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. 2024 Nov 28;14:29627. doi: 10.1038/s41598-024-81304-2

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© The Author(s) 2024

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.

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Fig. 3 — S-Allylmercaptocysteine (SAMC) down-regulates the phosphorylation of mRNA splicing-related proteins. (a-c) Gene ontology term annotation for cellular component (a) and biological process (b) and Wikipathway analysis (c) of the phosphoproteins increased by lipopolysaccharide (LPS) treatment (≥ 1.5-fold vs. control) and decreased by SAMC treatment (≤ 0.75-fold vs. LPS group). (d) MA plot of the phosphoproteins downregulated by SAMC. (e) Protein-protein interactions among the spliceosome-related proteins in (d) were represented by Markov Cluster Algorithm clustering performed by STRING database. The proteins associated with U2 snRNP and other spliceosomes excepting U2 snRNP were shown as blue and red spheres, respectively.