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杆状病毒极晚期基因表达相关基因vlf-1的鉴定与特性分析

Identification and characterization of vlf-1, a baculovirus gene involved in very late gene expression.

作者信息

McLachlin J R, Miller L K

机构信息

Department of Entomology, University of Georgia, Athens 30602.

出版信息

J Virol. 1994 Dec;68(12):7746-56. doi: 10.1128/JVI.68.12.7746-7756.1994.

Abstract

We have identified a gene required for strong expression of the polyhedrin gene by characterizing a mutant, tsB837, of the baculovirus Autographa californica nuclear polyhedrosis virus (AcMNPV) which is temperature sensitive (ts) for occluded virus production at the nonpermissive temperature. Marker rescue experiments utilizing an overlapping set of AcMNPV genomic clones revealed that the gene responsible for the ts mutant phenotype mapped to a region between 46 and 48 map units. Fragments (2.2 kb) from both wild-type AcMNPV and tsB837 genomes spanning the mutated region were sequenced, and a single nucleotide difference was observed. This mutation is predicted to substitute a single amino acid within a 44.4-kDa polypeptide. Analysis of protein synthesis in wild-type- and mutant-infected cells at the nonpermissive temperature indicated that polyhedrin synthesis was dramatically reduced in the mutant. Northern (RNA) blot analysis revealed that the mutant had markedly reduced levels of polyhedrin transcripts. Transcripts of another very late gene, p10, were also reduced but to a lesser degree. The transcription of two late genes (603 ORF and vp39) was neither reduced nor temporally delayed. Thus, the gene encoding this very late expression factor, designated vlf-1, regulates the levels of very late gene transcripts, and the tsB837 mutation affects the levels of polyhedrin gene transcripts more strongly than those of p10 transcripts. The product of the newly identified gene has a surprising but significant relationship to a family of integrases and resolvases.

摘要

我们通过对杆状病毒苜蓿银纹夜蛾核型多角体病毒(AcMNPV)的一个突变体tsB837进行特性分析,鉴定出了一个对多角体蛋白基因强表达所必需的基因。该突变体在非允许温度下对包涵体病毒的产生具有温度敏感性(ts)。利用一组重叠的AcMNPV基因组克隆进行的标记拯救实验表明,导致ts突变体表型的基因定位于46至48个图距单位之间的区域。对野生型AcMNPV和tsB837基因组跨越突变区域的片段(2.2 kb)进行了测序,发现了一个单核苷酸差异。预计该突变会在一个44.4 kDa的多肽内替换一个氨基酸。在非允许温度下对野生型和突变体感染细胞中的蛋白质合成进行分析表明,突变体中多角体蛋白的合成显著减少。Northern(RNA)印迹分析显示,突变体中多角体蛋白转录本的水平明显降低。另一个极晚期基因p10的转录本也有所减少,但程度较轻。两个晚期基因(603 ORF和vp39)的转录既没有减少也没有出现时间延迟。因此,编码这个极晚期表达因子的基因,命名为vlf-1,调节极晚期基因转录本的水平,并且tsB837突变对多角体蛋白基因转录本水平的影响比对p10转录本的影响更强。新鉴定基因的产物与整合酶和解旋酶家族有着惊人但重要的关系。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7b64/237236/5a8d8d6d7c7c/jvirol00021-0097-a.jpg

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