共查询到20条相似文献,搜索用时 656 毫秒
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Background and Aims
The Arabidopsis thaliana pollen cell wall is a complex structure consisting of an outer sporopollenin framework and lipid-rich coat, as well as an inner cellulosic wall. Although mutant analysis has been a useful tool to study pollen cell walls, the ultrastructure of the arabidopsis anther has proved to be challenging to preserve for electron microscopy.Methods
In this work, high-pressure freezing/freeze substitution and transmission electron microscopy were used to examine the sequence of developmental events in the anther that lead to sporopollenin deposition to form the exine and the dramatic differentiation and death of the tapetum, which produces the pollen coat.Key Results
Cryo-fixation revealed a new view of the interplay between sporophytic anther tissues and gametophytic microspores over the course of pollen development, especially with respect to the intact microspore/pollen wall and the continuous tapetum epithelium. These data reveal the ultrastructure of tapetosomes and elaioplasts, highly specialized tapetum organelles that accumulate pollen coat components. The tapetum and middle layer of the anther also remain intact into the tricellular pollen and late uninucleate microspore stages, respectively.Conclusions
This high-quality structural information, interpreted in the context of recent functional studies, provides the groundwork for future mutant studies where tapetum and microspore ultrastructure is assessed. 相似文献3.
OsABCG15 encodes a membrane protein that plays an important role in anther cuticle and pollen exine formation in rice 总被引:1,自引:0,他引:1
Lina Wu Yusheng Guan Zigang Wu Kun Yang Jun Lv Richard Converse Yuanxin Huang Jinxiong Mao Yong Zhao Zhongwei Wang Hengqi Min Dongyang Kan Yi Zhang 《Plant cell reports》2014,33(11):1881-1899
Key message
An ABC transporter gene ( OsABCG15 ) was proven to be involved in pollen development in rice. The corresponding protein was localized on the plasma membrane using subcellular localization.Abstract
Wax, cutin, and sporopollenin are important for normal development of the anther cuticle and pollen exine, respectively. Their lipid soluble precursors, which are produced in the tapetum, are then secreted and transferred to the anther and microspore surface for polymerization. However, little is known about the mechanisms underlying the transport of these precursors. Here, we identified and characterized a member of the G subfamily of ATP-binding cassette (ABC) transporters, OsABCG15, which is required for the secretion of these lipid-soluble precursors in rice. Using map-based cloning, we found a spontaneous A-to-C transition in the fourth exon of OsABCG15 that caused an amino acid substitution of Thr-to-Pro in the predicted ATP-binding domain of the protein sequence. This osabcg15 mutant failed to produce any viable pollen and was completely male sterile. Histological analysis indicated that osabcg15 exhibited an undeveloped anther cuticle, enlarged middle layer, abnormal Ubisch body development, tapetum degeneration with a falling apart style, and collapsed pollen grains without detectable exine. OsABCG15 was expressed preferentially in the tapetum, and the fused GFP-OsABCG15 protein was localized to the plasma membrane. Our results suggested that OsABCG15 played an essential role in the formation of the rice anther cuticle and pollen exine. This role may include the secretion of the lipid precursors from the tapetum to facilitate the transfer of precursors to the surface of the anther epidermis as well as to microspores. 相似文献4.
