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Addgene inc u6 expression vectors
U6 Expression Vectors, supplied by Addgene inc, used in various techniques. Bioz Stars score: 93/100, based on 12 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/sgrna+expression+vectors/SpCas9_sgRNA_expression_in_pBluescript+(Plasmid+%23122089)/pmc12957561-33-23-26
Average 93 stars, based on 12 article reviews

u6 expression vectors - by Bioz Stars, 2026-09

93/100 stars

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Infection:

Article Title: Identification of a Distal Enhancer That Regulates TGF-β-Induced SNAI1 Expression.
Article Snippet: .. A549 and NMuMG cells were first infected with KRAB- dCas9 and sgRNA- expression vectors (pCRISPRia- v2), followed by puromycin selection. pHR- SFFV- KRAB- dCas9P2A- mCherry (Addgene plasmid #60954; http:// n2t. net/ addge ne: 60954 ; RRID: Addgene_60,954) [37] and pCRISPRia- v2 (Addgene plasmid #84832; http:// n2t. net/ addge ne: 84832 ; RRID: Addgene_84,832) [38] were gifts from Dr. Jonathan Weissman. ..

Expressing:

Article Title: Compact RNA editors with natural miniature Cas13j nucleases.
Article Snippet: Clustered regularly interspaced short palindromic repeats–Cas13 effectors are used for RNA editing but the adeno-associated virus (AAV) packaging limitations because of their big sizes hinder their therapeutic application.. Here we report the identification of the Cas13j family, with LepCas13j (529 aa) and ChiCas13j (424 aa) being the smallest and most highly efficient variants for RNA interference.. The miniaturized Cas13j proteins enable the development of compact RNA base editors.

Article Title: BOD1L mediates chromatin binding and non-canonical function of H3K4 methyltransferase SETD1A
Article Snippet: The dCas9-VP64_GFP plasmid was obtained from Addgene (#61422), and VP64 was replaced with FRB or BOD1L fragments using restriction enzymes (BamHI and NheI) and a DNA Ligation Kit (Takara, #6023). .. For sgRNA constructs, annealed sgRNA oligos were ligated into sgRNA expression vectors, pLKO5.sgRNA.EFS.GFP (Addgene #57822) and lenti-sgRNA hygro (Addgene #104991). ..

Article Title: In vivo perturb-seq of cancer and microenvironment cells dissects oncologic drivers and radiotherapy responses in glioblastoma
Article Snippet: .. Protospacer sequences were selected from the optimized mouse CRISPRi v2 library [ ] by their predicted rank order, and the top 3 sgRNAs were individually cloned into single sgRNA expression vectors with direct capture cs1 sequences (Addgene # 122238) [ ] using restriction digest (BstXI and BlpI) and T4 ligation (NEB # M0202M). ..

Article Title: Chemical perturbations impacting histone acetylation govern colorectal cancer differentiation
Article Snippet: .. To generate lentiviruses, HEK293T cells were co-transfected with sgRNA expression vectors and lentiviral packaging constructs psPAX2 (Addgene #12260; RRID:Addgene_12260) and pMD2.G (Addgene #12259; RRID:Addgene_12259) in a 2:1:1 ratio using X-tremeGENE HP DNA Transfection Reagent (Roche) according to the manufacturer’s instructions. .. Cell culture media was changed the following day and lentiviral supernatant was harvested 24 h and 48 h later and filtered through a 0.45 μm filter (Celltreat).

Article Title: Identification of a distal enhancer of Ucp1 essential for thermogenesis and mitochondrial function in brown fat
Article Snippet: For the dCas9-KRAB expressing construct, we used KRAB-dCas9 (Addgene #112195) , for transient expression. .. To generate sgRNA expression vectors, oligonucleotides were annealed and inserted into the BsaI site of the pGL3-U6-sgRNA-PGK-puromycin vector (Addgene #51133). .. On the 4th day after the induction of differentiation, differentiated brown adipocytes were cotransfected using Lipofectamine 3000 (Invitrogen) with KRAB-dCas9 vector and pGL3-U6-sgRNA-PGK-puromycin vector.

Article Title: Identification of a distal enhancer of Ucp1 essential for thermogenesis and mitochondrial function in brown fat.
Article Snippet: For the dCas9-KRAB expressing construct, we used KRAB-dCas9 (Addgene #112195)90,91 for transient expression. .. To generate sgRNA expression vectors, oligonucleotides were annealed and inserted into the BsaI site of the pGL3-U6-sgRNA-PGK-puromycin vector (Addgene #51133). .. On the 4th day after the induction of differentiation, differentiated brown adipocytes were cotransfected using Lipofectamine 3000 (Invitrogen) with KRAB-dCas9 vector and pGL3-U6-sgRNA-PGK-puromycin vector.

Article Title: mTORC1 activity licenses its own release from the lysosomal surface.
Article Snippet: Plasmid DNA transfections in HEK293FT cells were performed using Effectene transfection reagent (#301425, QIAGEN), according to the manufacturer’s instructions. .. Generation of knockout cell lines The HEK293FT Rag quadruple knockout cell line (qKO)18 and the base-edited, rapamycin-resistant mTOR cell line (mTORRR) have been described previously.31 The HEK293FT RHEB, NPRL3, and FLCN knockout cell lines were generated using the pX459-based CRISPR/Cas9 method, as described elsewhere.60 The sgRNA expression vectors were generated by cloning appropriate DNA oligonucleotides (Table S2) into the BbsI restriction sites of the pX459 vector (#62988, Addgene). ..

Selection:

Plasmid Preparation:

Synthesized:

Clone Assay:

Construct:

Ligation:

Transfection:

Knock-Out:

Quadruple Knockout:

Generated:

CRISPR:

Cloning:

Image Search Results

A. Schematic of the XBP1-Venus IRE1 splicing reporter. B . Expression, measured by qPCR, of the IRE1/XBP1s target genes XBP1s and ERDJ4/DNAJB9 in HEK293 cells expressing non-targeting or SLC33A1 shRNA and treated for 4 h with Tg (0.5 µM) or IXA4 (10 µM). C . Expression, measured by qPCR, of the IRE1 target genes Xbp1s and Erdj4/Dnajb9 , the ATF6 target gene BiP , and the PERK target gene Chop in MEF cells CRISPR-deleted of Slc33a1 using two distinct sgRNA and treated for 4 h with IXA4 (10 µM). MEF cells expressing two distinct non-targeting sgRNAs are shown as a control. D . Expression, measured by qPCR, of the IRE1 target gene XBP1s in non-targeting HEK293 cells or HEK293 cells lacking SLC33A1 transfected with mock or wild-type SLC33A1, as indicated, and then treated for 4 h with Tg (0.5 µM) or IXA4 (10 µM). E . Immunoblots of the indicated proteins in HEK293T cells expressing non-targeting or SLC33A1 sgRNAs treated for 4 h with IXA4 (10 µM). Black asterisks in ( C ) represent comparisons between vehicle-treated control cells expressing NT sgRNA #1 and mutant cells treated with or without IXA4. Red asterisks in ( C ) indicate comparisons between vehicle and IXA4-treated samples. *p<0.05, **p<0.01, ***p<0.005, one-way ANOVA.

Journal: bioRxiv

Article Title: Pharmacological Inhibition of SLC33A1 Promotes Endoplasmic Reticulum Hyperoxidation and Induces Adaptive IRE1/XBP1s Signaling

doi: 10.64898/2026.02.17.706344

Figure Lengend Snippet: A. Schematic of the XBP1-Venus IRE1 splicing reporter. B . Expression, measured by qPCR, of the IRE1/XBP1s target genes XBP1s and ERDJ4/DNAJB9 in HEK293 cells expressing non-targeting or SLC33A1 shRNA and treated for 4 h with Tg (0.5 µM) or IXA4 (10 µM). C . Expression, measured by qPCR, of the IRE1 target genes Xbp1s and Erdj4/Dnajb9 , the ATF6 target gene BiP , and the PERK target gene Chop in MEF cells CRISPR-deleted of Slc33a1 using two distinct sgRNA and treated for 4 h with IXA4 (10 µM). MEF cells expressing two distinct non-targeting sgRNAs are shown as a control. D . Expression, measured by qPCR, of the IRE1 target gene XBP1s in non-targeting HEK293 cells or HEK293 cells lacking SLC33A1 transfected with mock or wild-type SLC33A1, as indicated, and then treated for 4 h with Tg (0.5 µM) or IXA4 (10 µM). E . Immunoblots of the indicated proteins in HEK293T cells expressing non-targeting or SLC33A1 sgRNAs treated for 4 h with IXA4 (10 µM). Black asterisks in ( C ) represent comparisons between vehicle-treated control cells expressing NT sgRNA #1 and mutant cells treated with or without IXA4. Red asterisks in ( C ) indicate comparisons between vehicle and IXA4-treated samples. *p<0.05, **p<0.01, ***p<0.005, one-way ANOVA.

