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Vector Laboratories texas red avidin dcs
Texas Red Avidin Dcs, supplied by Vector Laboratories, used in various techniques. Bioz Stars score: 93/100, based on 122 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/A-2016-1/Texas+Red+Avidin+DCS%2C+Cell+Sorting+Grade/pm41270342-92-21-25
Average 93 stars, based on 122 article reviews

texas red avidin dcs - by Bioz Stars, 2026-11

93/100 stars

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Avidin-Biotin Assay:

Article Title: Transcription decouples estrogen-dependent changes in enhancer-promoter contact frequencies and spatial proximity
Article Snippet: For 2-color detection (either with fosmid or 10 kb derived probes), the following antibody dilutions were made: anti-digoxigenin-Rhodamine FAB fragments (Roche, cat. no. 11207750910) 1:20; Texas Red anti-sheep 1:100 (Abcam ab6745) and Avidin-FITC1:500 (Vector Laboratories A-2011); biotinylated anti-avidin (Vector Laboratories, cat. no. BA-0300) 1:100, and Avidin-FITC 1:500. .. For 3-color detection the following antibody dilutions were made: anti-digoxigenin (Roche, cat. 11333089001) 1:10; AF647 anti-sheep (Invitrogen, cat. A-21448) 1:10 and Texas Red avidin (Vector Laboratories, cat. no. A-2016) 1:500; biotinylated anti-avidin (Vector Laboratories) 1:100; Texas Red avidin (Vector Laboratories, cat. no. A-2016) 1:500. ..

Article Title: Chronic Cigarette Smoke Causes Oxidative Damage and Apoptosis to Retinal Pigmented Epithelial Cells in Mice
Article Snippet: Sections were exposed to a monoclonal anti-8-OHdG antibody (1:20; Japan Institute for the Control of Aging, Shizuoka, Japan) or mouse IgG1 for 30 minutes at room temperature. .. Sections were then incubated with Biotinylated Anti-Mouse IgG (Vector Labs) for 10 minutes at room temperature, and then with Texas Red Avidin DCS (10 μg/ml, Vector Labs). .. Sections were counterstained with DAPI (Vector Labs) and imaged with a confocal microscope (Zeiss 510 META confocal microscope, Carl Zeiss Micro Imaging, Inc., Thornwood, NY) at wavelengths 405/460 nm for DAPI and 633/650 nm for Texas Red.

Article Title: Unique Signatures of Natural Background Radiation on Human Y Chromosomes from Kerala, India
Article Snippet: .. Biotynilated anti-fluorescein and anti-Texas red antibodies coupled with fluorescein and Texas red avidin DCS (Vector Labs) were used in dual probe FISH experiments. ..

Article Title: AXL inhibition improves the therapeutic efficacy of trastuzumab in high-risk endometrial cancer.
Article Snippet: • AXL and HER2 colocalize in high-risk endometrial cancer cells and are inhibited by batiraxcept and trastuzu-

Article Title: Genomic relationships among diploid and polyploid species of the genus Ludwigia L. section Jussiaea using a combination of cytogenetic, morphological, and crossing investigations
Article Snippet: .. Biotinylated probes were immunodetected by Texas Red avidin DCS (Vector Laboratories, Burlingame, CA, USA) and the signal was amplified with biotinylated anti-avidin D (Vector Laboratories). .. The chromosomes were mounted and counterstained in Vectashield (Vector Laboratories) containing 2.5μg/mL 4’,6-diamidino-2-phenylindole (DAPI).

Article Title: Playing with the ploidy level enables to switch on and off the strict recombination control even in the vicinity of Brassica centromeres
Article Snippet: .. Biotinylated probe was immunodetected by Texas Red avidin DCS (Vector Laboratories) and the signal was amplified with biotinylated anti-avidin D (Vector Laboratories). .. The chromosomes were mounted and counterstained in Vectashield (Vector Laboratories) containing 2.5μg/mL 4’,6-diamidino-2-phenylindole (DAPI).

Article Title: Transcription decouples estrogen-dependent changes in enhancer-promoter contact frequencies and physical proximity
Article Snippet: For 2-color detection (either with fosmid or 10 kb derived probes), the following antibody dilutions were made: anti-digoxigenin-Rhodamine FAB fragments (Roche, cat. no. 11207750910) 1:20; Texas Red anti-sheep 1:100 (Abcam ab6745) and Avidin-FITC1:500 (Vector Laboratories A-2011); biotinylated anti-avidin (Vector Laboratories, cat. no. BA-0300) 1:100, and Avidin-FITC 1:500. .. For 3-color detection the following antibody dilutions were made: anti-digoxigenin (Roche, cat. 11333089001) 1:10; AF647 anti-seep (Invitrogen, cat. A-21448) 1:10 and Texas Red avidin (Vector Laboratories, cat. no. A-2016) 1:500; biotinylated anti-avidin (Vector Laboratories) 1:100; Texas Red avidin (Vector Laboratories, cat. no. A-2016) 1:500. ..

