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Breakpoints of t(4;11) translocations in the human MLL and AF4 genes in ALL patients are preferentially clustered outside of high‐affinity matrix attachment regions
Author(s) -
Hensel Jan Patrick,
Gillert Esther,
Fey Georg H.,
Marschalek Rolf
Publication year - 2001
Publication title -
journal of cellular biochemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.028
H-Index - 165
eISSN - 1097-4644
pISSN - 0730-2312
DOI - 10.1002/jcb.1161
Subject(s) - chromosomal translocation , breakpoint , gene , nuclear matrix , biology , scaffold/matrix attachment region , dna , genetics , microbiology and biotechnology , gene expression , chromatin , chromatin remodeling
Chromosomal translocations t(4;11) are based on illegitimate recombinations between the human MLL and AF4 genes, and are associated with high‐risk acute leukemias of infants and young children. Here, the question was asked, whether a correlation exists between the location of translocation breakpoints within both genes and the location of S/MARs. In “halo mapping experiments” (to define SARs ), about 20 kb of MLL DNA was found to be attached to the nuclear matrix. Similar experiments performed for the translocation partner gene AF4 revealed that SARs are spanning nearly the complete breakpoint cluster region of the AF4 gene. By using short DNA fragments in “scaffold reassociation experiments” (to define MARs ), similar results were obtained for both genes. However, Distamycin A competition experiments in combination with “scaffold reassociation experiments” revealed specific differences in the affinity of each tested DNA fragment to bind the isolated nuclear matrix proteins. When the latter data were compared with the known location of chromosomal breakpoints for both genes, an unexpected correlation was observed. DNA areas with strong MAR affinity contained fewer translocation breakpoints, while areas with weak or absent MAR affinity showed a higher density of chromosomal breakpoints. J. Cell. Biochem. 82: 299–309, 2001. © 2001 Wiley‐Liss, Inc.