Relevant bibliographies by topics / GSK-3 Shaggy kinase

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  2. Dissertations / Theses

Academic literature on the topic 'GSK-3 Shaggy kinase'

Author: Grafiati
Published: 11 March 2023
Last updated: 31 July 2025

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Journal articles on the topic "GSK-3 Shaggy kinase"

1

Bianchi, Michèle W., Dominique Guivarc'h, and Martin Kreis. "Arabidopsishomologues of the shaggy/GSK-3 protein kinase." Acta Botanica Gallica 140, no. 6 (1993): 708. http://dx.doi.org/10.1080/12538078.1993.10515652.

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Kloc, Yuliya, Marta Dmochowska-Boguta, Andrzej Zielezinski, Anna Nadolska-Orczyk, Wojciech M. Karlowski, and Waclaw Orczyk. "Silencing of HvGSK1.1—A GSK3/SHAGGY-Like Kinase–Enhances Barley (Hordeum vulgare L.) Growth in Normal and in Salt Stress Conditions." International Journal of Molecular Sciences 21, no. 18 (2020): 6616. http://dx.doi.org/10.3390/ijms21186616.

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Glycogen synthase kinase 3 (GSK3) is a highly conserved kinase present in all eukaryotes and functions as a key regulator of a wide range of physiological and developmental processes. The kinase, known in land plants as GSK3/SHAGGY-like kinase (GSK), is a key player in the brassinosteroid (BR) signaling pathway. The GSK genes, through the BRs, affect diverse developmental processes and modulate responses to environmental factors. In this work, we describe functional analysis of HvGSK1.1, which is one of the GSK3/SHAGGY-like orthologs in barley. The RNAi-mediated silencing of the target HvGSK1.
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Wilson, K. S., P. Stoeva-Popova, and D. Dimaculangan. "Characterization ofLpSK6: ALycopersiconGroup Three GSK-3/SHAGGY-Like Protein Kinase." Biotechnology & Biotechnological Equipment 18, no. 3 (2004): 20–26. http://dx.doi.org/10.1080/13102818.2004.10817115.

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Papadopoulou, Deppie, Michele Wolfe Bianchi, and Marc Bourouis. "Functional Studies of Shaggy/Glycogen Synthase Kinase 3 Phosphorylation Sites in Drosophila melanogaster." Molecular and Cellular Biology 24, no. 11 (2004): 4909–19. http://dx.doi.org/10.1128/mcb.24.11.4909-4919.2004.

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ABSTRACT Early studies of glycogen synthase kinase 3 (GSK-3) in mammalian systems focused on its pivotal role in glycogen metabolism and insulin-mediated signaling. It is now recognized that GSK-3 is central to a number of diverse signaling systems. Here, we show that the major form of the kinase Shaggy (Sgg), the GSK-3 fly ortholog, is negatively regulated during insulin-like/phosphatidylinositol 3-kinase (PI3K) signaling in vivo. Since genetic studies of Drosophila melanogaster had previously shown that Wingless (Wg) signaling also acts to antagonize Sgg, we investigate how the kinase might
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Tichtinsky, Gabrielle, Raquel Tavares, Alain Takvorian, Nicole Schwebel-Dugué, David Twell, and Martin Kreis. "An evolutionary conserved group of plant GSK-3/shaggy-like protein kinase genes preferentially expressed in developing pollen." Biochimica et Biophysica Acta (BBA) - Gene Structure and Expression 1442, no. 2-3 (1998): 261–73. http://dx.doi.org/10.1016/s0167-4781(98)00187-0.

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Trostnikov, M. V., E. R. Veselkina, Y. A. Andreev, A. Y. Khryachkova, N. V. Roshina, and E. G. Pasyukova. "The Effect of the <i>aPKC</i> Gene Encoding Atypical Protein Kinase C on the Lifespan of <i>Drosophila melanogaster</i> Depends on the Expression Level of Protein Kinase GSK3." Генетика 59, no. 1 (2023): 26–38. http://dx.doi.org/10.31857/s0016675823010125.

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Drosophila melanogaster shaggy and aPKC genes encode highly conserved GSK3 (Glycogen Syntase Kinase 3) and aPKC (Protein Kinase C) proteinkinases that play key roles in many cellular processes. We previously demonstrated that changes in shaggy expression in neurons affect lifespan. In this article we show that changing the expression of the aPKC gene in neurons also affects lifespan. Changing the expression of the two protein kinases in all male or female neurons and in male motoneurons led to changes in lifespan, indicating that aPKC has no effect on GSK3 and GSK3 has a possible inhibitory ef
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Itoh, K., T. L. Tang, B. G. Neel, and S. Y. Sokol. "Specific modulation of ectodermal cell fates in Xenopus embryos by glycogen synthase kinase." Development 121, no. 12 (1995): 3979–88. http://dx.doi.org/10.1242/dev.121.12.3979.

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Shaggy is a downstream component of the wingless and Notch signaling pathways which operate during Drosophila development. To address the role of glycogen synthase kinase 3 beta (GSK3 beta), a mammalian homologue of Shaggy, in vertebrate embryogenesis, it was overexpressed in Xenopus embryos. Microinjection of rat GSK3 beta mRNA into animal ventral blastomeres of 8-cell-stage embryos triggered development of ectopic cement glands with an adjacent anterior neural tissue as evidenced by in situ hybridization with Xotx2, a fore/midbrain marker, and NCAM, a pan-neural marker. In contrast, animal d
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DiAngelo, Justin R., and Morris J. Birnbaum. "Regulation of Fat Cell Mass by Insulin in Drosophila melanogaster." Molecular and Cellular Biology 29, no. 24 (2009): 6341–52. http://dx.doi.org/10.1128/mcb.00675-09.

