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植物生长调节剂对细胞周期的调控:生长素和细胞分裂素参与矮牵牛原生质体重新进入细胞周期的过程。

Cell cycle regulation by plant growth regulators: involvement of auxin and cytokinin in the re-entry of Petunia protoplasts into the cell cycle.

作者信息

Tréhin C, Planchais S, Glab N, Perennes C, Tregear J, Bergounioux C

机构信息

Institut de Biotechnologie des Plantes, CNRS ERS 569, Université de Paris-Sud, Orsay, France.

出版信息

Planta. 1998 Oct;206(2):215-24. doi: 10.1007/s004250050393.

Abstract

In order to understand the mode of action of auxins and cytokinins in the induction of cell division, the effects of the two plant growth regulators 2,4-dichlorophenoxyacetic acid (2,4-D) and N6-benzyladenine (BA) were investigated using mesophyll protoplasts of Petunia hybrida, cultivated in either complete medium or in medium deficient in cytokinin, auxin or both. Firstly we studied DNA synthesis, using 5-bromodeoxyuridine/bisbenzimide Hoechst/propidium iodide flow cytometry analyses and by the monitoring of histone H4 transcript levels. Roscovitine, a cyclin-dependent kinase (CDK) inhibitor, was found to block the cell cycle prior to entry into the S and M phases in the cultured P. hybrida protoplasts. This suggests that in Petunia cell there is a requirement for CDK activity in order to complete the G1 and G2 phases. Further experiments using roscovitine showed that neither 2,4-D nor BA were individually able to induce cell cycle progression beyond the roscovitine G1 arrest. We also monitored the phytohormonal induction of S phase by studying variations in transcript levels of the gene for mitogenactivated protein kinase (PMEK1) and transcript levels of the cell division cycle gene cdc2Pet. Only 2,4-D, and not BA, was able to stimulate PMEK1 gene transcription; thus, the more rapid S-phase induction in 2,4-D-treated protoplasts may be attributable to the activation of this transduction pathway. In contrast, both plant growth regulators were required to induce the appearance of cdc2Pet mRNA transcripts prior to S-phase engagement.

摘要

为了了解生长素和细胞分裂素在诱导细胞分裂中的作用模式,我们使用矮牵牛的叶肉原生质体研究了两种植物生长调节剂2,4-二氯苯氧乙酸(2,4-D)和N⁶-苄基腺嘌呤(BA)的作用,这些原生质体在完全培养基或缺乏细胞分裂素、生长素或两者的培养基中培养。首先,我们使用5-溴脱氧尿苷/双苯并咪唑Hoechst/碘化丙啶流式细胞术分析并通过监测组蛋白H4转录水平来研究DNA合成。发现细胞周期蛋白依赖性激酶(CDK)抑制剂roscovitine在培养的矮牵牛原生质体进入S期和M期之前阻断细胞周期。这表明在矮牵牛细胞中,为了完成G1期和G2期需要CDK活性。使用roscovitine的进一步实验表明,2,4-D和BA单独都不能诱导细胞周期在roscovitine引起的G1期停滞之后继续进行。我们还通过研究丝裂原活化蛋白激酶(PMEK1)基因的转录水平变化和细胞分裂周期基因cdc2Pet的转录水平来监测S期的植物激素诱导。只有2,4-D能够刺激PMEK1基因转录;因此,在2,4-D处理的原生质体中更快的S期诱导可能归因于该转导途径的激活。相比之下,在进入S期之前,两种植物生长调节剂都需要诱导cdc2Pet mRNA转录本的出现。

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