Complex biallelic IGH rearrangements in IgM-expressing Z-138 cell line:: Involvement of downstream immunoglobulin class switch recombination

被引:9
作者
Guikema, JEJ
Fenton, JAL
de Boer, C
Kleiverda, K
Brink, AATP
Raap, AK
Estrov, Z
Schuuring, E
Kluin, PM
机构
[1] Univ Groningen, Ctr Med, Dept Pathol & Lab Med, NL-9700 RB Groningen, Netherlands
[2] Univ Leeds, Dept Haematol, Leeds, W Yorkshire, England
[3] Leiden Univ, Ctr Med, Dept Pathol, Leiden, Netherlands
[4] Leiden Univ, Ctr Med, Dept Mol Cell Biol, Leiden, Netherlands
[5] Univ Texas, MD Anderson Canc Ctr, Dept Bioimmunotherapy, Houston, TX 77030 USA
关键词
D O I
10.1002/gcc.20132
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Chromosomal translocations involving the immunoglobulin (Ig) receptor loci usually disrupt and silence these loci. On the basis of observations in follicular lymphoma (FL) with downstream Ig heavy chain (IGH) class switch recombination (CSR), we hypothesized that downstream CSR-mediated chromosomal translocations would leave the V(D)J-Cmu transcription unit intact, thereby still allowing IgM expression from the IGH allele involved in the translocation. To test this hypothesis, we analyzed biallelic IGH translocations in the IgM-expressing cell line Z-138 by interphase FISH, DNA fiber-FISH, long-distance vectorette PCR, and DNA sequencing. One IGH allele was involved in a t(11;14), showing a break in the JH region that juxtaposed the El,L enhancer and the 3' Calpha enhancers to the cyclin D1 gene. The other IGH allele contained a t(8; 14) breakpoint involving the 3' end of a Sgamma region, whereas the reciprocal breakpoint at 8q24 was approximately 40 kb centromeric of MYC. Molecular analysis showed that this IGH allele harbored a normal V(D)J-Cmu complex, which is responsible for IgM expression. These data show that chromosomal breakpoints such as the t(8; 14) can occur in downstream IGH constant regions and do not necessarily interfere with Ig expression. (C) 2004 Wiley-Liss, Inc.
引用
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页码:164 / 169
页数:6
相关论文
共 33 条
[1]  
Avet-Loiseau H, 1998, CANCER RES, V58, P5640
[2]   Chromosome translocations in multiple myeloma [J].
Bergsagel, PL ;
Kuehl, WM .
ONCOGENE, 2001, 20 (40) :5611-5622
[3]   Promiscuous translocations into immunoglobulin heavy chain switch regions in multiple myeloma [J].
Bergsagel, PL ;
Chesi, M ;
Nardini, E ;
Brents, LA ;
Kirby, SL ;
Kuehl, WM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (24) :13931-13936
[4]   Transcription-targeted DNA deamination by the AID antibody diversification enzyme [J].
Chaudhuri, J ;
Tian, M ;
Khuong, C ;
Chua, K ;
Pinaud, E ;
Alt, FW .
NATURE, 2003, 422 (6933) :726-730
[5]   Deregulation of FCGR2B expression by 1q21 rearrangements in follicular lymphomas [J].
Chen, WY ;
Palanisamy, N ;
Schmidt, H ;
Teruya-Feldstein, J ;
Jhanwar, SC ;
Zelenetz, AD ;
Houldsworth, J ;
Chaganti, RSK .
ONCOGENE, 2001, 20 (52) :7686-7693
[6]   The t(4;14) translocation in myeloma dysregulates both FGFR3 and a novel gene, MMSET, resulting in IgH/MMSET hybrid transcripts [J].
Chesi, M ;
Nardini, E ;
Lim, RSC ;
Smith, KD ;
Kuehl, WM ;
Bergsagel, PL .
BLOOD, 1998, 92 (09) :3025-3034
[7]   Frequent dysregulation of the c-maf proto-oncogene at 16q23 by translocation to an Ig locus in multiple myeloma [J].
Chesi, M ;
Bergsagel, PL ;
Shonukan, OO ;
Martelli, ML ;
Brents, LA ;
Chen, T ;
Schröck, E ;
Ried, T ;
Kuehl, VM .
BLOOD, 1998, 91 (12) :4457-4463
[8]   Visualization of mono-allelic chromosomal aberrations 3' and 5' of the cyclin D1 gene in mantle cell lymphoma using DNA fiber fluorescence in situ hybridization [J].
deBoer, CJ ;
Vaandrager, JW ;
vanKrieken, JHJM ;
Holmes, Z ;
Kluin, PM ;
Schuuring, E .
ONCOGENE, 1997, 15 (13) :1599-1603
[9]   TRANSLOCATION T(14-18) IN B-CELL LYMPHOMAS AS A CAUSE FOR DEFECTIVE IMMUNOGLOBULIN PRODUCTION [J].
DEJONG, D ;
VOETDIJK, BMH ;
VANOMMEN, GJB ;
KLUINNELEMANS, JC ;
BEVERSTOCK, GC ;
KLUIN, PM .
JOURNAL OF EXPERIMENTAL MEDICINE, 1989, 169 (03) :613-624
[10]   AID mediates hypermutation by deaminating single stranded DNA [J].
Dickerson, SK ;
Market, E ;
Besmer, E ;
Papavasiliou, EN .
JOURNAL OF EXPERIMENTAL MEDICINE, 2003, 197 (10) :1291-1296