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Table 1 Annotation of gene clusters using Gene Ontology (GO), KEGG and Ingenuity databases

From: Transcriptome profiling of the feeding-to-fasting transition in chicken liver

 

Biological process GO terms1

KEGG pathways2

Ingenuity pathways3

Cluster 1

Lipid metabolism

SLC27A4 -LYPLA2-ENPP6-DGAT2L4-CYP51A1-FASN-SULT4A1-CPNE7-ANGPTL3-ACACA-LSS-ACLY-PBX1-PIGH-PLCL1-PRKAG3-PRKAA2-SCD -SBF2-PLA2G12B-MTMR3-PITPNM1

P = 5.E-04

Fatty acid biosynthesis

ACLY-FASN-ACACA-SCD

Fatty Acid Biosynthesis

FASN-ACACA-MCCC2 P = 5.E-04

277 genes

Lipid biosynthesis

DGAT2L4-CYP51A1-FASN-ACACA-LSS-ACLY-PBX1-PIGH-PRKAG3-PRKAA2-SCD P = 2.E-03

Fatty acid biosynthesis

FASN-ACACA-PRKAG3-PRKAA2-SCD

P = 6.E-03

Regulation of action potential

KCNMB2-SBF2-EIF2B4 P = 7.E-03

  

Cluster 2

95 genes

Lipid metabolism

PECI-DCTN6-CPT1A-FABP1-ACSL1-ACAA1-HADHA-HMGCS1-APOB-ACOX1-SCP2-ADIPOR2-PLCZ1

P = 3.E-06

Fatty acid metabolism

PECI-CPT1A-FABP1-ACSL1-ACAA1-HADHA-ACOX1-ADIPOR2 P = 2.E-07

Fatty acid oxidation

CPT1A-HADHA-ACOX1-ADIPOR2

P = 4.E-06

Fatty acid beta-oxidation

CPT1A-HADHA-ACOX1 P = 2.E-05

Energy derivation by oxidation of organic compounds

FBP1-IDH1-PCK1-FBP2-GYG2

P = 8.E-03

Gluconeogenesis

FBP1-PCK1-FBP2 P = 4.E-04

Fatty acid metabolism

ACAT1-PECI-ACAA1-ACOX1-HADHA-ACSL1

PPAR signalling pathway

PCK1-SCP2-FABP1-ACAA1-ACOX1-ACSL1

Synthesis and degradation of ketone bodies

ACAT1-HMGCL-ACAA1-HMGCS1

Citrate cycle TCA cycle

PCK1-ACAT1-HMGCL-IDH1-ACAA1

Gluconeogenesis

PCK1-ACAT1-HMGCL-FBP1

Valine.leucine and isoleucine degradation

ACAT1-HMGCL-ACAA1-HADHA-HMGCS1

Lysine degradation

ACAT1-BBOX1-HADHA

Fatty Acid Metabolism

CYP3A43-CYP4A22-CPT1A-ACAA1-CYP2C18-ACOX1-PECI-ACAT1-ACSL1-HADHA P = 2.E-11

Synthesis and Degradation of Ketone Bodies

1-06E01 6-42E-02 CYP3A43-CYP4A22-CPT1A-ACAA1-CYP2C18-ACOX1-PECI-CPT2-ACAT1-EHHADH-ACSL1-HADHA

ACAA1-ACAT1-HMGCL-HMGCS1-HADHA P = 2.E-11

Pyruvate Metabolism

ACAA1-ACAT1-PCK1-ACSL1-HADHA

P = 2.E-05

Valine- Leucine and Isoleucine Degradation

ACAA1-ACAT1-HMGCL-HMGCS1-HADHA P = 9.E-08 6-94E00 6-54E-02 ACAA1-ACAT1-HMGCL-HMGCS2-EHHADH-HMGCS1-HADHA

Lysine Degradation

BBOX1-ACAA1-ACAT1-MLL3-HADHA

P = 1.E-06

Tryptophan Metabolism

CYP3A43-CYP4A22-ACAA1-CYP2C18-ACAT1-HADHA P = 8.E-06

Propanoate Metabolism

ACAA1-ACAT1-ACSL1-HADHA

P = 1.E-05 1-36E00 2-02E-02 EHHADH-HADHA 8-54E-01 1-69E-02 PCK1-IGFBP1

Cluster 3

517 genes

Cell cycl e

MPHOSPH9-TRIM13-TADA3L-YWHAQ-ESCO2-DBC1-E2F6-ERN1-FGF6-SH3BP4-FRAP1-GAS2-APBB2-KRAS-MAD2L1-MDM2-MLH1-MUTYH-NRAS-NDE1-PPP1CB-CDC37L1-PBK-PRKG2-PTMS-BARD1-CLSPN-NEK4-YWHAH-MAD1L1-MCM8-CCNH-PRC1-MTSS1-CUL7-DCLRE1A-CDC34 P = 9.E-03

