Effect of large targeted deletions on the mitotic stability of an extra chromosome mediating drug resistance in Leishmania

Pascal Dubessay, Christophe Ravel, Patrick Bastien, Marie Françoise Lignon, Buddy Ullman, Michel Pagès, Christine Blaineau

Research output: Contribution to journalArticle

21 Citations (Scopus)

Abstract

A mitotically stable linear extra chromosome obtained in a Leishmania donovani strain rendered mycophenolic acid-resistant has been physically mapped. This 290-kb chromosome has an inverted duplicated structure around a central inversion region, and is derived from a conservative amplification event of a Ο140-kb subtelomeric end of chromosome 19. Large-sized targeted deletions of the central region were performed through homologous recombination using three specific transfection vectors. The size of the extra chromosome was thus successfully reduced from 290 to 260, 200 and 120 kb respectively. The mitotic stability of these chromosomes was then analysed in drug-free cultures over > 140 days. Results differed according to the deletion created. By contrast with the smallest deletion the two largest deletions altered mitotic stability, leading to progressive loss of the size-reduced chromosomes with similar kinetics in both mutants. The 30-kb region common to both deletions may therefore be considered as involved in mitotic stability. A 44-kb contig covering this region could be assembled and sequenced. The analysis of this sequence did not reveal any sequence elements typical of centromeric DNA. By contrast, its enrichment in homopolymer tracts suggests that this region might contain an origin of replication.

Original languageEnglish (US)
Pages (from-to)3231-3240
Number of pages10
JournalNucleic Acids Research
Volume29
Issue number15
StatePublished - Aug 1 2001

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Chromosomal Instability
Leishmania
Drug Resistance
Chromosomes
Mycophenolic Acid
Chromosomes, Human, Pair 19
Leishmania donovani
Replication Origin
Homologous Recombination
Transfection
Sequence Analysis
DNA
Pharmaceutical Preparations

ASJC Scopus subject areas

  • Genetics

Cite this

Dubessay, P., Ravel, C., Bastien, P., Lignon, M. F., Ullman, B., Pagès, M., & Blaineau, C. (2001). Effect of large targeted deletions on the mitotic stability of an extra chromosome mediating drug resistance in Leishmania. Nucleic Acids Research, 29(15), 3231-3240.

Effect of large targeted deletions on the mitotic stability of an extra chromosome mediating drug resistance in Leishmania. / Dubessay, Pascal; Ravel, Christophe; Bastien, Patrick; Lignon, Marie Françoise; Ullman, Buddy; Pagès, Michel; Blaineau, Christine.

In: Nucleic Acids Research, Vol. 29, No. 15, 01.08.2001, p. 3231-3240.

Research output: Contribution to journalArticle

Dubessay, P, Ravel, C, Bastien, P, Lignon, MF, Ullman, B, Pagès, M & Blaineau, C 2001, 'Effect of large targeted deletions on the mitotic stability of an extra chromosome mediating drug resistance in Leishmania', Nucleic Acids Research, vol. 29, no. 15, pp. 3231-3240.
Dubessay P, Ravel C, Bastien P, Lignon MF, Ullman B, Pagès M et al. Effect of large targeted deletions on the mitotic stability of an extra chromosome mediating drug resistance in Leishmania. Nucleic Acids Research. 2001 Aug 1;29(15):3231-3240.
Dubessay, Pascal ; Ravel, Christophe ; Bastien, Patrick ; Lignon, Marie Françoise ; Ullman, Buddy ; Pagès, Michel ; Blaineau, Christine. / Effect of large targeted deletions on the mitotic stability of an extra chromosome mediating drug resistance in Leishmania. In: Nucleic Acids Research. 2001 ; Vol. 29, No. 15. pp. 3231-3240.
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