共查询到19条相似文献,搜索用时 62 毫秒
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高等植物通过调节顶端分生组织和侧生分生组织的活性建立地上株型系统, 分生组织的活性受环境信号、发育阶段和遗传因素的综合调控, 植物激素参与这些信号的整合。顶端优势是植物分枝调控的核心问题, 而生长素对顶端优势的形成和维持发挥关键作用。本文综述了近几年与植物地上部分株型形成相关的生长素合成代谢、极性运输及信号转导领域的研究进展, 并提出了展望。 相似文献
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生长素的极性运输及其在植物发育调控中的作用 总被引:6,自引:0,他引:6
生长素是已知的植物激素中唯一具有极性运输方式的激素。利用生长素极性运输抑制物和生长素极性运输突变体,使人们获得大量有关生长素及其极性运输在植物生长发育调控中具有重要作用的资料。与生长素极性运输有关的基因的克隆及其表达调控的研究将进而在分子水平上阐明其作用的机理。 相似文献
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生长素信号转导研究进展 总被引:11,自引:0,他引:11
长素的信号转导是一个复杂的网络系统,在信号的感知上,除了存在ABPI介导的膜上感知途径外,还有其他的感知途径。G蛋白参与诱导生长素信号的胞内传递,生长素信号转导的第二信使包括离子型第二信使、磷酯酶A2、脂活化蛋白激酶、MAPK和PINOIND等。AUX/IAA蛋白的泛素化降解在生长素反应中发挥关键性作用,ARF和AUX/IAA蛋白相互作用调节生长素响应基因的转录。 相似文献
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植物生长素极性运输调控机理的研究进展 总被引:7,自引:2,他引:5
生长素极性运输特异地调控植物器官发生、发育和向性反应等生理过程。本文综述和分析了生长素极性运输的调控机制。分子遗传和生理学研究证明极性运输这一过程是由生长素输入载体和输出载体活性控制的。小G蛋白ARF附属蛋白GEF和GAP分别调控输出载体(PINI)和输入载体(AUX1)的定位和活性。并影响高尔基体等介导的细胞囊泡运输系统,小G蛋白ROP也参与输出载体PIN2活性的调节。本文基于作者的研究工作提出小G蛋白在调控生长素极性运输中的可能作用模式。 相似文献
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植物生长素极性运输调控机理的研究进展 总被引:1,自引:0,他引:1
生长素极性运输特异地调控植物器官发生、发育和向性反应等生理过程。本文综述和分析了生长素极性运输的调控机制。分子遗传和生理学研究证明极性运输这一过程是由生长素输入载体和输出载体活性控制的。小G蛋白ARF附属蛋白GEF和GAP分别调控输出载体(PIN1)和输入载体(AUX1)的定位和活性, 并影响高尔基体等介导的细胞囊泡运输系统, 小G蛋白ROP也参与输出载体PIN2活性的调节。本
文基于作者的研究工作提出小G蛋白在调控生长素极性运输中的可能作用模式。 相似文献
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生长素极性运输机理的研究现状朱广廉(北京大学生命科学院100871)1932年温特(Went,F.W.)用燕麦胚芽鞘切段进行的有关生长素运输的经典实验,发现生长素在胚芽鞘节段内的传导具有极性,即只能从其形态学的顶端向基部移动,被后人称为极性运输。现在... 相似文献
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生长素信号调控植物生长发育的各个方面。该文综述了生长素信号在植物根尖的研究进展概况,从生长素在根尖的运输与分布、生长素信号对根尖细胞命运的影响及静止中心细胞的生长素信号研究三个方面进行了阐述,并对未来该领域的研究方向进行了展望。 相似文献
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双子叶植物种子在土壤中萌发后,其下胚轴顶端会形成弯钩的特化结构,保护子叶和顶端分生组织在破土过程中不受土壤机械力的破坏,保证幼苗顺利破土.顶端弯钩的发育过程分为弯钩形成、维持及打开3个阶段,其核心在于内外两侧细胞的差异性生长导致弯钩结构.近年来研究表明,植物激素及环境信号对顶端弯钩发育各个过程起着至关重要的调控作用.然... 相似文献
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生长素极性运输研究进展 总被引:25,自引:0,他引:25
高等植物的生长发育受激素的广泛调控,其中生长素的作用尤为独特,因为生长素在植物组织内的浓度梯度是由其极性运输维持的,而正是激素在植物组织的相对含量决定了该组织的发育命运。高等植物体内存在可运输的化学信使的概念首先由Darwin父子提出。通过对金丝鸟木亡草(Phalarisca nariensis)幼苗的向光性的研究,他们认为植物的向光性受到一种可运输的物质的调控[1]。后来发现这一物质是生长素,在自然界中主要存在的形式是IAA。到本世纪 30年代,禾谷类植物中的生长素的极性运输得到证实,后来发现所有… 相似文献
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生长素极性运输研究进展 总被引:2,自引:0,他引:2
Recent advances in dissecting polar auxin transport, i.e., the physiological characteristics and regulation of polar auxin transport, the chemiosmotic hypothesis for polar auxin transport, and the role of polar auxin transport in plant growth and development were reviewed. The authors here focus on the progress of new supports-isolation and function analysis of the genes encoding putative auxin carriers, for the old model of polar auxin transport. 相似文献
