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PMID: 7671237 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Chromosome band 11q23 translocation breakpoints are DNA topoisomerase II cleavage sites.

Cancer research ·Vol. 55 ·No. 19 ·1995-10-01 ·Pages 4287-92

Felix CA, Lange BJ, Hosler MR, Fertala J, Bjornsti MA

Abstract

Human leukemias with 11q23 translocations occur sporadically and after cancer treatment with DNA topoisomerase II-targeted drugs. To investigate this process, we examined DNA topoisomerase II cleavage in vitro in subclones of the normal 11q23 genomic homologue and a t(9;11) translocation breakpoint junction. Cleavage was assayed with limiting dilutions of enzyme in the presence or absence of epipodophyllotoxin and ATP. The strongest sites of cleavage coincided with the t(9;11) breakpoint site and two other translocation breakpoint sites within the normal homologue. These results support the involvement of DNA topoisomerase II in the translocation process at chromosome band 11q23.

MeSH Terms
Base Sequence Chromosomes, Human, Pair 11 Chromosomes, Human, Pair 9 DNA Topoisomerases, Type II/physiology DNA-Binding Proteins/genetics Histone-Lysine N-Methyltransferase Humans Introns Molecular Sequence Data Myeloid-Lymphoid Leukemia Protein Proto-Oncogenes Transcription Factors Translocation, Genetic
Chemicals
DNA-Binding Proteins KMT2A protein, human Transcription Factors Myeloid-Lymphoid Leukemia Protein Histone-Lysine N-Methyltransferase DNA Topoisomerases, Type II
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Felix C A
Department of Pediatrics, Children's Hospital of Philadelphia, University of Pennsylvania School of Medicine, Pennsylvania 19104, USA.
Lange B J
Hosler M R
Fertala J
Bjornsti M A
Article Info
Journal
Cancer research
Abbr.
Cancer Res
ISSN
0008-5472
Published
1995-10-01
Pages
4287-92
Language
English
Region
United States
NLM ID
2984705R
Subset
IM
Grants
NCI NIH HHS · CA58755 · United States
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