Article Snippet: To clone individual sgRNAs, top and bottom oligonucleotides (IDT) were annealed and ligated to lentiviral sgRNA expression vectors LentiGuide-puromycin (Addgene #52963), LentiCRISPRv2-puromycin (Addgene #98290), or LentiCRISPRv2-blasticidin (Addgene #98293)).

Techniques: Expressing, shRNA, CRISPR, Control, Transfection, Western Blot, Mutagenesis

A . XBP1-Venus reporter signal, measured by flow cytometry, in HEK293 cells stably expressing Cas9 and transduced with lentivirus encoding non-targeting (NT) or IRE1 sgRNA treated for 14 h with vehicle or IXA4 (10 µM). B . CRISPR screen used to identify genes whose deletion blocks IXA4-induced IRE1 activation. C . Plot showing gene score (DMSO) vs. gene score (IXA4), quantified as previously defined , from genome-wide CRISPR screen. D . XBP1-Venus signal, measured by flow cytometry, in HEK293 cells stably expressing Cas9 and transduced with lentivirus encoding non-targeting (NT) or SLC33A1 sgRNA treated for 14 h with vehicle or IXA4 (10 µM). E . Expression, measured by qPCR, of the IRE1 target genes XBP1s and DNAJB9 , the ATF6 target gene BiP, and the PERK target gene CHOP in HEK293 cells stably expressing Cas9 transduced with lentivirus encoding NT or SLC33A1 sgRNA treated for 4 h with vehicle, IXA4 (10 µM) or Tg (0.5 µM). *p<0.05, ***p<0.005 one-way ANOVA.

Journal: bioRxiv

Article Title: Pharmacological Inhibition of SLC33A1 Promotes Endoplasmic Reticulum Hyperoxidation and Induces Adaptive IRE1/XBP1s Signaling

doi: 10.64898/2026.02.17.706344

Figure Lengend Snippet: A . XBP1-Venus reporter signal, measured by flow cytometry, in HEK293 cells stably expressing Cas9 and transduced with lentivirus encoding non-targeting (NT) or IRE1 sgRNA treated for 14 h with vehicle or IXA4 (10 µM). B . CRISPR screen used to identify genes whose deletion blocks IXA4-induced IRE1 activation. C . Plot showing gene score (DMSO) vs. gene score (IXA4), quantified as previously defined , from genome-wide CRISPR screen. D . XBP1-Venus signal, measured by flow cytometry, in HEK293 cells stably expressing Cas9 and transduced with lentivirus encoding non-targeting (NT) or SLC33A1 sgRNA treated for 14 h with vehicle or IXA4 (10 µM). E . Expression, measured by qPCR, of the IRE1 target genes XBP1s and DNAJB9 , the ATF6 target gene BiP, and the PERK target gene CHOP in HEK293 cells stably expressing Cas9 transduced with lentivirus encoding NT or SLC33A1 sgRNA treated for 4 h with vehicle, IXA4 (10 µM) or Tg (0.5 µM). *p<0.05, ***p<0.005 one-way ANOVA.