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Image Search Results

HAT1 is essential for DEN/CCl 4 -induced hepatocarcinogenesis. (A) The scheme depicting the experimental outline of the DEN/CCl 4 -induced HCC mouse model was shown. The wild type (WT) and liver-specific Hat1 knockout C57BL/6 mice ( Hat1 −/− ) mice were administered DEN (25 mg/kg) by i.p. injection on Day 14 after birth and then were administered CCl 4 (0.5 mL/kg) by intraperitoneal injection for 20 weeks after administration of DEN. The mice were analyzed at 48 weeks. (B) The expression of HAT1 was examined by Western blot analysis in liver tissues of WT ( n = 6) and Hat1 −/− mice ( n = 6) from DEN/CCl 4 -induced HCC model. (C) Representative PET/CT images of WT and Hat1 −/− mice from the DEN/CCl 4 -induced HCC mouse model were shown, and the SUV max values were analyzed in the mice. (D) Representative livers from WT and Hat1 −/− mice of DEN/CCl4-induced HCC model were shown. H&E staining and IHC staining of HAT1 and Ki-67 were determined in liver tissues from the mice. Scale bar, 50 μm. (E) The total tumor number and the tumor number (>3 mm) were calculated in the liver of WT ( n = 6) and Hat1 −/− mice from the DEN/CCl 4 -induced HCC model ( n = 6). Each point is one mouse. (F) The liver/body weight ratio was tested in WT and Hat1 −/− mice from the DEN/CCl 4 -induced HCC model. (G, H) Untargeted metabolomics were performed in liver tissues from WT and Hat1 −/− mice of DEN/CCl 4 -induced HCC model. (G) Volcano plot depicting the different levels of metabolites (fold change >1.5, or fold change <0.67, P < 0.05). (H) Enriched Kyoto Encyclopaedia of Genes and Genomes (KEGG) pathways of differently expressed metabolites were presented. Data are presented as mean ± SD. Student's t -test, ∗∗∗ P < 0.001. HAT1: histone acetyltransferase 1, DEN: diethylnitrosamine, CCl 4 : carbon tetrachloride, HCC: hepatocellular carcinoma, WT: wild type, H&E: hematoxylin and eosin (H&E), IHC: immunohistochemistry, KEGG: Kyoto Encyclopaedia of Genes and Genomes.

Journal: Acta Pharmaceutica Sinica. B

Article Title: Succinylation of tumor suppressor PPP2R1A K541 by HAT1 converses the role in modulation of gluconeogenesis/lipogenesis remodeling to display oncogene function

doi: 10.1016/j.apsb.2025.07.040

Figure Lengend Snippet: HAT1 is essential for DEN/CCl 4 -induced hepatocarcinogenesis. (A) The scheme depicting the experimental outline of the DEN/CCl 4 -induced HCC mouse model was shown. The wild type (WT) and liver-specific Hat1 knockout C57BL/6 mice ( Hat1 −/− ) mice were administered DEN (25 mg/kg) by i.p. injection on Day 14 after birth and then were administered CCl 4 (0.5 mL/kg) by intraperitoneal injection for 20 weeks after administration of DEN. The mice were analyzed at 48 weeks. (B) The expression of HAT1 was examined by Western blot analysis in liver tissues of WT ( n = 6) and Hat1 −/− mice ( n = 6) from DEN/CCl 4 -induced HCC model. (C) Representative PET/CT images of WT and Hat1 −/− mice from the DEN/CCl 4 -induced HCC mouse model were shown, and the SUV max values were analyzed in the mice. (D) Representative livers from WT and Hat1 −/− mice of DEN/CCl4-induced HCC model were shown. H&E staining and IHC staining of HAT1 and Ki-67 were determined in liver tissues from the mice. Scale bar, 50 μm. (E) The total tumor number and the tumor number (>3 mm) were calculated in the liver of WT ( n = 6) and Hat1 −/− mice from the DEN/CCl 4 -induced HCC model ( n = 6). Each point is one mouse. (F) The liver/body weight ratio was tested in WT and Hat1 −/− mice from the DEN/CCl 4 -induced HCC model. (G, H) Untargeted metabolomics were performed in liver tissues from WT and Hat1 −/− mice of DEN/CCl 4 -induced HCC model. (G) Volcano plot depicting the different levels of metabolites (fold change >1.5, or fold change <0.67, P < 0.05). (H) Enriched Kyoto Encyclopaedia of Genes and Genomes (KEGG) pathways of differently expressed metabolites were presented. Data are presented as mean ± SD. Student's t -test, ∗∗∗ P < 0.001. HAT1: histone acetyltransferase 1, DEN: diethylnitrosamine, CCl 4 : carbon tetrachloride, HCC: hepatocellular carcinoma, WT: wild type, H&E: hematoxylin and eosin (H&E), IHC: immunohistochemistry, KEGG: Kyoto Encyclopaedia of Genes and Genomes.

Article Snippet: Histone acetyltransferase 1 (HAT1) inhibitor JG-2016 was purchased from MCE (Shanghai, China).

