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Biology subjects

Saltini, M.

Publications and source records attributed to Saltini, M..

9 recordsLinked to original sources

Selective contexts favouring asymmetry: a theoretical and empirical study of pollen transfer in mirror-image flowers

Reciprocal herkogamy has evolved multiple times in flowering plants and is thought to enhance cross-pollination and reduce reproductive interference. Mirror-image flowers represent a form of reciprocal herkogamy in which plants have either right-or left-deflected styles (dimorphic enantiostyly) or produce both stylar orientations (monomorphic enantiostyly). The ecological conditions under which these two forms of enantiostyly originate and persist remain poorly understood. Here, we investigate how floral asymmetry affects pollen transfer dynamics and mating outcomes, and under which conditions enantiostyly provides a fitness advantage over straight-styled floral morphologies. We integrate field observations of dimorphic enantiostylous Wachendorfia paniculata with a mathematical model simulating pollen transfer in plants with straight-styled, monomorphic, and dimorphic enantiostylous flowers. The model incorporates pollinator pathways, pollen carryover, and floral display size, and was parameterized using our ecological data. Enantiostylous flowers received more outcrossed pollen than straight-styled flowers, with dimorphism outperforming monomorphism. However, enantiostyly increased stochasticity in pollen transfer due to variation in pollinator pathways. Intrafloral self-pollination was extremely low in enantiostylous flowers and did not differ between monomorphic and dimorphic forms. Dimorphic enantiostylous plants exhibited longer pollen carryover curves and exported more pollen to more mates potentially increasing siring success and mate diversity. Enantiostyly, particularly in dimorphic systems, can provide a selective advantage by improving pollen receipt and export components of fitness through enhanced outcrossing. This mating advantage may be reduced under conditions of pollen limitation or when autogamy in straight-styled flowers is low. Our findings clarify the functional significance of enantiostyly and offer a framework for understanding the evolution of floral asymmetry in angiosperms.

evolutionary biology↗

Supergene control of chiral development in mirror-image flowers

How genes determine the left-versus right-handed development of chiral structures is a fascinating question. The reciprocal placement of female and male organs on opposite sides of the midline in mirror-image flowers limits selfing and promotes efficient cross-pollination. Here we identify the molecular and developmental basis of floral handedness in butterfly lilies. Female and male organs deflect by a combination of genetically controlled chirality and gravitropism, orienting left and right with respect to an external rather than internal reference axis. Coordinated organ placement is controlled by a hemizygous supergene containing two causal loci, MIR156-R and YUCCA-R, responsible for opposite female and male organ orientation, respectively. This genomic architecture results in differential placement of the supergene alleles on the pollinators and maintenance of the reproductive polymorphism.

plant biology↗

Style deflection is determined by the handedness of phyllotaxis and differential cell elongation in a species with mirror-image flowers

Many animals and plants show left-right (LR) asymmetry. In some animal systems, handedness has a simple genetic basis, which has allowed identifying how handedness is determined at the molecular level, even if its functional relevance often remains unclear. Mirror-image flowers represent an example of LR asymmetry of clear functional significance, with the reciprocal placement of male and female organs in left- versus right-handed flowers promoting cross-pollination. Here, we use the South African geophyte Cyanella alba to study how handedness of its mirror-image flowers is determined and elaborated during development. Inflorescences of C. alba produce flowers with a largely consistent handedness. However, we find that this handedness has no simple genetic basis, and individual plants can switch their predominant handedness between years. Rather, it is the direction of the phyllotactic spiral that determines floral handedness. Cellular analysis combined with biophysical modelling demonstrates that style deflection is driven by increased cell expansion in the adaxial carpel facing the next oldest flower compared to the other adaxial carpel. The more expanding carpel shows transcriptional signatures of increased auxin signaling compared to the less expanding one, and auxin application to the latter can reverse the orientation of style deflection. We propose that a recently described inherent LR auxin asymmetry in the initiating organs of spiral phyllotaxis determines handedness in C. alba, representing a conserved non-genetic mechanism for creating a stable floral polymorphism. This mechanism links chirality across different levels of plant development and exploits a developmental constraint in a core patterning process to produce morphological variation of ecological relevance.

plant biology↗

Protoxylem microtubule patterning requires ROP pattern co-alignment, realistic microtubule-based nucleation, and sufficient microtubule flexibility.

The development of the water transporting xylem tissue in plants involves an intricate interplay of Rho-of-Plants (ROP) proteins and cortical microtubules to generate highly functional secondary cell wall patterns, such as the ringed or spiral patterns in early-developing protoxylem. We study the requirements of protoxylem microtubule band formation with simulations in CorticalSim, extended to include finite microtubule persistence length and a novel algorithm for microtubule-based nucleation. We find that microtubule flexibility is required to facilitate pattern formation for all realistic degrees of mismatch between array and pattern orientation. At the same time, flexibility leads to more density loss, both from collisions and the microtubule-hostile gap regions, making it harder to maintain microtubule bands. Microtubule-dependent nucleation helps to counteract this effect by gradually shifting nucleation from the gap regions to the bands as microtubules disappear from the gaps. Our results reveal the main mechanisms required for efficient protoxylem band formation.

