Lizardi P M, Mahdavi V, Shields D, Candelas G
Proc Natl Acad Sci U S A. 1979 Dec;76(12):6211-5. doi: 10.1073/pnas.76.12.6211.
Silk fibroin mRNA was translated in a rabbit reticulocyte cell-free system. Addition of tRNA from silk glands was essential for complete translation of the fibroin polypeptide. (Mr approximately 400,000). Synthesis of full-sized product took at least 85 min. In addition to full-size product, a large number of smaller polypeptides were observed upon analysis by sodium dodecyl sulfate/polyacrylamide gel electrophoresis. Evidence is presented that these smaller polypeptides are growing fibroin chains that transiently accumulate as discrete size classes due to discontinuities in the translation process. These discontinuities, or pauses, occur at specific sites in the fibroin mRNA template. The relative duration of the pauses can be experimentally modulated by changing the source of the supplementary tRNA added to the in vitro system. Silk glands were incubated in organ culture under conditions where essentially exclusive labeling of newly synthesized fibroins was attained. Analysis in sodium dodecyl sulfate gels showed that the labeling pattern of nascent silk fibroins is similar to the pattern observed in the reticulocyte cell-free system. This result suggests that discontinuities or pauses in polypeptide chain elongation also occur in vivo under conditions of organ culture.
丝素mRNA在兔网织红细胞无细胞体系中进行翻译。添加来自丝腺的tRNA对于丝素多肽的完全翻译至关重要。(分子量约为400,000)。全长产物的合成至少需要85分钟。通过十二烷基硫酸钠/聚丙烯酰胺凝胶电泳分析,除了全长产物外,还观察到大量较小的多肽。有证据表明,这些较小的多肽是正在生长的丝素链,由于翻译过程中的间断,它们作为离散的大小类别短暂积累。这些间断或停顿发生在丝素mRNA模板的特定位点。通过改变添加到体外系统中的补充tRNA的来源,可以通过实验调节停顿的相对持续时间。在基本上实现新合成丝素的专一性标记的条件下,将丝腺进行器官培养。十二烷基硫酸钠凝胶分析表明,新生丝素的标记模式与在网织红细胞无细胞体系中观察到的模式相似。这一结果表明,在器官培养条件下,体内多肽链延伸过程中也会出现间断或停顿。