MLL-SEPT6 fusion transcript with a novel sequence in an infant with acute myeloid leukemia
- PMID: 16843108
- DOI: 10.1016/j.cancergencyto.2006.02.020
MLL-SEPT6 fusion transcript with a novel sequence in an infant with acute myeloid leukemia
Abstract
The MLL gene at 11q23 is a site of frequent rearrangement in acute leukemia with multiple fusion partners. A relatively uncommon rearrangement, associated with infant AML-M4, fuses the MLL and SEPT6 genes. SEPT6, located at Xq24, is a member of a family of mammalian septins involved in diverse functions such as cytokinesis, cell polarity, and oncogenesis. We describe the case of an infant with acute myelogenous leukemia who showed cytogenetic evidence of rearrangement between 11q23 and Xq24 regions. Fluorescence in situ hybridization analysis suggested a possible break in the MLL gene, and molecular analysis using reverse transcriptase-polymerase chain reaction followed by sequencing confirmed the expression of an MLL-SEPT6 fusion transcript with a novel sequence. The findings emphasize the importance of combined cytogenetic and molecular analyses in the workup of acute leukemia, especially in those leukemias that occur infrequently.
Similar articles
-
Molecular characterization of the MLL-SEPT6 fusion gene in acute myeloid leukemia: identification of novel fusion transcripts and cloning of genomic breakpoint junctions.Haematologica. 2008 Jul;93(7):1076-80. doi: 10.3324/haematol.12594. Epub 2008 May 19. Haematologica. 2008. PMID: 18492691
-
Molecular analysis of t(X;11)(q24;q23) in an infant with AML-M4.Genes Chromosomes Cancer. 2003 Nov;38(3):253-9. doi: 10.1002/gcc.10272. Genes Chromosomes Cancer. 2003. PMID: 14506700
-
Expression pattern of the septin gene family in acute myeloid leukemias with and without MLL-SEPT fusion genes.Leuk Res. 2010 May;34(5):615-21. doi: 10.1016/j.leukres.2009.08.018. Epub 2009 Sep 12. Leuk Res. 2010. PMID: 19748670
-
MLL-MLLT10 fusion gene in pediatric acute megakaryoblastic leukemia.Leuk Res. 2005 Oct;29(10):1223-6. doi: 10.1016/j.leukres.2005.03.008. Epub 2005 Apr 11. Leuk Res. 2005. PMID: 16111539 Review.
-
MLL/SEPTIN6 chimeric transcript from inv ins(X;11)(q24;q23q13) in acute monocytic leukemia: report of a case and review of the literature.Genes Chromosomes Cancer. 2003 Sep;38(1):8-12. doi: 10.1002/gcc.10235. Genes Chromosomes Cancer. 2003. PMID: 12874781 Review.
Cited by
-
Congenital X-linked neutropenia with myelodysplasia and somatic tetraploidy due to a germline mutation in SEPT6.Am J Hematol. 2022 Jan 1;97(1):18-29. doi: 10.1002/ajh.26382. Epub 2021 Nov 3. Am J Hematol. 2022. PMID: 34677878 Free PMC article.
-
Co-existence of KMT2A::SEPTIN6 fusion and DIS3 variant in a pediatric case with acute myeloid leukemia: a case report and literature review.Front Oncol. 2023 Dec 13;13:1308786. doi: 10.3389/fonc.2023.1308786. eCollection 2023. Front Oncol. 2023. PMID: 38152368 Free PMC article.
-
HYBRIDdb: a database of hybrid genes in the human genome.BMC Genomics. 2007 May 23;8:128. doi: 10.1186/1471-2164-8-128. BMC Genomics. 2007. PMID: 17519042 Free PMC article.
-
Clinical profile in KMT2A-SEPT6-positive acute myeloid leukemia: Does it often co-occur with NRAS mutations?Front Med (Lausanne). 2022 Sep 21;9:890959. doi: 10.3389/fmed.2022.890959. eCollection 2022. Front Med (Lausanne). 2022. PMID: 36213638 Free PMC article.
-
Pediatric M5 acute myeloid leukemia with MLL-SEPT6 fusion and a favorable outcome.Leuk Res Rep. 2021 Oct 26;16:100277. doi: 10.1016/j.lrr.2021.100277. eCollection 2021. Leuk Res Rep. 2021. PMID: 34760618 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical