Peunova N I, Samarina O P, Georgiev G P
Mol Biol (Mosk). 1980;14(1):212-22.
Triphosphorylated 5'-end fragments about 100 nucleotides long were prepared from purified nuclear pre-mRNA using a modified hydroxyapatite method. These fragments as well as fragments of total pre-mRNA were polyadenylated by ATP:RNA adenyl-transferase and used as templates for the synthesis of [32P]cDNA by reverse transcriptase in the presence of an oligo(dT)-primer, cDNA transcribed from total fragments of pre-mRNA and from 5'-end fragments (5'-cDNA) were hybridized with excess of nuclear pre-mRNA. The extent of hybridization was 65-70 and 80-85% in different experiments. 18% of total cDNA and 35% of 5'-cDNA hybridized with mRNA from polysomes. A high homology between mRNA and triphosphorylated 5'-ends of pre-mRNA may be explained in the terms of splicing. The sequences adjacent to the triphosphorylated 5'-ends of pre-mRNA represent a specific class with complexity about 2.10(5) nucleotides. Less than 30% of 5'-cDNA hybridized with intermediately repetitive DNA, while the main portion hybridized with unique DNA sequences. About 15% of 5'-cDNA contain oligo (dA) sequences, originated from oligo (U) in the pre-mRNA.
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'端片段。这些片段以及总前体mRNA的片段通过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,从总前体mRNA片段和5'端片段转录的cDNA(5'-cDNA)与过量的核前体mRNA杂交。在不同实验中,杂交程度为65-70%和80-85%。18%的总cDNA和35%的5'-cDNA与多核糖体的mRNA杂交。mRNA与前体mRNA的三磷酸化5'端之间的高度同源性可以用剪接来解释。与前体mRNA的三磷酸化5'端相邻的序列代表一类复杂性约为2.10(5)个核苷酸的特定序列。不到30%的5'-cDNA与中度重复DNA杂交,而主要部分与独特的DNA序列杂交。约15%的5'-cDNA含有源自前体mRNA中寡聚(U)的寡聚(dA)序列。