Braam J, Ulmanen I, Krug R M
Cell. 1983 Sep;34(2):609-18. doi: 10.1016/0092-8674(83)90393-8.
We present a model for the functions and movements of the influenza virus P proteins (PB1, PB2, and PA) as they transcribe the virion RNAs (vRNAs) into messenger RNAs (mRNAs). Using ultraviolet-light-induced crosslinking, we show that the P proteins as a complex move from the 3' ends of the vRNA templates down the elongating mRNAs. PB2 binds the cap 1 structure of heterologous RNAs, which are cleaved to generate capped primer fragments. PB1, initially found at the first residue added onto the primer, moves to the 3' ends of the growing mRNA chains, indicating that it most likely catalyzes each nucleotide addition. PA and PB2 move down the growing chains in concert with PB1. PB2 is also associated with the cap during the first 11-15 nucleotides of chain growth, but then dissociates from the cap as the P protein complex moves further down the mRNA chains.
我们提出了一个关于流感病毒P蛋白(PB1、PB2和PA)功能与运动的模型,这些蛋白在将病毒粒子RNA(vRNA)转录为信使RNA(mRNA)的过程中发挥作用。通过紫外线诱导交联,我们发现P蛋白作为一个复合体从vRNA模板的3'端沿着正在延长的mRNA移动。PB2结合异源RNA的帽1结构,这些异源RNA被切割以产生带帽引物片段。最初在添加到引物上的第一个残基处发现的PB1,移动到正在生长的mRNA链的3'端,这表明它很可能催化每个核苷酸的添加。PA和PB2与PB1协同沿着正在生长的链移动。在链生长的前11 - 15个核苷酸期间,PB2也与帽相关联,但随着P蛋白复合体进一步沿着mRNA链移动,它会从帽上解离。