Ghendon Y Z, Markushin S G, Klimov A I, Hay A J
J Gen Virol. 1982 Nov;63 (Pt 1):103-11. doi: 10.1099/0022-1317-63-1-103.
Two fowl plague virus temperature-sensitive (ts) mutants belonging to different complementation groups were studied. Both were defective in the syntheses of unpolyadenylated complementary RNA [A(-)cRNA] and virus RNA (vRNA) at non-permissive temperature whereas primary transcription was unaffected. In addition, ts 29, in which the ts mutation is in gene 1 coding for polypeptide P3, has a defect in 'secondary' synthesis of mRNA at non-permissive temperature whereas inhibition of mRNA synthesis by ts 131, in which the ts mutation is in gene 2 coding for polypeptide P1, appeared to result from a defect in vRNA synthesis. These results indicate, therefore, that different enzymes are responsible for the syntheses of virus mRNAs and A(-)cRNAs, which is consistent with the apparent differences in initiation and termination of transcription in the two reactions. The patterns of synthesis of the various types of virus RNA during infection are discussed.
研究了属于不同互补群的两种禽瘟病毒温度敏感(ts)突变体。在非允许温度下,两者在非聚腺苷酸化互补RNA [A(-)cRNA]和病毒RNA(vRNA)的合成中均存在缺陷,而初级转录不受影响。此外,ts29的ts突变位于编码多肽P3的基因1中,在非允许温度下mRNA的“二级”合成存在缺陷,而ts131(其ts突变位于编码多肽P1的基因2中)对mRNA合成的抑制似乎是由vRNA合成缺陷导致的。因此,这些结果表明,不同的酶负责病毒mRNA和A(-)cRNA的合成,这与两种反应中转录起始和终止的明显差异一致。文中还讨论了感染过程中各种病毒RNA的合成模式。