The in vitro phenylalanine incorporation by polyribosomes of peach flower buds (Prunus persica Stokes) during dormancy, dormancy break and flowering was investigated. Protein synthesis was measured using as catalyst either calf liver soluble factors or the ribosomal supernatant from the peach flower buds in the presence or the absence of the synthetic mRNA, polyuridylic acid. In the presence of polyuridylic acid, the activity of protein synthesis of dormant ribosomes is the same as that of ribosomes during dormancy break and flowering. The absence of synthetic messenger did not cause a change in activity. The ribosomal supernatant of dormant buds, but not of flowering buds, reduces the phenylalanine incorporation by polyribosomes from buds harvested at dormancy break. 相似文献
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Sang-Gyu Kim Sangmin Lee Youn-Sung Kim Dae-Jin Yun Je-Chang Woo Chung-Mo Park 《Plant molecular biology》2010,74(4-5):337-351
The tapetum is a layer of cells covering the inner surface of pollen sac wall. It contributes to anther development by providing enzymes and materials for pollen coat biosynthesis and nutrients for pollen development. At the end of anther development, the tapetum is degenerated, and the anther is dehisced, releasing mature pollen grains. In Arabidopsis, several genes are known to regulate tapetum formation and pollen development. However, little is known about how tapetum degeneration and anther dehiscence are regulated. Here, we show that an activation-tagged mutant of the S HI-R ELATED S EQUENCE 7 (SRS7) gene exhibits disrupted anther dehiscence and abnormal floral organ development in addition to its dwarfed growth with small, curled leaves. In the mutant hypocotyls, cell elongation was reduced, and gibberellic acid sensitivity was diminished. Whereas anther development was normal, its dehiscence was suppressed in the dominant srs7-1D mutant. In wild-type anthers, the tapetum disappeared at anther development stages 11 and 12. In contrast, tapetum degeneration was not completed at these stages, and anther dehiscence was inhibited, causing male sterility in the mutant. The SRS7 gene was expressed mainly in the filaments of flowers, where the DEFECTIVE-IN-ANTHER-DEHISCENCE 1 (DAD1) enzyme catalyzing jasmonic acid (JA) biosynthesis is accumulated immediately before flower opening. The DAD1 gene was induced in the srs7-1D floral buds. In fully open flowers, the SRS7 gene was also expressed in pollen grains. It is therefore possible that the abnormal anther dehiscence and floral development of the srs7-1D mutant would be related with JA. 相似文献
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Background and Aims
In temperate woody perennials, flower bud development is halted during the winter, when the buds enter dormancy. This dormant period is a prerequisite for adequate flowering, is genetically regulated, and plays a clear role in possibly adapting species and cultivars to climatic areas. However, information on the biological events underpinning dormancy is lacking. Stamen development, with clear differentiated stages, appears as a good framework to put dormancy in a developmental context. Here, stamen developmental changes are characterized in apricot (Prunus armeniaca) and are related to dormancy.Methods
Stamen development was characterized cytochemically from the end of August to March, over 4 years. Developmental changes were related to dormancy, using the existing empirical information on chilling requirements.Key Results
Stamen development continued during the autumn, and the flower buds entered dormancy with a fully developed sporogenous tissue. Although no anatomical changes were observed during dormancy, breaking of dormancy occurred following a clear sequence of events. Starch accumulated in particular places, pre-empting further development in those areas. Vascular bundles developed and pollen mother cells underwent meiosis followed by microspore development.Conclusions
Dormancy appears to mark a boundary between the development of the sporogenous tissue and the occurrence of meiosis for further microspore development. Breaking of dormancy occurs following a clear sequence of events, providing a developmental context in which to study winter dormancy and to evaluate differences in chilling requirements among genotypes. 相似文献9.
ABORTED MICROSPORES Acts as a Master Regulator of Pollen Wall Formation in Arabidopsis 总被引:3,自引:0,他引:3
Jie Xu Zhiwen Ding Gema Vizcay-Barrena Jianxin Shi Wanqi Liang Zheng Yuan Danièle Werck-Reichhart Lukas Schreiber Zoe A. Wilson Dabing Zhang 《The Plant cell》2014,26(4):1544-1556
Mature pollen is covered by durable cell walls, principally composed of sporopollenin, an evolutionary conserved, highly resilient, but not fully characterized, biopolymer of aliphatic and aromatic components. Here, we report that ABORTED MICROSPORES (AMS) acts as a master regulator coordinating pollen wall development and sporopollenin biosynthesis in Arabidopsis thaliana. Genome-wide coexpression analysis revealed 98 candidate genes with specific expression in the anther and 70 that showed reduced expression in ams. Among these 70 members, we showed that AMS can directly regulate 23 genes implicated in callose dissociation, fatty acids elongation, formation of phenolic compounds, and lipidic transport putatively involved in sporopollenin precursor synthesis. Consistently, ams mutants showed defective microspore release, a lack of sporopollenin deposition, and a dramatic reduction in total phenolic compounds and cutin monomers. The functional importance of the AMS pathway was further demonstrated by the observation of impaired pollen wall architecture in plant lines with reduced expression of several AMS targets: the abundant pollen coat protein extracellular lipases (EXL5 and EXL6), and CYP98A8 and CYP98A9, which are enzymes required for the production of phenolic precursors. These findings demonstrate the central role of AMS in coordinating sporopollenin biosynthesis and the secretion of materials for pollen wall patterning. 相似文献
