DNA breakage, repair, and lethality accompanying 125I decay in microorganisms.

R E Krisch, F Krasin, C J Sauri
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Abstract

Effects of 125I decay in DNA were investigated by measurements of strand breaks and lethal efficiencies of the decays. In bacteriophages T1 and T4, local decay effects were compared with effects of the emitted electrons by induction of both single (ssb) and double strand breaks (dsb) in the intact phage head and in extended free state DNA. Most dsbs were found to result from local decay effects whereas most real ssbs are caused by the electrons. A simple one-to-one relationship seems to exist in the phages between the decays of 125I, numbers of dsbs and lethal effects. In E. coli rec+ and recA repair of dsbs was studied in addition to lethal decay efficiencies. In rec+ more than 70% of the dsbs were repaired within 1 h at 37 degrees C. No repair was observed in recA. The probability of lethality per 125I decay per completed genome was found to be 0.37 for rec+ and 0.93 for recA cells. The number of lethal events per unrepaired dsb was found to be practically equal to unity. Unrepaired dsbs thus seem to be the primary mechanism of lethality caused by 125I decay, and all unrepaired dsbs seem to be lethal.

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微生物中伴随125I衰变的DNA断裂、修复和致死。
125I衰变在DNA中的影响通过测量链断裂和衰变的致死效率来研究。在T1和T4噬菌体中,比较了在完整噬菌体头部和延伸自由状态DNA中诱导单链断裂(ssb)和双链断裂(dsb)发射电子的局部衰减效应。大多数的dsbs被发现是由局部衰变效应引起的,而大多数真正的ssbs是由电子引起的。在噬菌体中,125I的衰变、dsb的数量和致死效应之间似乎存在着简单的一对一关系。在大肠杆菌中,除了致命的衰变效率外,还研究了recA和recA对dsbs的修复。在recA +中,超过70%的dsb在37℃下1小时内修复。发现rec+细胞每完成基因组每125I衰变的致死率为0.37,recA细胞为0.93。每个未修复的dsb的致命事件数量几乎等于1。因此,未修复的dsb似乎是由125I衰变引起的主要致死机制,所有未修复的dsb似乎都是致命的。
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