ArticleImmunogenetics1994
Molecular characterization of three Mhc class II B haplotypes in the ring-necked pheasant.
Article in Immunogenetics, 1994. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.
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Who cites it
12 citing papers in PubMed.
- Review
- MHC class II B diversity in blue tits: a preliminary study.Ecology and evolution · 2013Article
- Article
- Patterns of variation of the major histocompatibility complex class IIB loci in Chinese goose (Anser Cygnoides).Immunogenetics · 2009Article
- Isolation and characterization of major histocompatibility complex (MHC) class II B genes in the Barn owl (Aves: Tyto alba).Immunogenetics · 2008Article
- Emergence of influenza A virus variants after prolonged shedding from pheasants.Journal of virology · 2007Article
- Characterization of Mhc genes in a multigenerational family of ring-necked pheasants.Immunogenetics · 1996Article
- Contrasting histories of avian and mammalian Mhc genes revealed by class II B sequences from songbirds.Proceedings of the National Academy of Sciences of the United States of America · 1995Article
- Isolation and characterization of cDNA clones for Japanese quail (Coturnix japonica) major histocompatibility complex (MhcCoja) class I molecules.Immunogenetics · 1995Article
- Molecular cloning of major histocompatibility complex class II B gene cDNA from the Bengalese finch Lonchura striata.Immunogenetics · 1995Article
- Rfp-Y-like sequences assort independently of pheasant Mhc genes.Immunogenetics · 1995Article
- Article
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Authors and funding
4 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
We investigated the class II B genes in a free-ranging population of the ring-necked pheasant Phasianus colchicus by a combination of restriction fragment length polymorphism (RFLP), polymerase chain reaction (PCR), and DNA sequencing. Special attention was paid to the variation in the second exon, which encodes the peptide-binding beta 1-domain. The population was introduced, but it still exhibited major histocompatibility complex polymorphism with at least three segregating class II B haplotypes and consequently six genotypes. We found two class II B genes associated with each haplotype. The class II B genes of birds had until then only been molecularly characterized in the domestic chicken. The pheasant genes were highly variable, although one of the amplified sequences was found in two different haplotypes. Taken together, the most polymorphic positions (residues 37 and 38) were not identical in any of the predicted protein sequences, but all except one of the motifs had already been found in the domestic chicken. Structurally important features in mammalian class II B genes were generally conserved also in the pheasant sequences, but the loss of a potential salt bridge constituent (Arg72) in several sequences may suggest a slightly different structure of the adjacent parts of the peptide-binding groove. The pheasant genes are most closely related to the so called B-LBII family in the chicken, indicating that this represents a major line of development among avian class II B genes.
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