Somatic mutations of immunoglobulin variable genes are restricted to the rearranged V gene

Science ◽  
1983 ◽  
Vol 220 (4602) ◽  
pp. 1179-1181 ◽  
Author(s):  
J Gorski ◽  
P Rollini ◽  
B Mach
Genetics ◽  
1987 ◽  
Vol 115 (1) ◽  
pp. 169-176
Author(s):  
G Brian Golding ◽  
Patricia J Gearhart ◽  
Barry W Glickman

ABSTRACT The mechanism responsible for somatic mutation in the variable genes of antibodies is unknown and may differ from previously described mechanisms that produce mutation in DNA. We have analyzed 421 somatic mutations from the rearranged immunoglobulin variable genes of mice to determine (1) if the nucleotide substitutions differ from those generated during meiosis and (2) if the presence of nearby direct and inverted repeated sequences could template mutations around the variable gene. The results reveal a difference in the pattern of substitutions obtained from somatic mutations vs. meiotic mutations. An increased frequency of T:A to C:G transitions and a decreased frequency of mutations involving a G in the somatic mutants compared to the meiotic mutants is indicated. This suggests that the mutational processes responsible for somatic mutation in antibody genes differs from that responsible for mutation during meiosis. An analysis of the local DNA sequences revealed many direct repeats and palindromic sequences that were capable of templating some of the known mutations. Although additional factors may be involved in targeting mutations to the variable gene, mistemplating by nearby repeats may provide a mechanism for the enhancement of somatic mutation.


10.1038/88740 ◽  
2001 ◽  
Vol 2 (6) ◽  
pp. 537-541 ◽  
Author(s):  
Xianmin Zeng ◽  
David B. Winter ◽  
Cynthia Kasmer ◽  
Kenneth H. Kraemer ◽  
Alan R. Lehmann ◽  
...  

Blood ◽  
2000 ◽  
Vol 95 (3) ◽  
pp. 1023-1031 ◽  
Author(s):  
Holger Kanzler ◽  
Ralf Küppers ◽  
Sabine Helmes ◽  
Hans-Heinrich Wacker ◽  
Andreas Chott ◽  
...  

In rare cases of B-cell chronic lymphocytic leukemia (B-CLL), large cells morphologically similar to or indistinguishable from Hodgkin/Reed-Sternberg (HRS) cells of Hodgkin's disease (HD) can be found in a background of otherwise typical B-CLL. To test these HRS-like cells for a potential clonal relationship to the B-CLL cells, single cells were micromanipulated from immunostained tissue sections, and rearranged immunoglobulin genes were amplified from HRS-like cells and B-CLL cells and sequenced. The same variable (V) gene rearrangements with shared and distinct somatic mutations were found in HRS-like and B-CLL cells from 1 patient, which indicates derivation of these cells from 2 distinct members of a germinal-center B-cell clone. Separate clonal Vgene rearrangements were amplified from HRS-like and B-CLL cells from 2 other patients, showing concomitant presence of 2 distinct expanded B-cell clones. Epstein-Barr virus (EBV) was detected in the HRS-like cells of these 2 latter cases, indicating clonal expansion of an EBV-harboring B cell in the setting of B-CLL. There is evidence that HRS-like cells in B-CLL, like HRS cells in HD, derive from germinal-center B cells. In all cases, somatic mutations have been detected in the rearranged V genes of the HRS-like cells, and in 1 of the EBV-positive HRS-like cell clones, somatic mutations rendered an originally functional V gene rearrangement nonfunctional. We speculate that the HRS-like cells in B-CLL represent potential precursors for HRS cells causing HD.


1996 ◽  
Vol 43 (3) ◽  
Author(s):  
AnupamK. Dattamajumdar ◽  
DavidP. Jacobson ◽  
LeroyE. Hood ◽  
GamalE. Osman

1998 ◽  
Vol 76 (2) ◽  
pp. 179-185 ◽  
Author(s):  
Georg F Weiller ◽  
Harald S Rothenfluh ◽  
Paula Zylstra ◽  
Lynn M Gay ◽  
Holger Averdunk ◽  
...  

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