Development of a stable episomal shuttle vector for Toxoplasma gondii

被引:30
作者
Black, MW [1 ]
Boothroyd, JC [1 ]
机构
[1] Stanford Univ, Sch Med, Dept Microbiol & Immunol, Stanford, CA 94305 USA
关键词
D O I
10.1074/jbc.273.7.3972
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
The rapid developments in the molecular genetics of Toxoplasma gondii have far reaching implications in treatment and vaccination strategies far this as well as closely related pathogens such as Plasmodium. Although stable transformation of this parasite through homologous and illegitimate genomic integration has provided many of the tools necessary for genetic analysis, subsequent manipulations of the DNA have proven laborious, This report-describes the selection and subsequent characterization of a Toxoplasma sequence that permits the episomal maintenance of bacterial plasmids in this parasite, This sequence was isolated from the Toxoplasma. genome through selection for episomal stability of a pUC19-based library in the absence of a selectable marker, A 500-base pair fragment was determined to possess the stabilization activity. Transformations of Toxoplasma using vectors possessing this fragment, referred to as EMS (episomal maintenance sequence), demonstrated an elevated stable transformation frequency compared with the vector alone, Mutants deficient in hyploxanthine-xanthine-guanine phosphoribosyltransferase activity were used as a test to see if this gene could be selected from a genomic library using a vector containing the EMS. The success of this test demonstrates the utility of EMS-containing vectors in complementation strategies and the ability of such constructs bearing large? fragments of the Toxoplasma genome to be maintained episomally.
引用
收藏
页码:3972 / 3979
页数:8
相关论文
共 23 条
[1]  
Bloch K. D., 1995, CURRENT PROTOCOLS MO, V1
[2]  
Boothroyd John C., 1995, MBL (Marine Biology Laboratory) Lectures in Biology, V12, P211
[3]   Insertional tagging, cloning, and expression of the Toxoplasma gondii hypoxanthine-xanthine-guanine phosphoribosyltransferase gene - Use as a selectable marker for stable transformation [J].
Donald, RGK ;
Carter, D ;
Ullman, B ;
Roos, DS .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (24) :14010-14019
[4]   HOMOLOGOUS RECOMBINATION AND GENE REPLACEMENT AT THE DIHYDROFOLATE REDUCTASE-THYMIDYLATE SYNTHASE LOCUS IN TOXOPLASMA-GONDII [J].
DONALD, RGK ;
ROOS, DS .
MOLECULAR AND BIOCHEMICAL PARASITOLOGY, 1994, 63 (02) :243-253
[5]   STABLE MOLECULAR-TRANSFORMATION OF TOXOPLASMA-GONDII - A SELECTABLE DIHYDROFOLATE REDUCTASE-THYMIDYLATE SYNTHASE MARKER BASED ON DRUG-RESISTANCE MUTATIONS IN MALARIA [J].
DONALD, RGK ;
ROOS, DS .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (24) :11703-11707
[6]  
GODBERG J, 1990, NUCLEIC ACIDS RES, V18, P5515
[7]   A SHUTTLE VECTOR WHICH FACILITATES THE EXPRESSION OF TRANSFECTED GENES IN TRYPANOSOMA-CRUZI AND LEISHMANIA [J].
KELLY, JM ;
WARD, HM ;
MILES, MA ;
KENDALL, G .
NUCLEIC ACIDS RESEARCH, 1992, 20 (15) :3963-3969
[8]  
KIM K, 1993, CLIN RES, V41, pA209
[9]   RAPID ISOLATION OF DNA FROM TRYPANOSOMATID PROTOZOA USING A SIMPLE MINI-PREP PROCEDURE [J].
MEDINAACOSTA, E ;
CROSS, GAM .
MOLECULAR AND BIOCHEMICAL PARASITOLOGY, 1993, 59 (02) :327-329
[10]   MITOCHONDRIAL-LIKE DNA-SEQUENCES FLANKED BY DIRECT AND INVERTED REPEATS IN THE NUCLEAR GENOME OF TOXOPLASMA-GONDII [J].
OSSORIO, PN ;
SIBLEY, LD ;
BOOTHROYD, JC .
JOURNAL OF MOLECULAR BIOLOGY, 1991, 222 (03) :525-536