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一种影响病毒粒子成分的痘苗病毒温度敏感互补组的遗传和分子生物学特性

Genetic and molecular biological characterization of a vaccinia virus temperature-sensitive complementation group affecting a virion component.

作者信息

Fathi Z, Condit R C

机构信息

Department of Biochemistry, State University of New York, Buffalo 14214.

出版信息

Virology. 1991 Mar;181(1):258-72. doi: 10.1016/0042-6822(91)90491-s.

Abstract

The gene affected by five previously isolated temperature-sensitive (ts) mutants (ts 10, ts 18, ts 38, ts 39, ts 44) of vaccinia virus strain WR constituting a single "normal" complementation group has been characterized. Marker rescue and DNA sequence analysis show that the five members of the complementation group map in an open reading frame, ORF 18R, which spans the HindIII I-G junction and has the capacity to encode a 77.6-kDa protein. The nucleotide sequence change responsible for temperature sensitivity in each of the five mutants was determined. Two of the mutants, ts 38 and ts 44, have the identical nucleotide change and may therefore be sisters. Northern blot analysis demonstrates that ORF 18R is transcribed at both early and late times during infection. Two distinct early transcripts have been observed which are 5' coterminal and which contain a 518 nucleotide 5' untranslated region. The long early transcript spans the entire 18R gene while the 3' end of the shorter early transcript maps to an early transcription termination signal contained within the 18R coding sequence. The 5' ends of the late transcripts have been mapped to a family of AUG proximal sites using both S1 nuclease and primer extension analysis. Primer extension analysis also identifies additional late 5' ends which map between nucleotides -500 and -1000 relative to the ORF 18R AUG.

摘要

已对受痘苗病毒WR株的五个先前分离出的温度敏感(ts)突变体(ts 10、ts 18、ts 38、ts 39、ts 44)影响的基因进行了表征,这五个突变体构成一个单一的“正常”互补群。标记拯救和DNA序列分析表明,互补群的五个成员定位于一个开放阅读框ORF 18R中,该阅读框跨越HindIII I-G连接点,有能力编码一种77.6 kDa的蛋白质。确定了五个突变体中每个突变体导致温度敏感性的核苷酸序列变化。其中两个突变体ts 38和ts 44具有相同的核苷酸变化,因此可能是姐妹突变体。Northern印迹分析表明,ORF 18R在感染的早期和晚期均有转录。观察到两种不同的早期转录本,它们5' 端共末端,并且包含一个518个核苷酸的5' 非翻译区。较长的早期转录本跨越整个18R基因,而较短的早期转录本的3' 端定位于18R编码序列内的一个早期转录终止信号。使用S1核酸酶和引物延伸分析,已将晚期转录本的5' 端定位于一个AUG近端位点家族。引物延伸分析还鉴定出了其他晚期5' 端,它们相对于ORF 18R的AUG定位于核苷酸-500至-1000之间。

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