebrafish have proven to be a very effective model for studying the biological functions of aGPCRs in both developmental and adult contexts. However, aGPCR repertoires have not been defined in any fish species, nor are aGPCR expression profiles in adult tissues known. Additionally, the expression profiles of the aGPCR family have never been extensively characterized over a developmental time-course in any species. Results: Here, we report that there are at least 59 aGPCRs in zebrafish that represent homologs of 24 of the 33 aGPCRs found in humans; compared to humans, zebrafish lack clear homologs of GPR110, GPR111, GPR114, GPR115, GPR116, EMR1, EMR2, EMR3,andEMR4. We find that several aGPCRs in zebrafish have multiple paralogs, in line with the teleost-specific genome duplication. Phylogenetic analysis suggests that most zebrafish aGPCRs cluster closely with their mammalian homologs, with the exception of three zebrafish-specific expansion events in Groups II, VI, and VIII. Using quantitative real-time PCR, we have defined the expression profiles of 59 zebrafish aGPCRs at 12 developmental time points and 10 adult tissues representing every major organ system. Importantly, expression profiles of zebrafish aGPCRs in adult tissues are similar to those previously reported in mouse, rat, and human, underscoring the evolutionary conservation of this family, and therefore the utility of the zebrafish for studying aGPCR biology. Conclusions: Our results support the notion that zebrafish are a potentially useful model to study the biology of aGPCRs from a functional perspective. The zebrafish aGPCR repertoire, classification, and nomenclature, together with their expression profiles during development and in adult tissues, provides a crucial foundation for elucidating aGPCR functions and pursuing aGPCRs as therapeutic targets. Keywords: Adhesion G protein-coupled receptors, Zebrafish genome, Expression profiling, High-throughput quantitative real-time PCR Background families: glutamate, rhodopsin, adhesion, frizzled/taste2, The G protein-coupled receptor (GPCR) superfamily and secretin (GRAFS classification) [2]. Adhesion comprises the largest class of cell membrane receptors GPCRs (aGPCRs) are the second largest of the five found in metazoan proteomes [1]. In humans, more than GPCR families, with 33 and 31 members in humans and 800 genes encoding different GPCRs have been identi- mice, respectively [3]. The aGPCRs are further subdi- fied and phylogenetically divided into five discrete vided into nine groups based on phylogenetic analysis of the 7-transmembrane domain (7TM) [4]. Although * Correspondence: [email protected] members of this family follow the same general struc- 1Department of Developmental Biology, Washington University School of tural pattern as other GPCRs, they differ in that they are Medicine, St. Louis, MO 63110, USA characterized by an extremely long N-terminus that con- 3Hope Center for Neurological Disorders, Washington University School of Medicine, St. Louis, MO 63110, USA tains the GPCR autoproteolysis-inducing (GAIN) do- Full list of author information is available at the end of the article main, [5] which encompasses the highly conserved © 2015 Harty et al.; licensee BioMed Central. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. Harty et al. BMC Genomics (2015) 16:62 Page 2 of 21 GPCR proteolytic site (GPS). Most aGPCRs undergo a developmental time-course, as well as in a wide collec- autoproteolysis at the GPS motif, which results in a pro- tion of adult tissues. Our studies demonstrate that there tein that is separated into an N-terminal fragment are at least 59 aGPCRs in zebrafish representing 24 of (NTF) and C-terminal fragment (CTF) that are thought the 33 human aGPCRs, with similar expression profiles to remain non-covalently attached at the cell surface [6]. as their mammalian homologs. The “adhesion” classification was given to this family of GPCRs due to the large number of classical cell adhe- Results and discussion sion domains found in the NTFs of many of these recep- Defining the zebrafish aGPCR repertoire tors [4,7]. In other proteins, these “adhesion” domains To define the zebrafish aGPCR repertoire, we first compiled (e.g., EGF-like domains and cadherin domains) are in- a list of nucleotide and protein sequences for 33 aGPCRs volved in protein-protein, cell-matrix, and cell-cell inter- annotated in the Zv8 release of the zebrafish genome using actions, leading to the idea that they perform similar three genomic databases: GenBank [24], Ensembl (release functions in aGPCRs [7]. Recent data for multiple 75) [25], and the zebrafish model organism database (ZFIN) aGPCRs suggests that these proteins can function as ad- [26]. Next, we used genome alignment and search tools - hesion molecules by virtue of the NTF, and as classical BLAST [27], UCSC Genome Browser [28], and Sequencher GPCRs that signal through G-proteins by virtue of the (http://www.genecodes.com) - to further mine the zebrafish CTF, in addition to the roles the NTF and CTF have in genome for additional predicted aGPCR sequences. We concert with one another [8-13]. conducted BLAST [27] searches using both the nucleotide In addition to their protein domain complexity, and amino acid sequences of all of the 33 previously anno- aGPCRs have been difficult to study due to their large tated zebrafish aGPCRs, as well as aGPCR sequences from size and complex genomic structures, with many small five additional species: stickleback (Gasterosteus aculeatus), exons separated by very large introns [4]. Additionally, mouse (Mus musculus), rat (Rattus norvegicus), dog (Canis aGPCRs have numerous splice isoforms, often lacking lupus familiaris), and human (Homo sapiens). With this one or more protein domains in the NTF, which may first pass of analysis, we obtained 40 putative aGPCRs have functional or regulatory roles [14]. The study of encoded in the zebrafish genome. aGPCRs is further complicated by the fact that this fam- Next, we took these 40 putative zebrafish aGPCR se- ily is identified primarily based on structural similarity at quences and BLASTed them a second time against the the protein level because, on a sequence level, aGPCRs zebrafish genome (Zv8). This step was essential for two can be extremely divergent from one another [4]. How- reasons: 1) to determine if multiple predicted aGPCR se- ever, despite the divergence between family members, quences could be consolidated because they actually rep- aGPCRs in general are evolutionarily ancient and highly resented the same gene, and 2) to search for more conserved, with a homolog found in social amoeba, divergent paralogous sequences (e.g., gene duplicates). Dictyostelium discoideum [15]. Indeed, further analysis of BLAST results suggested that In recent years, the zebrafish (Danio rerio) has become several of the initial predicted aGPCR sequences might a premiere model organism for the study of a wide var- belong to the same genes. For example, one predicted iety of physiological processes and disease states during sequence encoded the N-terminal domains and another development and in adult animals [16,17]. Moreover, encoded the GAIN and 7TM domains. In these in- zebrafish have proven to be useful models
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