生长素在微生物调控根发育过程中的作用

很多微生物通过分泌生长素和生长素前体与植物建立了有益的关系并改变植物根系的形态结构,此外,微生物分泌的其他代谢产物也能改变植物生长素信号通路。因此,生长素和生长素信号通路在微生物调控植物根系发育的过程中起着至关重要的作用。该文从生长素合成、生长素信号和生长素极性运输3个方面总结了生长素在微生物调控植物根系发育过程中的作用,主要包括微生物增加了植物内源生长素的含量、增强了生长素的信号和调控PIN蛋白的表达水平,进而如何调控植物生理和分子水平来适应微生物对其根系的改变,为进一步开展该方面的研究奠定了基础。     

Root formation in pea cuttings: Effects of combined application of auxin and cytokinin at different developmental stages

Cuttings of pea cv. Alaska and ov. Kelwo were both decapitated and disbudded at different time intervals after cutting. Auxin and cytokinin combined in different ratios were applied to the upper part of the decapitated and disbudded cuttings. The effects of different ratios of auxin and cytokinin were not the same when applied at different developmental stages of the root initiation phase. The results seem to demonstrate an interaction between auxin and cytokinin at different ratios throughout the root initiation phase. The effects of combined application of auxin and cytokinin suggest that different stages of the root initiation phase require different levels of auxin and cytokinin. A higher level of auxin and either lower or equal level of cytokinin may be needed only in the early stages. During the subsequent stages a lower level of auxin in combination with a higher level of cytokinin seems to be more conducive.     

丛枝菌根真菌、磷和生长素对枳侧根形成的调控效应

为探讨丛枝菌根真菌(AMF)、磷水平和生长素对植物侧根形成的影响,在两种磷水平下接种AMF(Rhizophagus irregularis BGC JX04B),施用IBA、生长素运输抑制剂(TIBA),观察AMF、磷水平和生长素对枳Poncirus trifoliata幼苗侧根形成的调控效应。结果表明,AMF对植株生物量及各级侧根数量无显著影响,但显著降低一级侧根长度;磷水平对植株生物量、侧根数量及长度无显著影响;TIBA显著降低植株生物量、侧根数量和侧根长度,而IBA对各项指标无显著影响。AMF和生长素对主根长度的影响存在显著互作;AMF、磷水平和生长素对二级和三级侧根数量的影响存在显著互作。因此,AMF对枳侧根形成的调控可能涉及生长素信号途径,而生长素运输是枳侧根形成的关键因素。     

The role of auxins in somatic embryogenesis of <Emphasis Type="Italic">Abies alba</Emphasis>

The somatic embryogenesis of conifers is a process susceptible to exogenous phytohormonal treatments. We report the effects of the synthetic auxin 2,4-dichlorophenoxyacetic acid (2,4-D) and the auxin inhibitor p-chlorophenoxyisobutyric acid (PCIB) on the endogenous level of the auxin indole-3-acetic acid (IAA) and on the anatomical composition of early somatic embryos of Abies alba (European silver fir). The embryogenic suspensor mass (ESM) of Abies alba proliferated on a medium supplemented by 2,4-D as well as on an auxin-free medium. The endogenous level of IAA was significantly higher in the ESM cultivated on a medium supplemented by 2,4-D. The decrease in the endogenous level of IAA in the first week of maturation is one of the most important stimuli responsible for the subsequent development of embryos. However, suppression of IAA synthesis by an auxin inhibitor did not stimulate the development of embryos. The maturation of somatic embryos from the globular to the cotyledonary stage occurs when the concentration of endogenous auxin in the ESM (including the embryos) increases. Early somatic embryos proliferating on a medium supplemented by auxin had an increased probability of maturing successfully. Exogenous auxin treatment during maturation did not compensate for the auxin deficiency during proliferation.     

