Biology subjects

Roeder, A. H. K.

Publications and source records attributed to Roeder, A. H. K..

At least 19 recordsLinked to original sources

bioRxiv2026

Stomatal patterning is shaped by the interplay with giant cell patterning in Arabidopsis

In developing tissues, cells differentiate into distinct cell types and form complex spatial patterns. How distinct patterning systems interact during tissue growth to shape tissue composition and spatial organization remains poorly understood. Here, we investigate this question in the abaxial leaf epidermis of Arabidopsis thaliana, in which the same pool of progenitor cells gives rise to stomata, pavement cells, and giant cells. Using a quantitative approach combining Euclidean and network-based spatial analysis, we show that stomatal number and density are robust to reduced endoreduplication, whereas forced endoreduplication actively competes with the stomatal lineage to reduce stomatal number. Furthermore, we show that the stomatal spatial pattern is also shaped by the broader tissue context such as cell growth, cell division, and giant cell patterning, with distinct consequences for stomatal spatial distribution and cellular arrangement. Our results highlight that the interplay between patterning systems must be considered to understand how tissue organization is established.

plant biology↗

bioRxiv2025

APETALA2 controls seed growth by regulating outer integument mechanical identity during seed coat differentiation

Organ morphogenesis requires differentiating cells to acquire mechanical properties that precisely regulate growth. In Arabidopsis thaliana, seed size and shape are largely controlled by the outer integument of the seed coat, whose two layers develop distinct mechanical behaviors critical for growth regulation. Here, we show that the cell identity factor APETALA2 (AP2) both promotes and restricts seed growth by coordinating the post-fertilization differentiation of these layers into distinct seed coat tissues. AP2 drives layer-specific remodeling of cell wall composition, notably affecting pectin and xyloglucan, thereby establishing contrasting mechanical properties between the two layers. Unexpectedly, these changes in wall composition and mechanics do not alter mechanosensitive responses, revealing a surprising uncoupling between cell wall remodeling and mechanotransduction. Our findings identify AP2 as a key coordinator of tissue-specific mechanical differentiation during organ morphogenesis.

plant biology↗

bioRxiv2025

Brassinosteroids mediate proper coordination of sepal elongation

Arabidopsis sepals must grow in a coordinated and robust fashion to a consistent size and shape to close and protect the developing flower bud. To understand how this robust coordination occurs, we use the loss of robustness mutant development related myb-like1 (drmy1), which exhibits variable sepal initiation and growth, causing failure of the sepals to close the flower bud. Specifically, drmy1 has overgrown outer (abaxial) sepals and undergrown inner (adaxial) sepals, leading to a large discrepancy in the sizes of different sepals within individual flower buds. Using single cell and spatial RNA-seq, we found changes in expression of key genes related to brassinosteroid (BR) signaling in drmy1, particularly in cell types important to young flower bud development such as epidermal cells, boundary cells, and meristematic cells. Confocal imaging of a BRI1-EMS-SUPPRESSOR1 (BES1) ratiometric reporter confirms that BR signaling is upregulated and more variable in young drmy1 sepals. Subsequently, we found that altering BR signaling in drmy1 by crossing with BR mutants or adding brassinolide (a potent brassinosteroid) or brassinazole (a brassinosteroid biosynthesis inhibitor) can partially rescue this elongation defect by differentially altering the relative growth of the inner and outer sepals. Increasing BR signaling rescues by increasing the growth of the inner sepal but not the outer sepal, while decreasing BR signaling rescues by decreasing the growth of the outer sepal but not the inner sepal. These results suggest that brassinosteroids mediate the robust coordination of the growth rates between inner and outer sepals during early development, ensuring proper flower bud closure.

