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3 protocols using plvx tet on advanced vector

1

Development of GFP-IBD Reporter Cell Lines

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The MCF7 Tet-On Advanced cell line was obtained from Clontech. The generation and characterization of the MCF7GFP-IBD cell line has been described (24 (link)) and was used with further authentication by IDEXX BioResearch within the last 6 months. Panc 02GFP-IBD, U-87 MGGFP-IBD, and hTERT-HME1GFP-IBD cell lines were developed similarly from parent cell lines purchased from American Type Culture Collection (ATCC). Briefly, GFP-IBD cloned into the pLVX-Tight-Puro vector was transfected along with pLVX-Tet-On Advanced vector (Clontech) into each cell line. Following G418 and puromycin selection, cells were induced with 1 μg/mL doxycycline and sorted to establish the IRIF reporter cell lines. The Panc 02GFP-IBD and U-87 MGGFP-IBD cell lines were maintained in RPMI (Invitrogen), supplemented with 10% Tet system approved FBS (Clontech). The hTERT-HME1GFP-IBD cell line was maintained in MEBM media supplemented with MEGM SingleQuot (Lonza). For studies requiring glucose and glutamine limitation, media was prepared using DMEM base, D-glucose (Sigma), and L-glutamine solutions (Gemini Bioproducts) at appropriate concentrations with 10% FBS.
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2

Inducible YAP Mutant Expression

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YAPS127A and YAPS94A cDNAs were subcloned from pQCXIH-Flag-YAP-S127A (Addgene#33092) and pQCXIH-Myc-YAP-S94A (Addgene#33094), respectively, into the pLVX-Tight-Puro vector (Clontech) with NotI-EcoRI. Cancer cell lines were transduced with lentiviral particles containing pLVX-Tight-Puro-vector with YAPS127A or YAPS94A and with pLVX-Tet-On Advanced vector (Clontech). For YAP knockdown, miR-E-shRNA sequences were cloned into lentiviral Tet-ON all-in-one LT3GEPIR as described [38 (link)]. All constructs were sequence verified, and lentiviral particles were produced using MISSION Lentiviral Packaging Mix (Sigma#SHP-001). For lentiviral transduction, cells were incubated overnight with infectious particles in the presence of 8 μg/ml polybrene (Santa Cruz Biotechnology#sc-134,220). After recovery in complete medium for 24 h cells were incubated in 1 μg/ml puromycin and 300 μg/mL G418 for YAP mutant expression or 1 μg/ml puromycin for YAP silencing. Efficiency was verified by immunoblotting and immunofluorescence.
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3

Inducible HBx Expression in Liver Cancer Cells

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The Bel-7402 and SMMC-7721 cell line was, first, transfected with pLVX Tet-On Advanced vector (Clontech Laboratories, Inc., Mountain View, CA) using Lipofectamine 2000 (Invitrogen), according to manufacturer's protocol. tTA (Tet-On) expressing Bel-7402 and SMMC-7721 cells were selected with G418 at 700 μg/mL and 400 μg/mL for 14 days, respectively. To obtain stable inducible HBx expressing cells, lentivirus containing full-length and C-terminal truncated HBx in Myc/pLVX-Tight Puro vector was infected into tTA expressing Bel-7402 and SMMC-7721 cells and selected with puromycin at 1 μg/mL for 7 days.
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