2002
DOI: 10.1046/j.1471-8286.2002.00315.x
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PCR‐based markers detect genetic variation at growth and immune function‐related loci in chinook salmon (Oncorhynchus tshawytscha)

Abstract: We developed seven polymerase chain reaction (PCR) based markers that detect genetic variation at loci related to growth (four) and immune function (three) in chinook salmon. One assay shows a length polymorphism following PCR; the others show restriction fragment length polymorphisms (PCR‐RFLP). Two alleles were detected in each assay, and the common alleles were found at frequencies of 0.67–0.95 in seven wild populations in British Columbia, Canada. These loci also amplified in other salmonid species. These … Show more

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Cited by 18 publications
(19 citation statements)
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“…The YIAL population was founded with gametes from the Robertson Creek hatchery on Vancouver Island, and has been maintained since 1986. MHC diversity in the YIAL population is comparable to other populations of Chinook salmon, in which three to six alleles have been identified within a population (Miller & Withler 1996;Kim et al 1999;Docker & Heath 2002;Pitcher & Neff 2006). YIAL has eliminated the male sex chromosome through the use of hormonal sex-reversal in female XX salmon.…”
Section: Methodssupporting
confidence: 51%
See 1 more Smart Citation
“…The YIAL population was founded with gametes from the Robertson Creek hatchery on Vancouver Island, and has been maintained since 1986. MHC diversity in the YIAL population is comparable to other populations of Chinook salmon, in which three to six alleles have been identified within a population (Miller & Withler 1996;Kim et al 1999;Docker & Heath 2002;Pitcher & Neff 2006). YIAL has eliminated the male sex chromosome through the use of hormonal sex-reversal in female XX salmon.…”
Section: Methodssupporting
confidence: 51%
“…Genotypes were determined for a 294 bp portion of the MHC class IIB gene (Docker & Heath 2002) using single strand conformational polymorphism (Amersham Biosciences) to identify unique banding patterns. Each unique pattern was then cloned from two individuals using a Promega pGEM-T easy vector kit and sequenced.…”
Section: Methodsmentioning
confidence: 99%
“…Primers were designed to amplify exons encoding the peptide binding region (PBR) located on the a 1 chain of the MHC class I and the ß 1 chain of the MHC class II. PCR was used to amplify each locus following the protocols outlined in Miller et al (1997) and Docker and Heath (2002). For both loci, PCR products were visualised using SSCP (single strand conformation polymorphism) electrophoresis on the Amersham-Biosciences SSCP system and gels were fixed and stained using a silver stain (GE Healthcare Bio-Sciences Corp., Piscataway, NJ, USA).…”
Section: Mhc Genotypingmentioning
confidence: 99%
“…Both the MHC class I and II studied are likely functional because they are transcribed in closely related species including the Atlantic salmon Hordvik et al, 1993). We used polymerase chain reaction (PCR) to amplify each locus following the protocols outlined in and Docker and Heath (2002). The MHC class I-A1 primers amplify either 222 or 228 bp, whereas the MHC class II-B1 primers amplify 213 bp.…”
Section: Mhc Genotypingmentioning
confidence: 99%