Techniques: Knock-Out, Injection, Expressing, Western Blot, Positron Emission Tomography-Computed Tomography, Staining, Immunohistochemistry

HAT1 confers the remodeling of gluconeogenesis/lipogenesis. (A) A model of HAT1 conferring PCK1-mediated remodeling of gluconeogenesis/lipogenesis. (B) The levels of PCK1 pS90, PCK1, HAT1, and β -actin were detected by Western blot analysis in the liver tissues from C57BL/6 mice treated with normal vehicle ( n = 6) or C57BL/6 mice of DEN/CCl 4 -induced HCC model ( n = 6). (C) The levels of PCK1 pS90, PCK1, HAT1, and β -actin were measured by Western blot analysis in liver tissues of WT ( n = 6) and Hat1 −/− mice ( n = 6) from DEN/CCl 4 -induced HCC model. (D) The levels of PCK1 pS90, PCK1, HAT1, and β -actin were determined by Western blot analysis in primary human hepatocytes (PHH), HepG2, and Huh7 cells. (E) The levels of PCK1 pS90, PCK1, HAT1, and β -actin were examined by Western blot analysis in WT HepG2 cells and HAT1 KO Clone 1 HepG2 cells (HAT1 KO #1). (F) The relative levels of PEP, citrate, triglyceride, and cholesterol were analyzed by the corresponding assay kits in the liver tissues of WT ( n = 6) and Hat1 −/− mice ( n = 6) from DEN/CCl 4 -induced HCC model, respectively. (G–J) The relative levels of PEP, citrate, triglyceride, and cholesterol were tested by the corresponding assay kits in WT HepG2 cells and HAT1 KO #1 HepG2 cells cultured in 25 or 0.1 mmol/L glucose conditions for 10 h, respectively. (K) The lipid accumulation was analyzed by Nile Red staining in WT HepG2 cells and HAT1 KO #1 HepG2 cells cultured in 25 or 0.1 mmol/L glucose conditions for 10 h, respectively. Scale bar, 5 μm. The relative Nile Red staining intensity was quantified. Data are presented as mean ± SD. Student's t -test, ∗∗ P < 0.01, ∗∗∗ P < 0.001. HAT1: histone acetyltransferase 1, PCK1: phosphoenolpyruvate carboxykinase 1, pS90: phosphorylation at serine 90, DEN: diethylnitrosamine, CCl 4 : carbon tetrachloride, HCC: hepatocellular carcinoma, WT: wild type, KO: knockout, PEP: phosphoenolpyruvate.

Journal: Acta Pharmaceutica Sinica. B

Article Title: Succinylation of tumor suppressor PPP2R1A K541 by HAT1 converses the role in modulation of gluconeogenesis/lipogenesis remodeling to display oncogene function

doi: 10.1016/j.apsb.2025.07.040

Figure Lengend Snippet: HAT1 confers the remodeling of gluconeogenesis/lipogenesis. (A) A model of HAT1 conferring PCK1-mediated remodeling of gluconeogenesis/lipogenesis. (B) The levels of PCK1 pS90, PCK1, HAT1, and β -actin were detected by Western blot analysis in the liver tissues from C57BL/6 mice treated with normal vehicle ( n = 6) or C57BL/6 mice of DEN/CCl 4 -induced HCC model ( n = 6). (C) The levels of PCK1 pS90, PCK1, HAT1, and β -actin were measured by Western blot analysis in liver tissues of WT ( n = 6) and Hat1 −/− mice ( n = 6) from DEN/CCl 4 -induced HCC model. (D) The levels of PCK1 pS90, PCK1, HAT1, and β -actin were determined by Western blot analysis in primary human hepatocytes (PHH), HepG2, and Huh7 cells. (E) The levels of PCK1 pS90, PCK1, HAT1, and β -actin were examined by Western blot analysis in WT HepG2 cells and HAT1 KO Clone 1 HepG2 cells (HAT1 KO #1). (F) The relative levels of PEP, citrate, triglyceride, and cholesterol were analyzed by the corresponding assay kits in the liver tissues of WT ( n = 6) and Hat1 −/− mice ( n = 6) from DEN/CCl 4 -induced HCC model, respectively. (G–J) The relative levels of PEP, citrate, triglyceride, and cholesterol were tested by the corresponding assay kits in WT HepG2 cells and HAT1 KO #1 HepG2 cells cultured in 25 or 0.1 mmol/L glucose conditions for 10 h, respectively. (K) The lipid accumulation was analyzed by Nile Red staining in WT HepG2 cells and HAT1 KO #1 HepG2 cells cultured in 25 or 0.1 mmol/L glucose conditions for 10 h, respectively. Scale bar, 5 μm. The relative Nile Red staining intensity was quantified. Data are presented as mean ± SD. Student's t -test, ∗∗ P < 0.01, ∗∗∗ P < 0.001. HAT1: histone acetyltransferase 1, PCK1: phosphoenolpyruvate carboxykinase 1, pS90: phosphorylation at serine 90, DEN: diethylnitrosamine, CCl 4 : carbon tetrachloride, HCC: hepatocellular carcinoma, WT: wild type, KO: knockout, PEP: phosphoenolpyruvate.

Article Snippet: Histone acetyltransferase 1 (HAT1) inhibitor JG-2016 was purchased from MCE (Shanghai, China).