Techniques: Flow Cytometry, Stable Transfection, Expressing, Transduction, CRISPR, Activation Assay, Genome Wide

A. XBP1-Rluc signal in HEK293 cells stably expressing XBP1-RLuc treated with the indicated concentration of IXA4 or PTG2018 in the presence or absence of the IRE1 RNAse inhibitor 4µ8c (32 µM) for 14 h. Data are normalized to the XBP1-RLuc signal seen in cells treated with thapsigargin (Tg; 0.5 µM). Error bars show SEM for n=3 replicates. B . Dose-dependent proteome labeling with PTG2018 (left, rhodamine fluorescence; right, Coomassie stain). PTG2018-labeled proteins were identified by appending TAMRA-azide to PTG2018 via click chemistry. C . Streptavidin affinity purification and proteomes (input) from HEK293T cells overexpressing FLAG-tagged EPHX1 and treated with the indicated concentration of PTG2018 and IXA4. PTG2018 labeling of FLAG-tagged EPHX1 was visualized by appending a biotin to the alkyne handle of PTG2018 using click chemistry and monitoring the recovery of FLAG-tagged protein in streptavidin isolates. Mock transfected cells are shown as a control. D . Streptavidin affinity purification and proteomes (input) from HEK293T cells treated with the indicated concentration of PTG2018 and IXA4. PTG2018 labeling of SOAT1 was visualized by appending biotin to the alkyne handle of PTG2018 via click chemistry and monitoring the recovery the recovery of endogenous SOAT1 in streptavidin isolates. E , F . XBP1-Venus signal, measured by flow cytometry, in HEK293 cell stably expressing Cas9 and transduced with lentivirus encoding non-targeting (NT), SOAT1 or EPHX1 sgRNA treated for 14 h with vehicle or IXA4 (10 µM).

Journal: bioRxiv

Article Title: Pharmacological Inhibition of SLC33A1 Promotes Endoplasmic Reticulum Hyperoxidation and Induces Adaptive IRE1/XBP1s Signaling

doi: 10.64898/2026.02.17.706344

Figure Lengend Snippet: A. XBP1-Rluc signal in HEK293 cells stably expressing XBP1-RLuc treated with the indicated concentration of IXA4 or PTG2018 in the presence or absence of the IRE1 RNAse inhibitor 4µ8c (32 µM) for 14 h. Data are normalized to the XBP1-RLuc signal seen in cells treated with thapsigargin (Tg; 0.5 µM). Error bars show SEM for n=3 replicates. B . Dose-dependent proteome labeling with PTG2018 (left, rhodamine fluorescence; right, Coomassie stain). PTG2018-labeled proteins were identified by appending TAMRA-azide to PTG2018 via click chemistry. C . Streptavidin affinity purification and proteomes (input) from HEK293T cells overexpressing FLAG-tagged EPHX1 and treated with the indicated concentration of PTG2018 and IXA4. PTG2018 labeling of FLAG-tagged EPHX1 was visualized by appending a biotin to the alkyne handle of PTG2018 using click chemistry and monitoring the recovery of FLAG-tagged protein in streptavidin isolates. Mock transfected cells are shown as a control. D . Streptavidin affinity purification and proteomes (input) from HEK293T cells treated with the indicated concentration of PTG2018 and IXA4. PTG2018 labeling of SOAT1 was visualized by appending biotin to the alkyne handle of PTG2018 via click chemistry and monitoring the recovery the recovery of endogenous SOAT1 in streptavidin isolates. E , F . XBP1-Venus signal, measured by flow cytometry, in HEK293 cell stably expressing Cas9 and transduced with lentivirus encoding non-targeting (NT), SOAT1 or EPHX1 sgRNA treated for 14 h with vehicle or IXA4 (10 µM).

Techniques: Stable Transfection, Expressing, Concentration Assay, Labeling, Fluorescence, Staining, Affinity Purification, Transfection, Control, Flow Cytometry, Transduction

