COEXISTENCE OF CIRCULAR AND MULTIPLE LINEAR AMPLICONS IN METHOTREXATE-RESISTANT LEISHMANIA

被引:25
作者
OLMO, A [1 ]
ARREBOLA, R [1 ]
BERNIER, V [1 ]
GONZALEZPACANOWSKA, D [1 ]
RUIZPEREZ, LR [1 ]
机构
[1] CONSEJO SUPER INVEST CIENT,INST PARASITOL & BIOMED,E-18001 GRANADA,SPAIN
关键词
D O I
10.1093/nar/23.15.2856
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Circular and linear amplicons were analyzed in detail in Leishmania tropica cells resistant to methotrexate (MTX). Both types of elements presented sequences related to the H locus and coexisted in resistant cells. The linear amplicons appeared first during the selection process (at 10 mu M MTX) and varied with regard to size and structure in cells exposed to increasing concentrations of drug. The circular element was evident at higher concentrations (50 mu M) but was the major amplified DNA in cells resistant to 1000 mu M MTX while the level of amplification of the linear elements remained low. The extrachromosomal DNAs were unstable in the absence of drug and their disappearance coincided with an increase in sensitivity to MTX. Mapping of the minichromosomes and the circular element showed that they were all constituted by inverted duplications. The circular amplicon contained an inverted repeat derived from the H locus that encompassed the pteridine reductase gene (PTR1) responsible for MTX resistance. The amplified segment in the linear amplicons was longer and included the pgpB and pgpC genes that encode P-glycoproteins of unknown function previously characterized in different Leishmania species.
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页码:2856 / 2864
页数:9
相关论文
共 43 条
[21]   STRUCTURAL ALTERATIONS OF CHROMOSOME-2 IN LEISHMANIA-MAJOR AS EVIDENCE FOR DIPLOIDY, INCLUDING SPONTANEOUS AMPLIFICATION OF THE MINI-EXON ARRAY [J].
IOVANNISCI, DM ;
BEVERLEY, SM .
MOLECULAR AND BIOCHEMICAL PARASITOLOGY, 1989, 34 (02) :177-188
[22]  
IOVANNISCI DM, 1983, J PARASITOL, V169, P633
[23]   RESTRICTION ENDONUCLEASE ANALYSIS OF LEISHMANIA KINETOPLAST DNA CHARACTERIZES PARASITES RESPONSIBLE FOR VISCERAL AND CUTANEOUS DISEASE [J].
JACKSON, PR ;
WOHLHIETER, JA ;
JACKSON, JE ;
SAYLES, P ;
DIGGS, CL ;
HOCKMEYER, WT .
AMERICAN JOURNAL OF TROPICAL MEDICINE AND HYGIENE, 1984, 33 (05) :808-819
[24]   H-DNA AMPLIFICATION IN LEISHMANIA RESISTANT TO BOTH ARSENITE AND METHOTREXATE [J].
KATAKURA, K ;
CHANG, KP .
MOLECULAR AND BIOCHEMICAL PARASITOLOGY, 1989, 34 (02) :189-191
[25]  
KAUR K, 1988, J BIOL CHEM, V263, P7050
[26]  
LGARE D, 1994, MOL BIOCHEM PARASIT, V68, P81
[27]   DYNAMICS AND SIZE POLYMORPHISMS OF MINICHROMOSOMES IN LEISHMANIA-MAJOR LV-561 CLONED LINES [J].
NAVARRO, M ;
MAINGON, R ;
HAMERS, R ;
SEGOVIA, M .
MOLECULAR AND BIOCHEMICAL PARASITOLOGY, 1992, 55 (1-2) :65-74
[28]   DIRECT AND INVERTED DNA REPEATS ASSOCIATED WITH P-GLYCOPROTEIN GENE AMPLIFICATION IN DRUG-RESISTANT LEISHMANIA [J].
OUELLETTE, M ;
HETTEMA, E ;
WUST, D ;
FASEFOWLER, F ;
BORST, P .
EMBO JOURNAL, 1991, 10 (04) :1009-1016
[29]   DRUG-RESISTANCE AND P-GLYCOPROTEIN GENE AMPLIFICATION IN THE PROTOZOAN PARASITE LEISHMANIA [J].
OUELLETTE, M ;
BORST, P .
RESEARCH IN MICROBIOLOGY, 1991, 142 (06) :737-746
[30]   THE AMPLIFIED H-CIRCLE OF METHOTREXATE-RESISTANT LEISHMANIA-TARENTOLAE CONTAINS A NOVEL P-GLYCOPROTEIN GENE [J].
OUELLETTE, M ;
FASEFOWLER, F ;
BORST, P .
EMBO JOURNAL, 1990, 9 (04) :1027-1033