Models of sequestration and receptor cross-talk for explaining multiple mutants in plant stem cell regulation

<p>Abstract</p> <p>Background</p> <p>Stem cells reside in a plant's shoot meristem throughout its life and are main regulators of above-ground plant development. The stem cell maintenance depends on a feedback network between the <it>CLAVATA </it>and <it>WUSCHEL </it>genes. The CLAVATA3 peptide binds to the CLAVATA1 receptor leading to WUSCHEL inhibition. WUSCHEL, on the other hand, activates CLAVATA3 expression. Recent experiments suggest a second pathway where CLAVATA3 inhibits WUSCHEL via the CORYNE receptor pathway. An interesting question, central for understanding the receptor signaling, is why the <it>clavata1-11 </it>null mutant has a weaker phenotype compared with the <it>clavata1-1 </it>non-null mutant. It has been suggested that this relies on interference from the mutated CLAVATA1 acting on the CORYNE pathway.</p> <p>Results</p> <p>We present two models for the CLAVATA-WUSCHEL feedback network including two receptor pathways for WUSCHEL repression and differing only by the hypothesized mechanisms for the <it>clavata1-1 </it>non-null mutant. The first model is an implementation of the previously suggested interference mechanism. The other model assumes an unaltered binding between CLAVATA3 and the mutated CLAVATA1 but with a loss of propagated signal into the cell. We optimize the models using data from wild type and four single receptor mutant experiments and use data from two receptor double mutant experiments in a validation step. Both models are able to explain all seven phenotypes and in addition qualitatively predict CLAVATA3 perturbations. The two models for the <it>clavata1-1 </it>mutant differ in the direct mechanism of the mutant, but they also predict other differences in the dynamics of the stem cell regulating network. We show that the interference hypothesis leads to an abundance of receptors, while the loss-of-signal hypothesis leads to sequestration of CLAVATA3 and relies on degradation or internalization of the bound CLAVATA1 receptor.</p> <p>Conclusions</p> <p>Using computational modeling, we show that an interference hypothesis and a more parsimonious loss-of-signal hypothesis for a <it>clavata1 </it>non-null mutant both lead to behaviors predicting wild type and six receptor mutant experiments. Although the two models have identical implementations of the unperturbed feedback network for stem cell regulation, we can point out model-predicted differences that may be resolved in future experiments.</p

Increasing model robustness for stem cell regulation in plant shoots

The transcription factor WUSCHEL and the peptide CLAVATA3 have key roles to plat in the regulatory network effecting the differentiation of the stem cells at the shoot apical meristem of Arabidopsis. The signal pathway of this network has been under investigation for several years and models utilizing the already identified parts of the network have been developed. Such models have however so far been unable to explain a buffering ability of WUSCHEL against certain perturbations made experimentally to the promoter strength of CLAVATA3. For this thesis several alternative models have been proposed and investigated. All of them have a basis in a previously published model and adds or replaces different connections in order to be able to produce the experimentally observed dynamics. These in silico experiments have yielded several new models that are able to explain the buffering capabilities of WUSCHEL. They also show that many types of self-activation of WUSCHEL can produce not only the WUSCHEL buffering dynamics, but also the dynamics of the additional six mutant experiments that were used as a basis for the previous model

Implementing the CRISPR/Cas9 technology in Eucalyptus hairy roots and functional characterization of auxin-dependent transcription factors involved in wood formation

