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猿猴轮状病毒SA11温度敏感突变体A、C、F和G组对基因组片段的分配

Assignment of simian rotavirus SA11 temperature-sensitive mutant groups A, C, F, and G to genome segments.

作者信息

Gombold J L, Ramig R F

机构信息

Department of Virology, Baylor College of Medicine, Houston, Texas 77030.

出版信息

Virology. 1987 Dec;161(2):463-73. doi: 10.1016/0042-6822(87)90140-1.

Abstract

Crosses were performed between prototype temperature-sensitive (ts) mutants of simian rotavirus SA11 representing reassortment groups A, C, F, and G and ts mutants of rhesus rotavirus RRV that belonged to different reassortment groups. Wild-type (ts+) reassortant progeny were identified by plaque formation at nonpermissive temperature (39 degrees), picked, and grown to high titer. The ts+ phenotype of the resulting progeny clones was verified by titration at 39 degrees and 31 degrees. The electropherotypes of the ts+ clones were determined by electrophoresis, and parental origin of each genome segment was assigned by comparison of segment mobility to parental markers. Analysis of the parental origin of genome segments in the ts+ reassortants derived from SA11 ts X RRV ts crosses revealed the following map locations of the SA11 prototype ts mutants: tsA(778), segment 4; tsC(606), segment 1; tsF(2124), segment 2; and tsG(2130), segment 6. The assignment of tsA was made on the basis of genome segment segregation in two independent crosses with each of two independent RRV ts mutants. The assignment of tsC was made on the basis of segregation in only a single cross with an RRV ts mutant; however, a larger number of progeny clones were examined from this cross. The lesion of tsF was mapped with data from three independent crosses using two different RRV ts mutants. The assignment of tsG was made on the basis of segregation in three independent crosses, two with RRV ts mutants and one with Wa. The assignments of tsA, tsC, and tsF were confirmed in crosses between RRV ts mutants representing those reassortment groups, and SA11 ts mutants in other reassortment groups.

摘要

将代表重配组A、C、F和G的猿猴轮状病毒SA11的原型温度敏感(ts)突变体与属于不同重配组的恒河猴轮状病毒RRV的ts突变体进行杂交。通过在非允许温度(39℃)下形成噬斑来鉴定野生型(ts +)重配后代,挑选出来并培养至高滴度。通过在39℃和31℃下滴定来验证所得后代克隆的ts +表型。通过电泳确定ts +克隆的电泳图谱类型,并通过将片段迁移率与亲本标记进行比较来确定每个基因组片段的亲本来源。对源自SA11 ts×RRV ts杂交的ts +重配体中基因组片段的亲本来源分析揭示了SA11原型ts突变体的以下图谱位置:tsA(778),第4节段;tsC(606),第1节段;tsF(2124),第2节段;和tsG(2130),第6节段。tsA的定位是基于与两个独立的RRV ts突变体中的每一个进行的两个独立杂交中的基因组片段分离。tsC的定位仅基于与一个RRV ts突变体的单次杂交中的分离;然而,从这次杂交中检查了大量的后代克隆。使用两个不同的RRV ts突变体,通过三个独立杂交的数据绘制了tsF的损伤图谱。tsG的定位是基于三个独立杂交中的分离,两个与RRV ts突变体杂交,一个与Wa杂交。在代表那些重配组的RRV ts突变体与其他重配组中的SA11 ts突变体之间的杂交中,证实了tsA、tsC和tsF的定位。

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