Silva Camila S, Silva Sérgio H, Pereira-Júnior Olavo S, Cabral Fernanda J, Costa-Cruz Julia M, Rodrigues Vanderlei
Department of Biochemistry and Immunology, School of Medicine, University of São Paulo, Av. Bandeirantes 3900, 14049-900, Ribeirão Preto, SP, Brazil.
Acta Trop. 2007 Oct;104(1):52-62. doi: 10.1016/j.actatropica.2007.07.006. Epub 2007 Jul 31.
DNA is often damaged by many environmental agents, which lead to the up-regulation of several genes involved in different repair pathways. Schistosoma mansoni has a complex life cycle, being exposed to a subset of DNA-damaging agents, such as those present in the environment and host immune response. Recently, studies showed that nucleotide excision repair (NER) is an indispensable mechanism for removing a broad spectrum of different DNA lesions. In the present report, we showed the gene expression of nucleotide excision repair factor 2 (NEF2) SmRad23 and SmRad4, in different developmental stages of S. mansoni, as well as the differential expression of these genes in S. mansoni adult worms treated with DNA-damaging agents. Furthermore, it was revealed the correlation of these genes with their orthologues in other eukaryotes. Our reports suggest that NER is an important repair pathway during the complex life cycle of S. mansoni.
DNA经常受到许多环境因素的损伤,这会导致参与不同修复途径的多个基因上调。曼氏血吸虫具有复杂的生命周期,会接触到一部分DNA损伤因素,比如存在于环境中的因素以及宿主的免疫反应。最近,研究表明核苷酸切除修复(NER)是去除多种不同DNA损伤的不可或缺的机制。在本报告中,我们展示了曼氏血吸虫不同发育阶段核苷酸切除修复因子2(NEF2)SmRad23和SmRad4的基因表达情况,以及这些基因在经DNA损伤剂处理的曼氏血吸虫成虫中的差异表达。此外,还揭示了这些基因与其在其他真核生物中的直系同源基因的相关性。我们的报告表明,NER是曼氏血吸虫复杂生命周期中的一条重要修复途径。