Disruption of the Crithidia fasciculata KAP1 gene results in structural rearrangement of the kinetoplast disc

被引:31
|
作者
Lukes, J
Hines, JC
Evans, CJ
Avliyakulov, NK
Prabhu, VP
Chen, JH
Ray, DS
机构
[1] Univ Calif Los Angeles, Inst Mol Biol, Los Angeles, CA 90095 USA
[2] Univ Calif Los Angeles, Dept Microbiol & Mol Genet, Los Angeles, CA 90095 USA
[3] Acad Sci Czech Republ, Inst Parasitol, CR-37005 Ceske Budejovice, Czech Republic
[4] Univ S Bohemia, Fac Biol, Ceske Budejovice 37005, Czech Republic
[5] Univ Calif Los Angeles, Dept Mol Cell & Dev Biol, Los Angeles, CA 90095 USA
[6] Univ Delaware, Dept Chem & Biochem, Newark, DE 19716 USA
关键词
kinetoplast; trypanosome; minicircle; histone-like; DNA-binding protein;
D O I
10.1016/S0166-6851(01)00348-6
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 mitochondrial DNA (kinetoplast DNA) in trypanosomatids exists as a highly organized nucleoprotein structure with the DNA consisting of thousands of interlocked circles. Four H1 histone-like proteins (KAP1, 2, 3 and 4) are associated with the kinetoplast DNA in the trypanosomatid Crithidia fasciculata. We have disrupted both alleles of the KAP1 gene in this diploid protozoan and shown that expression of the KAP1 protein is eliminated. The mutant strain is viable but has substantial rearrangement of the kinetoplast structure. Expression of the KAP1 protein from an episome restored expression of the KAP1 protein in the mutant strain and also restored a normal kinetoplast structure. These studies provide evidence that the KAP1 protein is involved in kinetoplast DNA organization in vivo but is nonessential for cell viability. (C) 2001 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:179 / 186
页数:8
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