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Transcriptional Regulation of an Iron-Inducible Gene by Differential and Alternate Promoter Entries of Multiple Myb Proteins in the Protozoan Parasite Trichomonas vaginalis

机译:铁诱导基因的转录调控通过原生动物寄生虫毛滴虫中多个Myb蛋白的差异和交替启动子输入。

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Iron-inducible transcription of a malic enzyme gene (also reputed to be ap65-1) in Trichomonas vaginalis was previously shown to involve a Myb1 repressor and a Myb2 activator, each of which may preferentially select two closely spaced promoter sites, MRE-1/MRE-2r, which comprises overlapping promoter elements, and MRE-2f. In the present study, an iron-inducible ~32-kDa Myb3 nuclear protein was demonstrated to bind only the MRE-1 element. Changes in the iron supply, which produced antagonistic effects on the levels of Myb2 and Myb3 expression, also resulted in temporal and alternate entries of Myb2 and Myb3 into the ap65-1 promoter. Repression or activation of basal and iron-inducible ap65-1 transcription was detected in transfected cells when Myb3 was, respectively, substantially knocked down or overexpressed. In the latter case, increased Myb3 promoter entry was detected with concomitant decrease in Myb2 promoter entry under specific conditions, while Myb3 promoter entry was inhibited under all test conditions in cells overexpressing Myb2. In contrast, concomitant promoter entries by Myb2 and Myb3 diminished in cells overexpressing Myb1, except that Myb3 promoter entry was slightly affected under prolonged iron depletion. Together, these results suggest that Myb2 and Myb3 may coactivate basal and iron-inducible ap65-1 transcription against Myb1 through conditional and competitive promoter entries.
机译:先前显示阴道毛滴虫中苹果酸酶基因(也称为 ap65-1 )的铁诱导转录涉及Myb1阻遏物和Myb2激活物,每个其可以优先选择两个紧密间隔的启动子位点,MRE-1 / MRE-2r,其包含重叠的启动子元件,和MRE-2f。在本研究中,铁诱导的〜32 kDa Myb3核蛋白被证明仅结合MRE-1元素。铁供应的变化对Myb2和Myb3表达水平产生拮抗作用,还导致Myb2和Myb3暂时和交替进入 ap65-1 启动子。当Myb3基本上被敲低或过表达时,在转染的细胞中检测到了基础和铁诱导的 ap65-1 转录的抑制或激活。在后一种情况下,在特定条件下检测到Myb3启动子进入增加,同时Myb2启动子进入减少,而在所有测试条件下,Myb3启动子进入在过表达Myb2的细胞中均受到抑制。相反,在过量表达Myb1的细胞中,Myb2和Myb3伴随的启动子进入减少了,除了在长时间的铁耗竭下Myb3启动子进入受到轻微影响。在一起,这些结果表明Myb2和Myb3可能通过有条件和竞争性启动子进入共同激活针对Myb1的基础和铁诱导的 ap65-1 转录。

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