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溶组织内阿米巴通过同源重组进行DNA修复过程中EhRAD54、EhRAD51和EhBLM蛋白的表达

Expression of EhRAD54, EhRAD51, and EhBLM proteins during DNA repair by homologous recombination in Entamoeba histolytica.

作者信息

Charcas-Lopez Ma del Socorro, Garcia-Morales Lorena, Pezet-Valdez Marisol, Lopez-Camarillo Cesar, Zamorano-Carrillo Absalom, Marchat Laurence A

机构信息

Programa Institucional de Biomedicina Molecular, Escuela Nacional de Medicina y Homeopatía del IPN, Guillermo Massieu Helguera No. 239, Fracc. La Escalera, Ticoman, México D.F., C.P. 07320, Mexico.

Posgrado en Ciencias Genómicas, Universidad Autónoma de la Ciudad de México, San Lorenzo No. 290, Col. del Valle, México D.F., C.P. 03110, Mexico.

出版信息

Parasite. 2014;21:7. doi: 10.1051/parasite/2014006. Epub 2014 Feb 19.

Abstract

Entamoeba histolytica, the protozoan responsible for human amoebiasis, exhibits a great genome plasticity that is probably related to homologous recombination events. It contains the RAD52 epistasis group genes, including Ehrad51 and Ehrad54, and the Ehblm gene, which are key homologous recombination factors in other organisms. Ehrad51 and Ehrad54 genes are differentially transcribed in trophozoites when DNA double-strand breaks are induced by ultraviolet-C irradiation. Moreover, the EhRAD51 recombinase is overexpressed at 30 min in the nucleus. Here, we extend our analysis of the homologous recombination mechanism in E. histolytica by studying EhRAD51, EhRAD54, and EhBLM expression in response to DNA damage. Bioinformatic analyses show that EhRAD54 has the molecular features of homologous proteins, indicating that it may have similar functions. Western blot assays evidence the differential expression of EhRAD51, EhRAD54, and EhBLM at different times after DNA damage, suggesting their potential roles in the different steps of homologous recombination in this protozoan.

摘要

溶组织内阿米巴是导致人类阿米巴病的原生动物,其基因组具有很大的可塑性,这可能与同源重组事件有关。它包含RAD52上位性群基因,包括Ehrad51和Ehrad54,以及Ehblm基因,这些都是其他生物中的关键同源重组因子。当用紫外线-C照射诱导DNA双链断裂时,Ehrad51和Ehrad54基因在滋养体中差异转录。此外,EhRAD51重组酶在细胞核中30分钟时过度表达。在这里,我们通过研究EhRAD51、EhRAD54和EhBLM对DNA损伤的反应表达,扩展了对溶组织内阿米巴同源重组机制的分析。生物信息学分析表明,EhRAD54具有同源蛋白的分子特征,表明它可能具有类似的功能。蛋白质印迹分析证明了DNA损伤后不同时间EhRAD51、EhRAD54和EhBLM的差异表达,表明它们在这种原生动物同源重组的不同步骤中具有潜在作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c97f/3927307/cb4181b9add7/parasite-21-7-fig1.jpg

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