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ABSTRACT A phylogenetically conserved response to nutritional abundance is an increase in insulin signaling, which initiates a set of biological responses dependent on the species. Consequences of augmented insulin signaling include developmental progression, cell and organ growth, and the storage of carbohydrates and lipids. Here, we address the evolutionary origins of insulin's positive effects on anabolic lipid metabolism by selectively modulating insulin signaling in the fat body of the fruit fly, Drosophila melanogaster. Analogous to the actions of insulin in higher vertebrates, those in
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Roshina, N. V., E. R. Veselkina, M. V. Trostnikov, and E. G. Pasyukova. "The <i>shaggy</i> Gene Encoding the GSK3 Protein Kinase Controls the Sex-Dependent Effects of Specific Clusters of D. <i>melanogaster</i> Dopaminergic Neurons on Lifespan." Genetika 60, no. 10 (2024): 122–28. https://doi.org/10.31857/s0016675824100127.

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Dopaminergic neurons control behavior, memory, and locomotion, and the causal relationship of their dysfunction to neurodegenerative diseases and aging has drawn attention to investigating the involvement of dopaminergic neurons in the regulation of lifespan. The highly conserved serine-threonine protein kinase GSK3 (Glycogen Syntase Kinase 3), one of the most important multifunctional cellular enzymes in higher organisms, which in Drosophila melanogaster is encoded by the shaggy gene, plays an important role in the function of dopaminergic neurons. This paper provides the first evidence that
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Veselkina, Ekaterina R., Mikhail V. Trostnikov, Natalia V. Roshina, and Elena G. Pasyukova. "The Effect of the Tau Protein on D. melanogaster Lifespan Depends on GSK3 Expression and Sex." International Journal of Molecular Sciences 24, no. 3 (2023): 2166. http://dx.doi.org/10.3390/ijms24032166.

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The microtubule-associated conserved protein tau has attracted significant attention because of its essential role in the formation of pathological changes in the nervous system, which can reduce longevity. The study of the effects caused by tau dysfunction and the molecular mechanisms underlying them is complicated because different forms of tau exist in humans and model organisms, and the changes in protein expression can be multidirectional. In this article, we show that an increase in the expression of the main isoform of the Drosophila melanogaster tau protein in the nervous system has di
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Dissertations / Theses on the topic "GSK-3 Shaggy kinase"

1

Bianchi, Michele. "Isolement et caracterisation d'homologues de la proteine kinase shaggy/gsk-3 chez arabidopsis thaliana et identification d'un gene correspondant chez saccharomyces cerevisiae." Paris 11, 1993. http://www.theses.fr/1993PA112322.

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Les proteines kinases (pks) sont les composants centraux du systeme cybernetique des cellules eucaryotes. L'identification d'homologues de pks conservees au cours de l'evolution peut constituer une approche complementaire aux techniques genetiques pour l'etude de voies de transduction importantes chez les plantes. Dans un premier temps, une approche de pcr (polymerase chain reaction) a permis d'identifier, chez arabidopsis thaliana, une famille de genes apparentes a (1) mck1 (meiosis and centromere regulatory kinase) de saccharomyces cerevisiae; (2) shaggy/zeste-white 3, impliquee dans le deve
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TAVARES, RAQUEL. "Contribution a la caracterisation de la sous-famille des proteines serine/threonine kinases du type shaggy/gsk-3 chez arabidopsis thaliana." Paris 11, 2000. http://www.theses.fr/2000PA112390.

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Chez les animaux, les proteines serine/threonine kinases de la famille shaggy/gsk-3 sont impliquees dans une grande variete de processus biologiques, comme la regulation de l'insuline et la determination de la destinee et de la proliferation cellulaires. Ce travail de these avait comme objectif de contribuer a l'elucidation des roles biologiques de ces proteines chez les plantes, plus particulierement a travers l'identification et l'etude d'un sous-groupe de cette famille chez arabidopsis. L'analyse des sequences des genes atsk (arabidopsis thaliana shaggy-like kinases) du groupe iii a permis
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Tichtinsky, Gabrielle. "Caracterisation d'un sous-groupe de proteines serine/threonine kinases vegetales de la famille shaggy/gsk-3. Mise en evidence de leur role au cours du developpement des plantes." Paris 11, 1998. http://www.theses.fr/1998PA112414.

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Les proteines serine/threonine kinases shaggy de d. Melanogaster et gsk-3 de mammiferes sont des composants majeurs des voies de signalisation wingless et wnt qui regulent de nombreux processus de developpement chez les animaux. Des genes vegetaux apparentes ont ete isoles chez p. Hybrida et n. Tabacum. Ils sont principalement exprimes dans le pollen et forment, parmi les genes vegetaux de la famille shaggy/gsk-3, un sous-groupe particulier auquel appartiennent aussi des genes isoles chez b. Napus et a. Thaliana. Tous les genes de ce sous-groupe codent pour des proteines kinases caracterisees
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DAL, SANTO SILVIA. "The role of GSK-3 kinases in Arabidopsis thaliana stress response." Doctoral thesis, 2009. http://hdl.handle.net/11562/345259.

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Disponibile in Tedesco<br>Redox adjustments are central to most stress responses. However, little is known about the mechanisms of how the antioxidant system is regulated by cellular signalling to counteract oxidative stress. High soil salinity is a major environmental constraint for plant growth and development. Salinity imposes a water-deficit as well as ion stress, which causes damaging effects including an over-production of reactive oxygen species (ROS). Glucose-6-phosphate dehydrogenase (G6PD) catalyzes a key step of the oxidative pentose phosphate pathway which provides NADPH for
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