developmental biology↗

bioRxiv2025

The Role of SIAMESE in G2 Checkpoint Regulation in Arabidopsis thaliana

In Arabidopsis, SIAMESE (SIM) is a cyclin-dependent kinase inhibitor that restricts progression through mitosis. SIM is well known as a regulator of endoreplication in trichomes and roots. Mathematical modeling of the cell cycle has indicated that SIM may also modulate the length of G2 during mitotic cycles, potentially replacing the WEE1/CDC25 circuit that regulates G2 timing in animals and fungi, which is absent in plants. The predictions of this model were tested in several ways. First, the root meristem is longer in sim mutant roots than in wild-type (WT) roots. Second, two independent methods of measuring cell cycle phases, long-term live-cell imaging using fluorescent protein cell cycle markers and 5-ethynyl-2-deoxyuridine (EdU) pulse-chase imaging, showed that the length of G2 in root meristem cortex cells is shorter in sim mutant plants compared to WT, consistent with the view that these changes in G2 length are due to greater G2 CDK activity in sim mutants. Additionally, the fluorescence of a CYCB:GFP fusion both rose and declined more sharply in the mutant than in wild-type. Because both transcription and degradation of this fusion are directly affected by G2 CDK activity, this result is consistent with sim mutants having greater G2 CDK activity. Taken together, these results suggest that, in addition to its known role in inducing endoreplication, SIM may play a role in regulating the length of G2 during mitotic cycles, at least partially replacing the absence of WEE1/CDC25 regulation of the mitotic cell cycle.

plant biology↗

bioRxiv2025

ROS inhibits microtubule dynamics and cell growth heterogeneity during Arabidopsis sepal morphogenesis

Developing organs grow to reproducible sizes and shapes yet the growth of their constituent cells can be highly heterogeneous and fluctuating. During wild-type Arabidopsis thaliana sepal development, the fluctuations in cell growth average such that the sepals grow to uniform sizes and shapes. The uniform size and shape of the sepals allow the flower bud to stay closed and protected until the floral organs are mature. In contrast, cell growth averaging is reduced in the ftsh4-5 mutant, and the sepals develop to variable sizes and shapes. FTSH4 encodes a mitochondrial i-AAA protease localized to the mitochondria. Reactive oxygen species (ROS) accumulate in ftsh4-5 mutants, and lowering ROS levels rescues the sepal size and shape variability. Here, we investigate the effects of ROS on cell growth heterogeneity and cortical microtubule dynamics. We find that elevated ROS suppresses cell growth heterogeneity and averaging. We also find that elevated ROS causes cortical microtubules to become more crisscrossed, as well as more stable. The growth of the cells with crisscrossed microtubules changes less in time, which impairs cell growth averaging. However, depolymerizing microtubules is insufficient to restore normal growth fluctuations. Altogether, our results suggest that ROS affects microtubule dynamics and cell growth fluctuations which are necessary for robust morphogenesis.

developmental biology↗

bioRxiv2025

Spatial ploidy inference using quantitative imaging

Polyploidy (whole-genome multiplication) is a common yet under-surveyed property of tissues across multicellular organisms. Polyploidy plays a critical role during tissue development, following acute stress, and during disease progression. Common methods to reveal polyploidy involve either destroying tissue architecture by cell isolation or by tedious identification of individual nuclei in intact tissue. Therefore, there is a critical need for rapid and high-throughput ploidy quantification using images of nuclei in intact tissues. Here, we present iSPy (Inferring Spatial Ploidy), a new unsupervised learning pipeline that is designed to create a spatial map of nuclear ploidy across a tissue of interest. We demonstrate the use of iSPy in Arabidopsis, Drosophila, and human tissue. iSPy can be adapted for a variety of tissue preparations, including whole mount and sectioned. This high-throughput pipeline will facilitate rapid and sensitive identification of nuclear ploidy in diverse biological contexts and organisms.

