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tRNA基因序列是溶组织内阿米巴转录沉默所必需的。

tRNA gene sequences are required for transcriptional silencing in Entamoeba histolytica.

作者信息

Irmer Henriette, Hennings Ina, Bruchhaus Iris, Tannich Egbert

机构信息

Grisebachstr. 8, Institute of Microbiology and Genetics, Department of Molecular Microbiology and Genetics, Georg-August-University, Göttingen, 37077 Göttingen, Germany.

出版信息

Eukaryot Cell. 2010 Feb;9(2):306-14. doi: 10.1128/EC.00248-09. Epub 2009 Dec 18.

Abstract

Transcriptional silencing by trans inactivation can contribute to the regulation of gene expression in eukaryotic cells. In the human intestinal protozoan parasite Entamoeba histolytica, trans inactivation of the amoebapore-A gene (AP-A) was recently achieved by episomal transfection of E. histolytica trophozoites with the plasmid psAP1. The mechanism of AP-A trans inactivation is largely unknown, though it was suggested that a partial short interspersed transposable element (SINE) is required. By systematic assessment of various E. histolytica isolates transfected with psAP1 derivates, trans inactivation of AP-A was restricted to the strain HM-1:IMSS (2411) but could not be achieved in other standard laboratory strains. Importantly, sequences of an E. histolytica tRNA array that were located on psAP1 in close proximity to the AP-A upstream region and comprising the glutamic acid (TTC) (E) and tyrosine (GTA) (Y) tRNA genes were indispensable for AP-A silencing. In contrast to the case described in previous reports, SINE was not required for AP-A trans inactivation. AP-A expression could be regained in silenced cells by episomal transfection under the control of a heterologous E. histolytica promoter, opening a way toward future silencing of individual genes of interest in E. histolytica. Our results indicate that tRNA gene-mediated silencing is not restricted to Saccharomyces cerevisiae.

摘要

通过反式失活实现的转录沉默有助于真核细胞中基因表达的调控。在人类肠道原生动物寄生虫溶组织内阿米巴中,最近通过用质粒psAP1对溶组织内阿米巴滋养体进行游离转染,实现了对溶组织内阿米巴穿孔素-A基因(AP-A)的反式失活。尽管有人提出需要一个部分短散在转座元件(SINE),但AP-A反式失活的机制在很大程度上尚不清楚。通过系统评估用psAP1衍生物转染的各种溶组织内阿米巴分离株,AP-A的反式失活仅限于菌株HM-1:IMSS(2411),而在其他标准实验室菌株中无法实现。重要的是,位于psAP1上与AP-A上游区域紧邻且包含谷氨酸(TTC)(E)和酪氨酸(GTA)(Y)tRNA基因的溶组织内阿米巴tRNA阵列序列对于AP-A沉默是不可或缺的。与先前报道中描述的情况相反,SINE对于AP-A反式失活不是必需的。通过在异源溶组织内阿米巴启动子的控制下进行游离转染,可以在沉默细胞中恢复AP-A的表达,这为未来沉默溶组织内阿米巴中感兴趣的单个基因开辟了道路。我们的结果表明,tRNA基因介导的沉默并不局限于酿酒酵母。

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