Fong Nova, Bird Gregory, Vigneron Marc, Bentley David L
Department of Biochemistry and Molecular Genetics, UCHSC, B121, 4200 E. 9th Avenue, Denver, CO 80262, USA.
EMBO J. 2003 Aug 15;22(16):4274-82. doi: 10.1093/emboj/cdg396.
The RNA polymerase II C-terminal heptad repeat domain (CTD) is essential for normal transcription and co-transcriptional processing of mRNA precursors. The mammalian CTD comprises 52 heptads whose consensus, YSPTSPS, is conserved throughout eukaryotes, followed by a 10 amino acid C-terminal sequence that is conserved only among vertebrates. Here we show that surprisingly, the heptad repeats are not sufficient to support efficient transcription, pre-mRNA processing or full cell viability. In addition to the heptads, the 10 amino acid C-terminal motif is essential for high level transcription, splicing and poly(A) site cleavage. Efficient mRNA synthesis from a transiently transfected reporter gene required the C-terminal motif plus between 16 and 25 heptad repeats from either the N- or C-terminal half of the CTD. Twenty-seven consensus heptads plus the C-terminal motif also supported efficient mRNA synthesis but not cell viability.
RNA聚合酶II的C末端七肽重复结构域(CTD)对于mRNA前体的正常转录和共转录加工至关重要。哺乳动物的CTD由52个七肽组成,其共有序列YSPTSPS在整个真核生物中保守,随后是一个仅在脊椎动物中保守的10个氨基酸的C末端序列。在这里我们惊人地发现,七肽重复序列不足以支持高效转录、前体mRNA加工或细胞的完全存活能力。除了七肽之外,10个氨基酸的C末端基序对于高水平转录、剪接和聚腺苷酸化位点切割至关重要。从瞬时转染的报告基因高效合成mRNA需要C末端基序加上CTD的N末端或C末端一半的16至25个七肽重复序列。27个共有七肽加上C末端基序也支持高效的mRNA合成,但不支持细胞存活。