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J. Biol. Chem., Vol. 276, Issue 15, 11662-11673, April 13, 2001
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From the Centre de Recherche en Infectiologie, Centre de Recherche
du CHUL et Département de Biologie Médicale, Faculté
de Médecine, Université Laval,
Québec G1V 4G2, Canada
We have used a telomere-associated chromosome
fragmentation strategy to induce internal chromosome-specific breakage
of Leishmania chromosomes. The integration of telomeric
repeats from the kinetoplastid Trypanosoma brucei into
defined positions of the Leishmania genome by homologous
recombination can induce chromosome breakage accompanied by the
deletion of the chromosomal part that is distal to the site of the
break. The cloned telomeric DNA at the end of the truncated chromosomes
is functional and it can seed the formation of new telomeric repeats.
We found that genome ploidy is often altered upon telomere-mediated
chromosome fragmentation events resulting in large chromosomal
deletions. In most cases diploidy is either preserved, or partial
trisomic cells are observed, but interestingly we report here the
generation of partial haploid mutants in this diploid organism. Partial
haploid Leishmania mutants should facilitate studies on the
function of chromosome-assigned genes. We also present several lines of
evidence for the presence of sequences involved in chromosome mitotic
stability and segregation during cell cycle in this parasitic
protozoan. Telomere-directed chromosome fragmentation studies in
Leishmania may constitute a useful tool to assay for
centromere function.
FRSQ (Fonds de Recherche en Santé de Québec) Junior 2 scholar and member of a CIHR (Canadian Institutes of Health Research) group on host-pathogen interactions. To whom correspondence should be
addressed: Centre de Recherche en Infectiologie, Centre de Recherche du
CHUL (CHUQ), 2705 boul. Laurier, Ste-Foy, Québec, Canada
G1V 4G2. Tel.: 418-654-2705; Fax: 418-654-2715; E-mail: Barbara.
Papadopoulou@crchul.ulaval.ca.
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