Molecular Cloning of Chicken Vasoactive Intestinal Polypeptide Receptor Complementary DNA, Tissue Distribution and Chromosomal Localization1

Kansaku, Norio; Shimada, Kiyoshi; Ohkubo, Tadayasu; Sakai, Noboru; Suzuki, Tomohiro; Matsuda, Yoichi; Zadworny, D.

doi:10.1095/biolreprod64.5.1575

Cited by 35 publications

(20 citation statements)

References 53 publications

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“…Accession numbers of the sequences are: mouse, P97751; rat, P97751; human, P32241; pig, Q28992; frog, Q9YHC6 and goldfish, Q90308. The chicken sequence is taken from Kansaku et al 2001. revealed the presence of seven conserved transmembrane domains (Fig. 4).…”

Section: Resultsmentioning

confidence: 99%

“…Names and abbreviations and accession numbers for all the sequences shown: rat VPAC 1 , P97751; rat VPAC 2 , P35000; rat PAC 1 , P32215; rat sec, P23811; human V PAC 1 , P32241; human VPAC 2 , P41587; human PAC 1 , P41586; human sec, P47872; human GHRH, P43220 (used as the outgroup); mouse VPAC 1 , P97751; mouse VPAC 2 , P41587; mouse PAC 1 , P70205; frog VPAC 1 , Q9YHC6; pig VPAC 1 , Q28992; goldfish VPAC 1 , Q90308; goldfish PAC 1 , O73769; cattle PAC 1 , Q29627; toad PAC 1 , Q9PTK1; Fugu VPAC 1 A, AJ296144; Fugu VPAC 1 B, AJ296143; Fugu VPAC 2 A, AJ408877; Fugu VPAC 2 B, AJ408878; Fugu PAC 1 A, AJ490804; Fugu PAC 1 B, AJ494861; rabbit sec, O46502. The chicken sequences for VPAC 1 and PAC 1 were taken from Kansaku et al 2001 andPeeters et al 1999 respectively. Sec, secretin receptor. receptors in humans and rats.…”

Section: Discussionmentioning

confidence: 99%

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Duplicated receptors for VIP and PACAP (VPAC1R and PAC1R) in a teleost fish, Fugu rubripes

Cardoso¹,

Power²,

Elgar³

et al. 2004

Journal of Molecular Endocrinology

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Two principal groups of receptors orthologous with human PAC 1 R and VPAC 1 R and were identified and characterised at the genomic level in the teleost fish Fugu rubripes. An additional group orthologous with VPAC 2 R was also identified and partially characterised. In Fugu, gene duplication of each of the PAC 1 Rs, VPAC 1 Rs and VPAC 2 Rs appears to have occurred. The topology of the tree surrounding the Fugu duplications and other isolated piscine sequences indicates that the duplication events for these six genes clearly preceded the speciation event leading to the Cypriniformes and Tetraodontiformes and is probably teleost-specific. Overall, the combined pattern of gene expression for each pair of duplicated genes mirrored the expression in other vertebrates. However, within each pair of duplicates further specialisation had occurred, with each demonstrating differential tissue distribution profiles suggesting they that may be responsible for the divergent action of the ligands, vasoactive intestinal peptide (VIP) and pituitary adenylate cyclase-activating peptide (PACAP). The Fugu VPAC 1 R gene regions showed conserved synteny with human chromosome 3p21·3 and also C. elegans chromosome X, indicating that the putative ancestral human chromosome 3 region may be equivalent to chromosome X in

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Section: Resultsmentioning

confidence: 99%

Section: Discussionmentioning

confidence: 99%

Duplicated receptors for VIP and PACAP (VPAC1R and PAC1R) in a teleost fish, Fugu rubripes

Cardoso¹,

Power²,

Elgar³

et al. 2004

Journal of Molecular Endocrinology

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“…A single VIP receptor has been cloned in turkeys and chickens that exhibits 55-65% sequence identity with VIP1 and VIP2 receptors in mammals (Kansaku et al, 2001;You et al, 2001). Using the same 125 I-VIP employed here (human/porcine/rat; Perkin-Elmer Life Sciences, 2 Sociality information for the 139 estrildids has been compiled into a table, available from J.L.G.…”

Section: Avian Neuropeptide Receptors and Selection Of Iodinated Ligandsmentioning

confidence: 99%

“…A single VIP receptor has been cloned in turkeys and chickens that exhibits 55-65% sequence identity with VIP1 and VIP2 receptors in mammals (Kansaku et al, 2001;You et al, 2001). Using the same 125 I-VIP employed here (human/porcine/rat; Perkin-Elmer Life Sciences, Boston MA), it has been shown that specific binding sites in turkey telencephalon exhibit a high affinity for both VIP and pituitary adenylate cyclase-activating polypeptide (PACAP) (Zawilska et al, 2004).…”

Section: Avian Neuropeptide Receptors and Selection Of Iodinated Ligandsmentioning

confidence: 99%

Neuropeptide binding reflects convergent and divergent evolution in species-typical group sizes

