Effects of cell number and cell size on petiole length variation in a stoloniferous herb

In stoloniferous species, the length of petioles is of pivotal importance because it determines the position of leaf blades within the canopy. From a mechanistic perspective, two developmental processes, cell division and cell elongation, are responsible for the length of a given petiole. This study aimed at quantifying the relative contributions of cell division and cell elongation to genotypic and plastic variation in petiole length of the stoloniferous herb Trifolium repens. Thirty-four genotypes of T. repens were grown under high light conditions and simulated canopy shade. Cells were counted and their lengths measured on epidermal prints from fully grown petioles of leaves that had been initiated in the experimental light conditions. Cell number was the main trait explaining petiole length differences among genotypes grown under high light, while both cell number and length changed in response to shading. Our study revealed a strong negative correlation between shade-induced changes in cell number and cell length: genotypes that responded to shading by increasing cell numbers hardly changed in cell length, and vice versa. Our results suggest that genotypic and phenotypic variation in petiole length results from a complex interplay between the developmental processes of cell elongation and cell division.     

LONGIFOLIA1 and LONGIFOLIA2, two homologous genes, regulate longitudinal cell elongation in Arabidopsis.

Plants have diversified their leaf morphologies to adapt to diverse ecological niches. The molecular components responsible for regulating leaf morphology, however, have not been fully elucidated. By screening Arabidopsis activation-tagging lines, we identified a dominant mutant, which we designated longifolia1-1D (lng1-1D). lng1-1D plants were characterized by long petioles, narrow but extremely long leaf blades with serrated margins, elongated floral organs, and elongated siliques. The elongated leaves of the mutant were due to increased polar cell elongation rather than increased cell proliferation. Molecular characterization revealed that this phenotype was caused by overexpression of the novel gene LNG1, which was found to have a homolog, LNG2,in Arabidopsis. To further examine the role of the LNG genes, we characterized lng1 and lng2 loss-of-function mutant lines. In contrast to the elongated leaves of lng1-1D plants, the lng1 and lng2 mutants showed slightly decreased leaf length. Furthermore, the lng1-3 lng2-1 double mutant showed further decreased leaf length associated with less longitudinal polar cell elongation. The leaf widths in lng1-3 lng2-1 mutant plants were similar to those in wild type, implying that the role of LNG1 and LNG2 on polar cell elongation is similar to that of ROTUNDIFOLIA3 (ROT3). However, analysis of a lng1-3 lng2-1 rot3-1 triple mutant and of a lng1-1D rot3-1 double mutant indicated that LNG1 and LNG2 promote longitudinal cell elongation independently of ROT3. Taken together, these findings indicate that LNG1 and LNG2 are new components that regulate leaf morphology by positively promoting longitudinal polar cell elongation independently of ROT3 in Arabidopsis.     

CYP90C1 and CYP90D1 are involved in different steps in the brassinosteroid biosynthesis pathway in Arabidopsis thaliana

Brassinosteroids (BRs) are plant hormones that are essential for a wide range of developmental processes in plants. Many of the genes responsible for the early reactions in the biosynthesis of BRs have recently been identified. However, several genes for enzymes that catalyze late steps in the biosynthesis pathways of BRs remain to be identified, and only a few genes responsible for the reactions that produce bioactive BRs have been identified. We found that the ROTUNDIFOLIA3 (ROT3) gene, encoding the enzyme CYP90C1, which was specifically involved in the regulation of leaf length in Arabidopsis thaliana, was required for the late steps in the BR biosynthesis pathway. ROT3 appears to be required for the conversion of typhasterol to castasterone, an activation step in the BR pathway. We also analyzed the gene most closely related to ROT3, CYP90D1, and found that double mutants for ROT3 and CYP90D1 had a severe dwarf phenotype, whereas cyp90d1 single knockout mutants did not. BR profiling in these mutants revealed that CYP90D1 was also involved in BR biosynthesis pathways. ROT3 and CYP90D1 were expressed differentially in leaves of A. thaliana, and the mutants for these two genes differed in their defects in elongation of hypocotyls under light conditions. The expression of CYP90D1 was strongly induced in leaf petioles in the dark. The results of the present study provide evidence that the two cytochrome P450s, CYP90C1 and CYP90D1, play distinct roles in organ-specific environmental regulation of the biosynthesis of BRs.     