cell biology↗

A realistic algorithm for microtubule-based nucleation reveals large sensitivity to cell geometry of the plant cortical array

Many plant cell functions, including cell morphogenesis and anisotropic growth, rely on the self-organisation of cortical microtubules into aligned arrays with the correct orientation. An important ongoing debate is how cell geometry, wall mechanical stresses, and other internal and external cues are integrated to determine the orientation of the cortical array. Here, we demonstrate that microtubule-based nucleation can markedly shift the balance between these often competing directional cues. For this, we developed a novel, more realistic model for microtubule-based nucleation in the simulation platform CorticalSim, which avoids the longstanding inhomogeneity problem stemming from previous, less realistic models for microtubule-based nucleation. We show that microtubule-based nucleation increases the sensitivity of the array to cell geometry, and extends the regime of spontaneous alignment compared to isotropic nucleation. In the case of cylindrical cell shapes, we show that this translates into a strong tendency to align in the transverse direction rather than along the vertical axis, and this is robust against small directional cues favouring the longitudinal direction. Comparing various cylinders and boxes, we show that different nucleation mechanisms result in different preferred array orientations, with the largest differences on cylinders. Our model provides a powerful tool for investigating how plant cells integrate multiple biases to orient their cortical arrays, offering new insights into the biophysical mechanisms underlying cell shape and growth.

biophysics↗

Evolution from mixed to fixed handedness in mirror-image flowers: insights from adaptive dynamics

Mirror-image flowers (enantiostyly) involve a form of sexual asymmetry in which a flowers style is deflected either to the left or right side, with a pollinating anther orientated in the opposite direction. This curious floral polymorphism, which was known but not studied by Charles Darwin, occurs in at least 11 unrelated angiosperm families and represents a striking example of adaptive convergence in form and function associated with cross-pollination by insects. In several lineages, dimorphic enantiostyly (one stylar orientation per plant, both forms occurring within populations) has evolved from monomorphic enantiostyly, in which all plants can produce both style orientations. We use a modelling approach to investigate the emergence of dimorphic enantiostyly from monomorphic enantiostyly under gradual evolution. We show using adaptive dynamics that depending on the balance between inbreeding depression following geitonogamy, pollination efficiency and plant density, dimorphism can evolve from an ancestral monomorphic population. In general, the newly emergent dimorphic population is stable against invasion of a monomorphic mutant. However, our model predicts that under certain ecological conditions, e.g., a decline of pollinators, dimorphic enantiostyly may revert to a monomorphic state. We demonstrate using population genetics simulations that the observed evolutionary transitions are possible assuming a plausible genetic architecture.

evolutionary biology↗

Consequences of life-cycle complexity to the potential for evolutionary branching

Complex life-cycles - that is, organismal development that unfolds across ecological niches - are pervasive in nature. In this work we set out to investigate the effects of complex life-cycles on the potential for diversification via evolutionary branching. We did this by analyzing a mathematical model of a consumer with two life-stages, each of which is characterized by a specific feeding efficiency trait that undergoes evolutionary change in response to ecological conditions such as resource competition. We find (i) that life-cycle complexity can favor diversification when compared to simple life-cycles, as there is a larger potential for evolutionary branching in the trait of the life-stage that has a higher population density; (ii) that evolution favors character displacement to minimize intra-stage resource competition; and (iii) that under certain parameters more than one evolutionary branching event can occur.

evolutionary biology↗

A plausible mechanism for longitudinal lock-in of cortical microtubule array after light-induced reorientation

The light-induced reorientation of the cortical microtubule array in dark-grown A. thaliana hypocotyl cells is a striking example of the dynamical plasticity of the microtubule cytoskeleton. A consensus model, based on katanin-mediated severing at microtubule crossovers, has been developed that successfully describes the onset of the observed switch between a transverse and longitudinal array orientation. However, we currently lack an understanding of why the newly-populated longitudinal array direction remains stable for longer times and re-equilibration effects would tend to drive the system back to a mixed orientation state. Using both simulations and analytical calculations, we show that the assumption of a small orientation-dependent shift in microtubule dynamics is sufficient to explain the long term lock-in of the longitudinal array orientation. Furthermore, we show that the natural alternative hypothesis that there is a selective advantage in severing longitudinal microtubules, is neither necessary nor sufficient to achieve cortical array reorientation, but is able to accelerate this process significantly.

plant biology↗

CLASP stabilizes microtubule plus ends after severing to facilitate light-induced microtubule reorientation

Central to building and reorganizing cytoskeletal arrays is the creation of new polymers. While nucleation has been the major focus of study for new microtubule generation, severing has been proposed as an alternative mechanism to create new polymers, a mechanism recently shown to drive the reorientation of cortical arrays of higher plants in response to blue light perception. As severing produces new plus ends behind the stabilizing GTP-cap, an important and unanswered question is how these are stabilized in vivo to promote net microtubule generation. Here we identify the conserved protein CLASP as a potent stabilizer of new plus ends created by katanin severing and find that CLASP is required for rapid cortical array reorientation. In clasp mutants both rescue of shrinking plus ends and the regrowth of plus ends immediately after severing are reduced, computational modeling reveals that it is the specific stabilization of severed ends that explains CLASPs function in promoting microtubule amplification by severing and cortical array reorientation.

cell biology↗