Les Eucalyptus sont les feuillus les plus plantés au monde pour les nombreuses utilisations industrielles de leurs bois tells que la pâte à papier et la production émergente de biocarburants. L'analyse du génome d'Eucalyptus grandis a conduit à l'identification de nombreux candidats impliqués dans la formation du bois, tells que des médiateurs clés de la signalization de l'auxine (Aux/IAA et Auxin Response Factor (ARF). La caractérisation fonctionnelle de ces gènes candidats a été retardée jusqu'à présent par la difficulté de supprimer leurs fonctions dans un système homologue. Pour pallier à cela, le premier objectif de mon travail a été de mettre au point le puissant outil d'édition de gènes "CRISPR/Cas9" en profitant de la transformation de "hairy roots" transgéniques médiée par A. rhizogenes, récemment développée dans l'équipe. Dans un deuxième temps, mon objectif était d'utiliser cette méthode d'édition de génome pour étudier les rôles potentiels de trois facteurs de transcription dépendant de l'auxine (IAA9A, IAA20 et ARF5) dans la formation du bois d'Eucalyptus. Premièrement, comme preuve de concept pour la mise en oeuvre de la technologie CRISPR/Cas9, nous avons ciblé la Cinnamoyl-CoA réductase1 (CCR1), un gène clé de la biosynthèse de la lignine dont les effets de "down-regulation" sont bien connus. Nous avons également utilisé le gène IAA9A comme cible. Presque toutes les lignées transgéniques ont été éditées, mais les taux et les profils d'édition alléliques variaient considérablement selon le gène ciblé. La plupart des événements d'édition ont généré des protéines tronquées. En utilisant une combinaison de spectroscopie à infrarouge transformée de Fourier (FT-IR) et d'analyse multivariée (PLS-DA), j'ai pu montrer que les lignées éditées pour CCR1, étaient clairement séparées des témoins. Les analyses histochimiques ont confirmé la diminution de la lignification et la présence de vaisseaux écrasés dans les lignées éditées pour CCR1, qui sont des caractéristiques de la déficience de ce gène. Bien que l'efficacité de l'édition puisse être améliorée, la méthode décrite ici est déjà un outil utile pour caractériser fonctionnellement des gènes chez l'Eucalyptus. Dans la deuxième partie de mon travail, j'ai utilisé cette méthode d'édition du génome pour muter deux Aux/IAAs (IAA9A et IAA20) ainsi que ARF5 afin de mieux appréhender le rôle de l'auxine dans la régulation de la formation du bois chez l'Eucalyptus. J'ai généré des "hairy roots" soit pour surexprimer ces gènes, soit pour les muter par CRISPR/Cas9. Malheureusement, toutes les plantes transgéniques surexprimant IAA9A et IAA20 (sous le contrôle du promoteur CaMV35S) sont mortes pendant la période de confinement liée au Covid19 et seules trois lignées CRISPR-IAA20 ont survécu. Par conséquent, je n'ai pu analyser que des plantes transgéniques éditées pour deux candidats. Les lignées IAA9A générées par CRISPR/Cas9 présentaient des taux de knock-out élevés de 92,3% avec 58,3% de mutations bialléliques. En revanche, les lignées ARF5 avaient des taux d'édition assez faibles (43%) et des mutations monoalléliques et/ou chimériques. Dans les lignées éditées pour IAA9A, nous avons observé un développement précoce du xylème et une augmentation du diamètre des vaisseaux du xylème. Enfin, j'ai participé au criblage d'une banque double hybride de xylème d'Eucalyptus (Y2H) pour trouver des partenaires potentiels de IAA9A et IAA20. Pour IAA9A, des candidats prometteurs ont été obtenus tels que Histone Linker (EgH1.3) et CCoAOMT2, connus comme étant impliqués dans la formation du xylème ; pour IAA20, l'interacteur principal est IAA9A, ce qui suggère que IAA20 et IAA9A forment des dimères pour réguler la formation du bois. Nous avons également utilisé la méthode double hybride ciblée pour confirmer les interactions protéine-protéine d'IAA9A et d'IAA20 avec ARF5 ainsi qu'avec d'autres candidats préférentiellement exprimés dans le xylème d'Eucalyptus.Eucalyptus is the most planted hardwood worldwide for many industrial end-uses such as pulp and paper and emerging biofuel production. The analysis of the Eucalyptus grandis genome led to many candidate genes involved in wood formation including key mediators of auxin signaling (Auxin/Indole-3-Acetic Acid (Aux/IAA) and Auxin Response Factor (ARF). The functional characterization of these candidate genes was hampered by the difficulty to general stable transgenic Eucalyptus and to knock out these genes. Taking advantage of rapid and efficient hairy root transformation mediated by A.rhizogenes, recently implemented by our team, the objectives of my work were to implement the powerful CRISPR/Cas9 gene editing tool and to use it to investigate the potential roles of three Eucalyptus auxin-dependent transcription factors (IAA9A, IAA20 and ARF5) in regulating wood formation. First, as a proof-of-concept for implementing CRISPR/Cas9, We targeted Cinnamoyl-CoA Reductase1 (CCR1), a key lignin biosynthetic gene whose down-regulation effects are well described in several plants. Almost all transgenic lines were edited but the allele-editing rates and profiles varied greatly depending on the genes targeted. Most edition events generated truncated proteins. The prevalent edition types were small deletions but large deletions were also observed. By using a combination of Fourier Transformed InfraRed (FT-IR) spectroscopy and multivariate analysis (partial least square analysis (PLS-DA), we showed that the CCR1-edited lines, which were clearly separated from the controls. The most discriminant wave-numbers were attributed to lignin. Histochemical analyses further confirmed the decreased lignification and the presence of collapsed vessels in CCR1-edited lines, which are characteristics of CCR1 deficiency. Although the efficiency of editing could be improved, the method described here is already a useful tool to functionally characterize eucalypts genes. In the second part of my work, we used this genome editing method to knock out two Aux/IAAs (IAA9A and IAA20) and one Auxin Response Factor (ARF5) in order to get more insights into the role of auxin in the regulation of wood formation in Eucalyptus. We generated transgenic Eucalyptus hairy root to overexpress and to knock out these genes. Unfortunately, all the transgenic plants overexpressing IAA9A and IAA20 (under the control of 35S promoter) died during the Covid19 lockdown period and only three IAA20-CRISPR lines survived. Therefore, we could only analyze CRISPR/Cas9 edited transgenic plants for two candidates (IAA9A and ARF5). Editing events were detected either by subcloning and/or webbased tools (DSDecode and ICE synthego). CRISPR/Cas9 generated IAA9A_lines had high knockout rates of 92.3% with 58.3% of biallelic mutations. In contrast, ARF5 lines had quite low editing rates (43%) showing monoallelic and chimera mutations. In IAA9A_edited lines we observed precocious xylem development and increased xylem vessel diameters, while no obvious phenotype was detected in ARF5_edited lines. Finally, we screened a Eucalyptus developing xylem Yeast Two-Hybrid (Y2H) library to find potential partners of IAA9A and IAA20. For IAA9A, we found some potentially promising candidates such as Histone Linker (EgH1.3), CCoAOMT2 previously reported to be involved in xylem formation; for IAA20 the main interactor revealed was IAA9A, suggesting that IAA20 and IAA9A form dimers in developing xylem to regulate wood formation. In addition, we used the yeast two hybrid method to confirm protein-protein interactions of EgrIAA9A and EgrIAA20 with EgrARF5 and other candidates preferentially expressed in Eucalyptus wood-forming tissue

