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RNA聚合酶II的C末端结构域是一个多价靶向序列,仅通过共有七肽支持果蝇发育。

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

作者信息

Lu Feiyue, Portz Bede, Gilmour David S

机构信息

Center for Eukaryotic Gene Regulation, Department of Biochemistry and Molecular Biology, The Pennsylvania State University, University Park, PA 16802, USA; The Huck Institutes of Life Sciences, The Pennsylvania State University, University Park, PA 16802, USA.

Center for Eukaryotic Gene Regulation, Department of Biochemistry and Molecular Biology, The Pennsylvania State University, University Park, PA 16802, USA.

出版信息

Mol Cell. 2019 Mar 21;73(6):1232-1242.e4. doi: 10.1016/j.molcel.2019.01.008. Epub 2019 Feb 11.

Abstract

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.

摘要

RNA聚合酶II(Pol II)的C末端结构域(CTD)由共有序列YSPTSPS的重复序列组成,是转录相关因子的重要结合支架。后生动物的CTD具有长度和序列组成高度保守的特点,这些特点源于不同基序的进化,被认为对发育至关重要。相反,我们发现仅由YSPTSPS重复序列组成的截短CTD能支持果蝇存活,但具有足够YSPTSPS重复序列以匹配野生型果蝇CTD长度的CTD却是有缺陷的。此外,缺乏Pol II其余部分的荧光标记CTD能动态进入转录区室,这表明CTD起到信号序列的作用。然而,具有过多YSPTSPS重复序列的CTD更容易定位于与染色体分离的静态核灶。我们提出,CTD的序列复杂性抵消了由过多重复序列引起的异常行为,同时又不影响其靶向功能。

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