Gopalakrishna Y, Sarkar N
J Biol Chem. 1982 Mar 25;257(6):2747-50.
We had shown earlier (Gopalakrishna, Y., Langley, D., Sarkar, N. (1981) Nucleic Acid Res. 9, 3545-3554) that a substantial fraction of mRNA of various bacterial species carries 3'-terminal polyadenylate sequences. In this paper, we show that poly(A)-containing RNA from Bacillus subtilis can serve as template for the synthesis of complementary DNA by avian myeloblastosis virus reverse transcriptase, provided that oligodeoxythymidylate is added as primer. Poly(A)-RNA purified by affinity chromatography on oligo(dT)-cellulose was 20 times more effective as template for cDNA formation than total bacterial RNA, whereas rRNA was inactive. The average chain length of the cDNA was 400 nucleotides (range = 230-800 nucleotides), and 95% of the cDNA could be degraded by the single-strand specific S1 nuclease after denaturation. The small fraction (5%) that was resistant to S1 nuclease may represent duplex hairpin structures. Annealing with poly(A)-RNA protected cDNA from degradation by S1 nuclease, indicating that cDNA indeed contains nucleotide sequences complementary to poly(A)-RNA. These results constitute independent evidence that a large fraction (about 40%) of B. subtilis mRNA is polyadenylated. Moreover, the synthesis of cDNA to bacterial mRNA provides an important new tool for the study of bacterial mRNA structure.
我们先前已经表明(戈帕拉克里希纳,Y.,兰利,D.,萨卡尔,N.(1981年)《核酸研究》9,3545 - 3554),各种细菌物种的很大一部分mRNA携带3' - 末端聚腺苷酸序列。在本文中,我们表明,来自枯草芽孢杆菌的含聚(A)RNA可以作为禽成髓细胞瘤病毒逆转录酶合成互补DNA的模板,前提是添加寡聚脱氧胸苷酸作为引物。通过在寡聚(dT) - 纤维素上进行亲和层析纯化的聚(A) - RNA作为cDNA形成模板的效率比总细菌RNA高20倍,而rRNA无活性。cDNA的平均链长为400个核苷酸(范围 = 230 - 800个核苷酸),并且95%的cDNA在变性后可被单链特异性S1核酸酶降解。对S1核酸酶有抗性的一小部分(5%)可能代表双链发夹结构。与聚(A) - RNA退火可保护cDNA不被S1核酸酶降解,表明cDNA确实包含与聚(A) - RNA互补的核苷酸序列。这些结果构成了独立的证据,证明很大一部分(约40%)的枯草芽孢杆菌mRNA是聚腺苷酸化的。此外,细菌mRNA的cDNA合成提供了一种研究细菌mRNA结构的重要新工具。