developmental biology↗

bioRxiv2024

Mechanical regulation of tissue flatness in Marchantia

The production of flat organs involves a tight regulation of tissue expansion. During growth, the cell wall is under mechanical tension and continuous remodelling, requiring mechanisms to sense and maintain cell wall integrity (CWI). Here we studied the link between CWI sensing and flatness of Marchantia polymorpha thalli. We considered FERONIA (FER), a CWI sensor, and assessed its role in the maintenance of thallus shape. We developed a pipeline to quantify flatness at multiple scales. We found that both abolishing and increasing FER expression leads to loss of flatness. Based on experiments that reduce cell wall tension and partially restore wild-type cell size and thallus morphology, we ascribe loss of flatness to under- or to over-reaction of plants to mechanical stress. Altogether, our results support the concept that responses to mechanical stress contribute to the robustness of morphogenesis

plant biology↗

bioRxiv2024

Mechanical properties are tuned during development with the fibrous network nature of the Arabidopsis cell wall

During plant development, the mechanical properties of the cell walls must be tuned to regulate the growth of the cells. Cell growth involves significant stretching of the cell walls, yet little is known about the mechanical properties of cell walls under such substantial deformation, or how these mechanical properties change to regulate development. Here, we investigated the mechanical behavior of the Arabidopsis leaf epidermal cells being stretched. We found that the mechanical properties arise from the cell wall, which behaves as a fibrous network material. The epidermis exhibited a non-linear stiffening behavior that fell into three regimes. Each regime corresponded to distinct nonlinear behaviors in terms of transverse deformation (i.e., Poisson effect) and unrecoverable deformation (i.e., plasticity). Using a model, we demonstrated that the transition from reorientation and bending-dominated to stretch-dominated deformation modes of cellulose microfibrils cause these nonlinear behaviors. We found the stiffening behavior is more pronounced at later developmental stages. Finally, we show the spiral2-2 mutant has anisotropic mechanical properties, likely contributing to the spiraling of leaves. Our findings reveal the fibrous network nature of cell walls gives a high degree of tunability in mechanical properties, which allows cells to adjust these properties to support proper development.

plant biology↗

bioRxiv2024

Stochastic Gene Expression in Auxin Signaling in the Floral Meristem of Arabidopsis thaliana

Cells display striking stochasticity in gene expression, which plays an important role in development, disease, and regeneration. Previous studies have found stochastic gene expression in bacteria, yeast, and from constitutive promoters in Arabidopsis. However, most promoters are non-constitutive. Stochastic gene expression from non-constitutive promoters in a multicellular organism, especially those with key developmental roles, remains largely uncharacterized. Here, we report stochastic expression of auxin responsive genes in the Arabidopsis floral meristem, using promoter reporters of DR5, ARABIDOPSIS HISTIDINE PHOSPHOTRANSFER PROTEIN6 (AHP6), and DNA BINDING WITH ONE FINGER5.8 (DOF5.8). We found highly variable DR5 expression patterns among younger meristems. Such variability is not attributed to heterogeneity in auxin perception, but to downstream stochastic expression of DR5, mainly influenced by cell-intrinsic molecular noise. Expression of AHP6 and DOF5.8 is also noisy, although their noise is lower and has distinct spatiotemporal patterns unlike DR5. Finally, we propose spatial averaging as a mechanism that buffers cellular gene expression noise, allowing the formation of robust global expression patterns. Our study reveals stochastic gene expression downstream of auxin signaling, a key developmental player. Thus, stochastic gene expression from non-constitutive promoters, including those involved in hormone signaling, is an ordinary part of multicellular life.

developmental biology↗

bioRxiv2024

The receptor-like kinase ALE2 promotes giant cell formation in the sepal epidermis