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Jia-Xi Liu Jiao Zhang Hong-Juan Liu Min Wang Zu-Keng Chen Yi-Zhen Xi 《Plant Systematics and Evolution》2011,297(3-4):253-260
Anther structure and pollen ontogeny of six species of Hosta Tratt. was studied to provide additional data for its classification. Microscopic observation found that their male gametogenesis has the following structural characteristics: (1) the four microsporangia are linearly arranged on introrse side of anther connective tissue; (2) mature anther wall is composed of an epidermis, endothecium, middle layer(s), and tapetum; (3) microsporogenesis is successive; (4) mature pollen grains are three-celled at anthesis, with a vegetative cell filled with large amounts of starch grains; (5) pollen ontogeny is obviously asynchronous; (6) each tepal has about 9?C13 vascular traces in cross-section view. The above observations suggest that genus H. Tratt. should be classified as family Hostaceae, in agreement with Dahlgren and Clifford (1982), Takhtajan (1997), and Wu et?al. (2003). 相似文献
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Background and Aims
Anther appendages play diverse roles in anther dehiscence and pollen dispersal. This study aims to explore the pollen-dispensing mechanism triggered by special anther appendages in Incarvillea arguta.Methods
Field studies were conducted to record floral characteristics, pollinator visitations, and flower–pollinator interactions. Measurements of flowers and pollinators were analysed statistically. Pollen counts following a series of floral manipulations were used to evaluate pollen dispensing efficiency and function of the anther appendages.Key Results
Field observations determined that two species of Bombus (bumble-bees) were the primary pollinators of I. arguta with a mean visiting frequency of 1·42 visitations per flower h−1. The results display a diminishing pollen dispensing pattern; the proportion of remaining pollen removed by pollinators decreased from 27 % to 10 % and 7 % in subsequent visits. Anther appendages act as a trigger mechanism to dispense pollen. The arrangement of the anthers and appendages function to control pollen load and timing. Mechanical stimulation experiments revealed that one set of appendages is only triggered by stimulation in the direction moving into the flower, while the other set is only triggered by stimulation in the opposite direction (exiting the flower).Conclusions
The anther appendage is a pollen-dispensing trigger mechanism. The configuration of the stamens and duel trigger system has evolved to allocate pollen in allotments to enhance male function.Key words: Incarvillea arguta, anther appendage, pollination biology, Bignoniaceae, stamen morphology, pollen dispensing 相似文献13.
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Exine, the sporopollenin-based outer layer of the pollen wall, forms through an unusual mechanism involving interactions between two anther cell types: developing pollen and tapetum. How sporopollenin precursors and other components required for exine formation are delivered from tapetum to pollen and assemble on the pollen surface is still largely unclear. Here, we characterized an Arabidopsis (Arabidopsis thaliana) mutant, thin exine2 (tex2), which develops pollen with abnormally thin exine. The TEX2 gene (also known as REPRESSOR OF CYTOKININ DEFICIENCY1 (ROCK1)) encodes a putative nucleotide–sugar transporter localized to the endoplasmic reticulum. Tapetal expression of TEX2 is sufficient for proper exine development. Loss of TEX2 leads to the formation of abnormal primexine, lack of primary exine elements, and subsequent failure of sporopollenin to correctly assemble into exine structures. Using immunohistochemistry, we investigated the carbohydrate composition of the tex2 primexine and found it accumulates increased amounts of arabinogalactans. Tapetum in tex2 accumulates prominent metabolic inclusions which depend on the sporopollenin polyketide biosynthesis and transport and likely correspond to a sporopollenin-like material. Even though such inclusions have not been previously reported, we show mutations in one of the known sporopollenin biosynthesis genes, LAP5/PKSB, but not in its paralog LAP6/PKSA, also lead to accumulation of similar inclusions, suggesting separate roles for the two paralogs. Finally, we show tex2 tapetal inclusions, as well as synthetic lethality in the double mutants of TEX2 and other exine genes, could be used as reporters when investigating genetic relationships between genes involved in exine formation.Genetic, microscopy, and immunohistochemistry analyses place the Arabidopsis THIN EXINE2 protein at the intersection of several processes involved in the formation of pollen exine. 相似文献
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Sara Basconsuelo Herminda Reinoso Eugenia Lorenzo Rubén Bottini 《Plant Growth Regulation》1995,16(2):113-119
