Salditt-Georgieff M, Darnell J E
Proc Natl Acad Sci U S A. 1983 Aug;80(15):4694-8. doi: 10.1073/pnas.80.15.4694.
Nascent labeled RNA from induced, globin-producing mouse erythroleukemia cells was hybridized to cloned regions of the beta major-globin gene. Transcription ceases about 1,000 bases downstream from the poly(A) site as indicated by protection from nuclease digestion of a discrete-sized RNA fragment that it shorter than the protecting cloned DNA fragment. This defines an apparently unique termination site for a protein-coding gene that is transcribed by RNA polymerase II.
从诱导产生珠蛋白的小鼠红白血病细胞中提取的新生标记RNA,与β-珠蛋白基因的克隆区域进行杂交。转录在多聚腺苷酸(poly(A))位点下游约1000个碱基处停止,这由一个离散大小的RNA片段免受核酸酶消化所表明,该RNA片段比保护性克隆DNA片段短。这确定了一个由RNA聚合酶II转录的蛋白质编码基因的明显独特的终止位点。