Leaf growth in dicots and monocots : so different yet so alike

In plants, most organs grow post-embryonically through cell division and cell expansion. The coordination of these two growth processes is generally considered to be different between dicots and monocots. In dicot plants, such as the model plant Arabidopsis, leaf growth is most often described as being temporally regulated with cell division ceasing earlier at the tip and continuing longer at the base of the leaf. Conversely, in monocot leaves, the organization of the growth processes is rather viewed as spatially regulated with dividing cells at the base of the leaf, followed by expanding cells and finally mature cells at the tip. As our understanding of the leaf growth processes in the two major classes of flowering plants expands, it becomes increasingly clear that the regulation of the growth processes is to a great extent conserved between dicots and monocots. In this review, we highlight how the temporal and spatial organization of cell division and cell expansion takes place in both dicot and monocot leaves. We also show that there are similarities in the molecular wiring that coordinates these two processes during leaf development

Emerging connections between small RNAs and phytohormones

Small RNAs (sRNAs), mainly including miRNAs and siRNAs, are ubiquitous in eukaryotes. sRNAs mostly negatively regulate gene expression via (post-)transcriptional gene silencing through DNA methylation, mRNA cleavage, or translation inhibition. The mechanisms of sRNA biogenesis and function in diverse biological processes, as well as the interactions between sRNAs and environmental factors, like (a)biotic stress, have been deeply explored. Phytohormones are central in the plant’s response to stress, and multiple recent studies highlight an emerging role for sRNAs in the direct response to, or the regulation of, plant hormonal pathways. In this review, we discuss recent progress on the unraveling of crossregulation between sRNAs and nine plant hormones

Control interno y el estrés laboral en Konecta Bto, S.L. Sucursal en Perú, Lima 2019

La presente investigación lleva por título “Control Interno Y El Estrés Laboral En Konecta Bto, S.L. Sucursal En Perú, Lima 2019”. El objetivo principal fue demostrar la relación del control interno y el estrés laboral en Konecta BTO, s.l. sucursal en Perú, Lima 2019. La muestra estuvo representada por 50 gestores. El muestreo fue censal puesto que se tomó a toda la población para realizar el estudio. La metodología utilizada fue hipotético-deductivo, tipo de investigación aplicada con diseño no experimental-transversal; además el nivel de investigación que se utilizó fue el Descriptivo Correlacional, ya que se trabajó con variables independientes y dependientes. Se usó el cuestionario como instrumento de recolección de datos y se aplicó como técnica la encuesta con 20 preguntas por cada variable sobre la muestra. Los datos fueron procesados utilizando el programa del SPSS Statistics v.24 y analizados por el método estadístico descriptivo e inferencial, se obtuvo como resultado que El control interno tiene relación con el estrés laboral en Konecta BTO, s.l. sucursal en Perú, Lima 2019

SCFSAP controls organ size by targeting PPD proteins for degradation in Arabidopsis thaliana

Control of organ size by cell proliferation and growth is a fundamental process, but the mechanisms that determine the final size of organs are largely elusive in plants. We have previously revealed that the ubiquitin receptor DA1 regulates organ size by repressing cell proliferation in Arabidopsis. Here we report that a mutant allele of STERILE APETALA (SAP) suppresses the da1-1 mutant phenotype. We show that SAP is an F-box protein that forms part of a SKP1/Cullin/F-box E3 ubiquitin ligase complex and controls organ size by promoting the proliferation of meristemoid cells. Genetic analyses suggest that SAP may act in the same pathway with PEAPOD1 and PEAPOD2, which are negative regulators of meristemoid proliferation, to control organ size, but does so independently of DA1. Further results reveal that SAP physically associates with PEAPOD1 and PEAPOD2, and targets them for degradation. These findings define a molecular mechanism by which SAP and PEAPOD control organ size

Biogeochemical budgets in three large reservoirs of the Seine basin (Marne, Seine & Aube reservoirs)

