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The C-Terminal Domain of RNA Polymerase II Is a Multivalent Targeting Sequence that Supports Drosophila Development with Only Consensus Heptads

机译:RNA聚合酶II的C末端结构域是一种多价靶向序列,其仅均有共有庚菌菌

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摘要

The C-terminal domain (CTD) of RNA polymerase II (Pol II) is composed of repeats of the consensus YSPTSPS and is an essential binding scaffold for transcription-associated factors. Metazoan CTDs have well-conserved lengths and sequence compositions arising from the evolution of divergent motifs, features thought to be essential for development. On the contrary, we show that a truncated CTD composed solely of YSPTSPS repeats supports Drosophila viability but that a CTD with enough YSPTSPS repeats to match the length of the wild-type Drosophila CTD is defective. Furthermore, a fluorescently tagged CTD lacking the rest of Pol II dynamically enters transcription compartments, indicating that the CTD functions as a signal sequence. However, CTDs with too many YSPTSPS repeats are more prone to localize to static nuclear foci separate from the chromosomes. We propose that the sequence complexity of the CTD offsets aberrant behavior caused by excessive repetitive sequences without compromising its targeting function.
机译:RNA聚合酶II(POL II)的C末端域(CTD)由共有ysptsps的重复组成,并且是用于转录相关因子的必要结合支架。美唑烷CTDS具有良好的储蓄长度和序列组合物,来自发散主题的演变,特征被认为是发展至关重要的。相反,我们表明,仅由Ysptsps重复组成的截短的CTD支持果蝇的活力,但是具有足够YSPTSPS的CTD重复匹配野生型果蝇CTD的长度有缺陷。此外,缺乏POL II的其余部分的荧光标记的CTD动态进入转录隔间,表明CTD用作信号序列。然而,具有太多YSPTSPS重复的CTD更容易达到与染色体分开的静态核心焦灶。我们提出CTD的序列复杂性偏移由过量的重复序列引起的异常行为而不会影响其靶向功能。

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  • 来源
    《Molecular cell》 |2019年第6期|共15页
  • 作者单位

    Penn State Univ Ctr Eukaryot Gene Regulat Dept Biochem &

    Mol Biol University Pk PA 16802 USA;

    Penn State Univ Ctr Eukaryot Gene Regulat Dept Biochem &

    Mol Biol University Pk PA 16802 USA;

    Penn State Univ Ctr Eukaryot Gene Regulat Dept Biochem &

    Mol Biol University Pk PA 16802 USA;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 细胞生物学;
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