SLOW MOTION Is Required for Within-Plant Auxin Homeostasis and Normal Timing of Lateral Organ Initiation at the Shoot Meristem in Arabidopsis

The regular arrangement of leaves and flowers around a plant''s stem is a fascinating expression of biological pattern formation. Based on current models, the spacing of lateral shoot organs is determined by transient local auxin maxima generated by polar auxin transport, with existing primordia draining auxin from their vicinity to restrict organ formation close by. It is unclear whether this mechanism encodes not only spatial information but also temporal information about the plastochron (i.e., the interval between the formation of successive primordia). Here, we identify the Arabidopsis thaliana F-box protein SLOW MOTION (SLOMO) as being required for a normal plastochron. SLOMO interacts genetically with components of polar auxin transport, and mutant shoot apices contain less free auxin. However, this reduced auxin level at the shoot apex is not due to increased polar auxin transport down the stem, suggesting that it results from reduced synthesis. Independently reducing the free auxin level in plants causes a similar lengthening of the plastochron as seen in slomo mutants, suggesting that the reduced auxin level in slomo mutant shoot apices delays the establishment of the next auxin maximum. SLOMO acts independently of other plastochron regulators, such as ALTERED MERISTEM PROGRAM1 or KLUH/CYP78A5. We propose that SLOMO contributes to auxin homeostasis in the shoot meristem, thus ensuring a normal rate of the formation of auxin maxima and organ initiation.     

'Evidence of an auxin signal pathway, microRNA167-ARF8-GH3, and its response to exogenous auxin in cultured rice cells'

MicroRNA167 (miR167) was shown to cleave auxin responsive factor 8 (ARF8) mRNA in cultured rice cells. MiR167 level was found to be controlled by the presence of auxin in the growth medium. When cells grew in auxin-free medium, miR167 level decreased, resulting in an increase in the level of ARF8 mRNA. Cells growing in the normal growth medium containing auxin showed a reversed trend. It was also shown that expression of OsGH3-2, an rice IAA-conjugating enzyme, was positively regulated by ARF8. Delivery of synthesized miR167 into cells led to decrease of both ARF8 mRNA and OsGH3-2 mRNA. This study provides an evidence in which the exogeneous auxin signal is transduced to OsGH3-2 through miR167 and ARF8 in sequence. This proposed auxin signal transduction pathway, auxin-miR167-ARF8-OsGH3-2, could be, in conjunction with the other microRNA-mediated auxin signals, an important one for responding to exogeneous auxin and for determining the cellular free auxin level which guides appropriate auxin responses.     

Calcium Could Be Involved in Auxin-Regulated Maintenance of the Quiescent Center in the <Emphasis Type="Italic">Arabidopsis</Emphasis> Root

Ca²⁺ transduces hormone and environmental signals to the Ca²⁺ sensors and relays them to the downstream target effectors in cells. During the post-embryonic developmental process, auxin plays a critical role in maintaining the mitotically inactive status of the quiescent center (QC) and the root growth and development that follows. In this report, we demonstrate that Ca²⁺ plays an important role in the maintenance of the QC, probably by regulating PIN1-mediated auxin transport. Perturbation of the intracellular Ca²⁺ levels with chemicals that modify the Ca²⁺ level decreases the endogenous auxin level and the size of the auxin maximum in the root tip and, at the same time, activates QC cell division and expansion. This decreased level of auxin is almost completely restored to the control level by the treatment of exogenous auxin. Interestingly, treatment with Ca²⁺ level modifying chemicals significantly decreased the PIN1 expression in the root vasculature. Taken together, we suggest that balancing Ca²⁺ homeostasis is one of contributing factors in establishing the proper auxin maximum in the root tip and maintaining the QC identity.     