During sepal development in Arabidopsis thaliana, epidermal pavement cells differentiate into small cells and large, highly endoreduplicated giant cells. While the placement of giant cells differs between sepals, the number of giant cells is fairly consistent. The HD-ZIP class IV transcription factor ATML1 has been found to promote giant cell formation. ATML1 protein fluctuates within epidermal nuclei of developing sepals and high ATML1 concentrations reached in the G2 phase of the cell cycle strongly correlates with giant cell fate specification. A genetic screen for reduced giant cell number identified the receptor-like kinase ABNORMAL LEAF SHAPE2 (ALE2) as being important for giant cell formation. We find that ALE2 functions genetically upstream of ATML1 in promoting the formation of giant cells. We observe that nuclear-localized mCitrine-ATML1 fluctuates in ale2 mutants much as it does in wild type and, importantly, nuclear mCitrine-ATML1 reaches similarly high peak concentrations in ale2-1 mutants as in wild type. This indicates that ALE2 functions upstream of ATML1 by affecting protein activity rather than gene expression or protein degradation. One function of ATML1 is to promote transcription of the CDK inhibitor LGO. We find that LGO transcription is delayed and decreased in ale2-1 mutants as compared to wild-type plants, consistent with ATML1 having impaired protein function in ale2 mutants. Overall, we find that the receptor-like kinase ALE2 is necessary to sensitize cells of the developing sepal epidermis to fluctuations of the transcription factor ATML1.

plant biology↗

bioRxiv2024

A common pathway controls cell size in the sepal and leaf epidermis leading to a non-random pattern of giant cells

Arabidopsis leaf epidermal cells have a wide range of sizes and ploidies, but the mechanisms patterning their size and spatial distribution remain unclear. Here, we show that the same genetic pathway creating giant cells in sepals also regulates cell size in the leaf epidermis, leading to the formation of giant cells. In both sepals and leaves, giant cells are scattered among smaller cells; therefore, we asked whether their spatial arrangement is random. By comparing sepal and leaf epidermises with computationally generated randomized tissues we show that the giant cell pattern becomes less random across the epidermis as the cells surrounding giant cells divide, leading to clustered patterns in mature tissues. Our cell-autonomous and stochastic computational model reproduces the giant cell organization, suggesting that random giant cell initiation together with the divisions of surrounding cells lead to the observed clustered pattern. These findings reveal that cell-size patterning is developmentally regulated by common mechanisms in leaves and sepals, and the spatial pattern of giant cells emerges from the interplay between stochastic cell- autonomous gene expression and tissue growth.

plant biology↗

bioRxiv2024

The transcription factor ATML1 maintains giant cell identity by inducing synthesis of its own (very) long-chain fatty acid-containing ligands

During development, cells not only adopt specialized identities but also maintain those identities. Endoreduplication is thought to maintain cell identity. High concentrations of ARABIDOPSIS THALIANA MERISTEM LAYER1 (ATML1) specify giant cell identity and induce endoreduplication in sepals. How different concentrations of ATML1 can specify different identities remains unclear. Here, we show that high concentrations of ATML1 induce the biosynthesis of both long-chain and very long-chain fatty acids (LCFAs/VLCFAs), and these fatty acids are required for the maintenance of giant cell identity. Inhibition of VLCFA biosynthesis causes endoreduplicated giant cells to resume division and lose their identity, indicating that endoreduplication is not sufficient to maintain cell identity. Structural predictions suggest that LCFA-containing lipids bind to the START domain 2 of ATML1, causing ATML1 dimerization and its auto-activation. Our data and modeling imply that ATML1 induces biosynthesis of its own lipid ligands in a positive feedback loop, shedding light on the intricate network dynamics that specify and maintain giant cell identity. Teaser: Endoreduplicated cells in Arabidopsis thaliana sepals divide and de-differentiate in the absence of VLCFA biosynthesis.

