Exploring in vitro Oryzalin-Induced Polyploidy in Astragalus membranaceus: Implications for Gene Expression

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This study explored oryzalin-induced polyploidy in Astragalus membranaceus, finding variable gene expression changes related to calycosin biosynthesis, with certain genotypes showing significant upregulation even after ex vitro cultivation.

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The study investigated how in vitro artificial polyploidisation of Astragalus membranaceus using the antimitotic agent oryzalin affects gene expression related to the calycosin and calycosin-7-O-β-D-glucoside biosynthesis pathway, comparing multiple genotypic lines under both in vitro and ex vitro (two years greenhouse) conditions. Across lines, gene expression responses varied, with genotype 54 showing statistically significant upregulation of all investigated genes in vitro (AmPAL, AmC4H, and AmI3′H), while genotype 16 displayed the highest expression levels after tetraploidy loss, with upregulation of AmPAL and AmC4H. Genotype 74 (a tetraploid) showed upregulation of AmI3′H and downregulation of AmC4H. The paper does not explicitly discuss limitations beyond reporting differential gene expression outcomes across genotypes and conditions, and it presents findings focused on a specific pathway/candidate genes rather than a genome-wide analysis. The paper does not explicitly discuss endometriosis or adenomyosis; it was included in the corpus via a keyword match in the upstream search index.

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Abstract This study investigates the effects of artificial in vitro polyploidisation of Astragalus membranaceus, focusing specifically on gene expression and metabolic pathway associated with the biosynthesis of calycosin and calycosin-7-O-β-D-glucoside. Using oryzalin as an antimitotic agent, we have systematically investigated different genotypic lines, under both in vitro and ex vitro conditions. Amid cases of reduced gene expression in certain lines, results showed a significant upregulation in specific lines, particularly in genotypes 16, 54, and 74. Genotype 54 showed an exceptional response, manifesting a statistically significant upregulation in all investigated genes studied under in vitro conditions (i.e. AmPAL, AmC4H and AmI3′H). Interestingly, even under ex vitro conditions after two years of greenhouse cultivation, certain lines showed significant variations in gene expression. Despite the loss of tetraploidy, genotype 16 exhibited the highest expression levels among the examined genotypes, with statistically significant upregulation of both the AmPAL and AmC4H genes. In addition, the tetraploid genotype 74 showed a significant upregulation of the AmI3′H gene and a concomitant downregulation of the AmC4H gene. These results highlight the complex regulatory mechanisms affected by the polyploidisation of Astragalus membranaceus and provide promising avenues for manipulating gene expression to enhance the production of pharmacologically significant compounds.
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Exploring in vitro Oryzalin-Induced Polyploidy in Astragalus membranaceus: Implications for Gene Expression | Research Square window.SnipcartSettings = { analytics: { enabled: false } }; (function() { var accessVector = localStorage.getItem('access_vector') || ''; window.dataLayer = window.dataLayer || []; if (accessVector) { window.dataLayer.push({ user: { profile: { profileInfo: { snid: accessVector } } } }); } })(); (function(w,d,s,l,i){w[l]=w[l]||[];w[l].push({'gtm.start':new Date().getTime(),event:'gtm.js'});var f=d.getElementsByTagName(s)[0],j=d.createElement(s),dl=l!='dataLayer'?'&l='+l:'';j.async=true;j.src='https://www.googletagmanager.com/gtm.js?id='+i+dl;f.parentNode.insertBefore(j,f);})(window,document,'script','dataLayer','GTM-K279D39R'); Browse Preprints In Review Journals COVID-19 Preprints AJE Video Bytes Research Tools Research Promotion AJE Professional Editing AJE Rubriq About Preprint Platform In Review Editorial Policies Our Team Advisory Board Help Center Sign In Submit a Preprint Cite Share Download PDF Research Article Exploring in vitro Oryzalin-Induced Polyploidy in Astragalus membranaceus: Implications for Gene Expression Josef Baltazar Šenkyřík, Božena Navrátilová, Barbora Fišerová, and 2 more This is a preprint; it has not been peer reviewed by a journal. https://doi.org/ 10.21203/rs.3.rs-3904212/v1 This work is licensed under a CC BY 4.0 License Status: Published Journal Publication published 28 Jun, 2024 Read the published version in Plant Cell, Tissue and Organ Culture (PCTOC) → Version 1 posted 3 You are reading this latest preprint version Abstract This study investigates the effects of artificial in vitro polyploidisation of Astragalus membranaceus, focusing specifically on gene expression and metabolic pathway associated with the biosynthesis of calycosin and calycosin-7-O-β-D-glucoside. Using oryzalin as an antimitotic agent, we have systematically investigated different genotypic lines, under both in vitro and ex vitro conditions. Amid cases of reduced gene expression in certain lines, results showed a significant upregulation in specific lines, particularly in genotypes 16, 54, and 74. Genotype 54 showed an exceptional response, manifesting a statistically significant upregulation in all investigated genes studied under in vitro conditions (i.e. AmPAL, AmC4H and AmI3′H). Interestingly, even under ex vitro conditions after two years of greenhouse cultivation, certain lines showed significant variations in gene expression. Despite the loss of tetraploidy, genotype 16 exhibited the highest expression levels among the examined genotypes, with statistically significant upregulation of both the AmPAL and AmC4H genes. In addition, the tetraploid genotype 74 showed a significant upregulation of the AmI3′H gene and a concomitant downregulation of the AmC4H gene. These results highlight the complex regulatory mechanisms affected by the polyploidisation of Astragalus membranaceus and provide promising avenues for manipulating gene expression to enhance the production of pharmacologically significant compounds. Antimitotic agent artificial polyploidy Astragalus membranaceus flow cytometry medicinal plants plant biotechnology Full Text Cite Share Download PDF Status: Published Journal Publication published 28 Jun, 2024 Read the published version in Plant Cell, Tissue and Organ Culture (PCTOC) → Version 1 posted Reviewers agreed at journal 15 Mar, 2024 Editor assigned by journal 29 Jan, 2024 First submitted to journal 26 Jan, 2024 You are reading this latest preprint version Research Square lets you share your work early, gain feedback from the community, and start making changes to your manuscript prior to peer review in a journal. As a division of Research Square Company, we’re committed to making research communication faster, fairer, and more useful. We do this by developing innovative software and high quality services for the global research community. Our growing team is made up of researchers and industry professionals working together to solve the most critical problems facing scientific publishing. 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