A. [ 3 H]-acetyl-CoA uptake by ER microsomes (50 µg protein) isolated from HEK293T cells treated with/without IXA4 (10 µM) during the uptake assay. B . [ 3 H]-acetyl-CoA uptake by ER microsomes (50 µg protein) isolated from HEK293T cells expressing Cas9 and non-targeting (NT) or SLC33A1 sgRNA. C , D . Relative acetyl-CoA abundance ( C ) and oxidized glutathione abundance (GSSG; D ) in whole cell or ER isolated from HEK293T cells with non-targeting (NT) sgRNA or sgRNA targeting SLC33A1. Cells were treated with IXA4 (10 µM) for 4 h before ER isolation and LC/MS analysis. E . Immunoblot of DNAJC10 and PDIA4 in proteomes prepared from HeLa cells treated for 1 h with IXA4 (10 µM), DTT (5 mM), or diamide (500 µM). Following lysis in the presence of alkylating agents, disulfides within these proteins were reduced and then labeled with PEG(5K)-maleimide (2 mM), allowing visualization of oxidized and reduced protein populations. F . Immunoblot of proteomes from Ire1 -/- MEFs reconstituted with wild-type or a C148S IRE1 mutant, treated for 2 h with IXA4 (10 µM) or thapsigargin (Tg; 0.5 µM), and separated on a non-reducing SDS-PAGE gel. Oxidized and reduced IRE1 populations are shown. G . XBP1s levels, measured by qPCR, in HEK293T cells pre-treated for 18 h with BSO (50 µM) and then treated for 3 h with IXA4 (10 µM). H . Viability, assessed with CellTiter-Glo, of KP and KPK cells treated for 3 days with IXA4 (10 µM) or thapsigargin (Tg; 0.5 µM). I . Viability, assessed with CellTiter-Glo, of KP and KPK cells treated for 3 days with IXA4 (10 µM), BSO (50 µM), and 4µ8c (32 µM). *p<0.05, ***p<0.005, one-way ANOVA.

Journal: bioRxiv

Article Title: Pharmacological Inhibition of SLC33A1 Promotes Endoplasmic Reticulum Hyperoxidation and Induces Adaptive IRE1/XBP1s Signaling

doi: 10.64898/2026.02.17.706344

Figure Lengend Snippet: A. [ 3 H]-acetyl-CoA uptake by ER microsomes (50 µg protein) isolated from HEK293T cells treated with/without IXA4 (10 µM) during the uptake assay. B . [ 3 H]-acetyl-CoA uptake by ER microsomes (50 µg protein) isolated from HEK293T cells expressing Cas9 and non-targeting (NT) or SLC33A1 sgRNA. C , D . Relative acetyl-CoA abundance ( C ) and oxidized glutathione abundance (GSSG; D ) in whole cell or ER isolated from HEK293T cells with non-targeting (NT) sgRNA or sgRNA targeting SLC33A1. Cells were treated with IXA4 (10 µM) for 4 h before ER isolation and LC/MS analysis. E . Immunoblot of DNAJC10 and PDIA4 in proteomes prepared from HeLa cells treated for 1 h with IXA4 (10 µM), DTT (5 mM), or diamide (500 µM). Following lysis in the presence of alkylating agents, disulfides within these proteins were reduced and then labeled with PEG(5K)-maleimide (2 mM), allowing visualization of oxidized and reduced protein populations. F . Immunoblot of proteomes from Ire1 -/- MEFs reconstituted with wild-type or a C148S IRE1 mutant, treated for 2 h with IXA4 (10 µM) or thapsigargin (Tg; 0.5 µM), and separated on a non-reducing SDS-PAGE gel. Oxidized and reduced IRE1 populations are shown. G . XBP1s levels, measured by qPCR, in HEK293T cells pre-treated for 18 h with BSO (50 µM) and then treated for 3 h with IXA4 (10 µM). H . Viability, assessed with CellTiter-Glo, of KP and KPK cells treated for 3 days with IXA4 (10 µM) or thapsigargin (Tg; 0.5 µM). I . Viability, assessed with CellTiter-Glo, of KP and KPK cells treated for 3 days with IXA4 (10 µM), BSO (50 µM), and 4µ8c (32 µM). *p<0.05, ***p<0.005, one-way ANOVA.