Goodson

Evans

Wang

2006

Hormones and Behavior

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Neuroendocrine factors that produce species differences in aggregation behavior ("sociality") are largely unknown, although relevant studies should yield important insights into mechanisms of affiliation and social evolution. We here focused on five species in the avian family Estrildidae that differ selectively in their species-typical group sizes (all species are monogamous and occupy similar habitats). These include two highly gregarious species that independently evolved coloniality; two territorial species that independently evolved territoriality; and an intermediate, modestly gregarious species that is a sympatric congener of one of the territorial species. Using males and females of each species, we examined binding sites for 125 I-vasoactive intestinal polypeptide (VIP), 125 I-sauvagine (SG; a ligand for corticotropin releasing factor, CRF, receptors) and a linear 125 I-V 1a vasopressin antagonist (to localize receptors for vasotocin, VT). VIP, CRF and VT are neuropeptides that influence stress, anxiety and/or various social behaviors. For numerous areas (particularly within the septal complex), binding densities in the territorial species differed significantly from binding in the more gregarious species, and in most of these cases, binding densities for the moderately greagarious species were either comparable to the two colonial species, or were intermediate to the territorial and colonial species. Such patterns were observed for 125 I-VIP binding in the medial bed nucleus of the stria terminalis, medial septum, septohippocampal septum, and subpallial zones of the lateral septum; for 125 I-SG binding in the infundibular hypothalamus, and lateral and medial divisions of the ventromedial hypothalamus; and for the linear 125 I-V 1a antagonist in the medial septum, and the pallial and subpallial zones of the caudal lateral septum. With the exception of 125 I-SG binding in the infundibular hypothalamus, binding densitites are positively related to sociality. Keywords lateral septum; hypothalamus; vasotocin; vasopressin; corticotropin releasing factor; vasoactive intestinal polypeptide; evolution; sociality; songbird Components of social organization can change rapidly during evolution, as suggested by the fact that many vertebrate groups exhibit substantial diversity in behavioral dimensions such as grouping, mating systems, patterns of parental care, philopatry and kin affiliation. Thus, a given form of behavior or social structure may have evolved independently many times in various vertebrate lineages. Somewhat inconveniently, the evolution of a given species-typical social structure could hypothetically be produced by more than one kind of evolutionary modification to the brain, reducing our ability to generalize across species. Species-typical group size ("sociality") provides a good example: Natural selection on aggregation behavior could conceivably act on neural mechanisms that relate to anxiety, stress, aggression, reward, bonding, and/or simple arousal to social stimuli 1 . Therefore, in...

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“…As a receptor of VIP, VIPR is activated by VIP to give rise to secretion and release of PRL (el Halawani et al, 1990). The VIPR gene has proved to be involved in the regulation of broodiness in avian, as evidenced by the endocrine mechanism of broodiness and expression in vivo and in vitro (Rozenboim and el Halawani, 1993;Kansaku et al, 2001;Chaiseha et al, 2004). The VIPR-1 gene was expressed in the hypothalamus and pituitary, primarily in the latter, and only the differential mRNA expression of the VIPR-1 gene in the pituitary was associated with reproductive changes (You et al, 2001), suggesting that the VIPR-1 gene is an important candidate gene for egg-laying quails.…”

Section: Introductionmentioning

confidence: 99%

Association of VIPR-1 gene polymorphisms and haplotypes with egg production in laying quails

et al. 2016

J. Zhejiang Univ. Sci. B

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Abstract:The laying quail is a worldwide breed which exhibits high economic value. In our current study, the vasoactive intestinal peptide receptor-1 (VIPR-1) was selected as the candidate gene for identifying traits of egg production. A single nucleotide polymorphism (SNP) detection was performed in 443 individual quails, including 196 quails from the H line, 202 quails from the L line, and 45 wild quails. The SNPs were genotyped using a polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP). Two mutations (G373T, A313G) were detected in all the tested quail populations. The associated analysis showed that the SNP genotypes of the VIPR-1 gene were significantly linked with the egg weight of G373T and A313G in 398 quails. The quails with the genotype GG always exhibited the largest egg weight for the two mutations in the H and L lines. Linkage disequilibrium (LD) analysis indicated that G373T and A313G loci showed the weakest LD. Seven main diplotypes from the four main reconstructed haplotypes were observed, indicating a significant association of diplotypes with egg weight. Quails with the h1h2 (GGGT) diplotype always exhibited the smallest egg weight and largest egg number at 20 weeks of age. The overall results suggest that the alterations in quails may be linked with potential major loci or genes affecting reproductive traits.

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Molecular Cloning of Chicken Vasoactive Intestinal Polypeptide Receptor Complementary DNA, Tissue Distribution and Chromosomal Localization1

Cited by 35 publications

References 53 publications

Duplicated receptors for VIP and PACAP (VPAC1R and PAC1R) in a teleost fish, Fugu rubripes

Duplicated receptors for VIP and PACAP (VPAC1R and PAC1R) in a teleost fish, Fugu rubripes

Neuropeptide binding reflects convergent and divergent evolution in species-typical group sizes

Association of VIPR-1 gene polymorphisms and haplotypes with egg production in laying quails

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