Peunova N I, Samarina O P, Georgiev G P
Nucleic Acids Res. 1979 Aug 10;6(11):3625-40. doi: 10.1093/nar/6.11.3625.
Triphosphorylated 5'-end fragments about 100 nucleotides long were prepared from purified nuclear pre-mRNA using a modified hydroxyapatite method /1/. These fragments as well as fragments of total pre-mRNA of the same size were polyadenylated in vitro by ATP:RNA adenyltransferase and used as templates for the synthesis of [32P] cDNA by reverse transcriptase in the presence of an oligo(dT) primer. The use of cDNA transcribed from the triphosphorylated 5'-end fragments of pre-mRNA (5'-cDNA) and from the total pre-mRNA fragments allows one to calculate the complexity of the 5'-end fraction pre-mRNA and to detect these sequences in polysomal mRNA. Sequences adjacent to 5'-phosphorylated ends of pre-mRNA represent a specific class of sequences with a complexity of about 200 kb. It was also found that about 25% of total pre-mRNA and about a half of sequences adjacent to triphosphorylated 5'-ends are present in polysomal mRNA. A high homology between triphosphorylated 5'-end fragments of pre-mRNA and mRNA sequences may be explained in terms of splicing. Less than 30% of 5'-cDNA hybridized to moderately repetitive DNA while most of them are represented by unique DNA sequences. About 15% of 5'-cDNA contained oligo(dA) sequences originated from oligo(U) in pre-mRNA from which it was transcribed.
使用改良的羟基磷灰石方法从纯化的核前体mRNA制备了长度约为100个核苷酸的三磷酸化5'-末端片段/1/。这些片段以及相同大小的总前体mRNA片段在体外通过ATP:RNA腺苷酸转移酶进行聚腺苷酸化,并在寡聚(dT)引物存在下用作逆转录酶合成[32P]cDNA的模板。使用从mRNA前体的三磷酸化5'-末端片段(5'-cDNA)和总前体mRNA片段转录的cDNA,可以计算前体mRNA 5'-末端部分的复杂度,并在多核糖体mRNA中检测这些序列。与前体mRNA 5'-磷酸化末端相邻的序列代表一类特定的序列,其复杂度约为200 kb。还发现,总前体mRNA的约25%和约一半与三磷酸化5'-末端相邻的序列存在于多核糖体mRNA中。前体mRNA的三磷酸化5'-末端片段与mRNA序列之间的高度同源性可以用剪接来解释。不到30%的5'-cDNA与中度重复DNA杂交,而它们中的大多数由独特的DNA序列代表。约15%的5'-cDNA含有源自其转录的前体mRNA中的寡聚(U)的寡聚(dA)序列。