Techniques: Isolation, Expressing, Liquid Chromatography with Mass Spectroscopy, Western Blot, Lysis, Labeling, Mutagenesis, SDS Page

$A . In-gel fluorescence of acetylated proteins in ER and mitochondrial fractions isolated from HEK293T cells treated for 3 h with IXA4 (10 µM) and then incubated for 1 h with 3-butynoic acid. Acetylated proteins were identified by appending a rhodamine tag onto the 3-butynoic acid probe via click chemistry. B . In-gel fluorescence of acetylated proteins in ER fractions isolated from HEK293T Cas9 cells expressing non-targeting (NT) or SLC33A1 sgRNA incubated for 1 h with the 3-butynoic acid probe. Acetylated proteins were then identified by appending a rhodamine tag onto the 3-butynoic acid probe via click chemistry. C . Expression (published DNA microarrays) of IRE1/XBP1s, ATF6, and PERK target genesets in HEK293T cells overexpressing the ER oxidase ERO1. Source data available in GEO (GSE40601). D . XBP1 mRNA splicing (RT-PCR) in IRE1 -deficient HeLa cells transfected with wild-type IRE1 or a C109S/C148S/C332S IRE1 triple mutant and treated for 2 h with IXA4 (10 µM) or thapsigargin (Tg; 0.5 µM). Unspliced (u), spliced (s), and hybrid (*), XBP1 are shown. E . Crystal violet stained KPK cells treated for 2 days with thapsigargin (Tg; 0.5 µM) or IXA4 (10 µM). F . Crystal violet stained KPK cells incubated for 2 days with IXA4 (10 µM) and/or BSO (50 µM). p<0.05, **p<0.01, ***p<0.005, one-way ANOVA.$

Journal: bioRxiv

Article Title: Pharmacological Inhibition of SLC33A1 Promotes Endoplasmic Reticulum Hyperoxidation and Induces Adaptive IRE1/XBP1s Signaling

doi: 10.64898/2026.02.17.706344

Figure Lengend Snippet: A . In-gel fluorescence of acetylated proteins in ER and mitochondrial fractions isolated from HEK293T cells treated for 3 h with IXA4 (10 µM) and then incubated for 1 h with 3-butynoic acid. Acetylated proteins were identified by appending a rhodamine tag onto the 3-butynoic acid probe via click chemistry. B . In-gel fluorescence of acetylated proteins in ER fractions isolated from HEK293T Cas9 cells expressing non-targeting (NT) or SLC33A1 sgRNA incubated for 1 h with the 3-butynoic acid probe. Acetylated proteins were then identified by appending a rhodamine tag onto the 3-butynoic acid probe via click chemistry. C . Expression (published DNA microarrays) of IRE1/XBP1s, ATF6, and PERK target genesets in HEK293T cells overexpressing the ER oxidase ERO1. Source data available in GEO (GSE40601). D . XBP1 mRNA splicing (RT-PCR) in IRE1 -deficient HeLa cells transfected with wild-type IRE1 or a C109S/C148S/C332S IRE1 triple mutant and treated for 2 h with IXA4 (10 µM) or thapsigargin (Tg; 0.5 µM). Unspliced (u), spliced (s), and hybrid (*), XBP1 are shown. E . Crystal violet stained KPK cells treated for 2 days with thapsigargin (Tg; 0.5 µM) or IXA4 (10 µM). F . Crystal violet stained KPK cells incubated for 2 days with IXA4 (10 µM) and/or BSO (50 µM). p<0.05, **p<0.01, ***p<0.005, one-way ANOVA.

Techniques: Fluorescence, Isolation, Incubation, Expressing, Reverse Transcription Polymerase Chain Reaction, Transfection, Mutagenesis, Staining

a , PEtn levels in parental KP sh and clonal KP sh cells expressing sgRNA and complemented with guide-resistant Pcyt2 cDNA as indicated cultured on or off dox for 6 days ( P values, left to right: 0.0183, 0.0341, 0.0068 and 0.0104). b , c , PCA of RNA-seq ( b ) and bubble plot of pathway overrepresentation for genes that are upregulated in KP sh Pcyt2 -KO cells relative to cells complemented with sgRNA-resistant Pcyt2 cDNA following 6 days of dox withdrawal to activate p53 ( c ). d , Representative transmission electron microscope images from Pcyt2 -KO or Pcyt2 -KO complemented with guide-resistant Pcyt2 cDNA KP sh cells cultured on or off dox for 6 days. Scale bars as indicated. e , Population doublings of Pcyt2 -KO or Pcyt2 -KO complemented with guide-resistant Pcyt2 cDNA KP sh cells cultured on or off dox for indicated times. f , g , Tumour growth curve ( f ) or endpoint tumour volumes ( g ) for Pcyt2 -KO and Pcyt2 -KO complemented with guide-resistant Pcyt2 cDNA KP sh cell line xenograft maintained on dox chow ( sgPcyt2 , n = 8; sgPcyt2 + cDNA, n = 10) or withdrawn from dox chow ( sgPcyt2 , n = 12; sgPcyt2 + cDNA, n = 12) for 3 weeks. Otherwise, data represent n = 3 independently treated wells. Data are presented as mean ± s.d. ( a , e and g ) or s.e.m. ( f ), and statistical significance was assessed by two-sided Holm–Šídák method for multiple unpaired t- tests ( a ), Fisher’s exact test and adjusted for multiple testing using the Benjamini–Hochberg false discovery rate ( c ) or unpaired, two-tailed Student’s t- test ( g ). * P < 0.05, ** P < 0.01.

