Kuebbing D, Liarakos C D
Nucleic Acids Res. 1978 Jul;5(7):2253-66. doi: 10.1093/nar/5.7.2253.
DNA-sequence analysis of 300 nucleotides from the region of cloned, double-stranded ovalbumin cDNA corresponding to the 5' end of ovalbumin messenger RNA was accomplished using the technique of Maxam and Gilbert (Proc. Nat. Acad. Sci. USA (1977) 74,560-564). The AUG initiation codon was located 52 nucleotides from the AT linkers used in cloning and immediately adjacent to the amino terminal peptide of ovalbumin, indicating the absence of a "signal peptide" in this protein. The nucleotide sequence coding for a phosphorylated peptide from ovalbumin was also found. These results demonstrate that the coding portion of mRNAov begins near the 5' end of the molecule leaving some 600 nucleotides of noncoding information at the 3' end.
利用马克萨姆和吉尔伯特的技术(《美国国家科学院院刊》(1977年)74卷,560 - 564页),对克隆的双链卵清蛋白cDNA中对应于卵清蛋白信使RNA 5'端区域的300个核苷酸进行了DNA序列分析。AUG起始密码子位于克隆时所用AT连接子下游52个核苷酸处,且紧邻卵清蛋白的氨基末端肽段,这表明该蛋白不存在“信号肽”。还发现了编码卵清蛋白磷酸化肽段的核苷酸序列。这些结果表明,卵清蛋白信使RNA的编码部分始于分子的5'端附近,在3'端留下约600个核苷酸的非编码信息。