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PMC0
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10.1038%2Fncb2464
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methods section
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Lrig1 KO mice>>23<<, Egfrwa-2 and Lgr5−EGFP-IRES-CreERT2 knock in mice14 have been described.
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Lrig1 KO mice23, Egfrwa-2 and Lgr5−EGFP-IRES-CreERT2 knock in mice>>14<< have been described.
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n3:17934449
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Analysis of Lgr5-GFP/Lrig1 and UEA-1/pEgfr was carried out as recently described>>22<<.
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RNA was isolated from homogenised intestine or flow-sorted cells and either used directly for microarray experiments or for qPCR as described>>20<<.
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Bead level data from all hybridizations was background corrected, using default parameters of the RMA algorithm>>37<<, and summarised using the beadarray package for the Bioconductor suite (http:
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In order to reduce errors associated with multiple hypothesis testing, the significance p-values obtained were converted to corrected q-values using the false discovery rate (FDR) method>>39<<, as implemented in the qvalue package for Bioconductor.
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n3:12883005
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For GSEA using Fisher’s exact test we obtained a crypt gene signature>>25<< (1,692 genes in reference list, 802 genes up-regulated; Supplementary Table 3) and a Myc dependent gene network30 (374 genes in reference list, 144 genes up-regulated; Supplementary Table 4).
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For GSEA using Fisher’s exact test we obtained a crypt gene signature25 (1,692 genes in reference list, 802 genes up-regulated; Supplementary Table 3) and a Myc dependent gene network>>30<< (374 genes in reference list, 144 genes up-regulated; Supplementary Table 4).
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DIG in situ hybridisation was carried out essentially as described before using IMAGE clones>>40<<.
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Intestinal epithelial cells were isolated as described>>22<<. To generate a single cell suspension, cells were incubated with trypsin22 or with 0.25mg/mL Thermolysin for 1 minute at 37°C in PBS supplemented with 1%BSA for trypsin sensitive antigens such as Lrig1.
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To generate a single cell suspension, cells were incubated with trypsin>>22<< or with 0.25mg/mL Thermolysin for 1 minute at 37°C in PBS supplemented with 1%BSA for trypsin sensitive antigens such as Lrig1.
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Primary crypts were cultured according to Sato et al.>>31<< using reduced concentrations of murine recombinant R-spondin1 (500ng/mL – R&D Systems) and varying concentrations of EGF (Peprotech).
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