Inoue A, Nakamura M, Nakanishi S, Hidaka S, Miura K, Numa S
Eur J Biochem. 1981 Jan;113(3):531-9. doi: 10.1111/j.1432-1033.1981.tb05095.x.
The complete 5'-terminal nucleotide sequence of the MRNA coding for the bovine common precursor of corticotropin and beta-lipotropin has been determined. The 5'-32P-labelled, 21-nucleotides-long, single-stranded DNA fragment complementary to a portion of the 5'-noncoding region of the mRNA was prepared from a cDNA clone and elongated by reverse transcriptase reaction with the mRNA as template. The DNA transcript formed was sequenced by the procedure of Maxam and Gilbert, and the resultant sequence was cross-checked by two-dimensional electrophoretic analysis of the partial alkaline digest of the 5'-32P-labelled mRNA. The 5'-terminal nucleotide residue was determined by two-dimensional thin-layer chromatography of the complete hydrolysis product of the 5'-32P-labelled mRNA. The nucleotide sequence determined, which partially overlaps the known sequence of the cloned cDNA, reveals the complete 5'-terminal sequence of the mRNA. This, in conjunction with our previous data, defines the complete primary structure of the mRNA. The mRNA is composed of 1098 nucleotides, including an unusually long 5'-noncoding sequence of 128 nucleotides. The presence of a 'cap' structure at the 5' terminus of the mRNA is suggested. The 5'-terminal 48 nucleotide residues of the mRNA are extremely purine-rich, having an A + G content of 83%, whereas all pyrimidine-rich segments are located downstream from there. Because the 5'-noncoding region of the mRNA contains three segments of potential secondary structure which partially overlap, it can exist in a number of alternative base-pairing configurations. However, its interaction with the 3'-terminal segment of 18-S rRNA at the site of maximal complementarity would fix the mRNA configuration in such a way as to bring the possible site of ribosome binding near the initiation codon.
已确定编码牛促肾上腺皮质激素和β-促脂素共同前体的mRNA完整的5'-末端核苷酸序列。与mRNA的5'-非编码区一部分互补的5'-32P标记的、21个核苷酸长的单链DNA片段是从一个cDNA克隆制备的,并以mRNA为模板通过逆转录酶反应进行延伸。形成的DNA转录本通过Maxam和Gilbert的方法进行测序,所得序列通过对5'-32P标记的mRNA部分碱性消化产物的二维电泳分析进行交叉核对。5'-末端核苷酸残基通过对5'-32P标记的mRNA完全水解产物的二维薄层层析来确定。所确定的核苷酸序列部分与克隆的cDNA的已知序列重叠,揭示了mRNA完整的5'-末端序列。这与我们之前的数据一起,确定了mRNA完整的一级结构。该mRNA由1098个核苷酸组成,包括一个异常长的128个核苷酸的5'-非编码序列。提示在mRNA的5'末端存在一个“帽”结构。mRNA的5'-末端48个核苷酸残基富含嘌呤,A + G含量为83%,而所有富含嘧啶的区段都位于其下游。由于mRNA的5'-非编码区包含三个部分重叠的潜在二级结构区段,它可以以多种替代的碱基配对构型存在。然而,它在最大互补位点与18-S rRNA的3'-末端区段的相互作用将以这样一种方式固定mRNA构型,即使核糖体结合的可能位点靠近起始密码子。