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溶组织内阿米巴中的EhPC4转录因子促进多核化和多核体形成。

Multinucleation and Polykaryon Formation is Promoted by the EhPC4 Transcription Factor in Entamoeba histolytica.

作者信息

Hernández de la Cruz Olga, Marchat Laurence A, Guillén Nancy, Weber Christian, López Rosas Itzel, Díaz-Chávez José, Herrera Luis, Rojo-Domínguez Arturo, Orozco Esther, López-Camarillo César

机构信息

Universidad Autonoma de la Ciudad de Mexico, Genomics Sciences Program, Mexico City, Mexico.

National Polytechnic Institute, National School of Medicine and Homeopathy, Institutional Program of Molecular Biomedicine, Biotechnology Program, Mexico City, Mexico.

出版信息

Sci Rep. 2016 Jan 21;6:19611. doi: 10.1038/srep19611.

Abstract

Entamoeba histolytica is the intestinal parasite responsible for human amoebiasis that is a leading cause of death in developing countries. In this protozoan, heterogeneity in DNA content, polyploidy and genome plasticity have been associated to alterations in mechanisms controlling DNA replication and cell division. Studying the function of the transcription factor EhPC4, we unexpectedly found that it is functionally related to DNA replication, and multinucleation. Site-directed mutagenesis on the FRFPKG motif revealed that the K127 residue is required for efficient EhPC4 DNA-binding activity. Remarkably, overexpression of EhPC4 significantly increased cell proliferation, DNA replication and DNA content of trophozoites. A dramatically increase in cell size resulting in the formation of giant multinucleated trophozoites (polykaryon) was also found. Multinucleation event was associated to cytokinesis failure leading to abortion of ongoing cell division. Consistently, genome-wide profiling of EhPC4 overexpressing trophozoites revealed the up-regulation of genes involved in carbohydrates and nucleic acids metabolism, chromosome segregation and cytokinesis. Forced overexpression of one of these genes, EhNUDC (nuclear movement protein), led to alterations in cytokinesis and partially recapitulated the multinucleation phenotype. These data indicate for the first time that EhPC4 is associated with events related to polyploidy and genome stability in E. histolytica.

摘要

溶组织内阿米巴是导致人类阿米巴病的肠道寄生虫,而阿米巴病是发展中国家的主要死因之一。在这种原生动物中,DNA含量的异质性、多倍体和基因组可塑性与控制DNA复制和细胞分裂的机制改变有关。在研究转录因子EhPC4的功能时,我们意外地发现它在功能上与DNA复制和多核化有关。对FRFPKG基序进行定点诱变表明,K127残基是EhPC4有效DNA结合活性所必需的。值得注意的是,EhPC4的过表达显著增加了滋养体的细胞增殖、DNA复制和DNA含量。还发现细胞大小显著增加,导致形成巨大的多核滋养体(多核体)。多核化事件与胞质分裂失败有关,导致正在进行的细胞分裂终止。一致地,对过表达EhPC4的滋养体进行全基因组分析发现,参与碳水化合物和核酸代谢、染色体分离和胞质分裂的基因上调。其中一个基因EhNUDC(核运动蛋白)的强制过表达导致胞质分裂改变,并部分重现了多核化表型。这些数据首次表明,EhPC4与溶组织内阿米巴的多倍体和基因组稳定性相关事件有关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/afe3/4726151/f2ba3cb6d7e4/srep19611-f1.jpg

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