Effects of leaf blade narrowness and petiole length on the light capture efficiency of a shoot

Effects of the length: width ratio of a leaf blade and petiole length on shoot light capture were studied with computer simulation. Both a larger length: width ratio and longer petiole contributed to larger light capture per unit leaf area due to a reduced aggregation of leaf area around the stem. Other conditions being equal, shoots with narrow leaves and no petioles and those with wide leaves with petioles showed similar light capture as long as the mean distance of the leaf blade from the stem was the same. In shoots with a short internode and/or distichous phyllotaxis, however, narrow leaves contributed more to avoiding mutual shading than wide leaves with petioles. The predominance of light coming from a higher angular altitude also favored narrow leaves. The possible consequences of these results in the adaptive geometry of plant architecture are discussed.     

The BLADE-ON-PETIOLE 1 gene controls leaf pattern formation through the modulation of meristematic activity in Arabidopsis

The plant leaf provides an ideal system to study the mechanisms of organ formation and morphogenesis. The key factors that control leaf morphogenesis include the timing, location and extent of meristematic activity during cell division and differentiation. We identified an Arabidopsis mutant in which the regulation of meristematic activities in leaves was aberrant. The recessive mutant allele blade-on-petiole1-1 (bop1-1) produced ectopic, lobed blades along the adaxial side of petioles of the cotyledon and rosette leaves. The ectopic organ, which has some of the characteristics of rosette leaf blades with formation of trichomes in a dorsoventrally dependent manner, was generated by prolonged and clustered cell division in the mutant petioles. Ectopic, lobed blades were also formed on the proximal part of cauline leaves that lacked a petiole. Thus, BOP1 regulates the meristematic activity of leaf cells in a proximodistally dependent manner. Manifestation of the phenotypes in the mutant leaves was dependent on the leaf position. Thus, BOP1 controls leaf morphogenesis through control of the ectopic meristematic activity but within the context of the leaf proximodistality, dorsoventrality and heteroblasty. BOP1 appears to regulate meristematic activity in organs other than leaves, since the mutation also causes some ectopic outgrowths on stem surfaces and at the base of floral organs. Three class I knox genes, i.e., KNAT1, KNAT2 and KNAT6, were expressed aberrantly in the leaves of the bop1-1 mutant. Furthermore, the bop1-1 mutation showed some synergistic effect in double mutants with as1-1 or as2-2 mutation that is known to be defective in the regulation of meristematic activity and class I knox gene expression in leaves. The bop1-1 mutation also showed a synergistic effect with the stm-1 mutation, a strong mutant allele of a class I knox gene, STM. We, thus, suggest that BOP1 promotes or maintains a developmentally determinate state in leaf cells through the regulation of class I knox genes.     

冬性植物红菜薹在不同温度处理下花青素积累的分子机制

芸薹属植物红菜薹（Brassica rapa）是一种常见的蔬菜,它的花茎和叶柄表皮中均积累有花青素。为了解红菜薹中花青素合成的分子机制,进行了花青素含量的测定和花青素合成相关基因的表达分析。研究结果表明,叶柄表皮中的花青素含量显著高于叶片（去主脉）的花青素含量。同时,叶柄表皮花青素合成相关基因的表达水平高于叶柄（去表皮）和叶片（去主脉）的表达水平,这表明红菜薹中花青素的合成调控发生在转录水平。BrMYBA1仅在叶柄表皮中表达,但BrbHLH1和BrWD40在叶片和叶柄表皮中均能检测到表达。因此,BrMYBA1的转录激活可能与红菜薹的花青素合成相关。连续低温处理时,红菜薹叶柄表皮中的花青素含量逐渐增加,而该组织中花青素合成的结构基因表达水平逐渐降低。     

Growth and development of Brassica genotypes differing in endogenous gibberellin content. I. Leaf and reproductive development

