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High-frequency representation of a single VH gene in the expressed human B cell repertoire [published erratum appears in J Exp Med 1993 Apr 1;177(4):following 1226]
Idiotype (Id) 16/6 marks a variable (V) region structure that occurs frequently in the human immunoglobulin repertoire. The basis of the Id has been traced to a germline heavy chain gene segment, VH18/2 (VH26). To pursue the molecular basis for the frequency of Id 16/6, we have analyzed polymerase c...
Formato: | Texto |
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Lenguaje: | English |
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The Rockefeller University Press
1993
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2190904/ https://www.ncbi.nlm.nih.gov/pubmed/8426111 |
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collection | PubMed |
description | Idiotype (Id) 16/6 marks a variable (V) region structure that occurs frequently in the human immunoglobulin repertoire. The basis of the Id has been traced to a germline heavy chain gene segment, VH18/2 (VH26). To pursue the molecular basis for the frequency of Id 16/6, we have analyzed polymerase chain reaction-generated C mu, C gamma, and VH3 family V gene libraries derived from the circulating and tonsillar B cells of four normal individuals and from the B cells of two patients with active systemic lupus erythematosus (SLE). The frequency of VH18/2 in these libraries was compared with three control VH genes, VH56P1, VH21/28, and VHA57. Plaque lifts from C mu and C gamma VH cDNA libraries were screened with gene-specific oligonucleotide probes. The frequency of VH18/2 ranged from 4 to 10% of JH+ plaques (two of five times that of control VH genes). In four VH3 family-specific libraries derived from rearranged DNA, VH18/2 represented 19-33% of VH3+ plaques. Hybridizing VH18/2 plaques were 98-100% homologous to the germline VH gene; mutations when present were often in framework 3. Extensive variation was seen in the complementarity determining region 3 sequences of these rearranged V genes. The high frequency of VH18/2 expression in the B cell repertoire was confirmed by sequencing randomly picked JH+ plaques. In two patients with active SLE the frequency of use of VH18/2 was not greater than that observed in normal subjects. These results show that VH18/2 is overrepresented in the B cell repertoire of normal subjects and suggest that the immune repertoire may be dominated by relatively few V genes. |
format | Text |
id | pubmed-2190904 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1993 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-21909042008-04-16 High-frequency representation of a single VH gene in the expressed human B cell repertoire [published erratum appears in J Exp Med 1993 Apr 1;177(4):following 1226] J Exp Med Articles Idiotype (Id) 16/6 marks a variable (V) region structure that occurs frequently in the human immunoglobulin repertoire. The basis of the Id has been traced to a germline heavy chain gene segment, VH18/2 (VH26). To pursue the molecular basis for the frequency of Id 16/6, we have analyzed polymerase chain reaction-generated C mu, C gamma, and VH3 family V gene libraries derived from the circulating and tonsillar B cells of four normal individuals and from the B cells of two patients with active systemic lupus erythematosus (SLE). The frequency of VH18/2 in these libraries was compared with three control VH genes, VH56P1, VH21/28, and VHA57. Plaque lifts from C mu and C gamma VH cDNA libraries were screened with gene-specific oligonucleotide probes. The frequency of VH18/2 ranged from 4 to 10% of JH+ plaques (two of five times that of control VH genes). In four VH3 family-specific libraries derived from rearranged DNA, VH18/2 represented 19-33% of VH3+ plaques. Hybridizing VH18/2 plaques were 98-100% homologous to the germline VH gene; mutations when present were often in framework 3. Extensive variation was seen in the complementarity determining region 3 sequences of these rearranged V genes. The high frequency of VH18/2 expression in the B cell repertoire was confirmed by sequencing randomly picked JH+ plaques. In two patients with active SLE the frequency of use of VH18/2 was not greater than that observed in normal subjects. These results show that VH18/2 is overrepresented in the B cell repertoire of normal subjects and suggest that the immune repertoire may be dominated by relatively few V genes. The Rockefeller University Press 1993-02-01 /pmc/articles/PMC2190904/ /pubmed/8426111 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 High-frequency representation of a single VH gene in the expressed human B cell repertoire [published erratum appears in J Exp Med 1993 Apr 1;177(4):following 1226] |
title | High-frequency representation of a single VH gene in the expressed human B cell repertoire [published erratum appears in J Exp Med 1993 Apr 1;177(4):following 1226] |
title_full | High-frequency representation of a single VH gene in the expressed human B cell repertoire [published erratum appears in J Exp Med 1993 Apr 1;177(4):following 1226] |
title_fullStr | High-frequency representation of a single VH gene in the expressed human B cell repertoire [published erratum appears in J Exp Med 1993 Apr 1;177(4):following 1226] |
title_full_unstemmed | High-frequency representation of a single VH gene in the expressed human B cell repertoire [published erratum appears in J Exp Med 1993 Apr 1;177(4):following 1226] |
title_short | High-frequency representation of a single VH gene in the expressed human B cell repertoire [published erratum appears in J Exp Med 1993 Apr 1;177(4):following 1226] |
title_sort | high-frequency representation of a single vh gene in the expressed human b cell repertoire [published erratum appears in j exp med 1993 apr 1;177(4):following 1226] |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2190904/ https://www.ncbi.nlm.nih.gov/pubmed/8426111 |