plant biology↗

bioRxiv2023

A 3-component module maintains sepal flatness in Arabidopsis

As in origami, morphogenesis in living systems heavily relies on tissue curving and folding, through the interplay between biochemical and biomechanical cues. In contrast, certain organs maintain their flat posture over several days. Here we identified a pathway, which is required for the maintenance of organ flatness, taking the sepal, the outermost floral organ, in Arabidopsis as a model system. Through genetic, cellular and mechanical approaches, our results demonstrate that global gene expression regulator VERNALIZATION INDEPENDENCE 4 (VIP4) fine-tunes the mechanical properties of sepal cell walls and maintains balanced growth on both sides of the sepals, mainly by orchestrating the distribution pattern of AUXIN RESPONSE FACTOR 3 (ARF3). vip4 mutation results in softer cell walls and faster cell growth on the adaxial sepal side, which eventually cause sepals to bend outward. Downstream of VIP4, ARF3 works through modulating auxin signaling to down-regulate pectin methylesterase VANGUARD1, resulting in decreased cell wall stiffness. Our work unravels a 3-component module, which relates hormonal patterns to organ curvature, and actively maintains sepal flatness during its growth.

plant biology↗

bioRxiv2023

Tradeoff Between Speed and Robustness in Primordium Initiation Mediated by Auxin-CUC1 Interaction

Robustness is the reproducible development of a phenotype despite stochastic noise. It often involves tradeoffs with other performance metrics, but the mechanisms underlying such tradeoffs were largely unknown. An Arabidopsis flower robustly develops four sepals from four precisely positioned auxin maxima. The development related myb-like 1 (drmy1) mutant generates noise in auxin signaling that disrupts robustness in sepal initiation. Here, we found that increased expression of CUP-SHAPED COTYLEDON1 (CUC1), a boundary specification transcription factor, in drmy1 underlies this loss of robustness. CUC1 surrounds and amplifies stochastic auxin noise in drmy1 to form variably positioned auxin maxima and sepal primordia. Removing CUC1 from drmy1 provides time for noisy auxin signaling to resolve into four precisely positioned auxin maxima, restoring robust sepal initiation. However, removing CUC1 decreases auxin maxima intensity and slows down sepal initiation. Thus, CUC1 increases morphogenesis speed but impairs robustness against auxin noise. Further, using a computational model, we found that the observed phenotype can be explained by the effect of CUC1 in repolarizing PIN FORMED1 (PIN1), a polar auxin transporter. Lastly, our model predicts that reducing global growth rate improves developmental robustness, which we validated experimentally. Thus, our study illustrates a tradeoff between speed and robustness during development.

developmental biology↗

bioRxiv2023

Growth couples temporal and spatial fluctuations of tissue properties during morphogenesis

Living tissues display fluctuations - random spatial and temporal variations of tissue properties around their reference values - at multiple scales. It is believed that such fluctuations may enable tissues to sense their state or their size. Recent theoretical studies developed specific models of fluctuations in growing tissues and predicted that fluctuations of growth show long-range correlations. Here we elaborated upon these predictions and we tested them using experimental data. We first introduced a minimal model for the fluctuations of any quantity that has some level of temporal persistence or memory, such as concentration of a molecule, local growth rate, or mechanical property. We found that long-range correlations are generic, applying to any such quantity, and that growth couples temporal and spatial fluctuations, through a mechanism that we call fluctuation stretching -- growth enlarges the lengthscale of variation of this quantity. We then analysed growth data from sepals of the model plant Arabidopsis and we quantified spatial and temporal fluctuations of cell growth using the previously developed Cellular Fourier Transform. Growth appears to have long-range correlations. We compared different genotypes and growth conditions: mutants with lower or higher response to mechanical stress have lower temporal correlations and longer-range spatial correlations than wild-type plants. Finally, we used theoretical predictions to merge experimental data from all conditions and developmental stages into an unifying curve, validating the notion that temporal and spatial fluctuations are coupled by growth. Altogether, our work reveals kinematic constraints on spatiotemporal fluctuations that have an impact on the robustness of morphogenesis. Significance StatementHow do organs and organisms grow and achieve robust shapes in the face of subcellular and cellular variability? In order to address this outstanding mystery, we investigated the variability of growth at multiple scales and we analysed experimental data from growing plant tissues. Our results support the prediction that tissue expansion couples temporal memory of growth with spatial variability of growth. Our work reveals a constraint on the spatial and temporal variability of growth that may impact the robustness of morphogenesis.

