Munkres K D
Mech Ageing Dev. 1979 May;10(3-4):249-60. doi: 10.1016/0047-6374(79)90039-3.
Ferrous ions were highly lethal and mutagenic to germinated conidia of Neurospora crassa. At comparable survival, treatment with 0.2 mM ferrous ions was 14- and 50-fold more mutagenic than ultra-violet irradiation or X-rays, respectively, in the reversion of an inositol auxotroph. Ascorbic acid alone (2 mM) was not reproducibly lethal and inhibited both the lethality and mutagenicity of ferrous ions. Bovine superoxide dismutase (SOD) completely inhibited the residual lethality of ferrous ascorbate. Protection by ascorbic acid and SOD indicates that superoxide radicals, generated by oxidation of Fe(II), are directly or indirectly mutagenic and lethal. Malondialdehyde (MDA) was lethal and appeared to be mutagenic; however, its action is probably different from that of superoxide. Therefore, superoxide-mediated production of endogenous MDA by way of peroxidation of polyunsaturated fatty acids is probably not an alternate mutagenic pathway, at least in the reversion of the allele of the inl locus examined. These results and the demonstration of superoxide-mediated decrease in the synthetic fidelity of DNA polymerase in vitro (Rana and Munkres, in preparation) warrant additional exploration of the hypothesis that endogenous cellular free radicals, generated by pre- and post-senescent metabolism, may enter into lethal and mutagenic reactions.
亚铁离子对粗糙脉孢菌的萌发分生孢子具有高度致死性和诱变性。在可比存活率下,在肌醇营养缺陷型回复突变中,用0.2 mM亚铁离子处理的诱变性分别比紫外线照射或X射线高14倍和50倍。单独的抗坏血酸(2 mM)没有可重复的致死性,并且抑制了亚铁离子的致死性和诱变性。牛超氧化物歧化酶(SOD)完全抑制了抗坏血酸亚铁的残余致死性。抗坏血酸和SOD的保护作用表明,由Fe(II)氧化产生的超氧自由基直接或间接具有诱变性和致死性。丙二醛(MDA)具有致死性,似乎也具有诱变性;然而,其作用可能与超氧自由基不同。因此,至少在所检测到的inl基因座等位基因的回复突变中,通过多不饱和脂肪酸过氧化作用由超氧自由基介导的内源性MDA产生可能不是一种替代的诱变途径。这些结果以及体外超氧自由基介导的DNA聚合酶合成保真度降低的证明(Rana和Munkres,正在准备中),使得有必要进一步探索这样一种假说,即衰老前后代谢产生的内源性细胞自由基可能参与致死性和诱变性反应。