Cho E J, Takagi T, Moore C R, Buratowski S
Department of Biological Chemistry and Molecular Pharmacology, Harvard Medical School, Boston, Massachusetts 02115, USA.
Genes Dev. 1997 Dec 15;11(24):3319-26. doi: 10.1101/gad.11.24.3319.
Capping of mRNA occurs shortly after transcription initiation, preceding other mRNA processing events such as mRNA splicing and polyadenylation. To determine the mechanism of coupling between transcription and capping, we tested for a physical interaction between capping enzyme and the transcription machinery. Capping enzyme is not stably associated with basal transcription factors or the RNA polymerase II (Pol II) holoenzyme. However, capping enzyme can directly and specifically interact with the phosphorylated form of the RNA polymerase carboxy-terminal domain (CTD). This association occurs in the context of the transcription initiation complex and is blocked by the CTD-kinase inhibitor H8. Furthermore, conditional truncation mutants of the Pol II CTD are lethal when combined with a capping enzyme mutant. Our results provide in vitro and in vivo evidence that capping enzyme is recruited to the transcription complex via phosphorylation of the RNA polymerase CTD.
mRNA加帽在转录起始后不久发生,先于其他mRNA加工事件,如mRNA剪接和聚腺苷酸化。为了确定转录与加帽之间的偶联机制,我们测试了加帽酶与转录机器之间的物理相互作用。加帽酶与基础转录因子或RNA聚合酶II(Pol II)全酶没有稳定的关联。然而,加帽酶可以直接且特异性地与RNA聚合酶羧基末端结构域(CTD)的磷酸化形式相互作用。这种关联发生在转录起始复合物的背景下,并被CTD激酶抑制剂H8阻断。此外,当与加帽酶突变体结合时,Pol II CTD的条件性截短突变体是致死的。我们的结果提供了体外和体内证据,表明加帽酶通过RNA聚合酶CTD的磷酸化被招募到转录复合物中。