Leaf and reproductive development were compared in 3 rapid cycling Brassica rapa genotypes grown for 4 weeks under greenhouse conditions. The dwarf mutant, rosette ( ros ), is gibberellin (GA)-deficient, while the tall mutant, elongated internode ( ein ), has enhanced endogenous GA levels. Germination was delayed in ros and a selection of a more severe form of ros , named dormant ( do ), has even more retarded germination and some seeds entirely fail to germinate. Seeds of do and ros respond to exogenous GA, by rapid germination.
The 3 genotypes, ros , normal and ein , displayed similar developmental sequences, although floral bud formation and subsequent floral development and anthesis were delayed in ros. Conversely, anthesis was slightly accelerated in ein . Individual leaf areas were reduced in both ros and ein relative to the normal genotype, but leaf numbers were similar in all 3 genotypes. Differences in leaf morphology (heterophylly) were also observed; the normal genotype and ein plants possessed uniform leaf shapes and relatively smooth leaf margins, although petiole length was increased in ein . The mutant ros had scalloped leaf margins and convoluted leaf blades in addition to shortened petioles. These phenotypes suggest a role for GA in the regulation of germination and reproductive and leaf development in Brassica.     

MOVEMENT AND DISTRIBUTION OF 14C WITHIN PETIOLES OF INTACT COLEUS BLUMEI (LABIATAE) AFTER APPLICATION OF INDOLE-3-(ACETIC ACID-2-14C) TO THE LEAF SURFACE

Auxin transport and immobilization were followed in the petioles of intact plants of Coleus blumei Benth. after application of IAA-2-¹⁴C at a physiological concentration as droplets to the upper surface near the base of the blades of leaves #3 and #5. After 14 hr transportable and immobilized radiocarbon was found all along the petioles. Moreover, about half the total amount of ¹⁴C detected within the plant (= uptake) had moved beyond the petioles. This was true for leaves of both ages although the younger #3 petioles were only about half as long as the older #5 petioles. Because the uptake of radiocarbon by the #3 petioles was roughly half that of the #5 petioles, the absolute amounts immobilized per unit length of section were essentially uniform in the two petioles. On the contrary, the fractions remaining transportable within the #3 petiole sections averaged half those of the #5 petiole sections. The distribution of the transportable and the immobilized radioactive fractions along the petioles was characterized by high values near the apical application point, a decrease toward the middle of the petioles, and an increase to the level of the apical part toward the base of the petioles, which includes the abscission layer. The results have been discussed in connection with measurements of the cross sectional areas and the lengths of the epidermal and subepidermal cells along the petioles. An auxin transport and immobilization model, which assumes there are two different immobilization systems of different strength in the differently aged tissues, is outlined to explain the observations.     

Genomic fingerprinting of Frankia strains by PCR-based techniques. Assessment of a primer based on the sequence of 16S rRNA gene of Escherichia coli

Submergence stimulates elongation of the leaves of Rumex palustris and under laboratory conditions the maximum final leaf length (of plants up to 7 weeks old) was obtained within a 9 day period. This elongation response, mainly determined by petiole elongation, depends on the availability of storage compounds and developmental stage of a leaf. A starch accumulating tap root and mature leaves and petioles were found to supply elongating leaves with substrates for polysaccharide synthesis in expanding cell walls. Changes in the composition of cell wall polysaccharides of elongated petioles suggest a substantial cell wall metabolism during cell extension. Reduced starch levels or removal of mature leaves caused a substantial limitation of submerged leaf growth. From the 5th leaf onward enough reserves were available to perform submerged leaf growth from early developmental stages. Very young petioles had a limited capacity to elongate. In slightly older petioles submergence resulted in the longest final leaf lengths and these values gradually decreased when submergence was started at more mature developmental stages. Submerged leaf growth is mainly a matter of petiole elongation in which cell elongation has a concurrent synthesis of xylem elements in the vascular tissue. Mature petioles still elongated (when submerged) by cell and tissue elongation only: the annular tracheary elements stretched enabling up to 70% petiole elongation.     

