Pre-early functions of bacteriophage T5 and its relatives

J. Davison
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引用次数: 34

Abstract

Summary Coliphage T5 injects its DNA in 2 steps: the first step transfer (FST) region 7.9% is injected and its genes are expressed and only then does the remainder (second step transfer, SST) of its DNA enter the cell. In the FST region, only 2 essential genes (A1 and A2) have been identified and a third (dmp) non-essential gene codes for a deoxyribonucleotide 5′ monophosphatase. Thirteen additional putative ORFs are present in the FST region. Numerous properties have been attributed to FST region, including SST, host DNA degradation, inhibition of host RNA and protein synthesis, restriction insensitivity and protection of T5 DNA. These effects do not occur following infection with an A1 mutant. The A2 gene seems only to be involved in SST transfer. This is puzzling since there are more seemingly unrelated effects than there are essential genes to accomplish them and it is possible that some important genes were not identified. This review attempts to analyze these problems that were first identified in the 1970–80 s. In particular, an attempt is made to determine which potential ORFs are conserved in evolution (and thus likely to be important); by comparing T5 to 10 newly isolated and completely sequenced T5-like phages. A similar approach is used to identify conserved repeats, inverted repeats and palindromes that occur in all T5-like phages in the region containing the injection stop signal (iss) and the terminase substrate. Finally, an attempt is made to re-analyze the mechanism whereby T5 protects itself from the enzymes that degrade host DNA, from the RecBCD nuclease and from restriction enzymes. For all of these FST effects new hypotheses and possible new genetic and biochemical approaches are envisaged.
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噬菌体T5及其近亲的早期功能
噬菌体T5分两步注射DNA:注射第一步转移(FST)区7.9%,表达基因,然后剩余的DNA(第二步转移,SST)进入细胞。在FST区,仅鉴定出2个必需基因(A1和A2),第三个(dmp)非必需基因编码脱氧核糖核苷酸5 '单磷酸酶。在FST区域还有另外13个假定的orf。FST区域具有许多特性,包括SST、宿主DNA降解、抑制宿主RNA和蛋白质合成、限制性限制不敏感和保护T5 DNA。这些影响在A1突变体感染后不会发生。A2基因似乎只参与SST的转移。这是令人困惑的,因为有更多的看似不相关的影响,而不是必要的基因来完成它们,有可能是一些重要的基因没有被识别出来。本文试图分析这些在1970-80年代首次发现的问题。特别是,试图确定哪些潜在的orf在进化中是保守的(因此可能是重要的);通过比较T5和10个新分离的完全测序的T5样噬菌体。采用类似的方法鉴定所有t5样噬菌体中含有注射停止信号(iss)和终止酶底物区域的保守重复序列、倒置重复序列和回文重复序列。最后,试图重新分析T5保护自身免受降解宿主DNA的酶、RecBCD核酸酶和限制性内切酶的影响的机制。对于所有这些FST效应,设想了新的假设和可能的新的遗传和生化方法。
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