The growing story of (ARABIDOPSIS) CRINKLY 4

Receptor kinases play important roles in plant growth and development, but only few of them have been functionally characterized in depth. Over the past decade CRINKLY 4 (CR4)-related research has peaked as a result of a newly discovered role of ARABIDOPSIS CR4 (ACR4) in the root. Here, we comprehensively review the available (A)CR4 literature and describe its role in embryo, seed, shoot, and root development, but we also flag an unexpected role in plant defence. In addition, we discuss ACR4 domains and protein structure, describe known ACR4-interacting proteins and substrates, and elaborate on the transcriptional regulation of ACR4. Finally, we address the missing knowledge in our understanding of ACR4 signalling

Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition)

This work was supported by the National Institute of General Medical Sciences [GM131919].In 2008, we published the first set of guidelines for standardizing research in autophagy. Since then, this topic has received increasing attention, and many scientists have entered the field. Our knowledge base and relevant new technologies have also been expanding. Thus, it is important to formulate on a regular basis updated guidelines for monitoring autophagy in different organisms. Despite numerous reviews, there continues to be confusion regarding acceptable methods to evaluate autophagy, especially in multicellular eukaryotes. Here, we present a set of guidelines for investigators to select and interpret methods to examine autophagy and related processes, and for reviewers to provide realistic and reasonable critiques of reports that are focused on these processes. These guidelines are not meant to be a dogmatic set of rules, because the appropriateness of any assay largely depends on the question being asked and the system being used. Moreover, no individual assay is perfect for every situation, calling for the use of multiple techniques to properly monitor autophagy in each experimental setting. Finally, several core components of the autophagy machinery have been implicated in distinct autophagic processes (canonical and noncanonical autophagy), implying that genetic approaches to block autophagy should rely on targeting two or more autophagy-related genes that ideally participate in distinct steps of the pathway. Along similar lines, because multiple proteins involved in autophagy also regulate other cellular pathways including apoptosis, not all of them can be used as a specific marker for bona fide autophagic responses. Here, we critically discuss current methods of assessing autophagy and the information they can, or cannot, provide. Our ultimate goal is to encourage intellectual and technical innovation in the field.PostprintPeer reviewe

