Literature DB >> 3182826

Extrachromosomal elements in the lower eukaryote Leishmania.

R C Hightower1, L M Ruiz-Perez, M L Wong, D V Santi.   

Abstract

Extrachromosomal DNA elements have been identified in wild-type populations of the parasitic protozoan Leishmania. Elements from L. major and L. tropica were detected using orthogonal-field-alternation-gel electrophoresis. They are nonhomologous, supercoiled circular DNA molecules derived from different chromosomes in the Leishmania genome. Electron microscopy revealed that the elements have very similar physical properties; both are 80-kilobase supercoiled DNA molecules that contain large inverted repeat structures. The extrachromosomal DNAs are amplified in the Leishmania populations and show a fluctuation in copy number, from undetectable to around 20 copies per cell. After exposure of the L. tropica population to the drug methotrexate (MTX), a second amplified DNA was observed that is homologous to the extrachromosomal DNA found in L. major. Furthermore, wild-type Leishmania populations containing extrachromosomal DNA adapt more readily to MTX selection than populations with no amplified DNA. From these observations, there appears to be a relationship between the presence of extrachromosomal elements in wild-type Leishmania and the genesis and maintenance of MTX resistance in these organisms.

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Year:  1988        PMID: 3182826

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  20 in total

1.  Inverted repeats as genetic elements for promoting DNA inverted duplication: implications in gene amplification.

Authors:  C T Lin; W H Lin; Y L Lyu; J Whang-Peng
Journal:  Nucleic Acids Res       Date:  2001-09-01       Impact factor: 16.971

2.  Structural and functional analysis of an amplification containing a PGPA gene in a glucantime-resistant Leishmania (Viannia) guyanensis cell line.

Authors:  Charles Anacleto; Maria C B Abdo; Adlane V B Ferreira; Silvane M F Murta; Alvaro J Romanha; Ana Paula Fernandes; Elizabeth S A Moreira
Journal:  Parasitol Res       Date:  2003-02-11       Impact factor: 2.289

3.  Extrachromosomal genetic complementation of surface metalloproteinase (gp63)-deficient Leishmania increases their binding to macrophages.

Authors:  X Liu; K P Chang
Journal:  Proc Natl Acad Sci U S A       Date:  1992-06-01       Impact factor: 11.205

4.  Linear amplicons as precursors of amplified circles in methotrexate-resistant Leishmania tarentolae.

Authors:  K Grondin; C Kündig; G Roy; M Ouellette
Journal:  Nucleic Acids Res       Date:  1998-07-15       Impact factor: 16.971

5.  Replication initiates at multiple dispersed sites in the ribosomal DNA plasmid of the protozoan parasite Entamoeba histolytica.

Authors:  S K Dhar; N R Choudhury; V Mittal; A Bhattacharya; S Bhattacharya
Journal:  Mol Cell Biol       Date:  1996-05       Impact factor: 4.272

6.  Induction of circles of heterogeneous sizes in carcinogen-treated cells: two-dimensional gel analysis of circular DNA molecules.

Authors:  S Cohen; S Lavi
Journal:  Mol Cell Biol       Date:  1996-05       Impact factor: 4.272

7.  Mechanisms of sod2 gene amplification in Schizosaccharomyces pombe.

Authors:  E B Albrecht; A B Hunyady; G R Stark; T E Patterson
Journal:  Mol Biol Cell       Date:  2000-03       Impact factor: 4.138

8.  Multidrug resistance in Leishmania donovani is conferred by amplification of a gene homologous to the mammalian mdr1 gene.

Authors:  D M Henderson; C D Sifri; M Rodgers; D F Wirth; N Hendrickson; B Ullman
Journal:  Mol Cell Biol       Date:  1992-06       Impact factor: 4.272

9.  Homologous recombination between direct repeat sequences yields P-glycoprotein containing amplicons in arsenite resistant Leishmania.

Authors:  K Grondin; B Papadopoulou; M Ouellette
Journal:  Nucleic Acids Res       Date:  1993-04-25       Impact factor: 16.971

10.  The 63-kilobase circular amplicon of tunicamycin-resistant Leishmania amazonensis contains a functional N-acetylglucosamine-1-phosphate transferase gene that can be used as a dominant selectable marker in transfection.

Authors:  X Liu; K P Chang
Journal:  Mol Cell Biol       Date:  1992-09       Impact factor: 4.272

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