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. 2019 Nov 14;10:1032. doi: 10.3389/fgene.2019.01032

Table 3.

Functional annotation of clusters derived from untreated and LPS treated F2 BMDM.

Cluster Number (number of nodes) Expression pattern Representative genes Enhanced terms (P value)
001 (1396) Unchanged by LPS ACTA2, ADAMTSs, ASPH, COL1A1, COL1A2, FBN1, FN1, MFAPs, TGFB3, TGFBR2/3, THBS1, THBS2 Protein processing in endoplasmic reticulum (5.5E-10); Poly(A) RNA binding (3.2E-8); Extracellular matrix (1.6E-6); Endoplasmic reticulum (8.7E-6); ER-Golgi transport (7.5E-5); Focal adhesion (1.5E-4)
002 (485) Unchanged by LPS COL9A1, COL10A1, COL11A1, FGFRs, FOXO6, IRX5/6, MEF2A/B/C, PAX3, RUNX2, SIX2/3, SMAD1, SOX5/8/9 Extracellular matrix (0.003); Secreted (0.007); Glycoprotein (0.012); Signal (0.038)
003 (389) Up with LPS ATF3, BHLHE40, CD274, CEBPB, FOSL2, GGCL1, GVIN1, IFIT5, IFIH1, IRF1, IRF8, IRF9, OASL, SOCS1 Zinc finger, RING/FYVE/PHD-type (0.02); Influenza A (0.01)
004 (259) Unchanged with LPS CPSF2, DDX6, LEO1, PAPD5, PAPOLA, PARN, PRPF38B, PRPF39, PRPF40A, PRPF6, SMU1, TOP2B, TOP3B, TOPBP1 Spliceosome (2.4E-9); Cytoplasmic mRNA processing body (0.0004)
005 (168) Down with LPS C3AR1, CD14, FAAH, MAOA, PEX16, PSEN2, TNFAIP8L1, TUBB1 Transmembrane helix (0.1); Aldolase-type TIM barrel (0.07)
006 (167) Unchanged by LPS BUB1, BUB1B, BUB3, centromere protein genes, kinesin genes, kinetochore complex components Cell cycle (4.9E-14); Mitosis (9.8E-13); Cell division (2.3E-11); Centromere (8.3E-11)
007 (160) Unchanged by LPS RPL and RPS genes, translation initiation and elongation genes Structural constituent of ribosome (3.6E-81); Ribosome (4.7E-79); Translation (1.2E-68); Protein biosynthesis (1.8E-7)
008 (137) Up with LPS BACH1, IRF6, KLF8, MAFK, REL, TLR15 No significant enrichment
009 (100) Down with LPS IGF2, KLF3, KLF13, MAF1, TAF12 No significant enhancement
010 (76) Unchanged by LPS AAR2, CNOT10, EXOC1, GABPA, POLR1A RNA recognition motif (0.002)
011 (71) Unchanged by LPS but one animal very high ACTG2, CDH11, COL7A1, ENPP2/3, FGF7, NPY, PDGFRA, VAV2 Calcium ion binding (0.2)
012 (65) No trend with LPS All unannotated ENSGALG
013 (59) Up with LPS CCL4, BATF6, FLT1, IL13RA1, IL1B, NFKB1, NFKB2, NFKBIA, TRAF2, TRAF3, ZC3H12A Toll-like receptor signaling pathway (0.0005); Cytosolic DNA sensing pathway (0.001); RIG-I-like receptor signaling pathway (0.001); Inflammatory response (0.01)
014 (57) Up with LPS CCNE1, FMR1, SMCHD1, TRAF6, USP16 Cell cycle (0.1)
015 (57) Down with LPS Mostly unannotated ENSGALG and LOC genes No significant enhancement
016 (52) Down with LPS ATP6AP1, ATP6AP2, ATP6V0D1, CASP9 No significant enrichment
017 (52) Unchanged with LPS ACTR1A, COG5, E4F1, EIF2AK4, INSIG2 No significant enrichment
018 (52) Variable response to LPS All unannotated ENSGALG
019 (51) Variable response to LPS ACOD1 (IRG1), IRF2, MAP2K3, TAOK1, TBK1, USP15 Protein ubiquitination involved in ubiquitin-dependent protein catabolic process (0.01)
020 (45) Unchanged with LPS CCT genes, HSP genes Positive regulation of protein localization to Cajal body (1.5E-10); Chaperonin TCP-1, conserved site (4.7E-10); Positive regulation of establishment of protein localization to telomere (2.7E-10); Chaperone (2.1E-9)
021 (45) Down with LPS in most CSF1R, IL2RG, IL6R, TLR4 No significant enrichment

Benjamini Hochberg corrected P values are presented. First 21 clusters only as number of genes becomes too low for meaningful analysis in smaller clusters. This analysis used DAVID (https://david.ncifcrf.gov/home.jsp) to determine enrichment for annotation terms.