Journal: Nature Cell Biology

Article Title: p53 increases phospholipid headgroup scavenging in senescence

doi: 10.1038/s41556-025-01853-0

Figure Lengend Snippet: a , PEtn levels in parental KP sh and clonal KP sh cells expressing sgRNA and complemented with guide-resistant Pcyt2 cDNA as indicated cultured on or off dox for 6 days ( P values, left to right: 0.0183, 0.0341, 0.0068 and 0.0104). b , c , PCA of RNA-seq ( b ) and bubble plot of pathway overrepresentation for genes that are upregulated in KP sh Pcyt2 -KO cells relative to cells complemented with sgRNA-resistant Pcyt2 cDNA following 6 days of dox withdrawal to activate p53 ( c ). d , Representative transmission electron microscope images from Pcyt2 -KO or Pcyt2 -KO complemented with guide-resistant Pcyt2 cDNA KP sh cells cultured on or off dox for 6 days. Scale bars as indicated. e , Population doublings of Pcyt2 -KO or Pcyt2 -KO complemented with guide-resistant Pcyt2 cDNA KP sh cells cultured on or off dox for indicated times. f , g , Tumour growth curve ( f ) or endpoint tumour volumes ( g ) for Pcyt2 -KO and Pcyt2 -KO complemented with guide-resistant Pcyt2 cDNA KP sh cell line xenograft maintained on dox chow ( sgPcyt2 , n = 8; sgPcyt2 + cDNA, n = 10) or withdrawn from dox chow ( sgPcyt2 , n = 12; sgPcyt2 + cDNA, n = 12) for 3 weeks. Otherwise, data represent n = 3 independently treated wells. Data are presented as mean ± s.d. ( a , e and g ) or s.e.m. ( f ), and statistical significance was assessed by two-sided Holm–Šídák method for multiple unpaired t- tests ( a ), Fisher’s exact test and adjusted for multiple testing using the Benjamini–Hochberg false discovery rate ( c ) or unpaired, two-tailed Student’s t- test ( g ). * P < 0.05, ** P < 0.01.

Article Snippet: Lentivirus was generated by cotransfection of viral vectors expressing sgRNA or cDNA of interest with packaging plasmids psPAX2 (Addgene, 12260) and pMD2.G (Addgene, 12259) into 293T cells.

Techniques: Expressing, Cell Culture, RNA Sequencing, Transmission Assay, Microscopy, Two Tailed Test

