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Open Access Research article

Sequence features of HLA-DRB1 locus define putative basis for gene conversion and point mutations

Jenny von Salomé234 and Jyrki P Kukkonen134*

Author Affiliations

1 University of Helsinki, Department of Basic Veterinary Sciences, Helsinki, Finland

2 Karolinska University Hospital, Department of Clinical Genetics, Stockholm, Sweden

3 Åbo Akademi University, Department of Biology, Turku, Finland

4 Uppsala University, Department of Neuroscience, Physiology, Uppsala, Sweden

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BMC Genomics 2008, 9:228  doi:10.1186/1471-2164-9-228

Published: 19 May 2008

Abstract

Background

HLA/MHC class II molecules show high degree of polymorphism in the human population. The individual polymorphic motifs have been suggested to be propagated and mixed by transfer of genetic material (recombination, gene conversion) between alleles, but no clear molecular basis for this has been identified as yet. A large number of MHC class II allele sequences is publicly available and could be used to analyze the sequence features behind the recombination, revealing possible basis for such recombination processes both in HLA class II genes and other genes, which recombination acts upon.

Results

In this study we analyzed the vast dataset of human allelic variants (49 full coding sequences, 374 full exon 2 sequences) of the most polymorphic MHC class II locus, HLA-DRB1, and identified many previously unknown sequence features possibly contributing to the recombination. The CpG-dinucleotide content of exon 2 (containing the antigen-binding sites and subsequently a high degree of polymorphism) was much elevated as compared to the other exons despite similar overall G+C content. Furthermore, the CpG pattern was highly conserved. We also identified more complex, highly conserved sequence motifs in exon 2. Some of these can be identified as putative recombination motifs previously found in other genes, but most are previously unidentified.

Conclusion

The identified sequence features could putatively act in recombination allowing either less (CpG dinucleotides) or more specific DNA cleavage (complex sequences) or homologous recombination (complex sequences).