I. Wlodarska et al., MOLECULAR MAPPING OF THE CHROMOSOME-II BREAKPOINT OF T(11 17)(Q13 Q21) IN A T(11 14)(Q13 Q32)-POSITIVE-B NON-HODGKINS-LYMPHOMA, Genes, chromosomes & cancer, 8(4), 1993, pp. 224-229
The FAU gene is the cellular homologue of the viral FOX sequences in t
he genome of the Finkel-Biskis-Reilly murine sarcoma virus (FBR-MuSV);
the viral FOX sequences have been shown to increase the transforming
capacity of FBR-MuSV in vitro. The human FAU gene has recently been is
olated, characterized, and mapped to chromosome band 11q13. Here, we r
eport results of fluorescence in situ hybridization (FISH) analysis wh
ich indicate that the FAU gene maps proximally to the putative oncogen
e BCLI at 11q13. Furthermore, we identified a t(11;17)(q13;q21) transl
ocation in tumor cells of a t(11;14)(q13;q32)-positive B-cell non-Hodg
kin's lymphoma patient by FISH analysis using a FAU containing cosmid
clone as molecular probe and by double-colour chromosome painting anal
ysis using chromosome 11 - and chromosome 17-specific painting probes.
The position of the chromosome 11 breakpoint of the t(11;17) transloc
ation was pinpointed to a human DNA region around the FAU gene of abou
t 40 kbp. (C) 1993 Wiley-Liss, Inc.