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BMC Evol Biol
2009 Feb 26;9:47. doi: 10.1186/1471-2148-9-47.
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Characterization of the neurohypophysial hormone gene loci in elephant shark and the Japanese lamprey: origin of the vertebrate neurohypophysial hormone genes.
Gwee PC, Tay BH, Brenner S, Venkatesh B.
???displayArticle.abstract??? Vasopressin and oxytocin are mammalian neurohypophysial hormones with distinct functions. Vasopressin is involved mainly in osmoregulation and oxytocin is involved primarily in parturition and lactation. Jawed vertebrates contain at least one homolog each of vasopressin and oxytocin, whereas only a vasopressin-family hormone, vasotocin, has been identified in jawless vertebrates. The genes encoding vasopressin and oxytocin are closely linked tail-to-tail in eutherian mammals whereas their homologs in chicken, Xenopus and coelacanth (vasotocin and mesotocin) are linked tail-to-head. In contrast, their pufferfish homologs, vasotocin and isotocin, are located on the same strand of DNA with isotocin located upstream of vasotocin and separated by five genes. These differences in the arrangement of the two genes in different bony vertebrate lineages raise questions about their origin and ancestral arrangement. To trace the origin of these genes, we have sequenced BAC clones from the neurohypophysial gene loci in a cartilaginous fish, the elephant shark (Callorhinchus milii), and in a jawless vertebrate, the Japanese lamprey (Lethenteron japonicum). We have also analyzed the neurohypophysial hormone gene locus in an invertebrate chordate, the amphioxus (Branchiostoma floridae). The elephant shark neurohypophysial hormone genes encode vasotocin and oxytocin, and are linked tail-to-head like their homologs in coelacanth and non-eutherian tetrapods. Besides the hypothalamus, the two genes are also expressed in the ovary. In addition, the vasotocin gene is expressed in the kidney, rectal gland and intestine. These expression profiles indicate a paracrine role for the two hormones. The lamprey locus contains a single neurohypophysial hormone gene, the vasotocin. The synteny of genes in the lamprey locus is conserved in elephant shark, coelacanth and tetrapods but disrupted in teleost fishes. The amphioxus locus encodes a single neurohypophysial hormone, designated as [Ile4]vasotocin. The vasopressin- and oxytocin-family of neurohypophysial hormones evolved in a common ancestor of jawed vertebrates through tandem duplication of the ancestral vasotocin gene. The duplicated genes were linked tail-to-head like their homologs in elephant shark, coelacanth and non-eutherian tetrapods. In contrast to the conserved linkage of the neurohypophysial genes in these vertebrates, the neurohypophysial hormone gene locus has experienced extensive rearrangements in the teleost lineage.
Figure 1. Organization of neurohypophysial hormone-genes in jawed vertebrates. Genes are shown as arrows. Only the neurohypophysial hormone-genes are labeled. The elephant shark genes were sequenced in this study. The arrangements of genes in other vertebrates are mainly from [8]. The neurohypophysial hormone-genes in chicken and Xenopus are arranged like their homologs in coelacanth.
Figure 2. The neurohypophysial gene locus in the elephant shark (A) and Japanese lamprey (B). The BACs used for generating the sequences are shown below. Arrows represent genes and indicate the direction of transcription. Coloured vertical lines represent repetitive sequences. VT, vasotocin gene; OT, oxytocin gene; ProSAPiP1, proline rich synapse associated protein interacting protein 1; UBOX5, U-box domain containing 5; GNRH2, gonadotropin-releasing hormone 2; PTPRA, protein tyrosine phosphatase, receptor type, A.
Figure 3. Comparison of nucleotide and deduced amino acid sequences of elephant shark vasotocin and oxytocin genes. Conserved nucleotides are indicated by an asterisk. N-glycosylation sites and Leu-rich core segment in the vasotocin precursor are boxed. Intronic sequences are shown in lower case.
Figure 4. Comparison of amino acid sequences of vasopressin family hormone precursors in vertebrates. The alignment was generated by ClustalX. Amino acid residues conserved in all vertebrates are marked with an asterisk. B. floridae, Branchiostoma floridae; X. tropicalis, Xenopus tropicalis; and T. scyllium, Triakis scyllium. VP, vasopressin and VT, vasotocin. Accession numbers of sequences used in the alignment: NP_000481.2 (human VP), BAA24026.1 (lungfish VT), O42499 (fugu VT), BAD27476.1 (T. scyllium VT) and BAA06669.1 (lamprey VT). Sequences for Xenopus tropicalis and coelacanth were generated in a previous study [8] while sequences for elephant shark (eshark) and amphioxus (B. floridae) were generated in this study.
