AI Article Synopsis

  • Eukaryotic cells use stress granules, formed by key proteins like TIAR, TTP, and G3BP, to manage protein synthesis during stress, affecting mRNA stability and thus influencing cell behavior.
  • The study investigates the roles of these proteins during the embryonic development of a solitary ascidian, applying techniques like CRISPR/Cas9 gene knockout and gene reporter assays under both normal and stress conditions.
  • Results reveal that these proteins are crucial for the development of specific tissue types in the ascidian embryo, particularly in response to stress from metals like iron and cadmium.

Article Abstract

Controlling global protein synthesis through the assembly of stress granules represents a strategy adopted by eukaryotic cells to face various stress conditions. TIA 1-related nucleolysin (TIAR), tristetraprolin (TTP), and Ras-GTPase-activating protein SH3-domain-binding protein (G3BP) are key components of stress granules, allowing the regulation of mRNA stability, and thus controlling not only stress responses but also cell proliferation and differentiation. In this study, we aimed at investigating the roles of , , and during embryogenesis of the solitary ascidian under both physiological and stress conditions. We carried out CRISPR/Cas9 to evaluate the effects of gene knockout on normal embryonic development, and gene reporter assay to study the time and tissue specificity of gene transcription, together with whole-mount hybridization and quantitative real time PCR. To induce acute stress conditions, we used iron and cadmium as "essential" and "non-essential" metals, respectively. Our results highlight, for the first time, the importance of , and in controlling the development of mesendodermal tissue derivatives during embryogenesis of an invertebrate chordate.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11324471PMC
http://dx.doi.org/10.3389/fcell.2024.1414759DOI Listing

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