Differential protein, mRNA, lncRNA and miRNA regulation by p53.

Slides:



Advertisements
Similar presentations
M. Fu, G. Huang, Z. Zhang, J. Liu, Z. Zhang, Z. Huang, B. Yu, F. Meng 
Advertisements

NSAF and GeneChip data have similar distribution properties.
Correlation of log-transformed signal intensity from two Affymetrix microarray hybridizations using platelet RNA. Plotted are those probesets with an average.
PLGEM fits equally well on NSAF and GeneChip datasets
Identification of differentially abundant proteins in the yeast growth phase NSAF dataset. Identification of differentially abundant proteins in the yeast.
NSAF and GeneChip datasets have a similar variance-versus-mean dependence.A–C, the rowMean and the rowS.D. of the abundance values for each transcript.
Global Mapping of Human RNA-RNA Interactions
Comparative analysis of RNA and protein profiles.
HIS-24 regulates expression of infection-inducible genes.
SAGA Is a General Cofactor for RNA Polymerase II Transcription
High-Resolution Expression Map of the Arabidopsis Root Reveals Alternative Splicing and lincRNA Regulation  Song Li, Masashi Yamada, Xinwei Han, Uwe Ohler,
Widespread Inhibition of Posttranscriptional Splicing Shapes the Cellular Transcriptome following Heat Shock  Reut Shalgi, Jessica A. Hurt, Susan Lindquist,
Figure 3. Genes differentially expressed in batch cultures during adaptation to low temperature. Genes differentially expressed in batch cultures during.
Plasma CEP adducts and autoantibodies by donor age.
Transcriptional Profiling of Quiescent Muscle Stem Cells In Vivo
The transcript profiles in the three human cell lines based on RNA sequencing (RNA‐seq). The transcript profiles in the three human cell lines based on.
Comparison of protein synthesis patterns of L
Frequency distribution of the GRAVY of the theoretical proteins (open bars) and of 110 genes encoding proteins identified on a 2-D electrophoresis gel,
Distributions of the ELDP values and Mascot scores for all protein identifications.a, frequency of ELDP value returned by correct (gray bars) and incorrect.
Significantly enriched phosphorylation motifs from up-regulated phosphopeptides by Motif-X analysis. Significantly enriched phosphorylation motifs from.
Epitope Mapping Performance using a single peptide microarray.
Novel p53 target genes identified by RNA-Seq, pSILAC and ChIP-Seq.
Workflow of the integrated proteomics approach to identify the abnormal network in NF1-KD PC12 cells. Workflow of the integrated proteomics approach to.
Relative abundance of proteins identified in MALDI IMS
Identification of de novo synthesized proteins in response to ER stress. Identification of de novo synthesized proteins in response to ER stress.A, HeLa.
Genome-wide analysis of p53 occupancy.
Representative example of LAXIC performance for complex plant phosphoproteome. Representative example of LAXIC performance for complex plant phosphoproteome.A.
Exemplary validation of newly identified p53 target genes.
NanoLC-MS/MS/based analysis of proteome differences between colonospheres and isogenic differentiated tumor cells. NanoLC-MS/MS/based analysis of proteome.
Cluster analysis and pathway-based characterization of differentially expressed genes and proteins from integrated proteomics. Cluster analysis and pathway-based.
Colonopshere-enriched proteins display functional interactions.
Identification of SUMO3peptides from 2D-LC-MS/MS analyses of a tryptic digest of HEK293-SUMO3 cells using DDA and DIA methods. Identification of SUMO3peptides.
Sequence similarity clusters of SET domain methyltransferases.
Schematic model of effector pathways that mediate tumor suppression by p53. Schematic model of effector pathways that mediate tumor suppression by p53.
MRNAs that show increased protein synthesis following UPF1 depletion are enriched for those with very long 3′UTRs. mRNAs that show increased protein synthesis.
High correlation of expression changes of NMD-regulated genes identified by both the pSILAC screen and previously reported global RNA screens after UPF1.
Validation of p53- and miRNA-mediated down-regulation
Putative targets of miRNAs directly induced by p53 with down-regulated mRNA- and de novo protein synthesis or reduced de novo protein synthesis only. Putative.
LC-MS/MS analyses of synthetic peptides with SUMO1 and SUMO3 remnant chains using ETD, CID, and HCD activation modes. LC-MS/MS analyses of synthetic peptides.
Distribution of the phosphoproteins based on GO analysis, including biological process (Left) and cellular component (Right). Distribution of the phosphoproteins.
The BRD4 bromodomain is critical for expression of SASP genes.
K-Means clustering of protein and mRNA expression patterns after PPAR agonists treatments. k-Means clustering of protein and mRNA expression patterns after.
Number of genes/antibodies included in the database.
Transcriptionally regulated genes in Δsaci_ptp and Δsaci_pp2a as compared with the strain MW001. Transcriptionally regulated genes in Δsaci_ptp and Δsaci_pp2a.
Bar plot representation of the transcriptomic changes in Δsaci_ptp and Δsaci_pp2a. Bar plot representation of the transcriptomic changes in Δsaci_ptp and.
Volume 9, Issue 5, Pages (November 2017)
Differential expression levels of archaella operon genes and respiratory chain genes in Δsaci_pp2a and Δsaci_ptp. Differential expression levels of archaella.
A and B, ROC curves of the proteomics panel diagnosis.
Baekgyu Kim, Kyowon Jeong, V. Narry Kim  Molecular Cell 
Changes in mRNA levels do not correlate with changes in protein levels in upf1Δ and xrn1Δ cells. Changes in mRNA levels do not correlate with changes in.
Comparison of proteomics and RNA‐Seq data.
Classification of the 1458 identified proteins into molecular functions. Classification of the 1458 identified proteins into molecular functions. The pie.
Separation of colonospheres from differentiated tumor cells by cluster analysis. Separation of colonospheres from differentiated tumor cells by cluster.
RNA-seq results at the SAM
Significant differences in translational efficiencies of DNA damage repair pathway genes between patient clusters. Significant differences in translational.
Comparison of N. gonorrhoeae gene expression in infected men in vivo and isolates grown in vitro. Comparison of N. gonorrhoeae gene expression in infected.
Volume 10, Issue 2, Pages (August 2011)
Overlap between changes in de novo protein synthesis after p53- or miR-34a-induction. Overlap between changes in de novo protein synthesis after p53- or.
GeneGoTM-based signaling pathway annotations of proteins identified in CD56+ NK cell subsets. GeneGoTM-based signaling pathway annotations of proteins.
Statistical evaluation of CD56+ NK cell subset data.
Changes in protein expression during distinct stages of NK cell differentiation. Changes in protein expression during distinct stages of NK cell differentiation.
UPF1 depletion specifically up-regulates components of the PERK/IRE1 ER stress response pathways. UPF1 depletion specifically up-regulates components of.
Brandon Ho, Anastasia Baryshnikova, Grant W. Brown  Cell Systems 
ACF1 loss perturbs gene expression in early embryos.
RNA expression data. RNA expression data. Heat maps comparing the normalized log2 of the ratios of Fur−, F90, and F1 signals on the cl20 control signal.
Fig. 3 Conserved genomic association of PRC1 activity in different leukemic cells. Conserved genomic association of PRC1 activity in different leukemic.
CD4+CLA+CD103+ T cells from human blood and skin share a transcriptional profile. CD4+CLA+CD103+ T cells from human blood and skin share a transcriptional.
BACE2 substrates in mouse CSF.
Fig. 3 The rs risk enhancer is a hub for intrachromosomal and interchromosomal interactions. The rs risk enhancer is a hub for intrachromosomal.
Fig. 3 Gene expression analysis in 48-plex drug treatment experiments.
Presentation transcript:

