de Magistris L, Stunnenberg H G
European Molecular Biology Laboratories, Heidelberg, FRG.
Nucleic Acids Res. 1988 Apr 25;16(8):3141-56. doi: 10.1093/nar/16.8.3141.
Mutations in the sequences flanking the conserved and essential TAAAT motif of vaccinia late gene promoters (consensus: T/A T/A TAAAT G Pu Pu) affect the level of expression. Introduction of a pyrimidine in the purine stretch downstream of the TAAAT motif reduces the level of RNA synthesis. Mature transcripts from the wild-type 11K late promoter have a non-contiguous 5' poly(A) leader of approximately 35 A-residues (referred to as a poly(A) head). We show here by RNA sequencing, primer extension and subsequent m7G cap selection of cDNA/RNA hybrids that the mutations affect the length of the poly(A) head but not the location of the junction between the poly(A) leader and sequences encoded in the genome. These results are consistent with a slippage mechanism underlying the process of 5' poly(A) addition, but are not in agreement with a splicing event.
痘苗病毒晚期基因启动子保守且必需的TAAAT基序(共有序列:T/A T/A TAAAT G Pu Pu)侧翼序列中的突变会影响表达水平。在TAAAT基序下游的嘌呤序列中引入嘧啶会降低RNA合成水平。野生型11K晚期启动子的成熟转录本具有约35个A残基的非连续5'聚腺苷酸前导序列(称为聚腺苷酸头部)。我们在此通过RNA测序、引物延伸以及随后对cDNA/RNA杂交体的m7G帽选择表明,这些突变会影响聚腺苷酸头部的长度,但不影响聚腺苷酸前导序列与基因组中编码序列之间连接点的位置。这些结果与5'聚腺苷酸添加过程中潜在的滑动机制一致,但与剪接事件不一致。