生物
药理学
甲烷磺酸盐
基因
DNA
分子生物学
DNA修复
药物耐受性
曼氏血吸虫
作者
Carolina Furtado,Carlos Gustavo Regis-da-Silva,Danielle G. Passos-Silva,Glória Regina Franco,Andrea M. Macedo,Sérgio Danilo Junho Pena,Carlos Renato Machado
标识
DOI:10.1016/j.exppara.2006.11.001
摘要
Using a functional complementation strategy, we have isolated a Schistosoma mansoni cDNA that complemented Escherichia coli mutant strains which are defective in the DNA base excision repair pathway. This cDNA partially complemented the MMS-sensitive phenotype of these strains. The sequence of the isolated cDNA was homologous to genes involved in the RNA metabolism pathway, especially ScIMP4 of Saccharomyces cerevisiae. To establish whether the S. mansoni cDNA clone could complement yeast ScIMP4-defective mutants, we constructed a yeast haploid strain that coded for a truncated Imp4p protein. This mutant strain was treated with different DNA damaging agents, but showed only MMS sensitivity. The functional homology between the ScIMP4 gene and the cDNA from S. mansoni was verified by partial complementation of the mutant yeast with the worm's gene. This gene appears to be involved in DNA repair and RNA metabolism in both S. mansoni and S. cerevisiae.
科研通智能强力驱动
Strongly Powered by AbleSci AI