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通过电子显微镜对酵母三小核核糖核蛋白中Prp8、Brr2、Snu114和U4/U6蛋白进行定位。

Localization of Prp8, Brr2, Snu114 and U4/U6 proteins in the yeast tri-snRNP by electron microscopy.

作者信息

Häcker Irina, Sander Bjoern, Golas Monika M, Wolf Elmar, Karagöz Elif, Kastner Berthold, Stark Holger, Fabrizio Patrizia, Lührmann Reinhard

机构信息

Department of Cellular Biochemistry, Max Planck Institute for Biophysical Chemistry, Am Fassberg 11, D-37077 Göttingen, Germany.

出版信息

Nat Struct Mol Biol. 2008 Nov;15(11):1206-12. doi: 10.1038/nsmb.1506. Epub 2008 Oct 26.

Abstract

The U4/U6-U5 tri-small nuclear ribonucleoprotein (snRNP) is a major, evolutionarily highly conserved spliceosome subunit. Unwinding of its U4/U6 snRNA duplex is a central event of spliceosome activation that requires several components of the U5 portion of the tri-snRNP, including the RNA helicase Brr2, Prp8 and the GTPase Snu114. Here we report the EM projection structure of the Saccharomyces cerevisiae tri-snRNP. It shows a modular organization comprising three extruding domains that contact one another in its central portion. We have visualized genetically tagged tri-snRNP proteins by EM and show here that U4/U6 snRNP forms a domain termed the arm. Conversely, a separate head domain adjacent to the arm harbors Brr2, whereas Prp8 and the GTPase Snu114 are located centrally. The head and arm adopt variable relative positions. This molecular organization and dynamics suggest possible scenarios for structural events during catalytic activation.

摘要

U4/U6-U5三小核核糖核蛋白(snRNP)是一种主要的、在进化上高度保守的剪接体亚基。其U4/U6 snRNA双链的解旋是剪接体激活的核心事件,这需要三snRNP的U5部分的几个组分参与,包括RNA解旋酶Brr2、Prp8和GTP酶Snu114。在此,我们报道了酿酒酵母三snRNP的电子显微镜投影结构。它呈现出一种模块化组织,由三个在其中心部分相互接触的突出结构域组成。我们通过电子显微镜观察了基因标记的三snRNP蛋白,并在此表明U4/U6 snRNP形成了一个称为臂的结构域。相反,与臂相邻的一个单独的头部结构域包含Brr2,而Prp8和GTP酶Snu114位于中心位置。头部和臂采用可变的相对位置。这种分子组织和动态变化提示了催化激活过程中结构事件的可能情形。

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