Hamlyn P H, Browniee G G, Cheng C C, Gait M J, Milstein C
Cell. 1978 Nov;15(3):1067-75. doi: 10.1016/0092-8674(78)90290-8.
Three synthetic oligonucleotides were prepared to be complementary to known regions of the mouse immunoglublin light chain mRNA, and their ability to prime the transcription of complementary DNA (cDNA) was studied. The sequence of the cDNA was determined by adapting for mRNA the DNA sequencing method of Sanger, Nicklen and Coulson (1977) which uses 2'3' dideoxy ribonucleotides. A continuous sequence of 532 nucleotides was obtained, 321 corresponding to the whole of the constant region of the mRNA and the remaining 211 being the complete 3' noncoding region of the mRNA. The termination codon U-A-G occurs at the expected position in the mRNA corresponding to the triplet following the C terminal cystine. The nucleotide sequence is partially corroborated by the sequence of fragments obtained previously from 32P-mRNA fingerprints and endonuclease IV digests of 32P-cDNA, and is in agreement with the amino acid sequence of the constant region, except for a rearrangement of four amino acids (between amino acid positions 163 and 166). A revision of the amino acid sequence confirms the nucleic acid sequence.
制备了三种合成寡核苷酸,使其与小鼠免疫球蛋白轻链mRNA的已知区域互补,并研究了它们引发互补DNA(cDNA)转录的能力。cDNA的序列是通过采用Sanger、Nicklen和Coulson(1977年)用于mRNA的DNA测序方法来确定的,该方法使用2'3'双脱氧核糖核苷酸。获得了一段532个核苷酸的连续序列,其中321个对应于mRNA整个恒定区,其余211个是mRNA完整的3'非编码区。终止密码子U-A-G出现在mRNA中对应于C末端胱氨酸之后三联体的预期位置。该核苷酸序列部分得到了先前从32P-mRNA指纹图谱和32P-cDNA的核酸内切酶IV消化片段序列的证实,并且除了四个氨基酸(在氨基酸位置163和166之间)的重排外,与恒定区的氨基酸序列一致。氨基酸序列的修订证实了核酸序列。