Alisher Touraev

Initiation of microspore embryogenesis by stress

Microspores have the remarkable capacity to develop into haploid plants via embryogenesis in vitro . Stress treatment acts as a trigger for inducing this sporophytic pathway, preventing the development of fertile pollen (gametophytic pathway). The doubled haploids generated are completely homozygous, and represent an important tool for research in plant genetics and breeding. In addition, microspore embryogenesis can be used to study plant embryogenesis and phase transitions during the alternation of generations in plants. Microspore culture also allows stress to be analyzed in the novel context of cell cycle regulation and plant development.

Efficient microspore embryogenesis in wheat (Triticum aestivum L.) induced by starvation at high temperature

We have established an efficient method to induce embryo formation from isolated wheat (Triticum aestivum L.) microspores. Culture of excised anthers under starvation and heat shock conditions induced the formation of embryogenic microspores at high frequency in nine Austrian winter wheat genotypes, including cultivars that had been considered as recalcitrant in anther culture. Percoll gradient centrifugation of the mechanically isolated microspores allowed us to obtain homogeneous populations of embryogenic microspores in all genotypes which, after transfer to a rich medium containing immature ovaries for conditioning, divided and produced globular embryos. Thousands of embryos were produced in one petri dish. Many of these embryos developed into plantlets after transfer to a solid medium without ovaries.

The microspore: A haploid multipurpose cell

Abstract The microspore is at the centre of a variety of topics in modern plant science and breeding. Isolated microspore cultures have the remarkable quality of resembling the alternation of generations in the life cycle of angiosperms, i.e. the change between the diploid sporophytec and the haploid gametophytec generation. Although the natural destination of microspore development is to differentiate into mature pollen and accomplish fertilization, isolated and in vitro cultured microspores or young pollen grains can either differentiate into mature, fertile pollen (the male gametophytes) by culture in a rich medium without stress, or divide repeatedly and develop into embryos (sporophytes) after a stress treatment. As experimental systems, microspore cultures are used to investigate pollen development and pollination, embryogenesis, totipotency, cytodifferentiation, cell cycle, phase change and the role of stress in development. As a tool in genetic engineering, they can be used to produce doubled haploids (recombinant inbreds) for plant breeding and gene mapping, to overcome crossing barriers (male sterility and self-incompatibility), to induce and select for mutants and to create transgenic plants. In this review genetic, cell biological and molecular aspects of in vitro microspore development are presented and put in the context of current basic and applied plant science.

A developmentally regulated MAP kinase activated by hydration in tobacco pollen.

A novel mitogen-activated protein (MAP) kinase signaling pathway has been identified in tobacco. This pathway is developmentally regulated during pollen maturation and is activated by hydration during pollen germination. Analysis of different stages of pollen development showed that transcriptional and translational induction of MAP kinase synthesis occurs at the mid-bicellular stage of pollen maturation. However, the MAP kinase is stored in an inactive form in the mature, dry pollen grain. Kinase activation is very rapid after hydration of the dry pollen, peaking at approximately 5 min and decreasing thereafter. Immunoprecipitation of the kinase activity by an anti-phosphotyrosine antibody is consistent with the activation of a MAP kinase. The kinetics of activation suggest that the MAP kinase plays a role in the activation of the pollen grain after hydration rather than in pollen tube growth.

Micro‐arrayed wheat seed and grass pollen allergens for component‐resolved diagnosis

Background:  Wheat is a potent allergen source and can cause baker’s asthma, food and pollen allergy. The aim of the study was to develop an allergen micro‐array for differential diagnosis of baker’s asthma, wheat‐induced food allergy and grass pollen allergy.

Stress-induced microspore embryogenesis in tobacco : an optimized system for molecular studies

SummarySpecific stress treatments applied to isolated tobacco (Nicotiana tabacum L.) microspores efficiently induced haploid embryo formation in vitro. A heat shock at 33 or 37°C in the presence of sugar, as well as sucrose-starvation at 25°C, resulted in the formation of embryogenic microspores. A combination of both treatments had an additive effect. Under optimal induction conditions all viable microspores in the culture were embryogenic and developed subsequently into pollen embryos by culture at 25°C in a sugar-containing medium, with induction frequencies of more than 70% with respect to the initial microspore population. A high fraction of the early pollen embryos continued their development in vitro, giving rise to haploid plants. In contrast to other available systems for microspore/pollen embryogenesis, the new protocol allows the production of homogeneous populations of embryogenic microspores and early globular embryos in large-scale cultures, without any purification step, and is therefore well suited for biochemical and molecular work.

