Apical Dominance is not Due to a Lack of Functional Xylem and Phloem in Inhibited Buds

Mature sieve tubes were located in inhibited cotyledonary budsof soybean plants. They were connected to the pholem systemof the stem and were shown to be functional by observing theirability to transport a phloem-mobile tracor. The associatedxylem system was also shown to be functional by using a decolourizedbasic dye tracer. The inhibited buds in the axils of the primaryleaves also contained sieve tubes and xylem elements which wereconnected to their counterparts in the stom. It is concludedthat in soybeans the inhibition of bud growth due to apicaldominance cannot be caused by an incomplete or non-functionalvascular system.     

拟南芥茎顶端分生组织相关突变体的表型与结构分析

以拟南芥野生型(C24)和T-DNA插入诱发的突变体(155系)为材料,通过表型分析、组织切片、GUS基因表达的组织化学定位等研究方法对155系的形态结构和生长发育进行了较为细致的观察分析,结果发现:(1)T-DNA插入诱发的155系突变体植株矮化,叶片等器官体积减小,营养生长阶段延长,发育较C24缓慢;(2)同一时期155系的茎顶端分生组织面积较C24减小,顶端平坦,细胞层数减少,两侧叶原基基部之间的距离缩短,呈现出发育迟缓、从茎顶端分生组织向花分生组织转变延迟等特征;(3)GUS基因特异性地在155系茎顶端分生组织和维管组织中表达.结果表明,T-DNA诱捕基因可能在茎顶端分生组织中发挥作用,由于T-DNA的插入使该基因的功能受到了影响,进而影响了155系中茎顶端分生组织的发育模式,产生了155系的一系列表型改变.     

The Presentation Time for Shoot Inversion Release of Apical Dominance in Pharbitis nil

The presentation time for shoot inversion release of apicaldominance in Pharbitis nil is between 1 and 1.5 d. Five to 6d of shoot inversion are required for persistent outgrowth ofthe highest lateral bud. Pharbitis nil, apical dominance, shoot inversion, lateral bud growth, presentation time     

Proteomic Analysis of Chrysanthemum Lateral Buds after Removing Apical Dominance Based on Label-Free Technology

Studying the genetic basis and regulatory mechanism of chrysanthemum lateral bud outgrowth is of great significance for reduction the production cost of cut chrysanthemum. To clarify the molecular basis of lateral bud elongation after removal of apical dominance in chrysanthemum, label-free quantification analysis was used to analyze the proteome changes after apical bud removal. Quantitative real-time PCR (qPCR) was used to analyze the changes in the expression of three plant hormone-related genes. A total of 440 differentially expressed proteins were successfully identified at three time points during the lateral bud elongation. The number of differentially expressed proteins in the three stages (24 h/0 h, 48 h/0 h, 48 h/24 h) were 219, 332, and 97, respectively. The difference in expressed proteins in the three comparison stages mainly involves RNA processing and modification; translation, ribosomal structure and biogenesis; Posttranslational modification, protein turnover, and chaperones. Path analysis showed that there was various physiological activities in the process of lateral bud dormancy breaking and elongation, which involved energy metabolism, biosynthesis, signal transduction and stress response in the growth process of lateral buds. qPCR indicated that the expression of cytokinin synthesis related gene was significantly increased after the removal of apical dominance, while the expression of strigolactones synthesis related gene experiences a dramatic fall to promote the development of the lateral buds. However, there was a drop before a slight increase in the expression of the auxin synthesis related gene, which was mainly due to the removal of apical dominance that led to the loss of indoleacetic acid in the main stem. However, with formation of the new apical source, indoleacetic acid can be released again.     

Some Observations on Factors Controlling Apical Dominance in the 'Rogue' Tomato

The rogue tomato differs from the normal plant in that it exhibitsa lesser degree of apical dominance. Grafting techniques andmeasurements of the endogenous levels of growth substances inthe two types have been used in order to establish whether thisdifference is due to an altered hormonal balance in the roguetype. The results suggest that root-produced cytokinins play no rolein the control of apical dominance in the tomato plant, andthat lateral bud out-growth is influenced by a balance betweenapically-produced auxin, abscisic acid produced at the sitesof bud development and cytokinins synthesized within the budsthemselves. Lycopersicon esculentum L., tomato, apical dominance, abscisic acid, auxins, cytokinins, growth regulation     

