Biology subjects

Dejean, M.

Publications and source records attributed to Dejean, M..

4 recordsLinked to original sources

bioRxiv2026

Uncovering genetic determinants of rice root anatomy using genome wide analysis

Root anatomy plays a critical role in water and nutrients acquisition and influences plant adaptation to abiotic stresses. A better understanding of the genetic control of anatomical traits is important to improve rice production, a staple crop for half of the worlds population. In this study, we measured eleven root anatomical traits in a collection of 185 Vietnamese rice landraces, and conducted genome-wide association studies to uncover the genetic architecture underlying these traits. A total of 24 significant small nucleotide polymorphisms were identified, corresponding to 19 quantitative trait loci for traits such as root cross section area, cortex area, metaxylem area or theoretical axial conductance. Interestingly, several root anatomical traits correlated with previously characterized root architectural traits measured within the same Vietnamese rice collection, and some genetic regions associated with anatomical traits and drought-tolerance-related traits colocalized. Candidate genes potentially involved in root development and cell wall patterning were identified within these QTLs regions. In particular, the significant SNP in qRA10.1 associated with metaxylem area induces an amino-acid change in the kinase domain of a wall associated kinase (WAK) receptor-like protein kinase (OsWAK111) with an extracellular epidermal growth factor (EGT)-containing domain that bind pectin, which presumably sense perturbations in this component to influence cell elongation during plant development. This study reveal key determinants of the genetic control of root anatomy in rice, which could be exploited to enhance tolerance to abiotic stresses such as drought.

plant biology↗

bioRxiv2021

Quantitative imaging of transcription in living Drosophila embryos reveals the impact of core promoter motifs on promoter state dynamics

Genes are expressed in stochastic transcriptional bursts linked to alternating active and inactive promoter states. A major challenge in transcription is understanding how promoter composition dictates bursting, particularly in multicellular organisms. We investigate two key Drosophila developmental promoter motifs, the TATA box (TATA) and the Initiator (INR). Using live imaging in Drosophila embryos and new computational methods, we demonstrate that bursting occurs on multiple timescales ranging from seconds to minutes. TATA-containing promoters and INR-containing promoters exhibit distinct dynamics, with one or two separate rate-limiting steps respectively. A TATA box is associated with long active states, high rates of polymerase initiation, and short-lived, infrequent inactive states. In contrast, the INR motif leads to two inactive states, one of which relates to promoter-proximal polymerase pausing. Surprisingly, the model suggests pausing is not obligatory, but occurs stochastically for a subset of polymerases. Overall, our results provide a rationale for promoter switching during zygotic genome activation.

molecular biology↗

bioRxiv2020

Imaging translation dynamics in live embryos reveals spatial heterogeneities

The translation of individual mRNA molecules is a key biological process, yet this multi-step process has never been imaged in living multicellular organisms. Here we deploy the recently developed Suntag method to visualize and quantify translation dynamics of single mRNAs in living Drosophila embryos. By focusing on the translation of the conserved major epithelial-mesenchymal transition (EMT)-inducing transcription factor Twist, we identified spatial heterogeneity in mRNA translation efficiency and reveal the existence of translation factories, where clustered mRNAs are co-translated preferentially at basal perinuclear regions. Simultaneous visualization of transcription and translation dynamics in a living multicellular organism opens exciting new avenues for understanding of gene regulation during development.

developmental biology↗

bioRxiv2018

Temporal Control of Transcription by Zelda in living Drosophila embryos

Abstract/introPioneer factors have the exquisite ability to engage their target sites at nucleosomal DNA, which leads to a local remodeling of chromatin and the establishment of a transcriptional competence. However, the direct impact of enhancer priming by pioneer factors on the temporal control of gene expression and on mitotic memory remains elusive. In Drosophila embryos, the maternally deposited activator Zelda (Zld) exhibits key pioneer factor properties and indeed regulates the awakening of the zygotic genome. The analysis of thousands of endogenous Zld bound regions in various genetic contexts, as well as the study of isolated synthetic enhancers with static approaches, led to the proposal that Zld could act as a quantitative developmental timer. Here we employ quantitative live imaging methods and mathematical modeling to directly test the effect of Zld on temporal coordination in gene activation and on mitotic memory. Using an automatic tracking software, we quantified the timing of activation in hundreds of nuclei and their progeny in Drosophila embryos. We demonstrate that increasing the number of Zld binding sites accelerates the kinetics of transcriptional activation regardless of their past transcriptional state. In spite of its known pioneering activities, we show that Zld is not a mitotic bookmarker and is neither necessary nor sufficient to foster mitotic memory. Fluorescent recovery after photo-bleaching and fluorescent correlation spectroscopy experiments reveal that, Zld is highly dynamic and exhibits transient binding to chromatin. We propose that Zld low binding rates could be compensated for by local accumulation of Zld in nuclear microenvironments in vivo, thus allowing rapid and coordinated gene activation.

developmental biology↗