biophysics↗

bioRxiv2023

Puzzle cell shape emerges from the interaction of growth with mechanical constraints

Puzzle-shaped epidermal cells not only reduce mechanical stress during organ growth but also record the expansion history of the tissue in their outlines. By combining mechanical simulations with time-lapse imaging, we show that transitions from directional to isotropic expansion induce new lobes to form along the previous growth axis, and that switching the order of anisotropic and isotropic phases yields hybrid shapes that reliably preserve those transitions. In maize, model predictions and live imaging coincide precisely, and in Ara-bidopsis, final lobe patterns correlate more with growth history than with cell size alone. Ge-netic or pharmacological disruption of lobe formation constrains leaf expansion or drives compensatory elongation, which underscores a mechanical function. A broad survey of living and fossil vascular plants reveals that the mechanism to make puzzle-shaped cells is both widespread and developmentally plastic, suggesting that single snapshots of leaves can give insight into their growth history. Together, these findings demonstrate that puzzle cells trans-form cell geometry into a living record of how tissues grow.

plant biology↗

bioRxiv2023

Growth directions and stiffness across cell layers determine whether tissues stay smooth or buckle

From smooth shapes to buckles, nature exhibits organs of various shapes and forms. How cells grow to produce smooth shaped leaves and sepals remain unclear. Here, we show that growth along the longitudinal axis during early developmental stages and comparable stiffness across both epidermal layers of Arabidopsis sepals are essential for smoothness, as seen in the wild type. We identified a mutant (as2-7D) with ectopic expression of ASYMMETRIC LEAVES 2 (AS2) on the outer epidermis. Our analysis reveals that ectopic AS2 expression causes the outer epidermis of as2-7D sepals to buckle during early stages of sepal development. We show that buckling of the outer epidermis occurs due to conflicting cell growth directions and unequal tissue stiffness across the epidermal layers. Overexpression of cyclin-dependent kinase (CDK) inhibitor Kip-related protein 1 (KRP1) in as2-7D restores sepal smoothness by aligning the growth directions of the outer epidermal cells along the longitudinal axis, while also increasing the overall stiffness of the outer epidermis. Furthermore, buckling is associated with the convergence of auxin efflux transporter protein PIN-FORMED 1 (PIN1) to generate outgrowth in the sepals at later stages, suggesting that buckling can initiate outgrowths. Our findings suggest that in addition to molecular cues influencing tissue mechanics, tissue mechanics can also modulate molecular signals, giving rise to well-defined shapes. One-Sentence SummaryThe asymmetric leaves 2-7D mutant sepals buckle due to discoordination of growth between the two epidermal layers.

developmental biology↗

bioRxiv2023

DRMY1 promotes robust morphogenesis by sustaining translation of a hormone signaling protein

Robustness is the invariant development of phenotype despite environmental changes and genetic perturbations. In the Arabidopsis flower bud, four sepals robustly initiate and grow to constant size to enclose and protect the inner floral organs. We previously characterized the mutant development related myb-like1 (drmy1), where 3-5 sepals initiate variably and grow to different sizes, compromising their protective function. The molecular mechanism underlying this loss of robustness was unclear. Here, we show that drmy1 has reduced TARGET OF RAPAMYCIN (TOR) activity, ribosomal content, and translation. Translation reduction decreases the protein level of ARABIDOPSIS RESPONSE REGULATOR7 (ARR7) and ARABIDOPSIS HISTIDINE PHOSPHOTRANSFER PROTEIN 6 (AHP6), two cytokinin signaling inhibitors that are normally rapidly produced before sepal initiation. The resultant upregulation of cytokinin signaling disrupts robust auxin patterning and sepal initiation. Our work shows that the homeostasis of translation, a ubiquitous cellular process, is crucial for the robust spatiotemporal patterning of organogenesis.

developmental biology↗