1. A common 93-kb duplicated DNA sequence at 1q21.2 in acute lymphoblastic leukemia and Burkitt lymphoma
- Author
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Massimo F. Martelli, Roberta La Starza, Maria Grazia Kropp, Valentina Pierini, Paolo Gorello, Barbara Crescenzi, Lucia Brandimarte, Silvia Romoli, Caterina Matteucci, Cristina Mecucci, and Gianluca Barba
- Subjects
clone (Java method) ,Male ,Cancer Research ,Myotubularin ,Chromosomal translocation ,Biology ,Gene Duplication ,Gene duplication ,Genetics ,medicine ,Humans ,Genes, Tumor Suppressor ,Child ,Molecular Biology ,Gene ,In Situ Hybridization, Fluorescence ,Chromosome Aberrations ,medicine.diagnostic_test ,Breakpoint ,Chromosome Mapping ,RNA-Binding Proteins ,Karyotype ,Middle Aged ,Precursor Cell Lymphoblastic Leukemia-Lymphoma ,Molecular biology ,Burkitt Lymphoma ,Chromosomes, Human, Pair 1 ,Child, Preschool ,Karyotyping ,Female ,RNA Splicing Factors ,Fluorescence in situ hybridization - Abstract
In three patients with acute lymphoblastic leukemia (ALL) and in another with Burkitt lymphoma (BL), conventional cytogenetics and fluorescence in situ hybridization (FISH), applied singly or in combination, showed 1q duplication in two cases of ALL with hyperdiploid karyotypes, 1q duplication resulting from an unbalanced translocation in a third case of ALL, and inv dup(1)(q) in a patient with BL. Centromeric or telomeric breakpoints and extension of the 1q duplicons varied in each case. FISH defined a minimal, common duplicated region of 93kb at band 1q21.2 corresponding to clone RP11-212K13. In this region three putative oncogenes or tumor suppressor genes have been mapped: SF3B4 (splicing factor 3b, subunit 4), OTUD7B (OTU domain containing 7B), and MTMR11 (myotubularin related protein 11). For the first time, a minimal common 1q21.2 duplicated sequence has been identified in lymphoid malignancies in a region where putative oncogenes or suppressor genes have been mapped. This finding elucidates the genomic background of ALL and BL with 1q duplication and provides the basis for molecular studies investigating which genes are involved in leukemogenesis or disease progression in these cases.
- Published
- 2006