Nucleic Acids Research, Vol 26, Issue 14 3447-3448, Copyright © 1998 by Oxford University Press
Y Kuroiwa, T Shinohara, T Notsu, K Tomizuka, H Yoshida, S Takeda, M Oshimura and I Ishida
Truncation of human chromosomes at desired sites by homologous
recombination techniques enables functional and structural analyses of
human chromosomes and development of human artificial chromosomes. However,
this targeted truncation has been inefficient. We describe here an
efficient method for targeted truncation in the chicken DT40 cells with a
high homologous recombination rate. The human chromosome 22 was transferred
into DT40 cells, where human telomeric repeat (TTAGGG)n was targeted to the
LIF locus on the chromosome. Molecular and cytogenetic analyses showed that
the predicted truncation at the LIF locus occurred in all of the targeted
clones.
ARTICLES
Efficient modification of a human chromosome by telomere-directed truncation in high homologous recombination-proficient chicken DT40 cells
Central Laboratories for Key Technology, Kirin Brewery Company Ltd, 1- 13-5 Fukuura, Kanazawa-ku, Yokohama, Kanagawa 236-0004, Japan.
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