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诱变剂4-硝基喹啉1-氧化物对盘基网柄菌孢子萌发的阶段特异性抑制作用

The stage specific inhibition of Dictyostelium discoideum spore germination by the mutagen 4-nitroquinoline 1-oxide.

作者信息

Hamer J E, Cotter D A, Demsar I H

出版信息

Chem Biol Interact. 1984 Jan;48(1):1-14. doi: 10.1016/0009-2797(84)90002-4.

DOI:10.1016/0009-2797(84)90002-4
PMID:6420082
Abstract

The drug 4-nitroquinoline 1-oxide (4NQO) is a potent inhibitor of Dictyostelium discoideum spore germination. This inexpensive, water soluble drug is active at a concentration of 5 micrograms/ml (26 microM) and permeates the spore at all stages in germination. Spores subjected to 4NQO treatment exhibit an irreversible blockage of myxamoebae emergence, but spore activation, post-activation lag, and swelling are not affected. Swollen 4NQO-treated spores lose the outer two spore walls but lack the ability to degrade the innermost wall. The drug does not affect oxygen uptake during post-activation lag or swelling, and only a stage specific depression in O2 uptake is observed when control spores begin to release myxamoebae. When added early in germination, 4NQO blocks the incorporation of [3H] uracil into a cold trichloroacetic acid (TCA) insoluble fraction by 98%. However, when the drug is added midway through germination and followed by a pulse labelling period of 1 h, only 65% inhibition of RNA synthesis is observed. This lack of complete inhibition may occur because the drug requires metabolic activation; thus, new rounds of RNA synthesis may have initiated before the drug became fully activated. 4NQO also blocks the de novo expression of beta-glucosidase activity when added early in germination. Additionally, we observe that vegetative cellular slime mold cells are 100 times more resistant than spores to 4NQO-induced damage. Taken together, our results support the observation that RNA synthesis is only required for the emergence stage of germination and that dormant D. discoideum spores may lack efficient excision repair mechanisms.

摘要

药物4-硝基喹啉1-氧化物(4NQO)是盘基网柄菌孢子萌发的有效抑制剂。这种价格低廉、水溶性的药物在浓度为5微克/毫升(26微摩尔)时具有活性,并且在萌发的各个阶段都能渗透到孢子中。经过4NQO处理的孢子表现出变形虫出现的不可逆阻断,但孢子激活、激活后延迟和肿胀不受影响。经4NQO处理的肿胀孢子失去了外层的两层孢子壁,但缺乏降解最内层壁的能力。该药物在激活后延迟或肿胀期间不影响氧气摄取,只有在对照孢子开始释放变形虫时才观察到氧气摄取的阶段特异性降低。在萌发早期添加4NQO时,它会使[3H]尿嘧啶掺入冷三氯乙酸(TCA)不溶性部分的量减少98%。然而,当在萌发中期添加该药物并随后进行1小时的脉冲标记期时,仅观察到RNA合成受到65%的抑制。这种不完全抑制可能是因为该药物需要代谢激活;因此,在药物完全激活之前可能已经启动了新一轮的RNA合成。在萌发早期添加4NQO时,它还会阻断β-葡萄糖苷酶活性的从头表达。此外,我们观察到营养型细胞黏菌细胞对4NQO诱导的损伤的抗性比孢子高100倍。综上所述,我们的结果支持以下观察结果:RNA合成仅在萌发的出现阶段是必需的,并且休眠的盘基网柄菌孢子可能缺乏有效的切除修复机制。

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