399 research outputs found
Differential spatial distribution of miR165/6 determines variability in plant root anatomy
A clear example of interspecific variation is the number of root cortical layers in plants. The genetic
mechanisms underlying this variability are poorly understood, partly due to the lack of a convenient
model. Here, we demonstrate that Cardamine hirsuta, unlike Arabidopsis thaliana, has two cortical
layers that are patterned during late embryogenesis. We show that a miR165/6-dependent
distribution of the HOMEODOMAIN LEUCINE ZIPPER III (HD-ZIPIII) transcription factor
PHABULOSA (PHB) controls this pattern. Our findings reveal that interspecies variation in
miRNA distribution can determine differences in anatomy in plants
Experiments on standing bubbles in a vertical pipe
We present a series of laboratory experiments in which a steady stream of air is supplied through a small hole in the wall of a vertical pipe of rectangular cross-section down which there is a steady flux of water. For a range of liquid flow rates, the air forms a steady standing bubble whose nose is attached to the point of air supply. The steady bubble sheds a flux of much smaller air bubbles at its base, located downstream of the air injection point. The minimum liquid speed for which steady standing bubbles develop occurs at a particular Froude number of the liquid flow, Frd = U/ = 0.38, where U is the upstream speed, g the acceleration due to gravity and d the width of the cell. These trapped bubbles are distinct from the freely rising Taylor bubble, in that the Froude number at the nose is variable. Also, on a length scale greater than that influenced by surface tension, we find that the bubble nose asymptotes to a cusp-like shape, with an angle that decreases with Frd. We show that numerical solutions of the potential flow equations replicate the bubble shape and angle of the cusp, which appear independent of the gas flux. We also find that there is a minimum gas flux for which these standing bubbles develop. As the gas flux decreases below this threshold, the standing bubbles become unstable and, instead, a much shorter oscillating bubble develops. This produces a wake which has similarities with that formed downstream of a cylinder in a confined channel, but which also carries bubbles downstream. We also find that with sufficiently small gas flux, no bubble develops. For liquid flow rates smaller than the critical value, Frd < 0.38, we find that the bubbles become unstable and detach from the injection point and rise up the tube
Alternate wiring of a KNOXI genetic network underlies differences in leaf development of A. thaliana and C. hirsuta
Two interrelated problems in biology are understanding the regulatory logic and predictability of morphological evolution. Here, we studied these problems by comparing Arabidopsis thaliana, which has simple leaves, and its relative, Cardamine hirsuta, which has dissected leaves comprising leaflets. By transferring genes between the two species, we provide evidence for an inverse relationship between the pleiotropy of SHOOTMERISTEMLESS (STM) and BREVIPEDICELLUS (BP) homeobox genes and their ability to modify leaf form. We further show that cis-regulatory divergence of BP results in two alternative configurations of the genetic networks controlling leaf development. In C. hirsuta, ChBP is repressed by the microRNA164A (MIR164A)/ChCUP-SHAPED COTYLEDON (ChCUC) module and ChASYMMETRIC LEAVES1 (ChAS1), thus creating cross-talk between MIR164A/CUC and AS1 that does not occur in A. thaliana. These different genetic architectures lead to divergent interactions of network components and growth regulation in each species. We suggest that certain regulatory genes with low pleiotropy are predisposed to readily integrate into or disengage from conserved genetic networks influencing organ geometry, thus rapidly altering their properties and contributing to morphological divergence
Cytokinin acts through the auxin influx carrier AUX1 to regulate cell elongation in the root
Hormonal interactions are critical for plant development. In Arabidopsis, cytokinins inhibit root growth through effects on cell proliferation and cell elongation. Here we define key mechanistic elements in a regulatory network by which cytokinin inhibits root cell elongation in concert with the hormones auxin and ethylene. The auxin importer AUX1 functions as a positive regulator of cytokinin responses in the root, AUX1 mutants specifically affecting the ability of cytokinin to inhibit cell elongation but not cell proliferation. AUX1 is required for cytokinin-dependent changes of auxin activity in the lateral root cap associated with the control of cell elongation. Cytokinin regulates root cell elongation through ethylene-dependent and independent mechanisms, both hormonal signals converging on AUX1 as a regulatory hub. An autoregulatory circuit is identified involving the control of ARR10 and AUX1 expression by cytokinin and auxin, this circuit potentially functioning as an oscillator to integrate the effects of these two hormones. Taken together, our results uncover several regulatory circuits controlling interactions of cytokinin with auxin and ethylene, and support a model in which cytokinin regulates shootward auxin transport to control cell elongation and root growth
Branching out in roots: uncovering form, function, and regulation
Root branching is critical for plants to secure anchorage and ensure the supply of water, minerals, and nutrients. To date, research on root branching has focused on lateral root development in young seedlings. However, many other programs of postembryonic root organogenesis exist in angiosperms. In cereal crops, the majority of the mature root system is composed of several classes of adventitious roots that include crown roots and brace roots. In this Update, we initially describe the diversity of postembryonic root forms. Next, we review recent advances in our understanding of the genes, signals, and mechanisms regulating lateral root and adventitious root branching in the plant models Arabidopsis (Arabidopsis thaliana), maize (Zea mays), and rice (Oryza sativa). While many common signals, regulatory components, and mechanisms have been identified that control the initiation, morphogenesis, and emergence of new lateral and adventitious root organs, much more remains to be done. We conclude by discussing the challenges and opportunities facing root branching research
