1994
DOI: 10.1002/cne.903470310
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Localization of salmon gonadotropin‐releasing hormone mRNA and peptide in the brain of atlantic salmon and rainbow trout

Abstract: The decapeptide gonadotropin-releasing hormone (GnRH) is a key hormone for the central regulation of reproduction. The distribution of salmon GnRH (sGnRH), which is the major form in salmonids, has been studied in different fish species by immunocytochemistry. Discrepancies in data concerning the distribution of sGnRH perikarya led us to investigate this problem in two species, the Atlantic salmon and the rainbow trout, with in situ hybridization of sGnRH messenger, a highly specific molecular tool. By Norther… Show more

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Cited by 39 publications
(25 citation statements)
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References 34 publications
(24 reference statements)
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“…The DNA probe which was used for hybridisation (AS1-UpGnRH 236 bp fragment) detected both transgenic antisense and endogenous sGnRH transcripts with a better specificity for sGnRH-antisense (100% homology, 236 bp of complementary sequence) than for rainbow trout sGnRH mRNA (50 bp of complementary sequence with three and one mismatches for sGnRH-I and -II respectively). The antisense RNA was only present in the brain of AS(+) males and females, whereas sGnRH messengers were also present in AS( ) fish, and their size (650-700 bp) corresponded to that reported previously (Bailhache et al 1994, Ashihara et al 1995). An additional smear band of approximately 900 bp was only detected in AS(+) fish and could be the sGnRH-antisense transcript.…”
Section: Pab-directed Expression Of Inserted Genes In Transgenic Troutsupporting
confidence: 66%
“…The DNA probe which was used for hybridisation (AS1-UpGnRH 236 bp fragment) detected both transgenic antisense and endogenous sGnRH transcripts with a better specificity for sGnRH-antisense (100% homology, 236 bp of complementary sequence) than for rainbow trout sGnRH mRNA (50 bp of complementary sequence with three and one mismatches for sGnRH-I and -II respectively). The antisense RNA was only present in the brain of AS(+) males and females, whereas sGnRH messengers were also present in AS( ) fish, and their size (650-700 bp) corresponded to that reported previously (Bailhache et al 1994, Ashihara et al 1995). An additional smear band of approximately 900 bp was only detected in AS(+) fish and could be the sGnRH-antisense transcript.…”
Section: Pab-directed Expression Of Inserted Genes In Transgenic Troutsupporting
confidence: 66%
“…In particular, Parhar et al (1996) could not localize GnRH mRNA by in situ hybridization to preoptic area cells in a cichlid (Oreochromis mossambicus) or salmon (O. nerka) using a probe for 5Trp 7 Leu 8 6GnRH mRNA, yet they readily demonstrated immunoreactivity to GnRH in this region. Similarly, in situ hybridization in masu salmon (Suzuki et al, 1992), rainbow trout, and Atlantic salmon (Bailhache et al, 1994), using 5Trp 7 Leu 8 6GnRH-specific probes, found robust GnRH gene expression in the terminal nerve region yet only weak expression in the preoptic area. Comparing the immunocytochemical staining of GnRH neurons by Amano et al (1991) in masu salmon and Bailhache et al (1994) in Atlantic salmon and rainbow trout with in situ labeling in these species shows significantly less labeling in the preoptic area with in situ probes.…”
Section: Surprising Similarity Between 5trp 7 Leu 8 6gnrh In H Burtomentioning
confidence: 88%
“…Similarly, in situ hybridization in masu salmon (Suzuki et al, 1992), rainbow trout, and Atlantic salmon (Bailhache et al, 1994), using 5Trp 7 Leu 8 6GnRH-specific probes, found robust GnRH gene expression in the terminal nerve region yet only weak expression in the preoptic area. Comparing the immunocytochemical staining of GnRH neurons by Amano et al (1991) in masu salmon and Bailhache et al (1994) in Atlantic salmon and rainbow trout with in situ labeling in these species shows significantly less labeling in the preoptic area with in situ probes. Indeed, Bailhache et al concluded that this could ''.…”
Section: Surprising Similarity Between 5trp 7 Leu 8 6gnrh In H Burtomentioning
confidence: 88%
“…In situ hybridization was performed according to Salbcrt et al [ 18] and Bailhache et al [19] either on paraffin or cryostat sections. In the case of paraffin sections, the tissue was rinsed first in RNAscfrec phosphate buffer (PB.…”
Section: In Situ Hybridizationmentioning
confidence: 99%