Source:http://linkedlifedata.com/resource/pubmed/id/11986957
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
5
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pubmed:dateCreated |
2002-5-2
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pubmed:abstractText |
The t(2;14)(p13;q32.3) involving the BCL11A and IGH genes is a rare but recurrent chromosomal aberration in B-cell malignancies. Hitherto, juxtaposition of BCL11A and IGH has only been described in B-cell chronic lymphocytic leukemia (B-CLL) and immunocytoma. As subgroups of B-CLL can be distinguished by the pattern of somatic mutation of immunoglobulin variable (V) genes we investigated four lymphomas with IGH/BCL11A involvement for IGH hypermutation. Clonal V(H) gene rearrangements were amplified; in all four cases, sequencing of the amplificates revealed the rearranged V(H) genes to lack somatic mutations. These results suggest that t(2;14)(p13;q32.3) is associated with a subset of B-CLL/immunocytoma characterized by non-mutated IG genes deriving from pre-germinal center B cells. As the translocations in both informative cases are targeted to the switch regions of the IGG2 gene, which is mainly used in T cell-independent immune responses, these translocations presumably occurred in activated B cells in the course of T cell-independent immune responses outside the germinal center.
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pubmed:grant | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/BCL11A protein, human,
http://linkedlifedata.com/resource/pubmed/chemical/Carrier Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Immunoglobulin Heavy Chains,
http://linkedlifedata.com/resource/pubmed/chemical/Immunoglobulin Variable Region,
http://linkedlifedata.com/resource/pubmed/chemical/Neoplasm Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Nuclear Proteins
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pubmed:status |
MEDLINE
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pubmed:month |
May
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pubmed:issn |
0887-6924
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
16
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
937-9
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pubmed:dateRevised |
2007-11-15
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pubmed:meshHeading |
pubmed-meshheading:11986957-Carrier Proteins,
pubmed-meshheading:11986957-Chromosomes, Human, Pair 14,
pubmed-meshheading:11986957-Chromosomes, Human, Pair 2,
pubmed-meshheading:11986957-Genes, Immunoglobulin,
pubmed-meshheading:11986957-Humans,
pubmed-meshheading:11986957-Immunoglobulin Heavy Chains,
pubmed-meshheading:11986957-Immunoglobulin Switch Region,
pubmed-meshheading:11986957-Immunoglobulin Variable Region,
pubmed-meshheading:11986957-Leukemia, Lymphocytic, Chronic, B-Cell,
pubmed-meshheading:11986957-Lymphoma, B-Cell,
pubmed-meshheading:11986957-Mutation,
pubmed-meshheading:11986957-Neoplasm Proteins,
pubmed-meshheading:11986957-Nuclear Proteins,
pubmed-meshheading:11986957-Sequence Analysis, DNA,
pubmed-meshheading:11986957-Translocation, Genetic
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pubmed:year |
2002
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pubmed:articleTitle |
Lack of somatic hypermutation of IG V(H) genes in lymphoid malignancies with t(2;14)(p13;q32) translocation involving the BCL11A gene.
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pubmed:affiliation |
Institute for Genetics, Department of Internal Medicine I, LFI E4 R706, University of Cologne, Joseph-Stelzmannstrasse 9, D-50931 Cologne, Germany.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.,
Research Support, Non-U.S. Gov't
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