以單分子研究 rpsO 基因 5’端未轉譯區的 RNA 結構重組

在細胞中，轉譯（translation）的過程是受到高度調控的。我們在此將焦點放在大腸桿菌（Escherichia coli）rpsO基因所轉譯的核醣體蛋白 S15（ecS15）上。核醣體蛋白 S15可以結合到自身的信使核醣核酸（mRNA）上5’端未轉譯區，並且在核醣體蛋白 S15過剩時抑制其轉譯的進行；此結合而抑制的效果發生在信使核醣核酸的這段摺疊成假結（pseudoknot）結構的區域，然而這段區域也可以摺疊成雙髮夾（double-hairpin）的結構。再者，SD序列（Shine-Dalgarno sequence）只會暴露在假結的構形上並允許核醣體結合且解開此構造來起始轉譯。當核醣體蛋白 S15表現過量時，它可以結合至假結的結構導致核醣體被困在前起始階段。 rpsO信使核醣核酸上5’端未轉譯區所形成的結構在過去研究已甚了解，但雙髮夾的形成角色並不知道。為了了解這段5’端未轉譯區結構上和動力學上的特性，我們利用光鉗（optical tweezers）解開此核醣核酸片段。這個技術讓我們可以觀察到單一核醣核酸分子的構形改變（conformational change）。我們發現雙髮夾的形成可以促使其重組成假結結構，儘管假結的摺疊也可以不經由雙髮夾的結構。此外，我們還發現其他的結構產生，他們在光鉗上所表現出來的特性和假結類似。從我們實驗的結果推論雙髮夾結構在摺疊過程中是一種中間物，需要其他因子或蛋白來協助假結的正確構成。

關鍵字

轉譯調控； rpsO 信使核醣核酸；結構重組；單分子；光鉗

並列摘要

Translation is a highly regulated process in the cell. Here, we have focused on the translational regulation of Escherichia coli ribosomal protein S15 (ecS15), which is encoded by the rpsO gene. The ecS15 can bind to the 5’ untranslated region (5’-UTR) of its own mRNA and repress its translation when the ecS15 is in excess; the binding repression occurs when this region of the mRNA folds into a unique pseudoknot structure, as opposed to an alternative double-hairpin structure. However, the Shine-Dalgarno (SD) sequence is only exposed on the pseudoknot form to allow the ribosome binding and melting this structure for the initiation of translation. When ecS15 is over expressed, it binds to the pseudoknot and leads to the ribosome trapped in the pre-initiation state. The 5’-UTR of the rpsO mRNA has been studied for alternative structure formation in the past, but the role of the double-hairpin structure is unknown. To characterize these structural and dynamic aspects, we used optical tweezers to unfold the 5’-UTR of the rpsO mRNA. This technique allows us to observe the conformational change of a single RNA molecule. We find that formation of the pseudoknot can be promoted from rearrangement of the double-hairpin structure. In addition, we also observed some other structures of which the full unfolding distance is similar to that of the pseudoknot. From our results, we suggest that the double-hairpin may be an intermediate on the folding pathway to the pseudoknot, and other factors or proteins are required to promote correct formation of the pseudoknot structure.

並列關鍵字

translational regulation ； rpsO mRNA ； structural rearrangement ； single-molecule ； optical tweezers

參考文獻

Abels, J. A., F. Moreno-Herrero, et al. (2005). "Single-molecule measurements of the persistence length of double-stranded RNA." Biophys J 88(4): 2737-2744.

Agalarov, S. C., G. Sridhar Prasad, et al. (2000). "Structure of the S15,S6,S18-rRNA complex: assembly of the 30S ribosome central domain." Science 288(5463): 107-113.

Allison, D. P., P. Hinterdorfer, et al. (2002). "Biomolecular force measurements and the atomic force microscope." Curr Opin Biotechnol 13(1): 47-51.

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Ban, N., P. Nissen, et al. (2000). "The complete atomic structure of the large ribosomal subunit at 2.4 A resolution." Science 289(5481): 905-920.

國際替代計量

以單分子研究 rpsO 基因 5’端未轉譯區的 RNA 結構重組

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