International audienc

Molecular networks regulating cell division during Arabidopsis leaf growth

Leaves are the primary organs for photosynthesis and as such have a pivotal role for plant growth and development. Leaf development is a multi-factorial and dynamic process involving many genes that regulate size, shape, and differentiation. The processes that mainly drive leaf development are cell proliferation and cell expansion, and numerous genes have been identified that, when ectopically expressed or down-regulated, increase cell number and/or cell size during leaf growth. Many of the genes regulating cell proliferation are functionally interconnected and can be grouped in regulatory modules. Here, we review our current understanding of six important gene regulatory modules affecting cell proliferation during Arabidopsis leaf growth: DA1-EOD1, GRF-GIF, SWI/SNF, GA-DELLA, KLU, and PEAPOD. Furthermore, we discuss how post-mitotic cell expansion and these six modules regulating cell proliferation make up final leaf size

Chloroplasts are central players in sugar-induced leaf growth

Leaves are the plant's powerhouses, providing energy for all organs through sugar production during photosynthesis. However, sugars serve not only as a metabolic energy source for sink tissues but also as signaling molecules, affecting gene expression through conserved signaling pathways to regulate plant growth and development. Here, we describe an in vitro experimental assay, allowing one to alter the sucrose (Suc) availability during early Arabidopsis (Arabidopsis thaliana) leaf development, with the aim to identify the affected cellular and molecular processes. The transfer of seedlings to Suc-containing medium showed a profound effect on leaf growth by stimulating cell proliferation and postponing the transition to cell expansion. Furthermore, rapidly after transfer to Suc, mesophyll cells contained fewer and smaller plastids, which are irregular in shape and contain fewer starch granules compared with control mesophyll cells. Short-term transcriptional responses after transfer to Suc revealed the repression of well-known sugar-responsive genes and multiple genes encoded by the plastid, on the one hand, and up-regulation of a GLUCOSE-6-PHOSPHATE TRANSPORTER (GPT2), on the other hand. Mutant gpt2 seedlings showed no stimulation of cell proliferation and no repression of chloroplast-encoded transcripts when transferred to Suc, suggesting that GPT2 plays a critical role in the Suc-mediated effects on early leaf growth. Our findings, therefore, suggest that induction of GPT2 expression by Suc increases the import of glucose-6-phosphate into the plastids that would repress chloroplast-encoded transcripts, restricting chloroplast differentiation. Retrograde signaling from the plastids would then delay the transition to cell expansion and stimulate cell proliferation

Immunoanalytical Approach for Detecting and Identifying Ancestral Peptide Biomarkers in Early Earth Analogue Environments

Several mass spectrometry and spectroscopic techniques have been used in the search for molecular biomarkers on Mars. A major constraint is their capability to detect and identify large and complex compounds such as peptides or other biopolymers. Multiplex immunoassays can detect these com-pounds, but antibodies must be produced for a large number of sequence-dependent molecular targets. Ancestral Sequence Re-construction (ASR) followed by protein "resurrection" in the lab can help to narrow the selection of targets. Herein, we propose an immunoanalytical method to identify ancient and universally conserved protein/peptide sequences as targets for identifying ancestral biomarkers in nature. We have developed, tested, and validated this approach by producing antibodies to eight previously described ancestral resurrected proteins (three beta-lactamases, three thioredoxins, one Elongation Factor Tu, and one RuBisCO, all of them theoretically dated as Precambrian), and used them as a proxy to search for any potential feature of them that could be present in current natural environments. By fluorescent sandwich microarray immunoassays (FSMI), we have detected positive immunoreactions with antibodies to the oldest beta-lactamase and thioredoxin proteins (ca. 4 Ga) in samples from a hydrothermal environment. Fine epitope mapping and inhibitory immunoassays allowed the identification of well-conserved epitope peptide sequences that resulted from ASR and were present in the sample. We corroborated these results by metagenomic sequencing and found several genes encoding analogue proteins with significant matches to the peptide epitopes identified with the antibodies. The results demonstrated that peptides inferred from ASR studies have true counterpart analogues in Nature, which validates and strengthens the well-known ASR/protein resurrection technique and our immunoanalytical approach for investigating ancient environments and metabolisms on Earth and elsewhere