Premium
Microclustering of TEL‐AML1 translocation breakpoints in childhood acute lymphoblastic leukemia
Author(s) -
Wiemels Joseph L.,
Alexander Freda E.,
Cazzaniga Giovanni,
Biondi Andrea,
Mayer Sharon P.,
Greaves Mel
Publication year - 2000
Publication title -
genes, chromosomes and cancer
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.754
H-Index - 119
eISSN - 1098-2264
pISSN - 1045-2257
DOI - 10.1002/1098-2264(2000)9999:9999<::aid-gcc1028>3.0.co;2-d
Subject(s) - breakpoint , chromosomal translocation , biology , genetics , intron , sequence (biology) , dna sequencing , computational biology , gene
TEL ‐ AML1 fusions are the most common chromosome translocations in childhood leukemia and often, if not always, occur in utero. We previously reported the genomic sequencing of nine TEL ‐ AML1 translocations and showed unique structural features of a breakpoint cluster region in TEL intron 5. We now report data on sequencing and mapping of TEL ‐ AML1 from an additional 11 patients and, using Monte Carlo statistical methods, have analyzed the intronic distribution of the 24 TEL ‐ AML1 fusion junctions sequenced to date. Compared to a null hypothesis of random breakpoint allocation within TEL intron 5 and AML1 introns 1 and 2, significant microclustering was evident on both TEL and AML1 . In contrast to previous reports, the two strongest microclusters on TEL were 3′ to an unstable repeat region. AML1 demonstrated four highly significant microclusters, two of which were proximal to exons. We note the necessity of sequencing multiple breakpoints before the description of putative microcluster regions. TEL ‐ AML1 breakpoints may be distributed into microclusters because of specific DNA sequence or chromatin features in susceptible cells. We also report on additional features of breakpoints, including a complex t(12;3;21) in one patient and an inverted sequence in another. © 2000 Wiley‐Liss, Inc.