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拓扑异构酶II以及其他DNA延迟和DNA阻滞突变在体内和体外都会损害噬菌体T4的DNA包装。

Topoisomerase II and other DNA-delay and DNA-arrest mutations impair bacteriophage T4 DNA packaging in vivo and in vitro.

作者信息

Zachary A, Black L W

出版信息

J Virol. 1986 Oct;60(1):97-104. doi: 10.1128/JVI.60.1.97-104.1986.

Abstract

A survey of DNA packaging in vivo and in vitro during infections caused by T4 DNA-delay and DNA-arrest amber mutants revealed a common DNA packaging-deficient phenotype. Electron microscopy revealed high proportions of proheads partially filled with DNA in vivo, indicating normal initiation but incomplete encapsidation. In contrast, exogenous mature T4 DNA was packaged in vitro by several early-gene mutant extracts. Detailed analysis of gene ts39 mutants (subunit of topoisomerase II) showed that in vivo packaging is defective, yet expression of late proteins appeared normal and the concatemeric DNA was not abnormally short or nicked. Although g39 amber mutant extracts packaged DNA in vitro, two of three ts39 mutant extracts prevented encapsidation of the exogenous DNA. The temperature-sensitive (ts) gp39 in a mutant topoisomerase II complex may have interfered with packaging in vivo and in vitro by interacting with DNA in an anomalous fashion, rendering it unfit for encapsidation. These results support the hypothesis that T4 DNA packaging is sensitive to DNA structure and discriminates against encapsidation of some types of defective DNA.

摘要

对T4 DNA延迟和DNA阻滞琥珀突变体引起的感染过程中体内和体外DNA包装的一项调查揭示了一种常见的DNA包装缺陷表型。电子显微镜显示,体内有高比例的原头部部分填充有DNA,表明起始正常但衣壳化不完全。相比之下,几种早期基因突变体提取物在体外能包装外源成熟T4 DNA。对基因ts39突变体(拓扑异构酶II亚基)的详细分析表明,体内包装存在缺陷,但晚期蛋白质的表达看起来正常,并且串联体DNA没有异常短或有切口。尽管g39琥珀突变体提取物在体外能包装DNA,但三个ts39突变体提取物中有两个阻止了外源DNA的衣壳化。突变拓扑异构酶II复合物中的温度敏感型(ts)gp39可能通过以异常方式与DNA相互作用而干扰了体内和体外的包装,使其不适合衣壳化。这些结果支持了这样的假说,即T4 DNA包装对DNA结构敏感,并能区分某些类型的缺陷DNA的衣壳化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7af1/253906/0394b96f0d2e/jvirol00104-0107-a.jpg

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