BRI1 signaling at the dividing cells restores overall root growth

Slides:



Advertisements
Similar presentations
Plants and algae Fungi Metazoa Protist Supplementary Figure 1. Phylogenetic analysis of GlsA1/ZRF orthologs in different organisms. Coloured background.
Advertisements

Microtubule perturbations cause Ste5 patches to form less reliably, delay patch formation, and cause patches to persist for less time Microtubule perturbations.
Microtubule perturbations affect pathway variability η2(P) and transmitted signal P at or upstream of the Ste5 recruitment step Microtubule perturbations.
A stochastic feedback loop model predicts the kinetics of DDR and growth arrest at the single cell level. A stochastic feedback loop model predicts the.
Constriction Rate Modulation Can Drive Cell Size Control and Homeostasis in C. crescentus  Ambroise Lambert, Aster Vanhecke, Anna Archetti, Seamus Holden,
Role of C-terminal phosphorylation in the subcellular localization of AtPIP2;1.A, the figure shows typical laser-scanning confocal micrographs of the fluorescence.
MOSPD2 recruitment to interorganelle contact sites depends on the interaction between the FFAT motif and the MSP domain MOSPD2 recruitment to interorganelle.
Sensitivity of RNA‐seq.
Dual allele labeling reveals a trans‐acting source for extrinsic noise
Volume 23, Issue 24, Pages (December 2013)
The TBON model. The TBON model. (A) Representative confocal images of E14Tg2A cells stained for Tcf3 (green), Nanog (red), Oct4 (magenta), and total β‐catenin.
Relationship between clinical data and latent factors
Skin proliferation kinetics and in vivo fibroblast lineage tracing during dermal maturation (related to Fig 4)‏ Skin proliferation kinetics and in vivo.
Volume 11, Issue 6, Pages (May 2015)
Dose response of pAGA1 and pFIG1 induction
Dual LGR5 and KI67 knock‐in PDOs enable separation of quiescent and cycling LGR5+ CRC cells Dual LGR5 and KI67 knock‐in PDOs enable separation of quiescent.
Volume 25, Issue 19, Pages (October 2015)
H3 Dynamics in Wild-Type and fas1-4 Mutant Roots.
Characterization of promoters relative to pAGA1
Spatiotemporal Brassinosteroid Signaling and Antagonism with Auxin Pattern Stem Cell Dynamics in Arabidopsis Roots  Juthamas Chaiwanon, Zhi-Yong Wang 
Dynamics and variability of SMAD2 signaling in single cells
Genomic profiling of fitness in periodic salt stress
Richard Sibout, Stéphanie Plantegenet, Christian S. Hardtke 
The PRS is robust to changes in receptor abundance
Expression of GFP‐Aub transgenes in GSCs, and GSC loss phenotype in armi mutant Expression of GFP‐Aub transgenes in GSCs, and GSC loss phenotype in armi.
BAM3 is a CLE45 receptor BAM3 is a CLE45 receptor Schematic overview of the BAM3 gene structure. bam3 loss‐of‐function mutations that were isolated as.
Bojan Gujas, Carlos Alonso-Blanco, Christian S. Hardtke 
Dermal architecture is defined by an inverse correlation between fibroblast proliferation and ECM deposition Dermal architecture is defined by an inverse.
FFAT motif‐dependent recruitment of MOSPD2 in ER–endosome contacts by STARD3NL FFAT motif‐dependent recruitment of MOSPD2 in ER–endosome contacts by STARD3NL.
RNAi causes widespread changes in cell population context leading to predictable changes in virus infection. RNAi causes widespread changes in cell population.
Mutants of the Group III have differentially impaired induction of pAGA1 and pFIG1 Mutants of the Group III have differentially impaired induction of pAGA1.
Ubiquitin-Specific Protease 14 (UBP14) Is Involved in Root Responses to Phosphate Deficiency in Arabidopsis  Li Wen-Feng , Perry Paula J. , Prafulla Nulu.
Volume 5, Issue 4, Pages e4 (October 2017)
Rhamnose-Containing Cell Wall Polymers Suppress Helical Plant Growth Independently of Microtubule Orientation  Adam M. Saffer, Nicholas C. Carpita, Vivian.
Lag time to division depends on the frequency of pulsed glucose for a subpopulation Lag time to division depends on the frequency of pulsed glucose for.
Experimental approach and reproducibility
Visualization of a global auxin‐response gradient in the root meristem
Nec‐1 inhibits the phosphorylation and aggregation of tau
Lysozyme expression in isolated Paneth cells and linage tracing of Notch1+ cells Lysozyme expression in isolated Paneth cells and linage tracing of Notch1+
Computational wound healing gradients and in vivo imaging of the wound bed at PW2 (related to Fig 6)‏ Computational wound healing gradients and in vivo.
DeathPro dyes Hoechst and PI do not affect organoid growth and drug responses DeathPro dyes Hoechst and PI do not affect organoid growth and drug responses.
Drug‐induced cell death and proliferation inhibition can be quantified from serial confocal images Drug‐induced cell death and proliferation inhibition.
Volume 19, Issue 14, Pages (July 2009)
Gibberellin Signaling Controls Cell Proliferation Rate in Arabidopsis
Dynamics of induction of mating promoters after pheromone stimulation
Impact of growth phase on the Escherichia coli meltome and proteome
Cbl protein levels in ago3, twin, and armi mutant GSCs
Intrinsic role of Aub in GSC self‐renewal and differentiation
Design and optimization of the computational model.
Distinct collagen structures in the upper and lower neonatal dermis (related to Fig 1)‏ Distinct collagen structures in the upper and lower neonatal dermis.
Reproducibility of DeathPro drug screens
Noise in hoxb1a/krox20 expression leads to boundary sharpening.
Characterising dermis expansion and gene expression changes during mouse development (related to Fig 1)‏ Characterising dermis expansion and gene expression.
In vivo imaging of the wound bed at later time points (related to Fig 7)‏ In vivo imaging of the wound bed at later time points (related to Fig 7) A–CRepresentative.
Antisense expression associates with larger gene expression variability. Antisense expression associates with larger gene expression variability. (A–D)
Volume 15, Issue 6, Pages (December 2008)
Correlation of flux and enzyme concentration (inferred from transcripts) changes for reactions in central metabolism. Correlation of flux and enzyme concentration.
The transcriptional behavior of GREB1 changes with estrogen dose and exhibits considerable cell‐to‐cell variation (see also Fig EV2 and Movie EV2)‏ The.
DIA1(R1204X) induces elongated and thick microvilli in HeLa cells
Perturbation of ligand depletion affects the ultrasensitivity of long‐term P‐Smad2 responses to different doses of TGF‐β stimulation. Perturbation of ligand.
(A) Observed significant protein fold‐changes during the fed–fasting transition in C57BL/6J (B6) and 129Sv (S9) mice fed with a normal diet (T0). (A) Observed.
Fraction of flux entering the PEP‐glyoxylate cycle as a function of hexose uptake rate in batch (A) and chemostat (B) cultures. Fraction of flux entering.
Topologies, synthetic implementations and expression profiles of the networks studied Topologies, synthetic implementations and expression profiles of.
Changes in fibroblast activation and proliferation outside the wound and CHP staining in the wound bed (related to Fig 5)‏ Changes in fibroblast activation.
Fig. 6. LR phenotype of plastid translation-defective mutants with/without Spec. LR phenotype of plastid translation-defective mutants with/without Spec.
Defective organ development in mab1 mutants.
Nutrient availability regulates growth of the X. laevis optic tectum.
Fig. 7. Analysis of dFMRP kinetics in dFMRP granules by FRAP
Volume 26, Issue 4, Pages (August 2013)
George D. Dickinson, Ian Parker  Biophysical Journal 
Presentation transcript:

