首页> 外文期刊>Molecular biology of the cell >All Small Nuclear RNAs (snRNAs) of the [U4/U6.U5] Tri-snRNP Localize to Nucleoli; Identification of the Nucleolar Localization Element of U6 snRNA
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All Small Nuclear RNAs (snRNAs) of the [U4/U6.U5] Tri-snRNP Localize to Nucleoli; Identification of the Nucleolar Localization Element of U6 snRNA

机译:[U4 / U6.U5] Tri-snRNP的所有小核RNA(snRNA)均位于核仁; U6 snRNA核仁定位元件的鉴定

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Previously, we showed that spliceosomal U6 small nuclear RNA (snRNA) transiently passes through the nucleolus. Herein, we report that all individual snRNAs of the [U4/U6.U5] tri-snRNP localize to nucleoli, demonstrated by fluorescence microscopy of nucleolar preparations after injection of fluorescein-labeled snRNA into Xenopus oocyte nuclei. Nucleolar localization of U6 is independent from [U4/U6] snRNP formation since sites of direct interaction of U6 snRNA with U4 snRNA are not nucleolar localization elements. Among all regions in U6, the only one required for nucleolar localization is its 3′ end, which associates with the La protein and subsequently during maturation of U6 is bound by Lsm proteins. This 3′-nucleolar localization element of U6 is both essential and sufficient for nucleolar localization and also required for localization to Cajal bodies. Conversion of the 3′ hydroxyl of U6 snRNA to a 3′ phosphate prevents association with the La protein but does not affect U6 localization to nucleoli or Cajal bodies.
机译:先前,我们显示了剪接体U6小核RNA(snRNA)瞬时通过核仁。在这里,我们报道[U4 / U6.U5] tri-snRNP的所有单个snRNA都定位于核仁,这是通过将荧光素标记的snRNA注入非洲爪蟾卵母细胞核后,通过核仁制剂的荧光显微镜检查证明的。 U6的核仁定位独立于[U4 / U6] snRNP的形成,因为U6 snRNA与U4 snRNA的直接相互作用的位点不是核仁定位元件。在U6的所有区域中,核仁定位所需的唯一区域是其3'末端,该末端与La蛋白结合,随后在U6成熟期间被Lsm蛋白结合。 U6的3'-核仁定位元件对于核仁定位既是必需的又是足够的,并且对于定位至Cajal体也是必需的。 U6 snRNA的3'羟基转化为3'磷酸可防止与La蛋白缔合,但不影响U6定位于核仁或Cajal体。

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