Follicular lymphomas' BCL-2/IgH junctions contain templated nucleotide insertions: novel insights into the mechanism of t(14;18) translocation

Citation
U. Jager et al., Follicular lymphomas' BCL-2/IgH junctions contain templated nucleotide insertions: novel insights into the mechanism of t(14;18) translocation, BLOOD, 95(11), 2000, pp. 3520-3529
Citations number
48
Categorie Soggetti
Hematology,"Cardiovascular & Hematology Research
Journal title
BLOOD
ISSN journal
00064971 → ACNP
Volume
95
Issue
11
Year of publication
2000
Pages
3520 - 3529
Database
ISI
SICI code
0006-4971(20000601)95:11<3520:FLBJCT>2.0.ZU;2-B
Abstract
The human t(14;18) chromosomal translocation is assumed to result from ille gitimate rearrangement between BCL-2 and D-H/J(H) gene segments during V(D) J recombination In early B cells. De novo nucleotides are found inserted in most breakpoints and have been thus far interpreted as nontemplated N regi on additions. In this report, we have analyzed both direct (BCL-2/J(H)) and reciprocal (D-H/BCL-2) breakpoints derived from 40 patients with follicula r lymphoma with t(14;18), Surprisingly, we found that more than 30% of the breakpoint junctions contain a novel type of templated nucleotide insertion s, consisting of short copies of the surrounding BCL-2, D-H, and J(H) seque nces. The features of these templated nucleotides, including multiplicity o f copies for 1 template and the occurrence of mismatches in the copies, sug gest the presence of a short-patch DNA synthesis, templated and error-prone . In addition, our analysis clearly shows that 1(14;18) occurs during a ver y restricted window of B-cell differentiation and involves 2 distinct mecha nisms: V(D)J recombination, mediating the breaks on chromosome 14 during an attempted secondary D-H to J(H) rearrangement, and an additional unidentif ied mechanism creating the initial breaks on chromosome 18. Altogether, the se data suggest that the 1(14;18) translocation is a more complex process t han previously thought, involving the interaction and/or subversion of V(D) J recombination with multiple enzymatic machineries. (Blood. 2000;95:3520-3 529) (C) 2000 by The American Society of Hematology.