Role of transcriptional regulation in auxin-mediated response to abiotic stresses
Global climate change (GCC) is posing a serious threat to organisms, particularly plants, which are sessile. Drought, salinity, and the accumulation of heavy metals alter soil composition and have detrimental effects on crops and wild plants. The hormone auxin plays a pivotal role in the response to stress conditions through the fine regulation of plant growth. Hence, rapid, tight, and coordinated regulation of its concentration is achieved by auxin modulation at multiple levels. Beyond the structural enzymes involved in auxin biosynthesis, transport, and signal transduction, transcription factors (TFs) can finely and rapidly drive auxin response in specific tissues. Auxin Response Factors (ARFs) such as the ARF4, 7, 8, 19 and many other TF families, such as WRKY and MADS, have been identified to play a role in modulating various auxin-mediated responses in recent times. Here, we review the most relevant and recent literature on TFs associated with the regulation of the biosynthetic, transport, and signalling auxin pathways and miRNA-related feedback loops in response to major abiotic stresses. Knowledge of the specific role of TFs may be of utmost importance in counteracting the effects of GCC on future agriculture and may pave the way for increased plant resilience
Proteomic Characterization of Collagen-Based Animal Glues for Restoration
Animal glues are widely used in restoration as adhesives, binders, and consolidants for organic and inorganic materials. Their variable performances are intrinsically linked to the adhesive properties of collagen, which determine the chemical, physical, and mechanical properties of the glue. We have molecularly characterized the protein components of a range of homemade and commercial glues using mass spectrometry techniques. A shotgun proteomic analysis provided animal origin, even when blended, and allowed us to distinguish between hide and bone glue on the basis of the presence of collagen type III, which is abundant in connective skin/leather tissues and poorly synthetized in bones. Furthermore, chemical modifications, a consequence of the preparation protocols from the original animal tissue, were thoroughly evaluated. Deamidation, methionine oxidation, and backbone cleavage have been analyzed as major collagen modifications, demonstrating their variability among different glues and showing that, on average, bone glues are less deamidated than hide glues, but more fragmented, and mixed-collagen glues are overall less deamidated than pure glues. We believe that these data may be of general analytical interest in the characterization of collagen-based materials and may help restorers in the selection of the most appropriate materials to be used in conservation treatments
Cytokinin promotes growth cessation in the Arabidopsis root
The Arabidopsis root offers good opportunities to investigate how regulated cellular growth shapes different
tissues and organs, a key question in developmental biology. Along the root’s longitudinal axis, cells sequentially occupy different developmental states. Proliferative meristematic cells give rise to differentiating cells,
which rapidly elongate in the elongation zone, then mature and stop growing in the differentiation zone. The
phytohormone cytokinin contributes to this zonation by positioning the boundary between the meristem and
the elongation zone, called the transition zone. However, the cellular growth profile underlying root zonation
is not well understood, and the cellular mechanisms that mediate growth cessation remain unclear. By using
time-lapse imaging, genetics, and computational analysis, we analyze the effect of cytokinin on root zonation
and cellular growth. We found that cytokinin promotes growth cessation in the distal (shootward) elongation
zone in conjunction with accelerating the transition from elongation to differentiation. We estimated cell-wall
stiffness by using osmotic treatment experiments and found that cytokinin-mediated growth cessation is
associated with cell-wall stiffening and requires the action of an auxin influx carrier, AUX1. Our measurement
of growth and cell-wall mechanical properties at a cellular resolution reveal mechanisms via which cytokinin
influences cell behavior to shape tissue patterns
Inhibition of Polycomb Repressive Complex2 activity reduces trimethylation of H3K27 and affects development in Arabidopsis seedlings
Background: Polycomb repressive complex 2 (PRC2) is an epigenetic transcriptional repression system, whose
catalytic subunit (ENHANCER OF ZESTE HOMOLOG 2, EZH2 in animals) is responsible for trimethylating histone H3
at lysine 27 (H3K27me3). In mammals, gain-of-function mutations as well as overexpression of EZH2 have been
associated with several tumors, therefore making this subunit a suitable target for the development of selective
inhibitors. Indeed, highly specific small-molecule inhibitors of EZH2 have been reported. In plants, mutations in
some PRC2 components lead to embryonic lethality, but no trial with any inhibitor has ever been reported.
Results: We show here that the 1,5-bis (3-bromo-4-methoxyphenyl)penta-1,4-dien-3-one compound (RDS 3434),
previously reported as an EZH2 inhibitor in human leukemia cells, is active on the Arabidopsis catalytic subunit of
PRC2, since treatment with the drug reduces the total amount of H3K27me3 in a dose-dependent fashion.
Consistently, we show that the expression level of two PRC2 targets is significantly increased following treatment
with the RDS 3434 compound. Finally, we show that impairment of H3K27 trimethylation in Arabidopsis seeds and
seedlings affects both seed germination and root growth.
Conclusions: Our results provide a useful tool for the plant community in investigating how PRC2 affects
transcriptional control in plant development
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