Fig. 1 Dcr-2 is required for Toll signaling in Drosophila S2 cells.

Slides:



Advertisements
Similar presentations
miR-133a positively regulated p53/p21 pathway.
Advertisements

Toshiaki Monkawa, Tadashi Yoshida, Matsuhiko Hayashi, Takao Saruta 
Interferon (IFN)-Induced Protein 35 (IFI35), a Type I Interferon-Dependent Transcript, Upregulates Inflammatory Signaling Pathways by Activating Toll-Like.
Differentiation of AZD4785 from MAPK pathway inhibitors in vitro
BET inhibition and depletion repress the expression of BRCA1 and RAD51
Volume 28, Issue 3, Pages (November 2007)
Expression and regulation of MD-2s.
Pioglitazone inhibits aromatase expression in human preadipocytes.
Simvastatin Protects Human Melanocytes from H2O2-Induced Oxidative Stress by Activating Nrf2  Yuqian Chang, Shuli Li, Weinan Guo, Yuqi Yang, Weigang Zhang,
Keratinocyte growth factor promotes goblet cell differentiation through regulation of goblet cell silencer inhibitor  Dai Iwakiri, Daniel K. Podolsky 
qRT-PCR validation of differential expression.
Autoantigen La Promotes Efficient RNAi, Antiviral Response, and Transposon Silencing by Facilitating Multiple-Turnover RISC Catalysis  Ying Liu, Huiling.
HIS-24 and HPL associate with promoters of antimicrobial genes.
Collagen Synthesis Is Suppressed in Dermal Fibroblasts by the Human Antimicrobial Peptide LL-37  Hyun Jeong Park, Dae Ho Cho, Hee Jung Kim, Jun Young.
Knockdown efficiency of different shRNAs.
Dnmt2 mutants show delayed immune responses and Dnmt2–EGFP relocalizes and interacts with DCV RNA during infection. Dnmt2 mutants show delayed immune responses.
Differentiation of AZD4785 from MAPK pathway inhibitors in vitro
Fig. 2 PRC1 activity is required for leukemic cell growth independently of p16 and p19 expression. PRC1 activity is required for leukemic cell growth independently.
Fig. 2 Endurance exercise up-regulates TERRA in human muscle.
Fig. 3. Coilin levels correlate with altered nascent U2 snRNA, hTR and rRNA levels.RNA isolated from HeLa or WI-38 cells following RNAi targeting coilin.
Identification of Z-FA-FMK as a potent compound that increases SMN protein expression in HEK293 and patient fibroblast cells. Identification of Z-FA-FMK.
Fig. 2 AdOPG transduction changes RANKL/OPG homeostasis in primary hMSCs differentiated on Col-GAG and MC-GAG. AdOPG transduction changes RANKL/OPG homeostasis.
Knocking down Wnt3 increases the cells' response to trastuzumab and reduces cells' invasiveness. Knocking down Wnt3 increases the cells' response to trastuzumab.
Cell viability tests. Cell viability tests. SEM images of (A) MC3T3-E1 cells and (B) MSCs on days 1, 3, and 5 of culture. (C) Survival rates of MC3T3-E1.
Fig. 1 TET2 is a coactivator of ERα.
Fig. 4 Gene disruption via chip.
Effects of Z-FA-FMK on SMN protein expression in type II SMA patient fibroblast cells (GM22592). Effects of Z-FA-FMK on SMN protein expression in type.
Inactivation of Tor2 mimics nitrogen starvation.
Fig. 3 E2F1 interacts with components of the splicing machinery.
Fig. 5 E2F1 also interacts with alternatively spliced transcripts from the MECOM gene. E2F1 also interacts with alternatively spliced transcripts from.
Caveolin-1 downregulated survivin expression in cells with enhanced or constitutive activity via the Wnt pathway. Caveolin-1 downregulated survivin expression.
PER is a substrate of CK1α.
Northern blot analysis of hY4 in CLL-derived exosomes and cells.
Fig. 5 EGLN2-mediated HIF1A down-regulation promotes ferroptosis.
PU.1 Expression Delineates Heterogeneity in Primary Th2 Cells
Fig. 4 Loss of Zic5 derepresses GLUT1/SLC2A1 gene expression.
Fig. 3 The rs risk enhancer is a hub for intrachromosomal and interchromosomal interactions. The rs risk enhancer is a hub for intrachromosomal.
Figure 2 LMNB1 mRNA expression
Fig. 2 Expressions of cll, abd-A, and Abd-B by qRT-PCR.