Figure 5. Comparison of amino acid sequences of oxytocin family hormone precursors in vertebrates. The alignment was generated by ClustalX. Amino acid residues conserved in all vertebrates are marked with an asterisk. X. tropicalis, Xenopus tropicalis; and T. scyllium, Triakis scyllium. OT, oxytocin; MT, mesotocin; IT, isotocin; ASV, asvatocin and PAI, phasitocin. Accession numbers of sequences used in the alignment: NP_000906.1 (human OT), BAA24027.1 (lungfish [Phe2]MT), O42493 (fugu IT), BAD27478.1 (T. scyllium phasitocin) and BAD27477.1 (T. scyllium asvatocin). Sequences for Xenopus tropicalis and coelacanth were generated in a previous study [8] while the sequence for elephant shark (eshark) was generated in this study.
Figure 6. Expression patterns of elephant shark neurohypophysial hormone genes. Expression patterns of the elephant shark vasotocin and oxytocin genes as determined by semi-quantitative RT-PCR. Expression of actin gene was analyzed as a control for the quality of RNA and cDNA.
Figure 7. Schematic diagram of neurohypophysial hormone gene loci in chordates. Arrows represent genes and indicate the orientation of transcription. ProSAPiP1, ProSAP-interacting protein 1 gene; UBOX5, U-box domain containing 5; [Lys8]VP, lysipressin gene; VT, vasotocin gene; MT, mesotocin gene; OT, oxytocin gene; IT, isotocin gene, GNRH2, gonadotropin-releasing hormone 2; PTPRA, protein tyrosine phosphatase receptor type A gene; CL1, chemokine CL1 gene; UGNT, UDP glucuronic acid/N-acetylglucosamine dual transporter gene; RNR, ribonucleotide reductase M2 polypeptide; St8sia2, alpha-2,8-sialyltransferase; RPS6KA3, ribosomal protein S6 kinase 90kDa polypeptide3; Ci-VP, Ciona-vasopressin; and CELSR3, cadherin EGF LAG seven-pass G-type receptor3.
Acher,
Unique evolution of neurohypophysial hormones in cartilaginous fishes: possible implications for urea-based osmoregulation.
1999, Pubmed
Acher,
Unique evolution of neurohypophysial hormones in cartilaginous fishes: possible implications for urea-based osmoregulation.
1999,
Pubmed Christoffels,
Fugu genome analysis provides evidence for a whole-genome duplication early during the evolution of ray-finned fishes.
2004,
Pubmed Cruz,
Invertebrate vasopressin/oxytocin homologs. Characterization of peptides from Conus geographus and Conus straitus venoms.
1987,
Pubmed Davies,
Further delineation of the sequences required for the expression and physiological regulation of the vasopressin gene in transgenic rat hypothalamic magnocellular neurones.
2003,
Pubmed Fairbrother,
Predictive identification of exonic splicing enhancers in human genes.
2002,
Pubmed Fields,
Regulatory domains in the intergenic region of the oxytocin and vasopressin genes that control their hypothalamus-specific expression in vitro.
2003,
Pubmed Foo,
Vasopressin and oxytocin gene expression in rat testis.
1991,
Pubmed Gimpl,
The oxytocin receptor system: structure, function, and regulation.
2001,
Pubmed Gwee,
Sequence and organization of coelacanth neurohypophysial hormone genes: evolutionary history of the vertebrate neurohypophysial hormone gene locus.
2008,
Pubmed
,
Xenbase Heierhorst,
Presence of a member of the Tc1-like transposon family from nematodes and Drosophila within the vasotocin gene of a primitive vertebrate, the Pacific hagfish Eptatretus stouti.
1992,
Pubmed Hoyle,
Neuropeptide families and their receptors: evolutionary perspectives.
1999,
Pubmed Hyodo,
Osmoregulation in elephant fish Callorhinchus milii (Holocephali), with special reference to the rectal gland.
2007,
Pubmed Hyodo,
Neurohypophysial hormones of dogfish, Triakis scyllium: structures and salinity-dependent secretion.
