Schrader A P, Westaway E G
Department of Microbiology, Monash University, Clayton, Victoria, Australia.
Virus Res. 1988 Mar;9(4):323-33. doi: 10.1016/0168-1702(88)90091-3.
Kunjin (KUN) virus-infected cells were synchronized in translation by reversal of hypertonic inhibition; cells were then pulse-labelled with [35S]methionine. Electrophoretic analyses defined the sequence of incorporation of label into all the known KUN gene products shown previously to be unique and unrelated. GP44 or NS1 was inadequately labelled for analysis and was assumed to be translated sequentially after E in the polyprotein sequence. The relationship of the KUN gene order obtained by translation mapping to that proposed by Rice et al. Science (1985) 229, 726-733 based on the nucleotide sequence of yellow fever virus is as follows: KUN: 5'-C.GP20.E.GP44.P19.P10.P71. (?).P21.P98-3' YF: 5'-C.prM.E.NS1.ns2a.ns2b.NS3.ns4a.ns4b. NS5-3'. These results eliminate the ambiguities in identities of the previously hypothetical ns2a, ns2b and ns4b. Although ns4a was not positively identified, a labelled protein of Mr 12,000 to 14,000 was observed in one experiment and it mapped in the appropriate position for ns4a. Variation occurred in translation of NS5 when the hypertonic treatment of 40 min at 37 degrees C was reduced in time or in temperature.
通过逆转高渗抑制作用使感染库京(KUN)病毒的细胞在翻译过程中同步化;然后用[35S]甲硫氨酸对细胞进行脉冲标记。电泳分析确定了标记掺入所有先前显示为独特且不相关的已知KUN基因产物的顺序。GP44或NS1标记不足无法进行分析,推测其在多聚蛋白序列中在E之后依次翻译。通过翻译图谱获得的KUN基因顺序与赖斯等人基于黄热病毒核苷酸序列提出的顺序(《科学》(1985年)229卷,726 - 733页)如下:KUN:5'-C.GP20.E.GP44.P19.P10.P71.(?).P21.P98-3';黄热病毒(YF):5'-C.prM.E.NS1.ns2a.ns2b.NS3.ns4a.ns4b.NS5-3'。这些结果消除了先前假设的ns2a、ns2b和ns4b身份的模糊性。尽管未明确鉴定出ns4a,但在一次实验中观察到一种分子量为12,000至14,000的标记蛋白,其在ns4a的合适位置定位。当37℃下40分钟的高渗处理时间缩短或温度降低时,NS5的翻译出现变化。