Phyto-gene therapy using antisense oligonucleotides to control cereal fungal disease by silencing virulence factors and their regulators

With increasing concerns regarding food security, alternative solutions are required for disease control in crops, including those caused by fungal pathogens. Antisense single stranded short oligodeoxynucleotides (ASO) based gene therapy is widely used in medicine but is still emerging in plant sciences. The ASO gene silencing approach using phosphorothioate modified oligodeoxynucleotides (asPTOs) delivered to excised barley leaves was first devised as a tool for in planta transient host induced gene silencing (HIGS) to query the virulence role of genes from the biotrophic fungal pathogen, Blumeria graminis f.sp. hordei (Bgh), the causal agent of barley powdery mildew. Following this, our project aimed at exploiting the HIGS approach for discovering new key players for virulence of Bgh and some of the major wheat pathogens, B. graminis f.sp. tritici (Bgt) and Fusarium graminearum, the causal agent of Fusarium head blight. The ASO gene silencing approach was also evaluated for its suitability to protect wheat against fungi by targeting host susceptibility genes. AsPTOs to silence vital Bgh genes (actin, GAPDH, 2-Glycosyl transferase) successfully reduced powdery mildew infection in several barley cultivars. Similarly, silencing the metallo-protease-like effector BEC1019 impacted on Bgh and Bgt virulence in barley and wheat respectively. Following promoter sequence analysis of Bgh effectors expressed in haustoria, the HIGS approach allowed to confirm the implication of ZAP1 and PacC transcription factors in regulating BEC1019 and BEC1011 effector expression, while affecting Bgh virulence. To adapt ASO based gene silencing for disease control, in planta gene silencing of F. graminearum known virulence genes was attempted but with no convincing impact. However, asPTOs to silence BEC1011 were delivered into whole barley seedlings by root uptake resulting in reduced powdery mildew infection. This suggests that asPTOs based HIGS could be further investigated as a strategy to control fungal diseases in crops. <br/

Tree Peony Species Are a Novel Resource for Production of α-Linolenic Acid

Tree peony is known worldwide for its excellent ornamental and medical values, but recent reports that their seeds contain over 40% α-linolenic acid (ALA), an essential fatty acid for humans drew additional interest of biochemists. To understand the key factors that contribute to this rich accumulation of ALA, we carried out a comprehensive study of oil accumulation in developing seeds of nine wild tree peony species. The fatty acid content and composition was highly variable among the nine species; however, we selected a high- (P. rockii) and low-oil (P. lutea) accumulating species for a comparative transcriptome analysis. Similar to other oilseed transcriptomic studies, upregulation of select genes involved in plastidial fatty acid synthesis, and acyl editing, desaturation and triacylglycerol assembly in the endoplasmic reticulum was noted in seeds of P. rockii relative to P. lutea. Also, in association with the ALA content, transcript levels for fatty acid desaturases (SAD, FAD2 and FAD3), which encode for enzymes necessary for polyunsaturated fatty acid synthesis were higher in P. rockii compared to P. lutea. We further showed that the overexpression of PrFAD2 and PrFAD3 in Arabidopsis increased linoleic and α-linolenic acid content, respectively and modulated their final ratio in the seed oil. In conclusion, we identified the key steps that contribute to efficient ALA synthesis and validated the necessary desaturases in P. rockii that are responsible for not only increasing oil content but also modulating 18:2/18:3 ratio in seeds. Together, these results will aid to improve essential fatty acid content in seeds of tree peonies and other crops of agronomic interest