Gravistimulus Direction, Ethylene Production and Shoot Elongation in the Release of Apical Dominance in Pharbitis nil

Prasad, T. K. and Cline, M. G. 1985. Gravistimulus direction,ethylene production and shoot elongation in the release of apicaldominance in Pharbitis nil.—. exp. Bot. 36: 1969–1975.Release of apical dominance can be induced in Pharbitis nilby the inversion of the upper shoot. This promotion of outgrowthof the highest lateral bud adjacent to the bend of the stemappears to be mediated by ethylene inhibition of growth of theinverted main shoot. In the present investigation the existenceof a direct correlation between ethylene evolution and the directionof gravistimulus is demonstrated as well as an inverse correlationbetween ethylene production by the inverted upper shoot andits elongation. An inverse correlation also exists between elongationof the inverted upper shoot and the outgrowth of the highestlateral bud if the lower portion of the shoot (below the bend)is oriented in an upright position. The latent period for shoot–inversioninduction of ethylene production is about 2 h. These resultssupport the hypothesis of indirect ethylene control of apicaldominance release by retardation of elongation of the invertedshoot. Key words: Shoot inversion, gravistimulus, ethylene, latent period, bud outgrowth, pharbitis nil     

Apical Dominance in the 'Rogue' Tomato

The rogue tomato exhibits less apical dominance than the normalplant though the degree of correlative inhibition varies considerablybetween winter- and summer-sown plants. An examination of thelevel of endogenous hormones in both rogue and normal plantsat both times of year indicates that the degree of branchingis strongly associated with the levels of auxin in the tissue.It is suggested that this hormone has an effect on apical dominanceby virtue of its role in hormone-directed transport and by itseffect on the formation of abscisic acid in the region of thelateral buds. The results are discussed in relation to currenthypotheses of the mechanism of apical dominance.     

Apical Dominance Control in Ipomoea nil: The Influence of the Shoot Apex, Leaves and Stem

The outgrowth of lateral buds is known to be controlled by theupper shoot tissues, which include the apex, the young leavesand the upper stem. An analysis of the influence of these plantparts on axillary bud elongation in Ipomoea nil was carriedout by various treatments on these specific tissues. A restriction of elongation in the main shoot due to eitherdecapitation or shoot inversion resulted in the release of apicaldominance A non-linear type of compensating growth relationshipwas observed between the 13 cm apical growing region of thestem and the lateral buds. It was determined by decapitation,defoliation and AgNO₃ treatments that both the 13 cm stem-growthregion and the young leaves (1–5 cm in length) had a muchgreater inhibitory influence on the outgrowth of specified lateralbuds than did the stem apex (consisting of the terminal 0.5cm of the shoot). The specified lateral buds which were analyzedfor outgrowth were located a number of nodes below the shootapex. The intervening nodes were debudded. Although the importanceof young leaves in the control of apical dominance has beenpreviously recognized, the most significant result from thepresent study with Ipomoea was the strong influence of the 13cm apical growth region of the stem on the out growth of thelateral buds. Apical dominance, Ipomoea nil L., Pharbitis nil, growth region, lateral bud outgrowth, decapitation, defoliation, shoot inversion     

Apical Dominance in Vicia faba

Apical dominance phenomena have been studied in seedlings ofVicia faba particularly in relation to the movement about theplant of uracil-2-¹⁴C applied to the cotyledons. Decapitationjust below the second node releases the growth of the lowermostlateral bud and inhibition is completely reimposed by applicationof indole-3-acetic acid (IAA) to the cut surface. Uracil-2-¹⁴Capplied in solution to the cotyledons is distributed in thestems of all experimental seedlings with no consistent differencesdue to decapitation or IAA application. On the other hand, decapitationresults in a rapid increase in uracil-2-¹⁴C content in the lateralbuds which far exceeds their promoted growth. This uptake iscompletely suppressed by IAA application. A ring of tri-iodobenzoicacid (TIBA)-lanolin paste around the stem above the bud suppressesIAA action both in bud growth and on uracil-2-¹⁴C uptake, andalso on the movement of IAA-1-¹⁴C down the stem. TIBA-application to the base of the bud does not prevent IAAaction on bud growth, but also does not prevent the movementof IAA-1-¹⁴C (or a water soluble product of its metabolism)into the bud. Direct application of kinetin to the lateral bud of intact plantscauses a short-lived release of growth. Gibberellic acid producesa smaller and scarcely significant increase which is additiveto the kinetin effect. Neither has any effect on uracil-2-¹⁴Cmovement into the bud. The implications of these findings are discussed in relationto various existing theories of the mode of auxin action inapical dominance and it is concluded that their strongest supportis for a mechanism involving the suppression of phloem differentiationin the vascular supply to the bud.     