Techniques: Western Blot, Cell Culture, Staining, Phospho-proteomics, Knock-Out

HAT1 triggers the remodeling of gluconeogenesis/lipogenesis by modulating the levels of phosphorylation of PCK1 Ser90. (A–H) HepG2 cells were transfected with plasmids overexpressing HAT1, or co-transfected with plasmids overexpressing HAT1 and PCK1, PCK1 mutant (S90D), or PCK1 mutant (S90A), respectively. (A) The relative PCK1 activity was analyzed by the corresponding assay kit in the cells. (B) The nuclear accumulation of SREBP1 was observed by confocal immunofluorescence analysis in the cells. Scale bar, 5 μm. (C) The mRNA expression levels of SREBP1 target genes, including FASN , SCD , ACACA , and GPAM , were analyzed by RT-qPCR in the cells. (D–G) The relative levels of PEP, citrate, triglyceride, and cholesterol were measured by the corresponding assay kits in the cells cultured in 25 or 0.1 mmol/L glucose conditions for 10 h, respectively. (H) The lipid accumulation was showed by Nile Red staining in the cells cultured in 25 or 0.1 mmol/L glucose conditions for 10 h, respectively. Scale bar, 5 μm. The relative Nile Red staining intensity was quantified. Data are presented as mean ± SD. Student's t -test, ∗∗ P < 0.01, ∗∗∗ P < 0.001. HAT1: histone acetyltransferase 1, PCK1: phosphoenolpyruvate carboxykinase 1, pS90: phosphorylation at serine 90, SREBP1: sterol regulatory element-binding protein 1, FASN: fatty acid synthase, SCD: stearoyl-CoA desaturase, ACACA: acetyl-CoA carboxylase alpha, GPAM: glycerol-3-phosphate acyltransferase 1.

Journal: Acta Pharmaceutica Sinica. B

Article Title: Succinylation of tumor suppressor PPP2R1A K541 by HAT1 converses the role in modulation of gluconeogenesis/lipogenesis remodeling to display oncogene function

doi: 10.1016/j.apsb.2025.07.040

Figure Lengend Snippet: HAT1 triggers the remodeling of gluconeogenesis/lipogenesis by modulating the levels of phosphorylation of PCK1 Ser90. (A–H) HepG2 cells were transfected with plasmids overexpressing HAT1, or co-transfected with plasmids overexpressing HAT1 and PCK1, PCK1 mutant (S90D), or PCK1 mutant (S90A), respectively. (A) The relative PCK1 activity was analyzed by the corresponding assay kit in the cells. (B) The nuclear accumulation of SREBP1 was observed by confocal immunofluorescence analysis in the cells. Scale bar, 5 μm. (C) The mRNA expression levels of SREBP1 target genes, including FASN , SCD , ACACA , and GPAM , were analyzed by RT-qPCR in the cells. (D–G) The relative levels of PEP, citrate, triglyceride, and cholesterol were measured by the corresponding assay kits in the cells cultured in 25 or 0.1 mmol/L glucose conditions for 10 h, respectively. (H) The lipid accumulation was showed by Nile Red staining in the cells cultured in 25 or 0.1 mmol/L glucose conditions for 10 h, respectively. Scale bar, 5 μm. The relative Nile Red staining intensity was quantified. Data are presented as mean ± SD. Student's t -test, ∗∗ P < 0.01, ∗∗∗ P < 0.001. HAT1: histone acetyltransferase 1, PCK1: phosphoenolpyruvate carboxykinase 1, pS90: phosphorylation at serine 90, SREBP1: sterol regulatory element-binding protein 1, FASN: fatty acid synthase, SCD: stearoyl-CoA desaturase, ACACA: acetyl-CoA carboxylase alpha, GPAM: glycerol-3-phosphate acyltransferase 1.

Article Snippet: Histone acetyltransferase 1 (HAT1) inhibitor JG-2016 was purchased from MCE (Shanghai, China).

Techniques: Phospho-proteomics, Transfection, Mutagenesis, Activity Assay, Immunofluorescence, Expressing, Quantitative RT-PCR, Cell Culture, Staining, Binding Assay