Plasticity of petioles of white clover (Trifolium repens) to blue light

Petiole response of white clover to variations in blue light (BL) was studied on the main axis and on primary and secondary branches. The objectives of the present work were to determine (1) the time course of petiole response to BL and (2) whether these responses were dependent on petiole location. Under BL, clover had shorter petioles, and the switch to conditions without BL increased the length of forthcoming petioles. The fitting of a logistic function was used to compare the effect of BL on final petiole length, maximum elongation rate and the duration of petiole elongation between axes and phytomers. Petiole response to BL was not dependent on its location within the plant (axis type or phytomer position along the axis). A reduction in BL induced a rapid increase in leaf elongation rate, despite a small decrease in the duration of petiole elongation. Moreover, petiole response was dependent on petiole stage of development: the increase in the maximum rate of petiole elongation was inversely proportional to the petiole stage of development at the time of the switch. We conclude that the effects of BL on petiole elongation were not dependent on its position within the plant, whereas internode elongation resulted from the integration of light environment at the plant level. The difference between the responses of orthotropic and plagiotropic organs of clover to BL is discussed in relation to their structural function and localisation in the canopy.     

裂叶悬钩子组织培养研究 Ⅰ.裂叶悬钩子叶外植体培养直接再生不定芽及植物激素对它的影响

本文首次报道裂叶悬钩子(Rubus laciniatus Wild)叶外植体培养在改良的NN~(69)培养基上附加2—4mg/1 6-BA和0.1mg/1 NAA或1—3mg/1 2,4-D和0.1mg/1 NAA,两者都可直接从完整叶片、叶片下切段或叶柄诱导出不定芽。诱导频率达20—48%。而不定芽绝大部分发生在叶轴处或叶柄基部。完整叶片的不定芽诱导率与叶片下切段无差别,但比叶柄基部诱导率要高。6-BA对叶轴处不定芽诱导率比2,4-D的要高。此外,不需继代培养,不定芽数可达10—20个,继代培养一个月左右,每个不定芽能形成丛生芽数可达40一60个。另外,本文还讨论了细胞分化过程中的极性现象。     

Shade suppresses wound-induced leaf repositioning through a mechanism involving PHYTOCHROME KINASE SUBSTRATE (PKS) genes

Shaded plants challenged with herbivores or pathogens prioritize growth over defense. However, most experiments have focused on the effect of shading light cues on defense responses. To investigate the potential interaction between shade-avoidance and wounding-induced Jasmonate (JA)-mediated signaling on leaf growth and movement, we used repetitive mechanical wounding of leaf blades to mimic herbivore attacks. Phenotyping experiments with combined treatments on Arabidopsis thaliana rosettes revealed that shade strongly inhibits the wound effect on leaf elevation. By contrast, petiole length is reduced by wounding both in the sun and in the shade. Thus, the relationship between the shade and wounding/JA pathways varies depending on the physiological response, implying that leaf growth and movement can be uncoupled. Using RNA-sequencing, we identified genes with expression patterns matching the hyponastic response (opposite regulation by both stimuli, interaction between treatments with shade dominating the wound signal). Among them were genes from the PKS (Phytochrome Kinase Substrate) family, which was previously studied for its role in phototropism and leaf positioning. Interestingly, we observed reduced shade suppression of the wounding effect in pks2pks4 double mutants while a PKS4 overexpressing line showed constitutively elevated leaves and was less sensitive to wounding. Our results indicate a trait-specific interrelationship between shade and wounding cues on Arabidopsis leaf growth and positioning. Moreover, we identify PKS genes as integrators of external cues in the control of leaf hyponasty further emphasizing the role of these genes in aerial organ positioning.     

The different growth responses of the Arabidopsis thaliana leaf blade and the petiole during shade avoidance are regulated by photoreceptors and sugar

During the shade-avoidance response, leaf blade expansion is inhibited and petiole elongation is enhanced. In this study, we examined the roles of photoreceptors and sugar on the differential growth of the leaf blade and petiole in shade conditions. Under the conditions examined, cell expansion, not cell division, played a major role in the differential leaf growth. The enhanced cell expansion in the leaf blade is associated with an increase in the ploidy level, whereas cell elongation was stimulated in the petiole in dark conditions without an increase in the ploidy level. Analysis of phytochrome, cryptochrome and phototropin mutants revealed that phytochromes and cryptochromes specifically regulate the contrasting growth patterns of the leaf blade and petiole in shade. Examination of the effects of photo-assimilated sucrose on the growth of the leaf blade and petiole revealed growth-promotional effects of sucrose that are highly dependent on the light conditions. The leaf blades of abscisic acid-deficient and sugar-insensitive mutants did not expand in blue light, but expanded normally in red light. These results suggest that both the regulation of light signals and the modulation of responses to sugar are important in the control of the differential photomorphogenesis of the leaf blade and petiole.     

