Fig. 5 E2F1 also interacts with alternatively spliced transcripts from the MECOM gene. E2F1 also interacts with alternatively spliced transcripts from.

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Fig. 5 Correlation of RNA expression and protein abundance.

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Fig. 5 E2F1 also interacts with alternatively spliced transcripts from the MECOM gene. E2F1 also interacts with alternatively spliced transcripts from the MECOM gene. (A) Schematic representation of exon structure for the MECOM gene. Each alternatively spliced transcript expressed from this gene is displayed, with primer binding sites used to detect specific transcript variants in subsequent experiments indicated with black arrows. Note that forward primers were designed to span exon junctions. Mining of the RIP-seq dataset for exon spanning peaks identified reads spanning exons 1 and 3 (indicated by the red numbering), which occurs in MECOM transcript V7 (highlighted in red text). (B) U2OS (i), MCF7 (ii), or HCT116 cells (iii) were treated with 5 μM PRMT5 inhibitor as indicated. An anti-E2F1 RIP was then performed, and coimmunoprecipitated MECOM transcript variant V7 was analyzed by qRT-PCR using specific primers. Input protein levels for the U2OS experiment are also included (iv), while the input protein levels for HCT116 and MCF7 cells are the same as those displayed in Fig. 3 (E and F). n = 2. (C) Examination of the promoter region of the MECOM gene identified an E2F1 DNA binding motif lying within the first intron of V7 or the second intron of V4 (E2F1 motif marked in red) (i). An E2F1 ChIP was performed in HCT116 or HCT116 E2F1 CRISPR cell lines. Immunoprecipitated chromatin was analyzed using primers spanning the identified E2F DNA binding motif in MECOM or against the known E2F motif in the promoter sequence of CDC6 (ii). Input protein levels are the same as those displayed in Fig. 4F. n = 3. (D) U2OS cells (i) or HCT116 cells (iii) were treated with 5 μM PRMT5 inhibitor, where indicated. RNA was then isolated from cells and analyzed by qRT-PCR using primers targeting specific MECOM transcript variants or total MECOM RNA. Average (mean) fold change of each RNA species as compared to untreated U2OS/HCT116 cells was calculated and displayed with SE. Statistical analysis for each condition compared to untreated cells is also displayed over each bar. Input protein levels for U2OS cells are also displayed (ii), while the input protein levels for HCT116 cells are the same as those displayed in Fig. 4E. n = 4. Alice Poppy Roworth et al. Sci Adv 2019;5:eaaw4640 Copyright © 2019 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution License 4.0 (CC BY).