Hardeland Ulrike, Hurt Ed
Biochemie-Zentrum der Universitat Heidelberg, INF328, D-69120 Heidelberg, Germany.
Traffic. 2006 Apr;7(4):465-73. doi: 10.1111/j.1600-0854.2006.00399.x.
Eukaryotic RNA polymerases are multisubunit assemblies, whose enzymatic function in the nucleus is intensively studied. However, little is known about the biogenesis of the three RNA polymerases and coupling to nucleo-cytoplasmic transport. Here, we show that Rpc128, the second largest subunit of RNA polymerase III, was mislocalized to the cytoplasm, when a short sequence in the N-terminal domain was deleted. Importantly, nuclear import of other, but not all, RNA polymerase III subunits was impaired in this RPC128DeltaN mutant. These data suggest that RNA polymerase III subunits are not imported independently into the nucleus but may require preassembly into cytoplasmic subcomplexes for coordinated nuclear uptake. We expect these studies to be a starting point to dissect the complex biogenesis pathway of eukaryotic RNA polymerases.
真核生物RNA聚合酶是多亚基复合体,其在细胞核中的酶功能已得到深入研究。然而,对于这三种RNA聚合酶的生物发生以及与核质运输的偶联却知之甚少。在此,我们发现,当RNA聚合酶III的第二大亚基Rpc128的N端结构域中的一段短序列被缺失时,它会错误定位于细胞质中。重要的是,在这个Rpc128DeltaN突变体中,其他(但并非所有)RNA聚合酶III亚基的核输入受到损害。这些数据表明,RNA聚合酶III亚基并非独立地导入细胞核,而是可能需要预先组装成细胞质亚复合体以进行协调的核摄取。我们期望这些研究能够成为剖析真核生物RNA聚合酶复杂生物发生途径的起点。