The endoplasmic reticulum localized PIN8 is a pollen-specific auxin carrier involved in intracellular auxin homeostasis

The plant hormone auxin is a mobile signal which affects nuclear transcription by regulating the stability of auxin/indole-3-acetic acid (IAA) repressor proteins. Auxin is transported polarly from cell to cell by auxin efflux proteins of the PIN family, but it is not as yet clear how auxin levels are regulated within cells and how access of auxin to the nucleus may be controlled. The Arabidopsis genome contains eight PINs, encoding proteins with a similar membrane topology. While five of the PINs are typically targeted polarly to the plasma membranes, the smallest members of the family, PIN5 and PIN8, seem to be located not at the plasma membrane but in endomembranes. Here we demonstrate by electron microscopy analysis that PIN8, which is specifically expressed in pollen, resides in the endoplasmic reticulum and that it remains internally localized during pollen tube growth. Transgenic Arabidopsis and tobacco plants were generated overexpressing or ectopically expressing functional PIN8, and its role in control of auxin homeostasis was studied. PIN8 ectopic expression resulted in strong auxin-related phenotypes. The severity of phenotypes depended on PIN8 protein levels, suggesting a rate-limiting activity for PIN8. The observed phenotypes correlated with elevated levels of free IAA and ester-conjugated IAA. Activation of the auxin-regulated synthetic DR5 promoter and of auxin response genes was strongly repressed in seedlings overexpressing PIN8 when exposed to 1-naphthalene acetic acid. Thus, our data show a functional role for endoplasmic reticulum-localized PIN8 and suggest a mechanism whereby PIN8 controls auxin thresholds and access of auxin to the nucleus, thereby regulating auxin-dependent transcriptional activity.

Tracking individual wheat microspores in vitro: identification of embryogenic microspores and body axis formation in the embryo

Abstract. The development of isolated, defined wheat microspores undergoing in vitro embryogenesis has been followed by cell tracking. Isolated wheat (Triticum aestivum L.). microspores were immobilized in Sea Plaque agarose supported by a polypropylene mesh at a low cell density and cultured in a hormone-free, maltose-containing medium in the presence of ovaries serving as a conditioning factor. Embryogenesis was followed in microspores isolated from immature anthers of freshly cut tillers or from heat- and starvation-treated, excised anthers. Three types of microspore were identified on the basis of their cytological features at the start of culture. Type-1 microspores had a big central vacuole and a nucleus close to the microspore wall, usually opposite to the germ pore. This type was identical to the late microspore stage in anthers developing in vivo. Microspores with a fragmented vacuole and a peripheral cytoplasmic pocket containing the nucleus were defined as type 2. In type-3 microspores the nucleus was positioned in a cytoplasmic pocket in the centre of the microspore. Tracking revealed that, irrespective of origin, type-1 microspores first developed into type 2 and then into type-3 microspores. After a few more days, type-3 microspores absorbed their vacuoles and differentiated into cytoplasm-rich and starch-accumulating cells, which then divided to form multicellular structures. Apparently the three types of microspore represent stages in a continuous process and not, as previously assumed, distinct classes of responding and non-responding microspores. The first cell division of the embryogenic microspores was always symmetric. Cell tracking also revealed that the original microspore wall opened opposite to a region in the multicellular microspore which consisted of cells containing starch grains while the remaining cells were starch grain-free. The starch-containing cells were located close to the germ pore of the microspore. In more advanced embryos the broken microspore wall was detected at the root pole of the embryo.

Stress as the major signal controlling the developmental fate of tobacco microspores: towards a unified model of induction of microspore/pollen embryogenesis

Specific stress treatments (sucrose starvation, alone or combined with a heat shock) applied to isolated tobacco (Nicotiana tabacum L.) microspores irreversibly blocked normal gametophytic development and induced the formation of embryogenic cells, which developed subsequently into pollen-derived embryos by culture at 25°C in a sugar-containing medium. A cold shock at 4°C did not inhibit microspore maturation in vitro and did not induce cell division activity, even when combined with a starvation treatment. In the absence of sucrose, microspores isolated in the G1 phase of the cell cycle replicated their DNA and accumulated in G2. Late microspores underwent miotosis during the first day of culture which resulted in a mixed population of bicellular pollen grains and uninucleate microspores, both embryogenic. After the inductive stress treatments the origin of the first multicellular structures, formed in the sugar-containing medium, could be traced to divisions of the microspore cell or divisions of the vegetative cell of bicellular pollen, indicating that the symmetry of microspore mitosis in vitro is not important for embryogenic induction. These results represent a step forward towards a unified model of induction of embryogenesis from microspores/pollen which, within a relatively wide developmental window, are competent to deviate from normal gametophytic development and initiate the alternative sporophytic programme, in response to specific stress signals.

Assessment of various stresses and carbohydrates for their effect on the induction of embryogenesis in isolated wheat microspores

Isolated microspores of flowering plants can undergo embryogenesis when cultured in vitro under appropriate conditions. This process is triggered by various stresses including cold, heat and starvation. We have studied the effects of these stresses on the induction of embryogenesis in wheat microspores isolated from freshly cut or cold pretreated tillers. We show that the stress can be applied directly to microspore cultures, and efficient induction of embryogenesis can be obtained from microspores using a variety of stresses, namely cold (4°C), heat (33°C) and carbohydrate/nitrogen starvation. Cold pretreatment of tillers was able to replace stresses applied to microspores. For the first time we report on embryo formation in true ab initio wheat microspore cultures, not requiring any pretreatment of anthers or tillers prior to culture, in a maltose-containing medium. The effect of maltose on the induction of wheat microspore embryogenesis was specific and can possibly be attributed to its slow hydrolysis by plant cells, exerting starvation conditions early in culture and stable osmolarity of the medium later on. A comparison of three protocols for the induction of wheat microspore embryogenesis and plant regeneration has revealed no significant difference in plant yield, but the ploidy of the plants obtained was affected.