Kilbey B J, Fraser I, McAleese S, Goman M, Ridley R G
Institute of Cell and Molecular Biology, University of Edinburgh, UK.
Nucleic Acids Res. 1993 Jan 25;21(2):239-43. doi: 10.1093/nar/21.2.239.
The gene encoding the malarial homologue of proliferating cell nuclear antigen, PCNA, has been identified and characterised. It is located on chromosome 13. The coding sequence of 825 nucleotides predicts a protein of 30,586 Da. There are no introns and northern analysis reveals a transcript of approximately 1.6kb. The conserved residues which characterise the PCNAs of human, Drosophila, Saccharomyces and Xenopus are present in PfPCNA but the overall identity of PfPCNA with human and yeast PCNAs is low; 34% and 31% respectively. PfPCNA is longer than the PCNAs of these other species by about 16 amino acids, most of which are present in a block near the carboxy terminus. Antibodies against a purified PfPCNA-glutathione-S-transferase fusion protein recognise a single band in western blots of parasite extracts at 32kDa. The same antiserum has been used to demonstrate that the expression of PfPCNA is regulated during the intraerythrocytic development of the parasite. Expression increases dramatically in late trophozoites and is maintained during the subsequent nuclear divisions which produce schizonts.
编码增殖细胞核抗原(PCNA)的疟原虫同源基因已被鉴定和表征。它位于13号染色体上。825个核苷酸的编码序列预测出一种分子量为30586道尔顿的蛋白质。该基因没有内含子,Northern分析显示有一个约1.6kb的转录本。表征人类、果蝇、酿酒酵母和非洲爪蟾PCNA的保守残基在恶性疟原虫PCNA(PfPCNA)中也存在,但PfPCNA与人类和酵母PCNA的总体一致性较低,分别为34%和31%。PfPCNA比其他物种的PCNA长约16个氨基酸,其中大部分位于羧基末端附近的一个区域。针对纯化的PfPCNA-谷胱甘肽-S-转移酶融合蛋白的抗体在疟原虫提取物的Western印迹中识别出一条32kDa的单一带。同一抗血清已被用于证明PfPCNA的表达在疟原虫红细胞内发育过程中受到调控。在晚期滋养体中表达急剧增加,并在随后产生裂殖体的核分裂过程中保持。