The Interrelation of RNA, Auxin and Auxin-oxidases in Lentil Roots

The correlation between auxin and RNA metabolism was investigated in lentil roots. IAA and NAA both cause a considerable rise in the RNA level of germinating lentil roots, though no effect of IAA was found on the DNA level. In untreated germinating roots various sections were isolated and a direct relation found between RNA and auxin content, and an indirect relation between RNA content and auxin oxidase activity. In excised roots, incubated for 24 hours, the loss of RNA is paralleled by a loss of endogenous auxin. Excised roots treated with 10^?4M IAA or M 10^?4 NAA loose little RNA. The findings suggest that in lentil roots the RNA levels may be controlled by auxin levels, which in turn may be controlled by the levels of auxin oxidase.     

Growth Regulators in Populus tremula

The seasonal variation in capacity to form suckers and in auxin level in bark and wood was determined in root segments of aspen (Populus tremula L.). Auxin occurred in the roots from May to October but not in November. The highest auxin level was found during the period of shoot growth. During this period the capacity of root segments to form suckers was low. Auxin level decreased in isolated root segments during the first 24 hours after excision and was low during the period of sucker induction. The relation of endogenous auxin level to control of sucker formation is discussed. The experiments do not exclude the possibility that the auxin effect is mediated through inhibitors.     

Inhibition of Auxin-induced Deoxyribonucleic Acid Synthesis and Chromatin Activity by 5-Fluorodeoxyuridine in Soybean Hypocotyl

Rootless soybean (Glycine max) seedlings were used as a test system to examine the action of auxin on chromatin-directed RNA synthesis. Chromatin from the basal tissue of rootless seedlings (both control and auxin-treated) had RNA synthetic capacity similar to that of chromatin from comparably treated intact seedlings. When DNA synthesis normally induced in the basal tissue by auxin was blocked in the rootless seedlings by 5-fluorodeoxyuridine, the auxin enhancement of chromatin activity was inhibited 70%. This level was still three times the control level, indicating that auxin influenced the synthetic activity of existing DNA template. Experiments with Escherichia coli RNA polymerase revealed that chromatin from both auxin- and auxin plus 5-fluorodeoxyuridine-treated tissue saturated at higher levels than chromatin from control tissue.     

Auxin level and regeneration of Begonia leaves

Summary As previously found, both the level of ether-extractable auxin (presumably indole-3-acetic acid) and the root-forming ability of B.xcheimantha leaves are increased under long-day conditions by high temperature, whereas the capacity for adventitious bud formation is reduced. However, this relation is present under relatively high light intensity only. Under the low light intensities in late fall neither auxin level nor regeneration ability were significantly affected by temperature.Dark treatment of detached leaves for 2 to 16 days greatly counteracted the inhibitory effect of high temperature on bud formation and reduced both the auxin level and the root-forming ability of the leaves.The great seasonal changes in the regeneration ability of Begonia leaves seem to be the result of a complex interaction of temperature, day-length, and daily light energy on the level of endogenous auxin and other growth regulators.     

Auxin dynamics after decapitation are not correlated with the initial growth of axillary buds

One of the first and most enduring roles identified for the plant hormone auxin is the mediation of apical dominance. Many reports have claimed that reduced stem indole-3-acetic acid (IAA) levels and/or reduced basipetal IAA transport directly or indirectly initiate bud growth in decapitated plants. We have tested whether auxin inhibits the initial stage of bud release, or subsequent stages, in garden pea (Pisum sativum) by providing a rigorous examination of the dynamics of auxin level, auxin transport, and axillary bud growth. We demonstrate that after decapitation, initial bud growth occurs prior to changes in IAA level or transport in surrounding stem tissue and is not prevented by an acropetal supply of exogenous auxin. We also show that auxin transport inhibitors cause a similar auxin depletion as decapitation, but do not stimulate bud growth within our experimental time-frame. These results indicate that decapitation may trigger initial bud growth via an auxin-independent mechanism. We propose that auxin operates after this initial stage, mediating apical dominance via autoregulation of buds that are already in transition toward sustained growth.     

Auxin transport in maize roots in response to localized nitrate supply

Background and Aims

Roots typically respond to localized nitrate by enhancing lateral-root growth. Polar auxin transport has important roles in lateral-root formation and growth; however, it is a matter of debate whether or how auxin plays a role in the localized response of lateral roots to nitrate.