Differential protein, mRNA, lncRNA and miRNA regulation by p53. Differential protein, mRNA, lncRNA and miRNA regulation by p53. SW480/pRTR-p53-VSV were subjected to pSILAC, mRNA- and miRNA-Seq analyses after 48, 40 and 16 h DOX treatment, respectively. A, Volcano plot classification of proteins quantified in pSILAC experiments. Log-transformed p values (-log2) are plotted against the mean log2 of the corresponding pSILAC abundance ratios (induced/noninduced) of proteins quantified in at least two out of six replicates. Significantly regulated proteins with a log2 fold change ≥ 0.3 are indicated in green, with a log2 fold change ≤ -0.3 are marked in red and with 0.3 > log2 fold change > −0.3 in black. Proteins with a p value > 0.05 are represented by gray dots. B, C, rpkm scatter plot depicting expression changes of protein-coding mRNAs (B) and lncRNAs (C) detected by RNA-Seq. Transcripts with an rpkm < 0.5 in both conditions are shown in gray. Transcripts with a log2 fold change ≥ 1 are shown in green, with a log2 fold change ≤ −1 in red and with 1 > log2 fold change > −1 in black. D, Venn diagram displaying the overlap between quantified mRNAs (with an rpkm ≥ 0.5 in at least one condition) (shown in gray) and proteins (with a p value < 0.05) (shown in blue) and differentially regulated mRNAs (log2 fold change ≤ −1 or ≥ 1) (shown in orange) and proteins (log2 fold change ≤ −0.3 or ≥ 0.3) (shown in green). Genes differentially expressed on the mRNA level and the level of de novo protein synthesis are indicated in yellow. E, Cumulative distribution plot displaying changes in mRNA expression of up- and down-regulated proteins compared with the normal distribution of all mRNAs detected by RNA-Seq after activation of p53. F, Normalized read count scatter plot depicting expression changes of mature miRNAs. miRNAs with a log2 fold change ≥ 1 are shown in green, with a log2 fold change ≤ −1 in red and with 1 > log2 fold change > −1 in black. Sabine Hünten et al. Mol Cell Proteomics 2015;14:2609-2629 © 2015 by The American Society for Biochemistry and Molecular Biology, Inc.