Gerbi Susan A, Lange Thilo Sascha
Division of Biology and Medicine, Brown University, Providence, Rhode Island 02912, USA.
Mol Biol Cell. 2002 Sep;13(9):3123-37. doi: 10.1091/mbc.01-12-0596.
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.
此前,我们发现剪接体U6小核RNA(snRNA)会短暂穿过核仁。在此,我们报告,通过将荧光素标记的snRNA注射到非洲爪蟾卵母细胞核中后对核仁制剂进行荧光显微镜观察,[U4/U6.U5]三snRNP的所有单个snRNA都定位于核仁。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成熟过程中被Lsm蛋白结合。U6的这种3' - 核仁定位元件对于核仁定位既是必需的也是充分的,并且也是定位于卡哈尔体所必需的。将U6 snRNA的3'羟基转化为3'磷酸会阻止其与La蛋白结合,但不会影响U6定位于核仁或卡哈尔体。