19 research outputs found

    Additional file 14 of Sorting and packaging of RNA into extracellular vesicles shape intracellular transcript levels

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    Additional file 14: Figure S6. (A) Gene Ontology analysis of protein-coding genes altered in cells by coculture. For each category the top 10 most significantly enriched GO terms (FDR < 0.05) are displayed. BP = Biological Process, CC = Cellular Compartment, MF = Molecular Function. Individual values can be found in Additional file 17. (B) Volcano plot of log2 fold changes by RNA-Seq of mRNA and lncRNA genes (combined) in EVs derived from tumor-exposed cells vs. EVs derived from unexposed cells. (C) Log2 fold change in tumor-exposed cells vs. unexposed cells and in EVs derived from tumor-exposed cells vs. EVs derived from unexposed cells for the most increased (left) and decreased (right) mRNA and lncRNA genes significantly changed in cells. Error bars represent standard error of log2 fold change. Individual values can be found in Additional file 17. (D-E) Depletion of E2F_TARGETS_V1 gene set (D) and G2M_TARGETS gene set (E) in tumor-exposed vs. unexposed cells and enrichment of the same gene set in EVs derived from tumor-exposed vs. unexposed cells. All analyses were performed using 3 EV and 3 cell samples

    Additional file 2 of Sorting and packaging of RNA into extracellular vesicles shape intracellular transcript levels

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    Additional file 2: Figure S2. (A) Plot of RNA-Seq reads from 3 EV and 3 cell samples that map to more than one genomic location. Reads mapping to rRNA are excluded. Individual values can be found in Additional file 17. (B) Hierarchical clustering of long RNA transcripts by abundance determined by RNA-Seq in 3 EV and 3 cell samples. Data are read counts transformed using the Variance Stabilizing Transformation, top 200 transcripts with the highest variance across samples are displayed. (C) RNA-Seq read coverage (top) and RT-PCR amplicons (bottom) of HNRNPA1 (D), ANP32B (E), RPL14 (F) and RPL41 (F) mRNA. (G) RNA-Seq read coverage (top) and RT-PCR amplicons (bottom) of lncRNA GAS5. NT = no template, no-RT = RNA without reverse transcriptase. Uncropped gel images can be found in Additional file 18

    Additional file 6 of Sorting and packaging of RNA into extracellular vesicles shape intracellular transcript levels

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    Additional file 6: Figure S5. (A) mRNA and (B) lncRNA abundance from RNA-Seq in VEGF-treated cells and their EVs. TPM = transcripts per million. TPM values are averaged across 3 replicates. (C) Gene Ontology analysis of genes altered in cells by VEGF treatment. For each GO category the ten significant (FDR < 0.05) terms with the lowest p-values are displayed. BP = Biological Process, CC = Cellular Component, MF = Molecular Function. Individual values can be found in Additional file 17. (D) Volcano plot of log2 fold changes by RNA-Seq of mRNA and lncRNA genes (combined) in EVs derived from VEGF-treated cells vs. EVs derived from untreated cells. (E) Volcano plot of log2 fold changes by RNA-Seq of mRNA and lncRNA genes in VEGF-treated cells vs. untreated cells. All analyses were performed using 3 EV and 3 cell samples
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