a , Schematic depicting the metabolism-focused CRISPR genetic screens in KP sh cells. Cells were sequenced at day 0 (prior to dox withdrawal) and then after 10 days of additional growth with or without dox. b , Scatter plot showing normalized counts for each gene at day 0 (x-axis) and log 2 foldchange in normalized counts between day 10 and day 0 (y axis). Left: p53 off, right: p53 on. Genes highlighted in orange are genes differentially essential in p53-on cells, as shown in Fig. . c , Scatter plot comparing changes in gene expression induced by p53 activation (x-axis, log 2 fold change in expression KP sh cells cultured -dox compared to cells cultured +dox) with changes in gene scores following p53 activation (y-axis, gene scores determined by comparing sgRNA abundance of cells following 10 days culture with or without dox). Pearson correlation (two-sided) r = −0.10, P < 5.2 ×10 −8 . Genes both induced by p53 and more essential following p53 activation (log 2 fold change > 0.4; screen enrichment difference < −0.2) are highlighted in orange. Data are available in Supplementary Table . d , Bubble plot of pathway enrichment for genes highlighted in ( c ). e , Volcano plot showing pathways from gene set enrichment analysis (GSEA) analysis of genes co-expressed with HNF4A in pancreatic cancer cell lines in DepMap. Each dot present one pathway. f , GSEA plot showing lipid metabolism related pathways enriched among genes exhibiting similar expression patterns as HNF4A . g,h , Normalized counts individual sgRNA targeting Cers2 ( g ) and Hnf4a ( h ) in indicated conditions from the screen (P value: g = 0.0469, h = 0.0078). i , Scatter plot of DepMap gene effect versus log2 fold change in gene score (-dox/+dox at day 10) in KP sh cells. Each dot represents a gene; Cers2 and Hnf4a are highlighted in cyan and blue. j,k , Western blot of KP sh cells expressing sgRNA targeting Cers2 ( j ) and Hnf4a ( k ). Statistical significance was assessed by Fisher’s Exact test and adjusted for multiple testing using the Benjamini-Hochberg false discovery rate ( d ), GSEA ( e ), or Wilcoxon matched-pairs two-tails signed rank test ( g, h ). Source numerical data and unprocessed blots are available in source data.

Journal: Nature Cell Biology

Article Title: p53 increases phospholipid headgroup scavenging in senescence

doi: 10.1038/s41556-025-01853-0

Figure Lengend Snippet: a , Schematic depicting the metabolism-focused CRISPR genetic screens in KP sh cells. Cells were sequenced at day 0 (prior to dox withdrawal) and then after 10 days of additional growth with or without dox. b , Scatter plot showing normalized counts for each gene at day 0 (x-axis) and log 2 foldchange in normalized counts between day 10 and day 0 (y axis). Left: p53 off, right: p53 on. Genes highlighted in orange are genes differentially essential in p53-on cells, as shown in Fig. . c , Scatter plot comparing changes in gene expression induced by p53 activation (x-axis, log 2 fold change in expression KP sh cells cultured -dox compared to cells cultured +dox) with changes in gene scores following p53 activation (y-axis, gene scores determined by comparing sgRNA abundance of cells following 10 days culture with or without dox). Pearson correlation (two-sided) r = −0.10, P < 5.2 ×10 −8 . Genes both induced by p53 and more essential following p53 activation (log 2 fold change > 0.4; screen enrichment difference < −0.2) are highlighted in orange. Data are available in Supplementary Table . d , Bubble plot of pathway enrichment for genes highlighted in ( c ). e , Volcano plot showing pathways from gene set enrichment analysis (GSEA) analysis of genes co-expressed with HNF4A in pancreatic cancer cell lines in DepMap. Each dot present one pathway. f , GSEA plot showing lipid metabolism related pathways enriched among genes exhibiting similar expression patterns as HNF4A . g,h , Normalized counts individual sgRNA targeting Cers2 ( g ) and Hnf4a ( h ) in indicated conditions from the screen (P value: g = 0.0469, h = 0.0078). i , Scatter plot of DepMap gene effect versus log2 fold change in gene score (-dox/+dox at day 10) in KP sh cells. Each dot represents a gene; Cers2 and Hnf4a are highlighted in cyan and blue. j,k , Western blot of KP sh cells expressing sgRNA targeting Cers2 ( j ) and Hnf4a ( k ). Statistical significance was assessed by Fisher’s Exact test and adjusted for multiple testing using the Benjamini-Hochberg false discovery rate ( d ), GSEA ( e ), or Wilcoxon matched-pairs two-tails signed rank test ( g, h ). Source numerical data and unprocessed blots are available in source data.

Techniques: CRISPR, Gene Expression, Activation Assay, Expressing, Cell Culture, Western Blot

Review

u6 expression vectors (Addgene inc)

Structured Review

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Infection:

Expressing:

Selection:

Plasmid Preparation:

Synthesized:

Clone Assay:

Construct:

Ligation:

Transfection:

Knock-Out:

Quadruple Knockout:

Generated:

CRISPR:

Cloning:

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