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Correction: RNAi-Dependent and Independent Control of LINE1 Accumulation and Mobility in Mouse Embryonic Stem Cells

机译:更正:RNAi依赖和独立控制的小鼠胚胎干细胞中的LINE1积累和移动性。

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Panel A in Fig 4 and panels A and F in S4 Fig are not presented correctly. The lanes in the corrected figures are separated by tracks for other mutants that are not relevant for the current work and can be seen in the original blots, provided here as S7 and S8 Figs. The authors apologise for the mistake and have provided corrected versions, along with the original blots that were used to create the figures. These errors do not affect the conclusions of this article. 10.1371/journal.pgen.1005247.g001 Fig 4 L1 mRNA levels and genomic copy-number in various knock-out and knock-down mESC lines. A. Western analysis of XRN2 and L1_ORF1 accumulation in WT and Xrn2 _KD mESCs; CM: Coomassie staining of total protein. B. qRT-PCR analysis of L1_ORF2 mRNA levels in WT and Xrn2 _KD mESCs. C. qPCR analysis of L1_Tf copy-number in WT and Xrn2 _KD mESCs. D–E. qRT-PCR analysis of miR-295 (D) and L1_ORF2 mRNA (E) levels in WT and Dgcr8 _KO mESCs. F. qPCR analysis of L1_Tf copy-number in WT and Dgcr8 _KO mESCs. G–H. qRT-PCR analysis of miR-295 (G) and L1_ORF2 mRNA (H) levels upon hAgo2 deletion in Tamoxifen-treated Ago1 , 2 , 3 , 4_KO mESCs. I. qPCR analysis of L1_Tf copy-number in Ago1 , 2 , 3 , 4_KO_hAgo2 mESCs before and after hAgo2 deletion. *: p-value<0.1. Supporting Information S4 Fig L1 expression and genomic copy-number in various knock-out and knock-down mESC lines. A. Western analysis of RRP6 and L1_ORF1 accumulation in WT and Rrp6 _KD mESCs; CM: Coomassie staining of total protein. B. Accumulation of Tf_5′-UTR (+) and (?) sRNAs detected by qRT-PCR in WT and Xrn2 _KD mESCs. C. qPCR analysis of L1_Tf copy-number in WT and Rrp6 _KD mESCs. D. L1_ORF2, Tf, Gf and A sub-type mRNAs accumulation detected by qRT-PCR in Xrn2 _KD and Rrp6 _KD mESCs. E. Accumulation of miR-320 detected by qRT-PCR in WT and Dgcr8 _KO mESCs. F. Western analysis of AGO2 accumulation in WT and Ago1 , 2 , 3 , 4_KO_hAgo2 mESCs before and after hAgo2 deletion induced by tamoxifen; CM: Coomassie staining of total protein. G. Accumulation of the Hmga2 and Btg2 mRNAs, respectively targeted by mmu-miR-196a and mmu-let-7a/mmu-miR-132, analyzed by qRT-PCR before and after deletion of h Ago2 . H. mRNA accumulation of L1_Tf, _Gf and _A sub-types detected by qRT-PCR before and after h Ago2 deletion. I. mRNA accumulation of a single Tf_L1 subtype located on chromosome 17, analyzed by semi-quantitative RT-PCR before and after h Ago2 deletion. (TIF) Click here for additional data file. S7 Fig Original Blots for Fig 4A . The red rectangles highlight the part of the gel presented in Fig 4A . CM: Coomassie staining of total protein. (TIF) Click here for additional data file. S8 Fig Original Blots for S4A and S4F Fig. A. Original blot for the S4A Fig . The red rectangles highlight the part of the gel presented in S4A Fig . B. The original blot for the S4F Fig is presented. CM: Coomassie staining of total protein. (TIF) Click here for additional data file.
机译:图4中的面板A和图S4中的面板A和F没有正确显示。校正图中的泳道由与当前工作无关的其他突变体的轨道隔开,可以在原始印迹中看到,此处提供为S7和S8。作者对此错误表示歉意,并提供了更正的版本以及用于创建图形的原始污点。这些错误不会影响本文的结论。 10.1371 / journal.pgen.1005247.g001图4各种敲除和敲除mESC系中的L1 mRNA水平和基因组拷贝数。 A. WT和Xrn2 _KD mESC中XRN2和L1_ORF1积累的Western分析; CM:总蛋白的考马斯染色。 B. WT和Xrn2 _KD mESC中L1_ORF2 mRNA水平的qRT-PCR分析。 C. WT和Xrn2 _KD mESC中L1_Tf拷贝数的qPCR分析。 D–E。 WT和Dgcr8 _KO mESC中miR-295(D)和L1_ORF2 mRNA(E)水平的qRT-PCR分析。 F.WT和Dgcr8_KOmESC中L1_Tf拷贝数的qPCR分析。 GH。在他莫昔芬治疗的Ago1、2、3、4_KO mESC中,hAgo2缺失后,miR-295(G)和L1_ORF2 mRNA(H)水平的qRT-PCR分析。 I. qPCR分析hAgo2缺失前后Ago1、2、3、4_KO_hAgo2 mESC中L1_Tf的拷贝数。 *:p值<0.1。支持信息S4图L1在各种敲除和敲除mESC品系中的表达和基因组拷贝数。 A. WT和Rrp6 _KD mESC中RRP6和L1_ORF1积累的Western分析; CM:总蛋白的考马斯染色。 B.通过qRT-PCR在WT和Xrn2 _KD mESC中检测到的Tf_5'-UTR(+)和(?)sRNA的积累。 C. WT和Rrp6 _KD mESC中L1_Tf拷贝数的qPCR分析。 D. L1_ORF2,Tf,Gf和QRT-PCR在Xrn2 _KD和Rrp6 _KD mESC中检测到亚型mRNA积累。 E.通过qRT-PCR在WT和Dgcr8_KO mESC中检测到miR-320的积累。 F.他莫昔芬诱导hAgo2缺失前后WT和Ago1、2、3、4_KO_hAgo2 mESC中AGO2积累的Western分析; CM:总蛋白的考马斯染色。 G.分别在缺失h Ago2之前和之后通过qRT-PCR分析分别由mmu-miR-196a和mmu-let-7a / mmu-miR-132靶向的Hmga2和Btg2 mRNA的积累。 H.Ago2缺失前后通过qRT-PCR检测到的L1_Tf,_Gf和_A亚型的H.mRNA积累。 I.位于h Ago2缺失前后的半定量RT-PCR分析位于染色体17上的单个Tf_L1亚型的mRNA积累。 (TIF)单击此处获取其他数据文件。 S7 Fig图4A的原始印迹。红色矩形突出显示了图4A中显示的凝胶部分。 CM:总蛋白的考马斯染色。 (TIF)单击此处获取其他数据文件。 S4A和S4F的原始印迹图A. S4A的原始印迹红色矩形突出显示了S4A中呈现的凝胶部分。 B.展示了S4F Fig的原始印迹。 CM:总蛋白的考马斯染色。 (TIF)单击此处获取其他数据文件。

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