Literature DB >> 15086412

t(11;18)(q21;q21) of mucosa-associated lymphoid tissue lymphoma results from illegitimate non-homologous end joining following double strand breaks.

Hongxiang Liu1, Rifat A Hamoudi, Hongtao Ye, Agnes Ruskone-Fourmestraux, Ahmet Dogan, Peter G Isaacson, Ming-Qing Du.   

Abstract

t(11;18)(q21;q21) is the most frequent chromosomal aberration specifically associated with mucosa-associated lymphoid tissue (MALT) lymphoma. The translocation fuses the API2 gene to the MALT1 gene and generates a functional API2-MALT1 transcript. The breakpoint of the fusion gene is well characterized at the transcript level but poorly understood at the genomic level and the mechanism underlying the translocation is unknown. We identified the genomic breakpoint in 19 t(11;18)-positive MALT lymphoma cases by polymerase chain reaction and sequencing and analysed the junctional sequences. The breakpoints were scattered in intron 7 and exon 8 of the API2 gene, and introns 4, 6, 7 and 8 of the MALT1 gene. Comparative sequence analysis between the API2-MALT1 fusion on der(11) and the MALT1-API2 fusion on der(18) showed extensive alterations including deletions, duplications and non-template-based insertions at the fusion junctions in all cases examined. An extensive sequence search failed to reveal any known sequence motifs that might be associated with chromosomal recombination or any novel consensus sequences at or near the breakpoints on both der(11) and der(18) except in one case, in which Alu repeats spanned the breakpoint of the MALT1-API2 fusion. Our results suggest that t(11;18) may result from illegitimate non-homologous end joining following double strand breaks.

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Year:  2004        PMID: 15086412     DOI: 10.1111/j.1365-2141.2004.04909.x

Source DB:  PubMed          Journal:  Br J Haematol        ISSN: 0007-1048            Impact factor:   6.998


  6 in total

1.  The t(14;18)(q32;q21)/IGH-MALT1 translocation in MALT lymphomas is a CpG-type translocation, but the t(11;18)(q21;q21)/API2-MALT1 translocation in MALT lymphomas is not.

Authors:  Albert G Tsai; Zhengfei Lu; Michael R Lieber
Journal:  Blood       Date:  2010-04-29       Impact factor: 22.113

2.  Expression of FOXP1 in mucosa-associated lymphoid tissue lymphoma suggests a large tumor cell transformation and predicts a poorer prognosis in the positive thyroid patients.

Authors:  Wei Jiang; Lei Li; Yuan Tang; Wen-yan Zhang; Wei-ping Liu; Gan-di Li
Journal:  Med Oncol       Date:  2012-06-27       Impact factor: 3.064

3.  Saccharomyces cerevisiae as a model system to define the chromosomal instability phenotype.

Authors:  Christopher D Putnam; Vincent Pennaneach; Richard D Kolodner
Journal:  Mol Cell Biol       Date:  2005-08       Impact factor: 4.272

4.  Large duplications at reciprocal translocation breakpoints that might be the counterpart of large deletions and could arise from stalled replication bubbles.

Authors:  Karen D Howarth; Jessica C M Pole; Juliet C Beavis; Elizabeth M Batty; Scott Newman; Graham R Bignell; Paul A W Edwards
Journal:  Genome Res       Date:  2011-01-20       Impact factor: 9.043

Review 5.  Molecular Pathogenesis of MALT Lymphoma.

Authors:  Katharina Troppan; Kerstin Wenzl; Peter Neumeister; Alexander Deutsch
Journal:  Gastroenterol Res Pract       Date:  2015-04-01       Impact factor: 2.260

6.  Auto-ubiquitination-induced degradation of MALT1-API2 prevents BCL10 destabilization in t(11;18)(q21;q21)-positive MALT lymphoma.

Authors:  Heidi Noels; Riet Somers; Hongxiang Liu; Hongtao Ye; Ming-Qing Du; Christiane De Wolf-Peeters; Peter Marynen; Mathijs Baens
Journal:  PLoS One       Date:  2009-03-12       Impact factor: 3.240

  6 in total

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