Fig. 4 Cdc42 enhances the cellular uptake of EVs.
BORIS mRNA expression in DNMT deficient HCT116 cell lines.
Fig. 1 NDR2 facilitates RNA virus–induced IFN-β, IL-6, and TNF-α production via a kinase activity–independent mechanism in macrophages. NDR2 facilitates.
Induction of CDCP1 is regulated by Ras in NSCLC cells.
HMRS integrated with a microfluidic system for multiple analyses
Competition between FLYWCH1/β-catenin and TCF4/β-catenin complexes for their interaction to Tcf-DNA-binding sites. Competition between FLYWCH1/β-catenin.
Fig. 8 C9orf72 knockdown results in an increase in autophagic flux.
TFAP2A knockdown inhibits cell growth by targeting HIF-1α signaling.
Radiation does not alter AKT and MTOR gene expression.
Fig. 2 Viperin promotes methionine oxidation of KSHV helicase.
Cell lines with aberrant expression of NRG1 are exquisitely sensitive to downregulation of ERBB3 signaling. Cell lines with aberrant expression of NRG1.
Microfluidic platform for cell phenotype and gene function analysis
EGFR signaling regulates transcription of PDGFRβ gene.
Fig. 6 Antitumor effect on tumor growth and pulmonary metastasis of CSSD-9 in vivo. Antitumor effect on tumor growth and pulmonary metastasis of CSSD-9.
Dcr-2 directly interacts with Toll 3′UTR via its PAZ domain in vitro
Fig. 5 C9orf72 knockdown disrupts autophagy induction.
Fig. 4 Dcr-2 binds to the 3′UTR of Toll mRNA.
Expression and induction of HER2 and HPSE in 231BMBC cells.
ER stress mediates postslippage AMPK activation.
Effect of dexamethasone on PCDGF/GP88 mRNA and protein expressions and effect of PCDGF/GP88 on dexamethasone-induced cell death. Effect of dexamethasone.
Fig. 3 Effects of ASO and eGLP1-ASO conjugates on gene expression and protein levels in vitro in cell lines and primary mouse islet cells. Effects of ASO.
Fig. 5 Dcr-2 directly binds to Toll 3′UTR.
Fig. 1 TLR2 expression is induced during OIS.
TbERP1, TbERP2, TbERP3, and TbERP8 are codependent for stability.
Fig. 1 A large number of DUBs are regulated by virus-induced type I IFN signaling at the transcriptional level. A large number of DUBs are regulated by.
Fig. 6 Methionine oxidation catalyzed by viperin increases the stability and function of RNA helicase RIG-I. Methionine oxidation catalyzed by viperin.
CREB1 binds at the proximal region of the TGFB2 promoter and induces its transcriptional activation. CREB1 binds at the proximal region of the TGFB2 promoter.
Fig. 2 Dcr-2 is required for Toll activation in adult flies.
Fig. 1 Cellular PFAS negatively regulates RTA-dependent transcriptional activation. Cellular PFAS negatively regulates RTA-dependent transcriptional activation.
Fig. 2 hTERT induces expression of heat shock protein genes through HSF1 and interacts with Hsp70-1. hTERT induces expression of heat shock protein genes.
Cxxc1-deficient TH17 cells exhibit a Treg cell–like expression profile
Presentation transcript:

Fig. 1 Dcr-2 is required for Toll signaling in Drosophila S2 cells. Dcr-2 is required for Toll signaling in Drosophila S2 cells. (A and B) Cultured S2 cells were transfected with dsRNAs against the indicated genes. Total RNA extracts were prepared from the cells and detected via Northern blots using the indicated probes. (C) Cultured S2 cells were transfected with dsRNAs against the indicated genes and treated with Lys-PGN (100 μg/ml; lanes 2 to 5) or water (lane 1) for 20 hours. Total RNA extracts were prepared from the cells and detected via Northern blots using the indicated probes. (D and E) Cultured S2 cells were transfected with dsRNAs and treated with Lys-PGN as indicated. Total RNA extracts were prepared for qRT-PCR assay of Dros (D) or Dipt (E) mRNA (normalized to Rp49; n = 3; *P < 0.05, two-tailed Student’s t test; error bars, SD). Zhaowei Wang et al. Sci Adv 2015;1:e1500228 Copyright © 2015, The Authors