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Detailed Molecular Delineation of 13q14.3 Loss in B-Cell Chronic
Lymphocytic Leukemia
Martin M. Corcoran,
Omid Rasool,
Yie Liu,
Arati Iyengar,
Dan Grander,
Rachel E. Ibbotson,
Mats Merup,
Xiushan Wu,
Vadim Brodyansky,
Anne C. Gardiner,
Gunnar Juliusson,
Robert M. Chapman,
Ganka Ivanova,
Mary Tiller,
Gosta Gahrton,
Nick Yankovsky,
Eugene Zabarovsky,
David G. Oscier, and
Stefan Einhorn
From the Molecular Biology Laboratory, Royal Bournemouth General
Hospital, Bournemouth, UK; Radiumhemmet, Karolinska Hospital, Stockholm
Sweden; the Department of Medicine, Huddinge Hospital, Huddinge,
Sweden; the Laboratory of Genome Analysis, Institute of General
Genetics, Russian Academy of Science, Moscow, Russia; and the
Microbiology and Tumorbiology Center, Karolinska Institute, Stockholm,
Sweden.
A region of chromosome 13q14.3, telomeric to the Retinoblastoma gene
RB-1 is frequently deleted in patients with B-cell chronic lymphocytic
leukemia (B-CLL). A cosmid and P1-derived artificial chromosome
(PAC) contig spanning over 600 kb has been constructed, which encompasses this locus. The contig clones have been used to order
a number of markers along the minimally deleted region and to localize
a series of CpG islands corresponding to possible candidate genes. A
novel polymorphic dinucleotide repeat, 6E3.2, present in one of the
ordered cosmid clones has been isolated for use in deletion mapping
studies of patient DNA. Leukemic samples from 229 CLL patients have
been screened for loss of heterozygosity using microsatellite markers
and analyzed for hemizygous and homozygous deletions by Southern blot
techniques using genomic probes selected from cosmids across the
region. Hemizygous deletions were found in 31% of cases with an
additional 10% showing homozygous loss. The use of these probes has
defined the commonly deleted area to less than 130 kb, centromeric to
the locus D13S272.
Blood, Vol. 91 No. 4 (February 15), 1998:
pp. 1382-1390
© 1998 by The American Society of Hematology.

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