Morphological studies were carried out with peach flower buds collected monthly in 1989 and 1990, from two months before leaf fall (7 March) until two to three weeks before bloom (7/8 August). Chilled (2–4°C for 30 days) and unchilled buds were exposed to 20 to 25°C, 100% RH and continuous light. Gibberellin A3 (3 ng or 30 ng) was applied to some of the non-chilled cuttings at three days intervals. Then, 12, 19, and 26 days after they were planted, the buds were sampled and processed for histological studies. Cultured flower buds (chilled or unchilled) had accelerated anther and gynoecium morphogenesis after 12 days under controlled conditions, compared to buds processed immediately after collection from the field. Chilling treatment augmented the bud culture effect, while Gibberellin A3 applications to the excised buds retarded bud morphogenesis to a stage comparable to that of buds collected directly from the field. This, suggests that the comparatively high levels of Gibberellin A1/3 we previously found in mid winter [15, 18] could be at least one of the factors that controls floral bud dormancy by retarding anther and gynoecium development. 相似文献
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R. Wiermann 《Planta》1969,88(4):311-320
Summary The changes in the content of flavonols, anthocyanins, and carotenoids which can be observed in the anther during microsporogenesis were followed in Narcissus pseudonarcissus and in the Darwin tulip Apeldoorn.The investigations revealed a distinct relationship between the process of pigmentation and the cytologic development in the anther. A marked increase in the production of flavonols occurs during and immediately after the separation of the microspores of the tetrad and seems to be connected in some specific manner with the presence of the immature pollen. In Narcissus, the total flavonol content of the anthers and their pollen and tapetum fraction reaches its highest value during the enclosure of the bud by the bulb and remains more or less unchanged until the flowers open. In contrast, an intense synthesis of flavonols does not begin in the tulip before the flower-bud has left bulb; then the flavonol content increases continuously until anthesis is reached.The colouring of the pollen by anthocyanins does not occur until the final stages of maturation.Without exceptions the production of carotenoids takes place after the separation of the microspores of the tetrad.
Untersuchungen zum Phenylpropanstoffwechsel des Pollens. II. 相似文献
Untersuchungen zum Phenylpropanstoffwechsel des Pollens. II. 相似文献
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Hamdi El-Jendoubi Ernesto Igartua Javier Abadía Anunciación Abadía 《Plant and Soil》2012,354(1-2):121-139
Background and Aims
The possibility of using tree materials in early phenological stages, such as dormant buds and flowers, for the prognosis of Fe deficiency occurring later in the year has been studied in peach and pear trees.Methods
Thirty-two peach trees and thirty pear trees with different Fe chlorosis degrees were sampled in different commercial orchards. In peach, samples included flower buds, vegetative buds, bud wood, flowers and leaves at 60 and 120?days after full bloom (DAFB). In pear, samples included buds, bud wood, flowers and leaves at 60 and 120?days DAFB. Leaf chlorophyll was assessed (SPAD) at 60 and 120 DAFB. Sampling was repeated for 3–5?years depending on the materials. Mineral nutrients measured were N, P, K, Ca, Mg, Fe, Mn, Zn and Cu.Results
The relationships between the nutrient concentrations in the different materials and leaf SPAD were assessed using four different statistical approaches: i) comparison of means depending on the chlorosis level, ii) correlation analysis, iii) principal component analysis, and iv) stepwise multiple regression. In all cases, significant associations between nutrients and SPAD were found. The best-fit multiple regression curves obtained for the multi-year data set provided good prediction in individual years.Conclusions
Results found indicate that it is possible to carry out the prognosis of Fe chlorosis using early materials such as buds and flowers. The relationships obtained were different from those obtained in previous studies using a single orchard. The different methods of analysis used provided complementary data. 相似文献19.
Sevil Tütüncü Konyar 《Plant Systematics and Evolution》2014,300(2):303-320
In the present study, microsporogenesis, microgametogenesis and pollen wall ontogeny in Campsis radicans (L.) Seem. were studied from sporogenous cell stage to mature pollen using transmission electron microscopy. To observe the ultrastructural changes that occur in sporogenous cells, microspores and pollen through progressive developmental stages, anthers at different stages of development were fixed and embedded in Araldite. Microspore and pollen development in C. radicans follows the basic scheme in angiosperms. Microsporocytes secrete callose wall before meiotic division. Meiocytes undergo meiosis and simultaneous cytokinesis which result in the formation of tetrads mostly with a tetrahedral arrangement. After the development of free and vacuolated microspores, respectively, first mitotic division occurs and two-celled pollen grain is produced. Pollen grains are shed from the anther at two-celled stage. Pollen wall formation in C. radicans starts at tetrad stage by the formation of exine template called primexine. By the accumulation of electron dense material, produced by microspore, in the special places of the primexine, first of all protectum then columellae of exine elements are formed on the reticulate-patterned plasma membrane. After free microspore stage, exine development is completed by the addition of sporopollenin from tapetum. Formation of intine layer of pollen wall starts at the late vacuolated stage of pollen development and continue through the bicellular pollen stage. 相似文献