BRI1 signaling at the dividing cells restores overall root growth BRI1 signaling at the dividing cells restores overall root growth AEight‐day‐old seedlings of WT, bri1‐116, and pRPS5a:BRI1:YFP;bri1‐116. Scale bar 1 cm.BRoot length measurements of 10‐day‐old bri1‐116, bes1‐D, and pRP5SA:BRI:YFP;bri1‐116 seedlings compared to the wild type. Symbols represent the mean of more than 20 plants, from three independent experiments. Error bars show standard deviation. Straight lines represent the linear regression applied to each curve starting with day 4 postgermination. In this way, the root growth rate can be extracted for each phenotype (see Table EV7).CJuxtaposed (red lines) confocal images of 8‐day‐old WT, bri1‐116, and pRP5SA:BRI:YFP;bri1‐116 roots stained with PI. Green lines label the end of the transition zone, and the yellow lines label the first root hair (end of elongation zone). The inset shows pRP5SA expression domain of an 8‐day‐old pRP5SA:BRI:YFP;bri1‐116 seedling. Green line labels the end of the meristematic zone, which coincides with the end of pRP5SA expression domain. Scale bars correspond to 100 μm.D–IMain relationships as in Fig 2C–E between experimental values of the phenotypic traits used to assess the mechanism of differentiation in bri1‐116 mutant (D, F, H) and pRP5SA:BRI:YFP;bri1‐116 line (E, G, I) for the epidermis (left large plot) and cortex (right inset plot). Each circle denotes data extracted from a single root (n = 126 (epidermis) and n = 25 (cortex) for bri1‐116 and n = 90 (epidermis) and n = 17 (cortex) for pRP5SA:BRI:YFP;bri1‐116, see Table EV1, pooled from 6‐, 8‐, and 10‐day‐old seedlings for epidermis and from day 6 for cortex [data in Table EV5)]. In (H, I), the slope of the linear regression for epidermal data is 2.13 ± 0.04 for bri1‐116 and 2.53 ± 0.04 for pRP5SA:BRI:YFP;bri1‐116. Pearson correlation coefficient r is indicated and P‐value (P, using standard Pearson correlation test). In (F), bri1‐116 epidermal data do not conform to normal distributions (Spearman correlation test results in (epidermis) r = −0.29, P = 0.00104 and (cortex) r = −0.54, P = 0.00546 for bri1‐116, and in (epidermis) r = −0.24, P = 0.020 and (cortex) r = −0.38, P = 0.136 for pRP5SA:BRI:YFP;bri1‐116). Irina Pavelescu et al. Mol Syst Biol 2018;14:e7687 © as stated in the article, figure or figure legend