Auxin at the Shoot Apical Meristem

Plants continuously generate new tissues and organs through the activity of populations of undifferentiated stem cells, called meristems. Here, we discuss the so-called shoot apical meristem (SAM), which generates all the aerial parts of the plant. It has been known for many years that auxin plays a central role in the functioning of this meristem. Auxin is not homogeneously distributed at the SAM and it is thought that this distribution is interpreted in terms of differential gene expression and patterned growth. In this context, auxin transporters of the PIN and AUX families, creating auxin maxima and minima, are crucial regulators. However, auxin transport is not the only factor involved. Auxin biosynthesis genes also show specific, patterned activities, and local auxin synthesis appears to be essential for meristem function as well. In addition, auxin perception and signal transduction defining the competence of cells to react to auxin, add further complexity to the issue. To unravel this intricate signaling network at the SAM, systems biology approaches, involving not only molecular genetics but also live imaging and computational modeling, have become increasingly important.Plants continuously generate new tissues and organs through the activity of populations of undifferentiated stem cells, called meristems. Because meristems can modulate their activity, they provide the developmental flexibility that allows plants to adapt their development in reaction to the environment (reviews: Lyndon 1998; Traas and Doonan 2001; Aida and Tasaka 2006; Sablowski 2007).Distinct meristems exist. Apical meristems, positioned at the tip of the shoots and roots, initiate aerial and underground organs, respectively. Along the stems and roots, more diffuse secondary meristems are responsible for secondary thickening of these structures.The plant hormone auxin plays an instrumental role in meristem biology and we discuss here its role in a particular meristem, the shoot apical meristem (SAM) that generates all the aerial organs including the floral meristems (Fig. 1A–C). In this context, we limit ourselves to the meristems in angiosperm that have been studied in most detail.Open in a separate windowFigure 1.The shoot apical meristem of Arabidopsis thaliana. (A) Aerial part of a wild-type plant of the Columbia ecotype (Col-0). The SAM is responsible for the production of rosette leaves and, after floral transition, for the production of the stem, cauline leaves, lateral meristems, and flowers of the inflorescence. (B) Details of the tip of the inflorescence, showing the highly organized positioning of flowers around the main axis (a spiral). (C) A dissected inflorescence meristem. Older flowers have been removed to expose the meristem surrounded by young floral buds. (D) Longitudinal section of an inflorescence meristem showing the layered organization (L1, L2, and L3 cell layers). L1 and L2 are also called the tunica and L3 to the corpus. The functional zones are also represented. At the meristem summit the central zone (CZ) contains the stem cells, whereas primordia are initiated in the peripheral zone (PZ). The rib zone (RZ) produces the internal part of the stem.     

The Role of Gravity in Apical Dominance : Effects of Clinostating on Shoot Inversion-Induced Ethylene Production, Shoot Elongation, and Lateral Bud Growth

Shoot inversion-induced release of apical dominance in Pharbitis nil is inhibited by rotating the plant at 0.42 revolutions per minute in a vertical plane perpendicular to the axis of rotation of a horizontal clinostat. Clinostating prevented lateral bud outgrowth, apparently by negating the restriction of the shoot elongation via reduction of ethylene production in the inverted shoot. Radial stem expansion was also decreased. Data from experiments with intact tissue and isolated segments indicated that shoot-inversion stimulates ethylene production by increasing the activity of 1-aminocyclopropane-1-carboxylic acid synthase. The results support the hypothesis that shoot inversion-induced release of apical dominance in Pharbitis nil is due to gravity stress and is mediated by ethylene-induced retardation of the elongation of the inverted shoot.     

Hormones and Apical Dominance in the Fern Davallia

Lateral buds of the fern Davallia trichomanoides are releasedfrom inhibition by the removal of the main shoot apex. However,auxin is not capable of substituting for the apex in decapitatedshoots nor can auxin in shoot tips be detected by bioassay orextraction and chromatography. Expanding leaves of this speciescontain auxin, but these organs are not responsible for inhibitionof lateral bud growth. The response of lateral buds to an exogenouslyapplied cytokinin does not result in initial bud break. It isconcluded that the hormonal factors known to govern apical dominancein seed plants are not responsible for the regulation of differentialbud expansion in this fern.     

