Source:http://linkedlifedata.com/resource/pubmed/id/10090615
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
2
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pubmed:dateCreated |
1999-6-7
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pubmed:databankReference |
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/AF056981,
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/AH006343,
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/AH006344,
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/U66250,
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/U75864,
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/U75865,
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/U76414,
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/U76415,
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/U90558,
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/U90559,
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/U90560,
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/U90561,
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/U90562
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pubmed:abstractText |
The HLA-B locus is the most polymorphic of the class I genes encoded within the human major histocompatibility complex. This polymorphism is mainly located in exons 2 and 3, which code for the molecule's alpha1 and alpha2 domains and includes the antigenic peptide binding site. However, information about adjacent non-coding regions (introns 1 and 2) has not been extensively reported but could be very important in establishing an understanding of the evolutionary mechanisms involved in the polymorphism generation of HLA-B and the Mhc loci. In the present work, introns 1 and 2 of 14 HLA-B alleles are studied and their significance is discussed; 10 have been sequenced in our own laboratory and the other 4 have been previously reported by others. Different serological families share the complete intron 1 sequence; at this region, 12 out of 14 HLA-B alleles could be included in four groups with the same intron 1 sequence: a) B*0702, B*4201, B*4801; b) B*27052, B*4002, B*4011; c) B*40012, B*4101, including B*4501, B*5001 (these latter two alleles have specific characteristics in both introns 1 and 2, which may reflect a common evolutionary pathway); and d) B*44031, B*44032. The other alleles, B*1402, and B*1801, do not have identical intron 1 sequences compared to any of the described groups, but share many similarities with them. The B*1801 evolutionary pathway seems to be very specific since it branches separately from other alleles both in intron 1 and intron 2 dendrograms. On the other hand, HLA-B allelic group distribution and similarities according to intron 1 sequences were not confirmed when using intron 2, especially in the cases of B*4002, B*4101 and B*4801. This would suggest that both point mutations fixed by genetic drift and gene conversion events are involved in HLA-B diversification. The latter events could be supported by the strong homology between intron 1 and, to a lesser extent, intron 2, and also the CG content within them. Finally, the precise knowledge of these non-coding regions could be important for developing DNA base typing strategies for the HLA-B alleles.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Feb
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pubmed:issn |
0001-2815
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
53
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
153-60
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:10090615-Alleles,
pubmed-meshheading:10090615-Base Sequence,
pubmed-meshheading:10090615-DNA, Complementary,
pubmed-meshheading:10090615-Evolution, Molecular,
pubmed-meshheading:10090615-HLA-B Antigens,
pubmed-meshheading:10090615-Humans,
pubmed-meshheading:10090615-Introns,
pubmed-meshheading:10090615-Molecular Sequence Data,
pubmed-meshheading:10090615-Sequence Homology, Nucleic Acid
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pubmed:year |
1999
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pubmed:articleTitle |
Evolutionary relationships between HLA-B alleles as indicated by an analysis of intron sequences.
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pubmed:affiliation |
Department of Immunology, Hospital 12 de Octubre, Universidad Complutense, Madrid, Spain.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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