2004,
Pubmed Jaillon,
Genome duplication in the teleost fish Tetraodon nigroviridis reveals the early vertebrate proto-karyotype.
2004,
Pubmed Janvier,
Palaeontology: modern look for ancient lamprey.
2006,
Pubmed Kawada,
Characterization of a novel vasopressin/oxytocin superfamily peptide and its receptor from an ascidian, Ciona intestinalis.
2008,
Pubmed
,
Xenbase Lane,
Arginine vasotocin from the pituitary gland of the lamprey (Petromyzon marinus): isolation and amino acid sequence.
1988,
Pubmed Li,
Genomics, transcriptomics, and peptidomics of neuropeptides and protein hormones in the red flour beetle Tribolium castaneum.
2008,
Pubmed McMaster,
A vasotocin-like peptide in Aplysia kurodai ganglia: HPLC and RIA evidence for its identity with Lys-conopressin G.
1992,
Pubmed Méchaly,
Identification and sequence analysis of arginine vasopressin mRNA in normal and Brattleboro rat aortic tissue.
1998,
Pubmed Michel,
Chemical identification of the mammalian oxytocin in a holocephalian fish, the ratfish (Hydrolagus colliei).
1993,
Pubmed Mohr,
Expression of the vasopressin and oxytocin genes in rats occurs in mutually exclusive sets of hypothalamic neurons.
1988,
Pubmed Murphy,
In vivo gene transfer studies on the regulation and function of the vasopressin and oxytocin genes.
2003,
Pubmed Nielsen,
Isolation of Lys-conopressin-G from the venom of the worm-hunting snail, Conus imperialis.
1994,
Pubmed Oumi,
Annetocin: an oxytocin-related peptide isolated from the earthworm, Eisenia foetida.
1994,
Pubmed Proux,
Identification of an arginine vasopressin-like diuretic hormone from Locusta migratoria.
1987,
Pubmed Putnam,
The amphioxus genome and the evolution of the chordate karyotype.
2008,
Pubmed Ravi,
Rapidly evolving fish genomes and teleost diversity.
2008,
Pubmed Reich,
A new peptide of the oxytocin/vasopressin family isolated from nerves of the cephalopod Octopus vulgaris.
1992,
Pubmed Richards,
The genome of the model beetle and pest Tribolium castaneum.
2008,
Pubmed Ruppert,
Recent gene conversion involving bovine vasopressin and oxytocin precursor genes suggested by nucleotide sequence.
,
Pubmed Salzet,
Isolation, structural characterization and biological function of a lysine-conopressin in the central nervous system of the pharyngobdellid leech Erpobdella octoculata.
1993,
Pubmed Simon,
Identification of vasopressin mRNA in rat aorta.
1995,
Pubmed Stafflinger,
Cloning and identification of an oxytocin/vasopressin-like receptor and its ligand from insects.
2008,
Pubmed Suzuki,
Sequence analysis of vasotocin cDNAs of the lamprey, Lampetra japonica, and the hagfish, Eptatretus burgeri: evolution of cyclostome vasotocin precursors.
1995,
Pubmed Takuwa-Kuroda,
Octopus, which owns the most advanced brain in invertebrates, has two members of vasopressin/oxytocin superfamily as in vertebrates.
2003,
Pubmed Thompson,
The CLUSTAL_X windows interface: flexible strategies for multiple sequence alignment aided by quality analysis tools.
1997,
Pubmed Ukena,
Unique form and osmoregulatory function of a neurohypophysial hormone in a urochordate.
2008,
Pubmed van Kesteren,
Evolution of the vasopressin/oxytocin superfamily: characterization of a cDNA encoding a vasopressin-related precursor, preproconopressin, from the mollusc Lymnaea stagnalis.
1992,
Pubmed van Kesteren,
A vasopressin-related peptide in the mollusc Lymnaea stagnalis: peptide structure, prohormone organization, evolutionary and functional aspects of Lymnaea conopressin.
1992,
Pubmed Venkatesh,
Survey sequencing and comparative analysis of the elephant shark (Callorhinchus milii) genome.
2007,
Pubmed Venkatesh,
A compact cartilaginous fish model genome.
2005,
Pubmed Young,
Transgenesis and the study of expression, cellular targeting and function of oxytocin, vasopressin and their receptors.
2003,
Pubmed