Kenten J H, Molgaard H V, Houghton M, Derbyshire R B, Viney J, Bell L O, Gould H J
Proc Natl Acad Sci U S A. 1982 Nov;79(21):6661-5. doi: 10.1073/pnas.79.21.6661.
Messenger RNA has been isolated from cells of the human myeloma line 266BL which synthesizes IgE of the myeloma ND. A fraction enriched in mRNA for the epsilon heavy chain was copied into DNA and the DNA was cloned in Escherichia coli. A chemically synthesized oligonucleotide probe, based on the experimentally determined sequence of the specific message, was used to screen colonies. The largest epsilon chain cDNA cloned, 2.0 kilobases, was characterized by restriction endonuclease mapping and DNA sequence analysis. It appears to encode the complete amino acid sequence of the epsilon chain, including a signal peptide at the NH2 terminus as well as untranslated sequences at the 5' and 3' ends of the mRNA. The missing part of the previously published amino acid sequence of the ND epsilon chain was determined from the DNA sequence.
信使核糖核酸已从人骨髓瘤细胞系266BL中分离出来,该细胞系能合成骨髓瘤ND的免疫球蛋白E。富含ε重链信使核糖核酸的部分被转录成脱氧核糖核酸,然后该脱氧核糖核酸被克隆到大肠杆菌中。根据实验确定的特定信使核糖核酸序列化学合成的寡核苷酸探针,用于筛选菌落。克隆得到的最大的ε链互补脱氧核糖核酸为2.0千碱基,通过限制性内切酶图谱分析和脱氧核糖核酸序列分析对其进行了表征。它似乎编码了ε链完整的氨基酸序列,包括氨基末端的信号肽以及信使核糖核酸5'和3'末端的非翻译序列。从脱氧核糖核酸序列中确定了先前发表的ND ε链氨基酸序列中缺失的部分。