Masters J N, Attardi G
Mol Cell Biol. 1985 Mar;5(3):493-500. doi: 10.1128/mcb.5.3.493-500.1985.
The 5' ends of dihydrofolate reductase (DHFR)-specific transcripts have been mapped in the 5'-flanking region of the amplified DHFR gene of the human methotrexate-resistant cell line 6A3 by primer extension and S1 protection experiments. The main 5' end, at position -71 relative to the first nucleotide of the DHFR reading frame, corresponds to the recently identified main transcription initiation site for the DHFR gene and pertains to transcripts representing approximately 99% of the DHFR-specific polysomal polyadenylic acid-containing RNA, and including the previously described DHFR mRNAs with sizes of 3.8, 1.0, and 0.8 kilobases. At least six other minor 5' ends have been mapped to nucleotide positions -449 to -480 upstream of the DHFR gene and pertain to approximately 1% of the DHFR-specific polysomal polyadenylic acid-containing RNA. These upstream initiating transcripts appear to include five major discrete species with sizes of 4.3, 3.8, 3.1, 2.1, and 1.0 kilobases and four minor ones with sizes of 7.3, 5.0, 1.4, and 0.8 kilobases. These species, with the exception of those of 3.1- and 2.1-kilobase sizes, also have been found in VA2-B cells, the parental line of 6A3, and in HeLa cells. The upstream initiating transcripts present in all three cell lines are increased in amount in 6A3 cells as compared with the other cell lines, in about the same proportion as the three identified DHFR mRNAs.
通过引物延伸和S1核酸酶保护实验,已将二氢叶酸还原酶(DHFR)特异性转录本的5'末端定位在人甲氨蝶呤抗性细胞系6A3的扩增DHFR基因的5'侧翼区域。相对于DHFR阅读框的第一个核苷酸,主要的5'末端位于-71位,对应于最近确定的DHFR基因的主要转录起始位点,并且属于代表约99%的DHFR特异性多核糖体含聚腺苷酸RNA的转录本,包括先前描述的大小为3.8、1.0和0.8千碱基的DHFR mRNA。至少还有六个其他次要的5'末端已定位在DHFR基因上游-449至-480的核苷酸位置,并且属于约1%的DHFR特异性多核糖体含聚腺苷酸RNA。这些上游起始转录本似乎包括五个主要的离散种类,大小分别为4.3、3.8、3.1、2.1和1.0千碱基,以及四个次要的,大小分别为7.3、5.0、1.4和0.8千碱基。除了3.1千碱基和2.1千碱基大小的那些转录本外,这些种类在6A3细胞的亲本系VA2-B细胞和HeLa细胞中也已被发现。与其他细胞系相比,在所有三种细胞系中都存在的上游起始转录本在6A3细胞中的量增加,增加比例与三种已鉴定的DHFR mRNA大致相同。