Zimmern D
Philos Trans R Soc Lond B Biol Sci. 1976 Nov 30;276(943):189-204. doi: 10.1098/rstb.1976.0110.
The interaction of TMV RNA with the disk aggregate of TMV protein at the initiation of assembly has been studied by using the techniques of RNA sequencing. The 5' end group has been identified, and shown not to be protected in the early stages of assembly from accessibility to nuclease digestion. A population of RNA fragments of average length 250 nucleotides, originating from a unique region of TMV RNA, is encapsidated by limited assembly, and sufficient sequence information is available to identify certain unusual features. The protected region does not contain highly reiterated simple repeating sequences, but may contain more complicated repeats. The length and complexity of the nucleation region may reflect adaptation to the efficient mediation of the conformational change from disk to helix of TMV protein, besides a requirement for binding to the disk, and this may be an important part of the mechanism of specificity in the nucleation of assembly.
利用RNA测序技术研究了装配起始时烟草花叶病毒(TMV)RNA与TMV蛋白质盘状聚集体的相互作用。已鉴定出5′端基团,并表明在装配早期它不受保护,可被核酸酶消化。通过有限装配,源自TMV RNA独特区域的平均长度为250个核苷酸的RNA片段群体被衣壳化,并且有足够的序列信息来识别某些异常特征。受保护区域不包含高度重复的简单重复序列,但可能包含更复杂的重复序列。成核区域的长度和复杂性除了反映与盘状结构结合的需求外,可能还反映了对TMV蛋白质从盘状构象高效介导到螺旋构象变化的适应性,这可能是装配成核特异性机制的重要组成部分。