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首页> 外文期刊>plant and cell physiology >Induction of DNA synthesis and callus formation from tuber tissue of Jerusalem artichoke by 2,4-dichlorophenoxyacetic acid
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Induction of DNA synthesis and callus formation from tuber tissue of Jerusalem artichoke by 2,4-dichlorophenoxyacetic acid

机译:2,4-二氯苯氧乙酸诱导菊芋块茎组织DNA合成和愈伤组织形成

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Cellus induction was observed from Jerusalem artichoke tuber tissue on a synthetic medium containing 2,4-D at 10−6, 10−5(optimum conc.) and 10−4M. The first DNA synthesis (thymidine incorporation) was observed only at 2,4-D concentrations of 10−5to 10−4M. In 10−5M2,4-D treated tissue, DNA synthesis increased after a 20 hr lag and reached a maximum at 36 hr, after which it decreased. Actinomycin D and 8-aza-guanine; inhibitors of RNA synthesis, inhibited DNA synthesis completely. 2,4-D caused the characteristic changes in RNA and protein syntheses. In comparison with the control, RNA and protein syntheses were first repressed then induced before the peak of DNA synthesis. Treatment with cycloheximide (10−4M) for one hour before inoculation inhibited protein synthesis completely for 12 hr; consequently DNA synthesis was also delayed. The results suggest that RNA and protein syntheses needed for callus induction are regulated by 2,4-D in the first
机译:在含有 10−6、10−5(最佳浓度)和 10−4M 的 2,4-D 的合成培养基上观察到菊芋块茎组织的 cellus 诱导。仅在10-5至10-4M的2,4-D浓度下观察到第一次DNA合成(胸苷掺入)。在10−5M2,4-D处理的组织中,DNA合成在滞后20小时后增加,在36小时时达到最大值,之后减少。放线菌素D和8-氮杂鸟嘌呤;RNA合成抑制剂,完全抑制DNA合成。2,4-D引起RNA和蛋白质合成的特征性变化。与对照组相比,RNA和蛋白质合成首先被抑制,然后在DNA合成达到峰值之前被诱导。接种前用环己酰亚胺(10-4M)处理1小时完全抑制蛋白质合成12小时;因此,DNA合成也被推迟了。结果表明,愈伤组织诱导所需的RNA和蛋白质合成首先受2,4-D调控

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