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Duplicated regions of AF-4 intron 4 at t(4;11) translocation breakpoints
- Source :
- Molecular diagnosis : a journal devoted to the understanding of human disease through the clinical application of molecular biology. 4(4)
- Publication Year :
- 2000
-
Abstract
- Background: AF-4 is a common partner gene of MLL. AF-4 breakpoints occur in introns, but most AF-4 introns are uncharacterized. Methods and Results: We cloned AF-4 intron 4 and examined the frequency of breakpoints in this intron. The 5.8-kb intron is rich in repeat sequences and was the site of translocation in 3 of 17 leukemias with t(4;11). We cloned the der (11) and der (4) breakpoints and isolated the fusion transcripts in the cell line MV4-11 and in a de novo acute lymphoblastic leukemia (ALL). Both translocations joined MLL intron 6 and AF-4 intron 4. In MV4-11, 249 bases from AF-4 were present in both derivative chromosomes, indicating duplication. In the de novo ALL, duplication of 446 bases from MLL and AF-4 occurred. Reciprocal fusion transcripts were expressed. Conclusions: Intronic sequence of AF-4 is useful for molecular diagnosis of t(4;11). Duplicated intronic regions suggest staggered chromosomal breakage.
- Subjects :
- Adult
Adolescent
Sequence analysis
Molecular Sequence Data
Alu element
Chromosomal translocation
Biology
Translocation, Genetic
Alu Elements
hemic and lymphatic diseases
Gene Duplication
Gene duplication
Tumor Cells, Cultured
Humans
Amino Acid Sequence
Child
Gene
In Situ Hybridization, Fluorescence
Aged
Genetics
Base Sequence
Reverse Transcriptase Polymerase Chain Reaction
Chromosomes, Human, Pair 11
Breakpoint
Intron
Infant, Newborn
Infant
Karyotype
General Medicine
Sequence Analysis, DNA
Precursor Cell Lymphoblastic Leukemia-Lymphoma
Molecular biology
Introns
Leukemia, Myeloid, Acute
Karyotyping
Chromosomes, Human, Pair 4
Sequence Alignment
Subjects
Details
- ISSN :
- 10848592
- Volume :
- 4
- Issue :
- 4
- Database :
- OpenAIRE
- Journal :
- Molecular diagnosis : a journal devoted to the understanding of human disease through the clinical application of molecular biology
- Accession number :
- edsair.doi.dedup.....0eb43e8367066a00e417439eb3468859