Skip Navigation

This Article
Right arrow FREE Full Text (PDF) Freely available
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in ISI Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrow Search for citing articles in:
ISI Web of Science (37)
Right arrowRequest Permissions
Google Scholar
Right arrow Articles by Edwards, S. V.
Right arrow Articles by March, M.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Edwards, S. V.
Right arrow Articles by March, M.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

Molecular Biology and Evolution, Vol 15, 236-250, Copyright © 1998 by Society for Molecular Biology and Evolution


ORIGINAL ARTICLE

Genomics and polymorphism of Agph-DAB1, an Mhc class II B gene in red- winged blackbirds (Agelaius phoeniceus)

SV Edwards, J Gasper and M March
Department of Zoology, University of Washington, Seattle 98195, USA. edwards@zoology.washington.edu

To further our understanding of the evolution of avian Mhc genes at the genomic level, we screened a cosmid library made from a red-winged blackbird (Agelaius phoeniceus) with a blackbird cDNA probe and subcloned from one of the Mhc-containing cosmids a gene which we designate Agph-DAB1. The structure of the gene is similar to that found for chicken class II B genes, except that the introns are surprisingly large, ranging from 98 to over 600 bp, making this the longest avian class II B gene to date. Using primers targeted toward the introns flanking the peptide-binding region (PBR), we amplified the entirety of the second exon and determined nucleotide sequences of 41 PCR products from eight individual blackbirds. The 10 sequence types found, among which were two probable pseudogene sequences, exhibit the classic hallmarks for evolution of PBRs, namely, an excess of nonsynonymous over synonymous substitutions and evidence of gene conversion events in polymorphic subdomains. Despite these patterns and our use of intron primers, the distribution of sequences among individuals suggests that more than one locus was amplified in most individuals, and the bushlike tree of sequences provides little information as to locus-specific clusters. These results imply a complex history of gene conversion, recent duplication, or possibly, concerted evolution among multiple loci, although Agph-DAB1, the first genomic Mhc sequence from a bird other than chicken, provides important clues in the quest for locus- specific Mhc primers in birds.
Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
J HeredHome page
A. Aguilar, S. V. Edwards, T. B. Smith, and R. K. Wayne
Patterns of Variation in MHC Class II {beta} Loci of the Little Greenbul (Andropadus virens) with Comments on MHC Evolution in Birds
J. Hered., March 1, 2006; 97(2): 133 - 142.
[Abstract] [Full Text] [PDF]


Home page
Mol Biol EvolHome page
S. V. Edwards, J. Gasper, D. Garrigan, D. Martindale, and B. F. Koop
A 39-kb Sequence Around a Blackbird Mhc Class II Gene: Ghost of Selection Past and Songbird Genome Architecture
Mol. Biol. Evol., September 1, 2000; 17(9): 1384 - 1395.
[Abstract] [Full Text] [PDF]


Home page
Genome ResHome page
C. M. Hess, J. Gasper, H. E. Hoekstra, C. E. Hill, and S. V. Edwards
MHC Class II Pseudogene and Genomic Signature of a 32-kb Cosmid in the House Finch (Carpodacus mexicanus)
Genome Res., May 1, 2000; 10(5): 613 - 623.
[Abstract] [Full Text]



Disclaimer: Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.