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通过标记拯救对温和型芽孢杆菌噬菌体phi 105的原噬菌体和成熟脱氧核糖核酸进行定位

Mapping of prophage and mature deoxyribonucleic acid from temperate Bacillus bacteriophage phi 105 by marker rescue.

作者信息

Armentrout R W, Rutberg L

出版信息

J Virol. 1970 Dec;6(6):760-7. doi: 10.1128/JVI.6.6.760-767.1970.

Abstract

By using temperature-sensitive (ts) and suppressor-sensitive (sus) mutants, 11 essential genes have been identified in phage phi105. The order of the genes has been established in two- and three-factor crosses. The genes can be arranged in a linear order; this order is identical in the vegetative phage and in the prophage. One gene essential for phage deoxyribonucleic acid (DNA) synthesis has been found. Marker rescue from prophage and mature DNA, taken up by competent bacteria, was studied by superinfection with phage carrying one sus and one ts mutation. In prophage DNA, all single markers studied are rescued at similar frequencies. The frequency of co-rescue of two markers is proportional to the recombinational distance between the markers. Thus, colinearity between the genetic map and the position on the DNA molecule of those mutations used to establish the map is demonstrated. The results indicate that the recombination frequencies observed in vegetative crosses are a relative measure of the physical distance between markers. All single markers are not rescued at equal frequencies from mature DNA. The frequency of co-rescue of two markers is related to the recombinational distance only over a distance about one-fourth or less of the genetic map. Markers separated by 10% recombination, or more, are co-rescued at 5 to 10% of the frequency of rescue of single markers. Shearing of mature DNA into half-sized molecules reduces the efficiency by which single markers are rescued by a factor of 5 to 10. The results of experiments on co-rescue of two markers from half-sized mature DNA indicate a preferred break-point near the middle of the genetic map; the results are compatible with a nonpermuted sequence in mature DNA. It is pointed out and discussed that mature DNA exhibits several anomalies in marker rescue experiments.

摘要

通过使用温度敏感(ts)和抑制敏感(sus)突变体,在噬菌体phi105中已鉴定出11个必需基因。这些基因的顺序已在双因子和三因子杂交中确定。这些基因可以按线性顺序排列;该顺序在营养噬菌体和原噬菌体中是相同的。已发现一个对噬菌体脱氧核糖核酸(DNA)合成至关重要的基因。通过用携带一个sus和一个ts突变的噬菌体进行超感染,研究了从原噬菌体和成熟DNA中被感受态细菌摄取的标记拯救。在原噬菌体DNA中,所研究的所有单个标记以相似的频率被拯救。两个标记共同拯救的频率与标记之间的重组距离成正比。因此,证明了遗传图谱与用于构建图谱的那些突变在DNA分子上的位置之间的共线性。结果表明,在营养杂交中观察到的重组频率是标记之间物理距离的相对度量。并非所有单个标记从成熟DNA中被拯救的频率都相等。两个标记共同拯救的频率仅在遗传图谱约四分之一或更小的距离范围内与重组距离相关。重组率为10%或更高的标记共同拯救的频率为单个标记拯救频率的5%至10%。将成熟DNA剪切成半大小的分子会使单个标记被拯救的效率降低5至10倍。从半大小的成熟DNA中对两个标记进行共同拯救的实验结果表明,在遗传图谱中间附近有一个优先的断点;结果与成熟DNA中的非置换序列一致。文中指出并讨论了成熟DNA在标记拯救实验中表现出的几个异常现象。

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