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Mutational hot spots in Ig V region genes of human follicular lymphomas

The genes coding for the Ig light chains expressed in two cases of human follicular lymphoma were cloned and sequenced. In each case, multiple independent isolates of the tumor population were compared. Although each tumor represented a single clone of B cells with a unique V/J joint, different cell...

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Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1988
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2188990/
https://www.ncbi.nlm.nih.gov/pubmed/3045247
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description The genes coding for the Ig light chains expressed in two cases of human follicular lymphoma were cloned and sequenced. In each case, multiple independent isolates of the tumor population were compared. Although each tumor represented a single clone of B cells with a unique V/J joint, different cells within each tumor had accumulated multiple point mutations in the V gene during clonal expansion. Most of the mutations observed were silent, but some resulted in amino acid replacements. Identical silent mutations were often observed in independent isolates of each tumor. By combining the current data with VH sequences obtained previously from the same cells, it was apparent that the repetitive silent mutations could not be explained solely by a genealogic tree. Such mutations could represent hot spots whose tendency to mutate may be influenced by neighboring DNA sequences or by the methylation of specific cytosine residues.
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spelling pubmed-21889902008-04-17 Mutational hot spots in Ig V region genes of human follicular lymphomas J Exp Med Articles The genes coding for the Ig light chains expressed in two cases of human follicular lymphoma were cloned and sequenced. In each case, multiple independent isolates of the tumor population were compared. Although each tumor represented a single clone of B cells with a unique V/J joint, different cells within each tumor had accumulated multiple point mutations in the V gene during clonal expansion. Most of the mutations observed were silent, but some resulted in amino acid replacements. Identical silent mutations were often observed in independent isolates of each tumor. By combining the current data with VH sequences obtained previously from the same cells, it was apparent that the repetitive silent mutations could not be explained solely by a genealogic tree. Such mutations could represent hot spots whose tendency to mutate may be influenced by neighboring DNA sequences or by the methylation of specific cytosine residues. The Rockefeller University Press 1988-08-01 /pmc/articles/PMC2188990/ /pubmed/3045247 Text en This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/).
spellingShingle Articles
Mutational hot spots in Ig V region genes of human follicular lymphomas
title Mutational hot spots in Ig V region genes of human follicular lymphomas
title_full Mutational hot spots in Ig V region genes of human follicular lymphomas
title_fullStr Mutational hot spots in Ig V region genes of human follicular lymphomas
title_full_unstemmed Mutational hot spots in Ig V region genes of human follicular lymphomas
title_short Mutational hot spots in Ig V region genes of human follicular lymphomas
title_sort mutational hot spots in ig v region genes of human follicular lymphomas
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2188990/
https://www.ncbi.nlm.nih.gov/pubmed/3045247