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Molecular assignment of a translocation breakpoint in acute myeloid leukemia with t(8;21).

作者信息

Shimizu K, Ichikawa H, Miyoshi H, Ohki M, Kobayashi H, Maseki N, Kaneko Y

机构信息

Department of Immunology and Virology, Saitama Cancer Center Research Institute, Japan.

出版信息

Genes Chromosomes Cancer. 1991 May;3(3):163-7. doi: 10.1002/gcc.2870030302.

Abstract

An 8;21 translocation is a common chromosome abnormality associated with acute myeloblastic leukemia with maturation (M2 of French-American-British (FAB) classification). We have isolated chromosome 21 Notl linking clones; pulsed field gel electrophoresis analysis with one clone (LL263) detected an altered fragment of Notl-digested leukemic cell DNA carrying t(8;21). The altered fragment was shown to be produced by the 8;21 translocation. The breakpoint in chromosome 21 was located about 13 kb to 100 kb proximal to the LL263 Notl site. Because the LL263 clone has a CpG island and is a short distance from the breakpoint, the clone itself may be considered as a candidate for part of the t(8;21) associated gene.

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