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Expression of the murine RanBP1 and Htf9-c genes is regulated from a shared bidirectional promoter during cell cycle progression

机译:小鼠RanBP1和Htf9-c基因的表达在细胞周期进程中受共享的双向启动子调控

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摘要

The murine Htf9-a/RanBP1 and Htf9-c genes are divergently transcribed from a bidirectional promoter. The Htf9-a gene encodes the RanBP1 protein, a major partner of the Ran GTPase. The divergently transcribed Htf9-c gene encodes a protein sharing similarity with yeast and bacterial nucleic acid-modifying enzymes. We report here that both mRNA species produced by the Htf9-associated genes are regulated during the cell cycle progression, peak in S phase and decrease during mitosis. Transient expression experiments with reporter constructs showed that cell cycle expression is controlled at the transcriptional level, because the bidirectional Htf9 promoter is downregulated in growth-arrested cells, is activated at the G(1)/S transition and reaches maximal activity in S phase, though with a different efficiency for each orientation. We have delimited specific promoter regions controlling S phase activity in one or both orientations: identified elements contain recognition sites for members belonging to both the E2F and Spl families of transcription factors. Together, the results suggest that the sharing of the regulatory region supports co-regulation of the Htf9-a/RanBP1 and Htf9-c genes in a common window of the cell cycle.
机译:鼠Htf9-a / RanBP1和Htf9-c基因是从双向启动子转录的。 Htf9-a基因编码RanGTP酶的主要伴侣RanBP1蛋白。差异转录的Htf9-c基因编码与酵母和细菌核酸修饰酶相似的蛋白质。我们在这里报告说,由Htf9相关基因产生的两种mRNA物种在细胞周期进程中受到调节,在S期达到峰值,在有丝分裂期间下降。使用报告子构建体的瞬时表达实验表明,细胞周期表达在转录水平受到控制,因为双向Htf9启动子在生长停滞的细胞中被下调,在G(1)/ S转变中被激活,并在S期达到最大活性,尽管每个方向的效率不同。我们已经确定了在一个或两个方向上控制S期活性的特定启动子区域:已识别的元件包含识别位点,该位点既属于转录因子的E2F家族又属于Spl家族。总之,结果表明调节区域的共享支持了在细胞周期的共同窗口中对Htf9-a / RanBP1和Htf9-c基因的共同调节。

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