Kim Minkyu, Ahn Seong-Hoon, Krogan Nevan J, Greenblatt Jack F, Buratowski Stephen
Department of Biological Chemistry and Molecular Pharmacology, Harvard Medical School, Boston, MA, USA.
EMBO J. 2004 Jan 28;23(2):354-64. doi: 10.1038/sj.emboj.7600053. Epub 2004 Jan 22.
To understand the factor interactions of transcribing RNA polymerase II (RNApII) in vivo, chromatin immunoprecipitations were used to map the crosslinking patterns of multiple elongation and polyadenylation factors across transcribed genes. Transcription through the polyadenylation site leads to a reduction in the levels of the Ctk1 kinase and its associated phosphorylation of the RNApII C-terminal domain. One group of elongation factors (Spt4/5, Spt6/Iws1, and Spt16/Pob3), thought to mediate transcription through chromatin, shows patterns matching that of RNApII. In contrast, the Paf and TREX/THO complexes partially overlap RNApII, but do not crosslink to transcribed regions downstream of polyadenylation sites. In a complementary pattern, polyadenylation factors crosslink strongly at the 3' ends of genes. Mutation of the 3' polyadenylation sequences or the Rna14 protein causes loss of polyadenylation factor crosslinking and read-through of termination sequences. Therefore, transcription termination and polyadenylation involve transitions at the 3' end of genes that may include an exchange of elongation and polyadenylation/termination factors.
为了解体内转录RNA聚合酶II(RNApII)的因子相互作用,采用染色质免疫沉淀法来绘制多个延伸和聚腺苷酸化因子在转录基因上的交联模式。通过聚腺苷酸化位点的转录会导致Ctk1激酶水平及其与RNApII C末端结构域相关磷酸化水平的降低。一组被认为介导通过染色质转录的延伸因子(Spt4/5、Spt6/Iws1和Spt16/Pob3)显示出与RNApII匹配的模式。相比之下,Paf和TREX/THO复合物与RNApII部分重叠,但不会与聚腺苷酸化位点下游的转录区域交联。以互补模式,聚腺苷酸化因子在基因的3'末端强烈交联。3'聚腺苷酸化序列或Rna14蛋白的突变会导致聚腺苷酸化因子交联的丧失以及终止序列的通读。因此,转录终止和聚腺苷酸化涉及基因3'末端的转变,这可能包括延伸因子与聚腺苷酸化/终止因子的交换。