The Mechanism of Apical Dominance in Coleus

The development of lateral buds in isolated stems of Coleus blumei is inhibited by low concentrations of indoleacetic acid or other auxins, just as in other plants. The inhibition can be fully reversed by kinetin, about 3 times as much kinetin as IAA being needed. However, the outgrowth of the same lateral buds on intact Coleus plants is sensitive to environmental conditions, well-nourished plants in full daylight often showing little inhibition by applied auxin. It is shown that (a) the solvent used for IAA, (b) the light intensity and (c) the nitrogen and phosphorus nutrition, all control the sensitivity of the buds to auxin inhibition. Using water instead of lanolin, lowering the light intensity or decreasing the supply of either nitrogen or phosphorus all increase the degree of apical dominance.     

Apical Dominance in Phaseolus vulgaris L.

Although determinations of the ABA content of lateral buds ofPhaseolus vulgaris revealed no difference between decapitatedand intact control plants in the first 12 h following decapitation,a relative decrease in the ABA content of lateral buds of decapitatedplants was detectable 24 h following decapitation. Shoot decapitationwas also observed to result in a decrease in the ABA contentof stem tissue. The application of IAA to the stem of decapitatedplants prevented these changes and increased the ABA contentof stem tissue relative to that of intact plants. The levelsof IAA and ABA were also determined in the stem tissue fromthe nodes of intact bean plants. The possible interdependenceof these two plant hormones was further investigated by a studyof [2_–14ClABA metabolism. The results are discussed inrelation to the possible role of these hormones in apical dominance. Key words: Apical dominance, Abscisic acid, Indole-3-acetic acid     

植物的顶端优势和水分上升机理新说

植物体有一个能量系统,由植物顶端、由植物顶端、形成层及其初生韧皮部和木质部、传递细胞等组成。这些细胞含线粒体量多质好,摘顶等刺激这些地方ＡＴＰ复合酶能产生大量能量,通过胞间连丝引起连锁反应并刺激和激活激素、营养物质等而产生生命活动、项端优势等。植物细胞的原生质是一种液晶,只需极少能量便能产生很大的作用。除去顶芽,刺激线粒体能产生大量能量供给侧芽,激活侧芽激素等而使侧芽生长,由于能量作功,逐渐减少,     

植物茎尖分生组织分化调控机制研究进展

茎尖分生组织是位于植物顶端具有持续分化能力的组织,通过细胞分裂、分化产生茎、叶和花等器官,形成植株地上部分。茎尖分生组织在分化过程中受外界环境因素、内源激素水平和分子调控等影响,表现出明显变化。该文综合国内外近年来有关茎尖分生组织分化调控的研究进展,从茎尖分生组织的形态结构和环境影响因素,以及激素调控和分子调控等方面,对茎尖分生组织分化活动的研究进行综述,并对目前研究现状存在问题及未来研究方向进行了分析和展望。     

Direct Adventitious Shoot Formation from Apical Shoot Explants of Euphorbia tirucalli

The induction of adventitious buds from apical shoot explants of Euphorbia tirucalli was studied. On average, 10.5 adventitious buds were efficiently induced in a ring on the segment from one apical explant on MS (Murashige and Skoog) medium supplemented with 0.5 mg l⁻¹ thidiazuron and 0.5 mg l⁻¹ benzylaminopurine. The adventitious buds could develop into adventitious shoots during subsequent cultures on hormone-free MS medium. For rooting, shoot clumps were cultured on half-strength MS medium containing 0.2 mg l⁻¹ α-naphthaleneacetic acid or indole-3-butyric acid. All the rooted plants survived establishment in soil within 2 months.     

乙烯在豌豆植株顶端优势中的作用

用人工合成细胞分裂素BAP和CPPU处理豌豆植株叶腋可诱导处理部位侧芽的生长,同时伴有大量乙烯产生;用乙烯合成抑制剂AVG处理或植株去顶同样可导致创芽生长,但乙烯释放量却明显少于对照,表明侧芽的生长与乙烯释放量的多少无关。而3种物质处理后诱导产生的侧芽的数目、长度及其鲜重与处理部位内源IAA含量的增加则呈正相关。