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Protein kinase A (PKA) plays a crucial and conserved role in various biological processes across species. Despite its significance, tissue-level regulatory networks controlling PKA activity remain incompletely characterized. In this study, we develop a live animal PKA sensor that can faithfully indicate changes in PKA activity in the intestines of Caenorhabditis elegans (C. elegans). Using complementary genome-wide and intestine-specific RNAi screens, we reveal both intestine-autonomous and non-autonomous regulators of intestinal PKA. Notably, we show that inhibiting mitochondrial oxidative phosphorylation, either through RNAi or chemical treatment, leads to a marked increase in intestinal PKA activity. Additionally, we demonstrate that the pyrimidine synthesis pathway serves as a critical autonomous regulator of PKA in the intestines of C. elegans, operating mechanistically in a cAMP-independent manner. Furthermore, this pathway holds a critical and conserved role in regulating PKA in cultured human cells. Overall, our study uncovers the first set of intestinal PKA regulators in C. elegans, with potential implications for PKA modulation under physiological or pathological conditions across species.
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http://dx.doi.org/10.1038/s42003-025-08718-0 | DOI Listing |
ACS Synth Biol
September 2025
ARC Centre of Excellence in Synthetic Biology, Queensland University of Technology, Brisbane, QLD 4000, Australia.
Fluorescent proteins (FPs) are commonly used as reporters to examine intracellular genetic, molecular, and biochemical status. Flow cytometry is a powerful technique for accurate quantification of single-cell fluorescent levels. Here, we characterize green, red, and blue FPs for use in yeast .
View Article and Find Full Text PDFJCI Insight
September 2025
Department of Pharmacology, University of Michigan, Ann Arbor, United States of America.
Cardiac hypertrophy is a common adaptation to cardiovascular stress and often a prelude to heart failure. We examined how S-palmitoylation of the small GTPase, Ras-related C3 botulinum toxin substrate 1 (Rac1), impacts cardiomyocyte stress signaling. Mutation of the cysteine-178 palmitoylation site impaired activation of Rac1 when overexpressed in cardiomyocytes.
View Article and Find Full Text PDFJ Am Chem Soc
September 2025
Department of Chemistry, Rutgers University-Newark, Newark, New Jersey 07102, United States.
Carbon-hydrogen bond activation is a pillar of synthetic chemistry. While it is generally accepted that Pd is more facile than Ni in C-H activation catalysis, there are no experimental platforms available to directly compare the magnitude of C-H bond weakening between Ni and Pd prior to bond scission. This work presents the first direct measurements of C(sp)-H bond acidity (p) and bond dissociation free energy (BDFE) for a species containing a ligated alkane-palladium interaction (RCH···Pd), also known as an agostic interaction.
View Article and Find Full Text PDFAllergol Immunopathol (Madr)
September 2025
Department of Respiratory and Critical Care Medicine, the Wenzhou Central Hospital and Dingli Clinical Institute of Wenzhou Medical University, Wenzhou, Zhejiang, China.
Background: Acute lung injury (ALI) is a critical clinical condition with high mortality, necessitating the development of more effective therapeutic strategies. Rho Guanine nucleotide dissociation inhibitor (GDP) beta (ARHGDIB) has been shown to exert protective effects against noxious stimuli in various disease models.
Objective: In this study, we investigated whether ARHGDIB knockdown had a protective effect on lipopolysaccharide (LPS)-induced injury in alveolar epithelial cells and elucidated its underlying molecular mechanisms.
Chemistry
September 2025
Institute for Advanced Study, Shenzhen University, Shenzhen, 518060, P. R. China.
The long-term visualization of intracellular Fe dynamics and lysosomal activity is crucial for investigating the physiological roles and functions of lysosomes during the growth of organisms. The lysosome-targeted fluorescent probe (RBH-EdC), derived from rhodamine-nucleoside conjugates, demonstrates a sophisticated dual-activation design: one is Fe⁺ response, triggering spirolactam ring-opening to form xanthine structures, resulting in ≥ 1000-fold fluorescence enhancement with visible colorimetric transition (colorless→pink). Another is pH sensitivity, demonstrating protonation-dependent fluorescence amplification at the dC at site N3 (pK= 2.
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