HAT1 succinylates PPP2R1A K541, leading to phosphorylation of PCK1 Ser90. (A) The levels of PPP2R1A succinylation and HAT1 were examined by immunoprecipitation and Western blot analysis as indicated in the liver tissues from C57BL/6 mice treated with normal vehicle ( n = 6) or tumor tissues from C57BL/6 mice of DEN/CCl 4 -induced HCC model ( n = 6). (B) The levels of PPP2R1A succinylation and HAT1 were measured by immunoprecipitation and Western blot analysis as indicated in tumor tissues of WT ( n = 6) and Hat1 −/− mice ( n = 6) from DEN/CCl 4 -induced HCC model, respectively. (C) The PPP2R1A succinylation levels and HAT1 were determined by immunoprecipitation and Western blot analysis as indicated in HepG2 cells (WT), HAT1 KO #1 HepG2 cells, HAT1 KO #1 HepG2 cells reconstituted with wild-type HAT1 or HAT1 mutant (T188A). (D) The levels of PPP2R1A K541 succinylation, PPP2R1A, and HAT1 were measured by Western blot analysis in HepG2 cells (WT), HAT1 KO #1 HepG2 cells, HAT1 KO #1 HepG2 cells reconstituted with wild-type HAT1 or HAT1 mutant (T188A). (E) HAT1-catalyzed PPP2R1A succinylation was analyzed by in vitro succinylation assays using purified HAT1, PPP2R1A, and succinyl-CoA/acetyl-CoA as indicated. Western blot analysis was performed using the indicated antibodies. (F) The interaction of PCK1 with PPP2R1A or PPP2CA was analyzed by immunoprecipitation and Western blot analysis as indicated in HepG2 cells (WT), HAT1 KO #1 HepG2 cells, HAT1 KO #1 HepG2 cells reconstituted with wild-type HAT1 or HAT1 mutant (T188A). (G) The interaction of flag-PPP2R1A or flag PPP2R1A mutant (K541R) with PCK1 or PPP2CA was examined by immunoprecipitation and Western blot analysis as indicated in HepG2 cells (WT), HAT1 KO #1 HepG2 cells, HAT1 KO #1 HepG2 cells reconstituted with wild-type HAT1 or HAT1 mutant (T188A). (H–M) HepG2 cells were transfected with plasmids overexpressing HAT1, or co-transfected with plasmids overexpressing HAT1 and PPP2R1A or PPP2R1A mutant (K541E), respectively. (H) The levels of PCK1 pS90, PCK1, HAT1, PPP2R1A, and β -actin were examined by Western blot analysis in the cells. (I) The relative PCK1 activity was detected by the corresponding assay kit in the cells. (J) The nuclear accumulation of SREBP1 was observed by confocal immunofluorescence analysis in the cells. Scale bar, 5 μm. (K) The mRNA expression levels of SREBP1 target genes, including FASN, SCD, ACACA, and GPAM, were analyzed by RT-qPCR in the cells. (L) The relative levels of PEP, citrate, triglyceride, and cholesterol were tested by the corresponding assay kits in the cells cultured in 25 or 0.1 mmol/L glucose conditions for 10 h, respectively. (M) The lipid accumulation was measured by Nile Red staining in the cells cultured in 25 or 0.1 mmol/L glucose conditions for 10 h, respectively. Scale bar, 5 μm. The relative Nile Red staining intensity was quantified. Data are presented as mean ± SD. Student's t -test, ∗∗∗ P < 0.001. HAT1: histone acetyltransferase 1, PCK1: phosphoenolpyruvate carboxykinase 1, pS90: phosphorylation at serine 90, DEN: diethylnitrosamine, CCl 4 : carbon tetrachloride, HCC: hepatocellular carcinoma, WT: wild type, KO: knockout, PPP2R1A: protein phosphatase 2 scaffold subunit alpha, PPP2CA: protein phosphatase 2 catalytic subunit alpha, PEP: phosphoenolpyruvate, SREBP1: sterol regulatory element-binding protein 1, FASN: fatty acid synthase, SCD: stearoyl-CoA desaturase, ACACA: acetyl-CoA carboxylase alpha, GPAM: glycerol-3-phosphate acyltransferase 1.

Journal: Acta Pharmaceutica Sinica. B

Article Title: Succinylation of tumor suppressor PPP2R1A K541 by HAT1 converses the role in modulation of gluconeogenesis/lipogenesis remodeling to display oncogene function

doi: 10.1016/j.apsb.2025.07.040

Figure Lengend Snippet: HAT1 succinylates PPP2R1A K541, leading to phosphorylation of PCK1 Ser90. (A) The levels of PPP2R1A succinylation and HAT1 were examined by immunoprecipitation and Western blot analysis as indicated in the liver tissues from C57BL/6 mice treated with normal vehicle ( n = 6) or tumor tissues from C57BL/6 mice of DEN/CCl 4 -induced HCC model ( n = 6). (B) The levels of PPP2R1A succinylation and HAT1 were measured by immunoprecipitation and Western blot analysis as indicated in tumor tissues of WT ( n = 6) and Hat1 −/− mice ( n = 6) from DEN/CCl 4 -induced HCC model, respectively. (C) The PPP2R1A succinylation levels and HAT1 were determined by immunoprecipitation and Western blot analysis as indicated in HepG2 cells (WT), HAT1 KO #1 HepG2 cells, HAT1 KO #1 HepG2 cells reconstituted with wild-type HAT1 or HAT1 mutant (T188A). (D) The levels of PPP2R1A K541 succinylation, PPP2R1A, and HAT1 were measured by Western blot analysis in HepG2 cells (WT), HAT1 KO #1 HepG2 cells, HAT1 KO #1 HepG2 cells reconstituted with wild-type HAT1 or HAT1 mutant (T188A). (E) HAT1-catalyzed PPP2R1A succinylation was analyzed by in vitro succinylation assays using purified HAT1, PPP2R1A, and succinyl-CoA/acetyl-CoA as indicated. Western blot analysis was performed using the indicated antibodies. (F) The interaction of PCK1 with PPP2R1A or PPP2CA was analyzed by immunoprecipitation and Western blot analysis as indicated in HepG2 cells (WT), HAT1 KO #1 HepG2 cells, HAT1 KO #1 HepG2 cells reconstituted with wild-type HAT1 or HAT1 mutant (T188A). (G) The interaction of flag-PPP2R1A or flag PPP2R1A mutant (K541R) with PCK1 or PPP2CA was examined by immunoprecipitation and Western blot analysis as indicated in HepG2 cells (WT), HAT1 KO #1 HepG2 cells, HAT1 KO #1 HepG2 cells reconstituted with wild-type HAT1 or HAT1 mutant (T188A). (H–M) HepG2 cells were transfected with plasmids overexpressing HAT1, or co-transfected with plasmids overexpressing HAT1 and PPP2R1A or PPP2R1A mutant (K541E), respectively. (H) The levels of PCK1 pS90, PCK1, HAT1, PPP2R1A, and β -actin were examined by Western blot analysis in the cells. (I) The relative PCK1 activity was detected by the corresponding assay kit in the cells. (J) The nuclear accumulation of SREBP1 was observed by confocal immunofluorescence analysis in the cells. Scale bar, 5 μm. (K) The mRNA expression levels of SREBP1 target genes, including FASN, SCD, ACACA, and GPAM, were analyzed by RT-qPCR in the cells. (L) The relative levels of PEP, citrate, triglyceride, and cholesterol were tested by the corresponding assay kits in the cells cultured in 25 or 0.1 mmol/L glucose conditions for 10 h, respectively. (M) The lipid accumulation was measured by Nile Red staining in the cells cultured in 25 or 0.1 mmol/L glucose conditions for 10 h, respectively. Scale bar, 5 μm. The relative Nile Red staining intensity was quantified. Data are presented as mean ± SD. Student's t -test, ∗∗∗ P < 0.001. HAT1: histone acetyltransferase 1, PCK1: phosphoenolpyruvate carboxykinase 1, pS90: phosphorylation at serine 90, DEN: diethylnitrosamine, CCl 4 : carbon tetrachloride, HCC: hepatocellular carcinoma, WT: wild type, KO: knockout, PPP2R1A: protein phosphatase 2 scaffold subunit alpha, PPP2CA: protein phosphatase 2 catalytic subunit alpha, PEP: phosphoenolpyruvate, SREBP1: sterol regulatory element-binding protein 1, FASN: fatty acid synthase, SCD: stearoyl-CoA desaturase, ACACA: acetyl-CoA carboxylase alpha, GPAM: glycerol-3-phosphate acyltransferase 1.

Article Snippet: Histone acetyltransferase 1 (HAT1) inhibitor JG-2016 was purchased from MCE (Shanghai, China).

Techniques: Phospho-proteomics, Immunoprecipitation, Western Blot, Mutagenesis, In Vitro, Purification, Transfection, Activity Assay, Immunofluorescence, Expressing, Quantitative RT-PCR, Cell Culture, Staining, Knock-Out, Binding Assay

PPP2R1A promotes gluconeogenesis and inhibits lipogenesis by dephosphorylation of PCK1 Ser90 to suppress tumor growth. (A–I) HepG2 cells were transfected with plasmids overexpressing PPP2R1A or PPP2R1A mutant (K541E), or co-transfected with plasmids overexpressing PCK1 or PCK1 mutant (S90A), respectively. (A) The levels of PCK1 pS90, PCK1, PPP2R1A, and β -actin were tested by Western blot analysis in the cells. (B) The relative PCK1 activity was analyzed by the corresponding assay kit in the cells. (C) The nuclear accumulation of SREBP1 was observed by confocal immunofluorescence analysis in the cells. Scale bar, 5 μm. (D) The mRNA expression levels of SREBP1 target genes, including FASN, SCD, ACACA, and GPAM, were examined by RT-qPCR in the cells. (E–H) The relative levels of PEP, citrate, triglyceride, and cholesterol were analyzed by the corresponding assay kits in the cells cultured in 25 or 0.1 mmol/L glucose conditions for 10 h, respectively. (I) The cell viability was determined by CCK-8 assays cultured in 25 or 0.1 mmol/L glucose conditions for 10 h, respectively. (J–N) HepG2 cells were transfected with plasmids overexpressing PPP2R1A or PPP2R1A mutant (K541E), or co-transfected with plasmids overexpressing PCK1 or PCK1 mutant (S90A), respectively. The cells were subcutaneously injected into athymic nude mice ( n = 6). (J) Representative images of tumors from the nude mice ( n = 6) are shown. Tumor volumes and average tumor weight were calculated. Scale bar, 1 cm. (K–N) The relative levels of PEP, citrate, triglyceride, and cholesterol were analyzed by the corresponding assay kits in the tumor tissues from the nude mice. Data are presented as mean ± SD. Student's t -test, ∗∗ P < 0.01, ∗∗∗ P < 0.001. HAT1: histone acetyltransferase 1, PCK1: phosphoenolpyruvate carboxykinase 1, pS90: phosphorylation at serine 90, PPP2R1A: protein phosphatase 2 scaffold subunit alpha, SREBP1: sterol regulatory element-binding protein 1, FASN: fatty acid synthase, SCD: stearoyl-CoA desaturase, ACACA: acetyl-CoA carboxylase alpha, GPAM: glycerol-3-phosphate acyltransferase 1.

Journal: Acta Pharmaceutica Sinica. B

Article Title: Succinylation of tumor suppressor PPP2R1A K541 by HAT1 converses the role in modulation of gluconeogenesis/lipogenesis remodeling to display oncogene function

doi: 10.1016/j.apsb.2025.07.040

Figure Lengend Snippet: PPP2R1A promotes gluconeogenesis and inhibits lipogenesis by dephosphorylation of PCK1 Ser90 to suppress tumor growth. (A–I) HepG2 cells were transfected with plasmids overexpressing PPP2R1A or PPP2R1A mutant (K541E), or co-transfected with plasmids overexpressing PCK1 or PCK1 mutant (S90A), respectively. (A) The levels of PCK1 pS90, PCK1, PPP2R1A, and β -actin were tested by Western blot analysis in the cells. (B) The relative PCK1 activity was analyzed by the corresponding assay kit in the cells. (C) The nuclear accumulation of SREBP1 was observed by confocal immunofluorescence analysis in the cells. Scale bar, 5 μm. (D) The mRNA expression levels of SREBP1 target genes, including FASN, SCD, ACACA, and GPAM, were examined by RT-qPCR in the cells. (E–H) The relative levels of PEP, citrate, triglyceride, and cholesterol were analyzed by the corresponding assay kits in the cells cultured in 25 or 0.1 mmol/L glucose conditions for 10 h, respectively. (I) The cell viability was determined by CCK-8 assays cultured in 25 or 0.1 mmol/L glucose conditions for 10 h, respectively. (J–N) HepG2 cells were transfected with plasmids overexpressing PPP2R1A or PPP2R1A mutant (K541E), or co-transfected with plasmids overexpressing PCK1 or PCK1 mutant (S90A), respectively. The cells were subcutaneously injected into athymic nude mice ( n = 6). (J) Representative images of tumors from the nude mice ( n = 6) are shown. Tumor volumes and average tumor weight were calculated. Scale bar, 1 cm. (K–N) The relative levels of PEP, citrate, triglyceride, and cholesterol were analyzed by the corresponding assay kits in the tumor tissues from the nude mice. Data are presented as mean ± SD. Student's t -test, ∗∗ P < 0.01, ∗∗∗ P < 0.001. HAT1: histone acetyltransferase 1, PCK1: phosphoenolpyruvate carboxykinase 1, pS90: phosphorylation at serine 90, PPP2R1A: protein phosphatase 2 scaffold subunit alpha, SREBP1: sterol regulatory element-binding protein 1, FASN: fatty acid synthase, SCD: stearoyl-CoA desaturase, ACACA: acetyl-CoA carboxylase alpha, GPAM: glycerol-3-phosphate acyltransferase 1.

Article Snippet: Histone acetyltransferase 1 (HAT1) inhibitor JG-2016 was purchased from MCE (Shanghai, China).

Techniques: De-Phosphorylation Assay, Transfection, Mutagenesis, Western Blot, Activity Assay, Immunofluorescence, Expressing, Quantitative RT-PCR, Cell Culture, CCK-8 Assay, Injection, Phospho-proteomics, Binding Assay

Succinylation of PPP2R1A by HAT1 converses the role in modulation of remodeling of gluconeogenesis/lipogenesis to support liver cancer. (A) The cell viability was analyzed by CCK-8 assays in HepG2 cells (WT), HAT1 KO #1 HepG2 cells, HAT1 KO #1 HepG2 cells reconstituted with wild-type HAT1 or HAT1 mutant (T188A), HAT1 KO #1 HepG2 cells co-reconstituted with wild-type HAT1 and PCK1, PCK1 mutant (S90A), PPP2R1A, or PPP2R1A mutant (K541R), respectively. (B–H) The athymic nude mice ( n = 6) were subcutaneously injected with HepG2 cells (WT), HAT1 KO #1 HepG2 cells, HAT1 KO #1 HepG2 cells reconstituted with wild-type HAT1 or HAT1 mutant (T188A), HAT1 KO #1 HepG2 cells co-reconstituted with wild-type HAT1 and PCK1, PCK1 mutant (S90A), PPP2R1A, or PPP2R1A mutant (K541R), respectively. (B) Representative images of tumors from the nude mice ( n = 6) were shown. Tumor volumes and average tumor weight were calculated. Scale bar = 1 cm. (C) The expression levels of Ki-67 were analyzed by IHC staining in the tumor tissues from the nude mice. Scale bar = 50 μm. (D) The levels of PCK1 pS90, PCK1, PPP2R1A, HAT1, and β -actin were examined by Western blot analysis in the tumor tissues from the nude mice. (E–H) The relative levels of PEP, citrate, triglyceride, and cholesterol were determined by the corresponding assay kits in the tumor tissues from the nude mice. Data are presented as mean ± SD. Student's t -test, ∗∗∗ P < 0.001. HAT1: histone acetyltransferase 1, PCK1: phosphoenolpyruvate carboxykinase 1, pS90: phosphorylation at serine 90, WT: wild type, KO: knockout, PPP2R1A: protein phosphatase 2 scaffold subunit alpha, IHC: immunohistochemistry, PEP: phosphoenolpyruvate.

Journal: Acta Pharmaceutica Sinica. B

Article Title: Succinylation of tumor suppressor PPP2R1A K541 by HAT1 converses the role in modulation of gluconeogenesis/lipogenesis remodeling to display oncogene function

doi: 10.1016/j.apsb.2025.07.040

Figure Lengend Snippet: Succinylation of PPP2R1A by HAT1 converses the role in modulation of remodeling of gluconeogenesis/lipogenesis to support liver cancer. (A) The cell viability was analyzed by CCK-8 assays in HepG2 cells (WT), HAT1 KO #1 HepG2 cells, HAT1 KO #1 HepG2 cells reconstituted with wild-type HAT1 or HAT1 mutant (T188A), HAT1 KO #1 HepG2 cells co-reconstituted with wild-type HAT1 and PCK1, PCK1 mutant (S90A), PPP2R1A, or PPP2R1A mutant (K541R), respectively. (B–H) The athymic nude mice ( n = 6) were subcutaneously injected with HepG2 cells (WT), HAT1 KO #1 HepG2 cells, HAT1 KO #1 HepG2 cells reconstituted with wild-type HAT1 or HAT1 mutant (T188A), HAT1 KO #1 HepG2 cells co-reconstituted with wild-type HAT1 and PCK1, PCK1 mutant (S90A), PPP2R1A, or PPP2R1A mutant (K541R), respectively. (B) Representative images of tumors from the nude mice ( n = 6) were shown. Tumor volumes and average tumor weight were calculated. Scale bar = 1 cm. (C) The expression levels of Ki-67 were analyzed by IHC staining in the tumor tissues from the nude mice. Scale bar = 50 μm. (D) The levels of PCK1 pS90, PCK1, PPP2R1A, HAT1, and β -actin were examined by Western blot analysis in the tumor tissues from the nude mice. (E–H) The relative levels of PEP, citrate, triglyceride, and cholesterol were determined by the corresponding assay kits in the tumor tissues from the nude mice. Data are presented as mean ± SD. Student's t -test, ∗∗∗ P < 0.001. HAT1: histone acetyltransferase 1, PCK1: phosphoenolpyruvate carboxykinase 1, pS90: phosphorylation at serine 90, WT: wild type, KO: knockout, PPP2R1A: protein phosphatase 2 scaffold subunit alpha, IHC: immunohistochemistry, PEP: phosphoenolpyruvate.

Article Snippet: Histone acetyltransferase 1 (HAT1) inhibitor JG-2016 was purchased from MCE (Shanghai, China).

Techniques: CCK-8 Assay, Mutagenesis, Injection, Expressing, Immunohistochemistry, Western Blot, Phospho-proteomics, Knock-Out

Succinylation of PPP2R1A lysine 541 by HAT1 converses the role in modulation of remodeling of gluconeogenesis/lipogenesis to support liver cancer. In this model, PP2A is a protein complex that contains 60 different holoenzymes, PPP2R1A and PPP2CA are representative members of A and C subunits of PP2A in hepatocytes. PPP2R1A is required for the assembly of the PP2A complex. PCK1 catalyzes the conversion of OAA to PEP in gluconeogenesis. PPP2R1A promotes gluconeogenesis and inhibits lipogenesis by de-phosphorylation of PCK1 Ser90, leading to the tumor suppression of liver cancer. HAT1 contributes to the remodeling of gluconeogenesis/lipogenesis in liver cancer. PPP2R1A is succinylated at K541 by HAT1, leading to the inhibition of assembly of PP2A in liver cancer. Inhibition of assembly of PP2A blocks the dephosphorylation of PCK1 Ser90, which induces lipogenesis but fails to catalyze the conversion of OAA to PEP in gluconeogenesis, contributing to the malignant progression of liver cancer. Thus, the succinylation of tumor suppressor PPP2R1A displays an oncogene function. HAT1: histone acetyltransferase 1, PCK1: phosphoenolpyruvate carboxykinase 1, PPP2R1A: protein phosphatase 2 scaffold subunit alpha, PPP2CA: protein phosphatase 2 catalytic subunit alpha, PP2A: protein phosphatase 2A, OAA: oxaloacetate, PEP: phosphoenolpyruvate, SREBP1: sterol regulatory element-binding protein 1.

Journal: Acta Pharmaceutica Sinica. B

Article Title: Succinylation of tumor suppressor PPP2R1A K541 by HAT1 converses the role in modulation of gluconeogenesis/lipogenesis remodeling to display oncogene function

doi: 10.1016/j.apsb.2025.07.040

Figure Lengend Snippet: Succinylation of PPP2R1A lysine 541 by HAT1 converses the role in modulation of remodeling of gluconeogenesis/lipogenesis to support liver cancer. In this model, PP2A is a protein complex that contains 60 different holoenzymes, PPP2R1A and PPP2CA are representative members of A and C subunits of PP2A in hepatocytes. PPP2R1A is required for the assembly of the PP2A complex. PCK1 catalyzes the conversion of OAA to PEP in gluconeogenesis. PPP2R1A promotes gluconeogenesis and inhibits lipogenesis by de-phosphorylation of PCK1 Ser90, leading to the tumor suppression of liver cancer. HAT1 contributes to the remodeling of gluconeogenesis/lipogenesis in liver cancer. PPP2R1A is succinylated at K541 by HAT1, leading to the inhibition of assembly of PP2A in liver cancer. Inhibition of assembly of PP2A blocks the dephosphorylation of PCK1 Ser90, which induces lipogenesis but fails to catalyze the conversion of OAA to PEP in gluconeogenesis, contributing to the malignant progression of liver cancer. Thus, the succinylation of tumor suppressor PPP2R1A displays an oncogene function. HAT1: histone acetyltransferase 1, PCK1: phosphoenolpyruvate carboxykinase 1, PPP2R1A: protein phosphatase 2 scaffold subunit alpha, PPP2CA: protein phosphatase 2 catalytic subunit alpha, PP2A: protein phosphatase 2A, OAA: oxaloacetate, PEP: phosphoenolpyruvate, SREBP1: sterol regulatory element-binding protein 1.

Article Snippet: Histone acetyltransferase 1 (HAT1) inhibitor JG-2016 was purchased from MCE (Shanghai, China).

Techniques: De-Phosphorylation Assay, Inhibition, Binding Assay

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