Leaf recruitment and elongation: an adaptive response to flooding in Villarsia reniformis

Villarsia reniformis (Menyanthaceae) responds to flooding by rapid leaf elongation and continual recruitment of young, submerged leaves (4.3–6.5 per week). Leaf production is influenced by nutrient availability and water depth. Leaves are submerged and die as the water level rises, but are replaced by younger leaves able to broach the surface. Young petioles may elongate at more than 10 cm per day, but lose the ability to elongate after the blades are exposed to air more than twice. Young petioles produce new cells and existing cells elongate, but in older petioles fewer new cells are produced and cell elongation, whilst limited, is the main mechanism for petiole elongation. Continual recruitment implies a high cost for production of structural tissue, but ensures that leaves capable of rapid extension are within reach of the water surface and the plants can respond quickly to flooding.     

The functional morphology of light capture and carbon gain in the Redwood forest understorey plant Adenocaulon bicolor Hook

1. A three-dimensional geometric simulation model of crown architecture was utilized to investigate the efficiency of light capture and its relationship to whole-plant CO₂ assimilation of Adenocaulon bicolor .
2. Positioning of the leaves by the combined effects of ontogenetic variations in petiole length and angle and leaf size, and the leaf divergence angles were shown to be effective in minimizing self shading. The efficiency of light absorption varied from 0·64 to 0·70 among individual plants that were sampled.
3. Plant to plant variation in simulated daily carbon gain was strongly influenced by variations in the direct and diffuse PFD received by the individual plants. When simulations were run for all plants under a single common light environment, the carbon gain was strongly dependent on the efficiencies of light absorption of the different plants.
4. Simulations in which petiole length was varied showed a non-linear dependence of light absorption efficiency on petiole length. When both petiole length and leaf size were varied in a way that maintained a constant biomass then an optimal petiole length that corresponded to the observed petiole length was apparent. The observed divergence angle between successive leaves also maximized light absorption efficiency as compared to greater or lesser angles, but increases in internode length had no significant effect.
5. The results of this study provide evidence for selection for an 'optimal design' of crown architecture in Adenocaulon bicolor that maximizes light capture.     

Shade induced changes in biomechanical petiole properties in the stoloniferous herb <Emphasis Type="Italic">Trifolium repens</Emphasis>

Increased cell number and cell length both contribute to shade induced elongation of petioles which enables stoloniferous plants to place their leaf lamina higher up in the canopy. Although petiole elongation is assumed to be beneficial, it may also imply costs in terms of decreased biomechanical stability. We test the hypothesis that shade induced elongation changes the biomechanical properties of petioles and that the underlying mechanisms, cell division and cell elongation, differentially affect biomechanical properties. This was done by subjecting 14 genotypes differing in the relative contribution of cell size and cell number to shade induced elongation responses to high light conditions and to simulated canopy shade. Developmental traits (cell size and cell number), morphological traits characterizing the petioles, as well as biomechanical characteristics were measured. Our results show that, comparable to stems of non-clonal plants, the rigidity of a petiole’s tissue (the Young’s modulus) increases, leading to increased flexural stiffness of petioles subjected to shading. Increased flexural stiffness proved to be associated with increased performance under shaded conditions. Our results also indicate that cell number affected the material properties and the flexural stiffness of petioles. However, the degree and pattern of the effects differed between light environments. Shade induced increase in cell number translated into shade induced increase of Young’s modulus and flexural stiffness. Genotypes producing relatively larger cells under shaded conditions experienced a decrease in tissue rigidity. In concert our results indicate that the pattern of selection on flexural stiffness, and thereby also on shade induced changes of cell number and cell size differs among light environments. An erratum to this article can be found at     

