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诱导马铃薯切片 DNA 合成:蛋白质合成的作用。

Induction of deoxyribonucleic Acid synthesis in potato tuber slices: role of protein synthesis.

机构信息

Institute for Biochemical Regulation, Faculty of Agriculture, Nagoya University, Chikusa-ku, Nagoya, Japan.

出版信息

Plant Physiol. 1976 Apr;57(4):568-71. doi: 10.1104/pp.57.4.568.

Abstract

Timing of protein synthesis which is a prerequisite to DNA synthesis induced in potato tuber tissue (Solanum tuberosum L.) by cut injury has been studied using cycloheximide. The induction of DNA synthesis which was measured by incorporation of (3)H-thymidine was completely inhibited when the inhibitor was applied to the tuber discs immediately after slicing. When the application of cycloheximide was delayed for 6 hours or more after slicing, DNA synthesis was observed but its rate was reduced to 20% of control. The inhibitory effect of cycloheximide, however, rapidly decreased when the inhibitor was applied at 6 or less hours immediately prior to determination of DNA synthesis. The effect of cycloheximide on the incorporation of (14)C-leucine suggests that the change in the effect of cycloheximide on the induction of DNA synthesis is not due to incomplete inhibition of protein synthesis. Cycloheximide did not have significant effects on either uptake or phosphorylation of (3)H-thymidine in the discs. Inhibition of both protein and DNA synthesis by cycloheximide was reversed by washing and further incubation of the discs. Almost no qualitative difference was detected by buoyant density analysis between DNA formed under inhibition of protein synthesis of the later stage and DNA synthesized under normal conditions. These results suggest that DNA synthesis induced in potato tuber tissue by cut injury requires continuous synthesis of new protein molecules in a characteristically programmed sequence.

摘要

利用环己亚胺研究了由切割损伤诱导的马铃薯块茎组织(Solanum tuberosum L.)中 DNA 合成的蛋白质合成的时间,这是 DNA 合成的先决条件。通过(3)H-胸腺嘧啶的掺入测量 DNA 合成的诱导,当抑制剂在切割后立即施加到块茎圆盘上时,完全抑制了 DNA 合成的诱导。当在切割后 6 小时或更长时间延迟施加环己亚胺时,观察到 DNA 合成,但合成率降低至对照的 20%。然而,当在 6 小时或更短时间之前立即施加抑制剂以确定 DNA 合成时,环己亚胺的抑制作用迅速降低。环己亚胺对(14)C-亮氨酸掺入的影响表明,环己亚胺对 DNA 合成诱导的作用的变化不是由于蛋白质合成的不完全抑制所致。环己亚胺对圆盘中(3)H-胸腺嘧啶的摄取或磷酸化均没有显着影响。环己亚胺对蛋白质和 DNA 合成的抑制作用可通过洗涤和进一步孵育圆盘来逆转。在抑制蛋白质合成的后期形成的 DNA 和在正常条件下合成的 DNA 之间,通过浮力密度分析几乎未检测到定性差异。这些结果表明,由切割损伤诱导的马铃薯块茎组织中的 DNA 合成需要新的蛋白质分子在特征性编程序列中连续合成。

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