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MLL leukemia-associated rearrangements in peripheral blood lymphocytes from healthy individuals
Brassesco, María Sol; Montaldi, Ana Paula; Gras, Diana Ester; Queiroz, Rosane Gomes de Paula; Martinez-Rossi, Nilce Maria; Tone, Luiz Gonzaga; Sakamoto-Hojo, Elza Tiemi.
Affiliation
  • Brassesco, María Sol; Universidade de São Paulo. Faculdade de Medicina de Ribeirão Preto. Departamento de Genética. Ribeirão Preto. BR
  • Montaldi, Ana Paula; Universidade de São Paulo. Faculdade de Medicina de Ribeirão Preto. Departamento de Genética. Ribeirão Preto. BR
  • Gras, Diana Ester; Universidade de São Paulo. Faculdade de Medicina de Ribeirão Preto. Departamento de Genética. Ribeirão Preto. BR
  • Queiroz, Rosane Gomes de Paula; Universidade de São Paulo. Faculdade de Medicina de Ribeirão Preto. Departamento de Puericultura e Pediatria. Ribeirão Preto. BR
  • Martinez-Rossi, Nilce Maria; Universidade de São Paulo. Faculdade de Medicina de Ribeirão Preto. Departamento de Genética. Ribeirão Preto. BR
  • Tone, Luiz Gonzaga; Universidade de São Paulo. Faculdade de Medicina de Ribeirão Preto. Departamento de Puericultura e Pediatria. Ribeirão Preto. BR
  • Sakamoto-Hojo, Elza Tiemi; Universidade de São Paulo. Faculdade de Medicina de Ribeirão Preto. Departamento de Genética. Ribeirão Preto. BR
Genet. mol. biol ; Genet. mol. biol;32(2): 234-241, 2009. ilus, tab
Article in Pt | LILACS | ID: lil-513965
Responsible library: BR1.1
ABSTRACT
Chromosomal translocations are characteristic of hematopoietic neoplasias and can lead to unregulated oncogene expression or the fusion of genes to yield novel functions. In recent years, different lymphoma/leukemia-associated rearrangements have been detected in healthy individuals. In this study, we used inverse PCR to screen peripheral lymphocytes from 100 healthy individuals for the presence of MLL (Mixed Lineage Leukemia) translocations. Forty-nine percent of the probands showed MLL rearrangements. Sequence analysis showed that these rearrangements were specific for MLL translocations that corresponded to t(4;11)(q21;q23) (66 percent) and t(9;11) (20 percent). However, RT-PCR failed to detect any expression of t(4;11)(q21;q23) in our population. We suggest that 11q23 rearrangements in peripheral lymphocytes from normal individuals may result from exposure to endogenous or exogenous DNA-damaging agents. In practical terms, the high susceptibility of the MLL gene to chemically-induced damage suggests that monitoring the aberrations associated with this gene in peripheral lymphocytes may be a sensitive assay for assessing genomic instability in individuals exposed to genotoxic stress.
Key words
Full text: 1 Index: LILACS Type of study: Risk_factors_studies Language: Pt Journal: Genet. mol. biol Journal subject: GENETICA Year: 2009 Type: Article
Full text: 1 Index: LILACS Type of study: Risk_factors_studies Language: Pt Journal: Genet. mol. biol Journal subject: GENETICA Year: 2009 Type: Article