Methods

Treating maize (Zea mays) in a split-root system, auxin levels were quantified directly and polar transport was assayed by the movement of [³H]IAA. The effects of exogenous auxin and polar auxin transport inhibitors were also examined.

Key Results

Auxin levels in roots decreased more in the nitrate-fed compartment than in the nitrate-free compartment and nitrate treatment appeared to inhibit shoot-to-root auxin transport. However, exogenous application of IAA only partially reduced the stimulatory effect of localized nitrate, and auxin level in the roots was similarly reduced by local applications of ammonium that did not stimulate lateral-root growth.

Conclusions

It is concluded that local applications of nitrate reduced shoot-to-root auxin transport and decreased auxin concentration in roots to a level more suitable for lateral-root growth. However, alteration of root auxin level alone is not sufficient to stimulate lateral-root growth.     

植物生长素受体蛋白研究现状

受体是研究生长素信号传导链的关键环节,因为只有生长素与生长素受体结合以后才会引起后续的级联反应,生长素受体的发现对探索和了解生长素调控机制是极其重要的.目前所发现的生长素结合蛋白(受体)有TIR1和ABP1.扼要的介绍生长素受体TIR1的结构及其与生长素的结合位点,阐述了TIR1在基因水平上的调控和AUX/IAA被泛素化后最终被26S蛋白酶体降解的过程.概述了ABPI的结构、活性位点、性质以及ABP1的作用机理的模型.     

Auxin Content and Auxin Catabolism in Relation to the Growth Polarity

The auxin level in the root fragments of carrot cultivated in vitro is inversely related to the auxin-oxidase activity. In the morphological basal region, auxin catabolism is low and, in consequence, auxin content is high. This accumulation of the endogenous auxin leads to the induction of callus. In such new tissues, IAA-oxidase activity is also very low and, similarly, the auxin content is high: thus, cells can growth rapidly. Consequently the growth polarity is directly related to the auxin catabolism.     

Auxin Stimulation of Cambial Activity in Pinus silvestris II. Dependence upon Basipetal Transport

Natural auxin content has been determined in the cambial region of large Pinus silvestris L. trees at various dates during the year. The tissue was collected from the stem of intact or ring-barked trees and from stumps remaining after the trees were cut down at breast height in early summer or late autumn. No seasonal decrease of concentration of the extractable auxin in the cambial region could be detected. Decapitation or ring-barking produced severe reduction in auxin content and arrested cambial division. In the next season the auxin level and the cambial activity remained completely depressed. It is concluded that without tissue continuity in the region external to xylem and without basipetal supply of substances, no mechanism operated by roots or remaining stem tissue near the tree base can ensure a high level of auxin in the cambial region or activate and maintain the cambial division. The activity of extracted pine auxin was found not to be identical with the stimulatory potential of authentic IAA determined by standard bioassays. The possibility of interaction with other extracted substances is discussed.     

Auxin-Induced Regulation of Protein Synthesis in Tobacco Mesophyll Protoplasts Cultivated In Vitro: II. Time Course and Level of Auxin Control

When protoplasts, previously cultivated in a medium lacking auxin, are transferred to complete medium, proteins whose synthesis is stimulated by the hormone become detectable after about 30 minutes and reach a constant level 2 to 4 hours after the beginning of hormonal treatment. In contrast, proteins whose level of synthesis is reduced by auxin, are only affected after 6 hours of treatment.

Short radioactive labelings in deficient medium followed by chases in complete medium show that auxin does not interfere with posttranslational processes.

Analysis of in vitro translation products of protoplast RNA shows that the time courses of auxin effects on protein synthesis and mRNA accumulation are perfectly superimposable. This allows us to exclude the possibility that auxin affects the translation process, but indicates that this hormone acts by regulating the concentration of the auxin-sensitive protein mRNAs.