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Functions of the sequences at the ends of the inverted repeats of pseudorabies virus.

机译:伪狂犬病病毒反向重复序列末端的序列功能。

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摘要

Two mutants were constructed to explore the functions of the sequences at the end of the S terminus of pseudorabies virus (PrV). In mutant vYa, 17 bp from the internal inverted repeat, as well as adjacent sequences from the L component, were deleted. In mutant v135/9, 143 bp from the internal inverted repeat (including sequences with homology to the pac-1 site of herpes simplex virus), as well as adjacent sequences from the L component, were deleted. Our aim in constructing these mutants was to ascertain whether equalization of the terminal regions of the S component would occur, whether genome termini that lack either the terminal 17 or 143 bp would be generated as a result of equalization of the repeats (thereby identifying the terminal nucleotides that may include cleavage signals), and whether inversion of the S component would occur (thereby ascertaining the importance of the deleted sequences in this process). The results obtained show the following (i) The removal of the terminal 17 or 143 bp of the internal S component, including the sequences with homology to the pac-1 site, does not affect the inversion of the Us. (ii) The equalization of both the vYa and the v135/9 inverted repeats occurs at high frequency, the terminal repeats being converted and becoming similar to the mutated internal inverted repeat. (iii) Mutants in which the 17 terminal base pairs (vYa) have been replaced by unrelated sequences are viable. However, the 143 terminal base pairs appear to be essential to virus survival; concatemeric v135/9 DNA with equalized, mutant-type, inverted repeats accumulates, but mature virions with such equalized repeats are not generated at high frequency. Since concatemeric DNA missing the 143 bp at both ends of the S component is not cleaved, the terminal 143 bp that include the sequences with homology to the pac-1 site are necessary for efficient cleavage. (iv) v135/9 intracellular DNA is composed mainly of arrays in which one S component (with two equalized inverted repeats both having the deletion) is bracketed by two L components in opposite orientations and in which two L components are in head-to-head alignment.(ABSTRACT TRUNCATED AT 250 WORDS)
机译:构建了两个突变体以探索伪狂犬病病毒(PrV)S末端的序列功能。在突变体vYa中,缺失了来自内部反向重复序列的17bp以及来自L组分的相邻序列。在突变体v135 / 9中,删除了来自内部反向重复序列的143 bp(包括与单纯疱疹病毒pac-1位点具有同源性的序列)以及L成分的相邻序列。我们构建这些突变体的目的是确定是否会发生S组分末端区域的均等化,是否会由于重复序列的均等化而产生缺少末端17或143 bp的基因组末端(从而鉴定末端)。可能包含切割信号的核苷酸),以及是否会发生S成分的倒置(从而确定该过程中缺失序列的重要性)。获得的结果显示以下结果:(i)除去内部S组分的末端17或143bp,包括与pac-1位点具有同源性的序列,不影响Us的倒置。 (ii)vYa和v135 / 9反向重复序列的均等化在高频发生,末端重复序列被转换并变得类似于突变的内部反向重复序列。 (iii)其中17个末端碱基对(vYa)已被无关序列取代的突变体是可行的。但是,143个末端碱基对似乎对病毒生存至关重要。具有均等突变体型,反向重复序列的串联v135 / 9 DNA会积累,但不会等高频率生成具有此类均等重复序列的成熟病毒体。由于没有切割在S组分的两个末端缺失143 bp的连体DNA,因此有效切割需要包含与pac-1位点具有同源性的序列的143 bp末端。 (iv)v135 / 9细胞内DNA主要由以下阵列组成:其中一个S成分(两个相等的反向重复序列均具有缺失)被两个相反方向的L成分包围,并且其中两个L成分从头到尾头部对齐(摘要以250字截断)

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