Premium
t(2;8) variant translocation in burkitt's lymphoma: Mapping of chromosomal breakpoints by in situ hybridization
Author(s) -
Adolph Sabine,
Hameister Horst,
Henglein Berthold,
Lipp Martin,
Hartl Peter,
Baas Frank,
Lenoir Gilbert,
Bornkamm Georg W.
Publication year - 1989
Publication title -
international journal of cancer
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.475
H-Index - 234
eISSN - 1097-0215
pISSN - 0020-7136
DOI - 10.1002/ijc.2910440213
Subject(s) - breakpoint , microbiology and biotechnology , chromosomal translocation , biology , gene mapping , fluorescence in situ hybridization , in situ hybridization , chromosome , karyotype , thyroglobulin , gene , genetics , gene expression , thyroid
In 6 different Burkitt lymphoma cell lines with t(2;8) variant translocations (JI. LY66, LY9I, BL21, BL64, JBL2) the breakpoints on chromosome 8q + were mapped in relation to each other and to c‐myc by in situ hybridization. The probes used were derived from chromosome 8q24 and comprised a c‐myc probe, a probe located 48 kb downstream of c‐myc , 3 probes adjacent to the chromosomal breakpoints of BL64, LY91 and JBL2, respectively, and 2 probes located in the 5′ and 3′ part of the thyroglobulin gene. The breakpoints of LY91 and JBL2 lie <200 kb and>200 kb downstream of c‐myc , whereas the distance to c‐myc of the BL64 breakpoint and of the thyroglobulin probes is unknown. By recording the hybridization signals specific for these probes on chromosomes 2p − and 8q + of each cell line it was possible to establish the order of breakpoints on band 8q24 relative to the c‐myc and thyroglobulin genes as follows: centromere—c‐myc—JI—BL64—BL21— LY91—JBL2—LY66—thyroglobulin—telomere. This information is essential for further mapping of this important chromosomal region.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom