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The regulation of ferroptosis by MESH1 through the activation of the integrative stress response

机译:通过综合应力反应的激活来对Mesh1调节Mesh1

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摘要

A Heatmap of the transcriptional difference between control or two independent MESH1 siRNA knockdown in RCC4 cells. MESH1 was silenced by siMESH1#1 or siMESH1#2 and profiled by RNA-seq. Color scale indicates log2-fold-change. B Top ten repressed Gene Ontology processes of the transcriptome of MESH1-silenced RCC4 cells. C, D GSEA analysis showed the enrichment of DNA replication geneset (C) and constituent of ribosome (D) in the MESH1 knockdown cells. E–H mRNA abundance of MESH1 (E), CDK2 (F), E2F1 (G), and RRM2 (H) as validated by rt-qPCR. mRNA abundance was determined by rt-qPCR, normalized by β-actin, and presented in relative ratio to siNT (non-targeting) treatment. n = 3 biological replicates. Statistical analysis: ANOVA with Tukey HSD post hoc test, **P < 0.01.
机译:在RCC4细胞中对照或两个独立网状物敲击之间的转录差异的热图。 Mesh1由Simesh1#1或Simesh1#2静音,并由RNA-SEQ分析。颜色刻度表示Log2-Foll-Change。 B顶部十大压抑基因本体本病程的网状物1沉默的RCC4细胞转录组。 C,D GSEA分析显示在网状1敲低细胞中富集DNA复制基因(C)和核糖体(D)的组成部分。通过RT-QPCR验证的Mesh1(e),CDK2(F),E2F1(G)和RRM2(H)的E-H mRNA丰富。通过RT-QPCR测定mRNA丰度,通过β-肌动蛋白标准化,并以与SINT(非靶向)处理的相对比率呈现。 n = 3生物重复。统计分析:具有Tukey HSD后HOC测试的ANOVA,** P <0.01。

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