Phytochromes A1 and B1 have distinct functions in the photoperiodic control of flowering in the obligate long-day plant Nicotiana sylvestris

The obligate long-day plant Nicotiana sylvestris with a nominal critical day length of 12 h was used to dissect the roles of two major phytochromes (phyA1 and phyB1) in the photoperiodic control of flowering using transgenic plants under-expressing PHYA1 (SUA2), over-expressing PHYB1 (SOB36), or cosuppressing the PHYB1 gene (SCB35). When tungsten filament lamps were used to extend an 8 h main photoperiod, SCB35 and SOB36 flowered earlier and later, respectively, than wild-type plants, while flowering was greatly delayed in SUA2. These results are consistent with those obtained with other long-day plants in that phyB has a negative role in the control of flowering, while phyA is required for sensing day-length extensions. However, evidence was obtained for a positive role for PHYB1 in the control of flowering. Firstly, transgenic plants under-expressing both PHYA1 and PHYB1 exhibited extreme insensitivity to day-length extensions. Secondly, flowering in SCB35 was completely repressed under 8 h extensions with far-red-deficient light from fluorescent lamps. This indicates that the dual requirement for both far-red and red for maximum floral induction is mediated by an interaction between phyA1 and phyB1. In addition, a diurnal periodicity to the sensitivity of both negative and positive light signals was observed. This is consistent with existing models in which photoperiodic time measurement is not based on the actual measurement of the duration of either the light or dark period, but rather the coincidence of endogenous rhythms of sensitivity - both positive and negative - and the presence of light cues.     

裂叶悬钩子组织培养研究——Ⅰ.裂叶悬钩子叶外植体培养直接再生不定芽及植物激素对它的影响

本文首次报道裂叶悬钩子(Rubus laciniatus Wild)叶外植体培养在改良的NN⁶⁹培养基上附加2—4mg/1 6-BA和0.1mg/1 NAA或1—3mg/1 2,4-D和0.1mg/1 NAA,两者都可直接从完整叶片、叶片下切段或叶柄诱导出不定芽。诱导频率达20—48%。而不定芽绝大部分发生在叶轴处或叶柄基部。完整叶片的不定芽诱导率与叶片下切段无差别,但比叶柄基部诱导率要高。6-BA对叶轴处不定芽诱导率比2,4-D的要高。此外,不需继代培养,不定芽数可达10—20个,继代培养一个月左右,每个不定芽能形成丛生芽数可达40一60个。另外,本文还讨论了细胞分化过程中的极性现象。     

The involvement of gibberellin 20-oxidase genes in phytochrome-regulated petiole elongation of Arabidopsis

Long day (LD) exposure of rosette plants causes rapid stem/petiole elongation, a more vertical growth habit, and flowering; all changes are suggestive of a role for the gibberellin (GA) plant growth regulators. For Arabidopsis (Arabidopsis thaliana) L. (Heynh), we show that enhancement of petiole elongation by a far-red (FR)-rich LD is mimicked by a brief (10 min) end-of-day (EOD) FR exposure in short day (SD). The EOD response shows red (R)/FR photoreversibility and is not affected in a phytochrome (PHY) A mutant so it is mediated by PHYB and related PHYs. FR photoconversion of PHYB to an inactive form activates a signaling pathway, leading to increased GA biosynthesis. Of 10 GA biosynthetic genes, expression of the 20-oxidase, AtGA20ox2, responded most to FR (up to a 40-fold increase within 3 h). AtGA20ox1 also responded but to a lesser extent. Stimulation of petiole elongation by EOD FR is reduced in a transgenic AtGA20ox2 hairpin gene silencing line. By contrast, it was only in SD that a T-DNA insertional mutant of AtGA20ox1 (ga5-3) showed reduced response. Circadian entrainment to a daytime pattern provides an explanation for the SD expression of AtGA20ox1. Conversely, the strong EOD/LD FR responses of AtGA20ox2 may reflect its independence of circadian regulation. While FR acting via PHYB increases expression of AtGA20ox2, other GA biosynthetic genes are known to respond to R rather than FR light and/or to other PHYs. Thus, there must be different signal transduction pathways, one at least showing a positive response to active PHYB and another showing a negative response.