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Experiments were performed on the first and second internodes and 4-cm-long apical segments of main roots of pea (Pisum sativum L.) seedlings, grown in the light and decapitated above the second node on the seventh day after seed germination. Endogenous phytohormones were measured by the enzyme-linked immunosorbent assay during three days after decapitation of seedlings. The IAA level in the internodes decreased 2–3 times on the second day after decapitation of seedlings while the cytokinin level increased 5–6 times for zeatin and zeatin riboside (Z and ZR) and 1.5–2 times for isopentenyl adenine and isopentenyl adenosine (IP and IPA). In contrast to internodes, the IP and IPA contents in the roots of decapitated seedlings did not change, but the levels of Z and ZR increased 1.5–2 times compared to intact plant roots. The IAA level in the apical region of root remained almost unchanged after the removal of shoot apex. It was concluded that the apical meristem of the main root is not the site of the cytokinin response to the auxin signal coming from the stem apex and that a slight accumulation of Z and ZR after decapitation is due to upper zones of the root. There was no difference in the content of gibberellin-like substances between the internodes of intact and decapitated seedlings. However, the content of gibberellins (GA) in the root tip decreased after decapitation of seedling, which suggests an essential role of apical bud in supplying the root with GA and/or intermediates for their biosynthesis. 相似文献
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The study of transgenic plants has greatly advanced our understanding of the control of development and metabolism. The ability to isolate and modify genes greatly extends the range of what is technically feasible. In the area of hormone biology, transgenic plants have helped to elucidate the pathways of synthesis, the metabolic control points, and the biological functions of the various phytohormones. This review covers the available genes that modulate the metabolism and perception of the phytohormones. One of the most significant conclusions coming out of transgenic plant work is the complex interaction among the different classes of phytohormones. For example, increasing the level of the auxin indole-3-acetic acid (IAA) in a plant has the secondary effect of inducing ethylene biosynthesis. This complication can be circumvented by combining transgenic plants modulating multiple hormones or through the use of available mutants. In this manner, transgenic plants have been utilized to unambiguously define the roles of auxin, cytokinin, and ethylene in the control of apical dominance. The power of transgenic plants as tools in hormone biology is perhaps best illustrated by work on ethylene. In this case, the modular characterization of genes led to elucidation of the biosynthetic pathway. Availability of the biosynthetic genes has permitted detailed analysis of the regulation of synthesis, definition of the role of ethylene in the control of several developmental processes, and the application of that knowledge for agricultural improvement. 相似文献