Glycolysis

DLAT-ENO1-OGDH-PGAM1-PKM2-UEVLD P = 8.E-03

Cytokinesis

CECR2-PRC1-ROCK2 P = 7.E-03

Ceramide metabolism

GALC-PRKAA1-SGPL1 P = 7.E-03

Regulation of protein catabolism

ATE1-MDM2-BARD1 P = 2.E-03

Insulin signalling pathway

PTPN1-PRKAA1-KRAS-FRAP1-PRKAB1-SORBS1-CRK-NRAS

ErbB signalling pathway _

CAMK2A-JUN-KRAS-FRAP1-PAK7-SRC-CRK-NRAS-

GnRH signalling pathway

CAMK2A-ADCY3-JUN-KRAS-CACNA1C-SRC-NRAS

Renal cell carcinoma _

JUN-SLC2A1-KRAS-PAK7-ARNT-CRK-NRAS-EGLN3

Tight junction _

JAM3-KRAS-CLDN16-SRC-MAGI1-NRAS-ACTB

Glioma _

CAMK2A-KRAS-FRAP1-MDM2-NRAS

Chemokine Signaling

ROCK2-SRC-PLCB4-CAMK2A-NRAS-JUN-MYL2-PPP1CB-KRAS P = 3.E-04

Ephrin Receptor Signaling

MAP3K14-SRC-NRAS-CREB3-SOS2-KRAS-CRK-ROCK2-AKT1-SORBS1-EFNB1-ACP1-ARPC4-PRKAA1-PAK7-MAK P = 6.E-04

B Cell Receptor Signaling

MAP3K14-FRAP1-AKT1-CAMK2A-NRAS-JUN-MAP3K7-CREB3-SOS2-PIK3AP1-KRAS P = 3.E-03

Estrogen Receptor Signaling

SRC-PRKDC-CCNH-NRAS-SOS2-KRAS-GTF2A1-MED4-ESR2 P = 3.E-03

PDGF Signaling

SRC-NRAS-JUN-ACP1-SOS2-KRAS-CRK P = 4.E-03

Wnt/ÃŽ 2 -catenin Signaling

SRC-AKT1-WIF1-MAP3K7-WNT7B-FZD3-DKK2-MDM2 (includes EG:4193)-WNT5B-WNT2-SOX5 (includes EG:6660) P = 6.E-03

Actin Cytoskeleton Signaling

ABI2-TIAM1-NRAS-MYL2-ACTB-SOS2-PPP1CB-KRAS-CRK-FGF6-ROCK2-ARPC4-PRKAA1-PAK7-MAK P = 6.E-03

JAK/Stat Signaling

FRAP1-AKT1-NRAS-SOS2-PTPN1-KRAS P = 8.E-03

Hypoxia Signaling in the Cardiovascular System

AKT1-JUN-COPS5-CREB3-MDM2 (includes EG:4193)-CDC34-UBE2I-ARNT

P = 6.E-04

Cluster 4

273 genes

 

TGF.beta signalling pathway

ACVR2A-PPP2R2A-RBL1

Complement and coagulation cascades

F13A1-C8B-F8-PLAU

Purine metabolism

ADSL-ITPA-ATIC-POLR1B-POLR3G-POLR2C

Gap junction

CDC2-PDGFA-MAP2K2-GNAI1

RNA_polymerase

POLR1B-POLR3G-POLR2C

Histidine_metabolism

ADSL-GAD1-ATIC

Long.term depression

RARB-CASP9-STK4-MAP2K2

Long.term_potentiation

GRIN2B-GRIN2A-MAP2K2

cAMP-mediated Signaling

CNGA4-MAP2K2-GNAO1-GNAI1-HTR1A-RGS12-CNGA1-CHRM3-CHRM5

P = 1.E-03 1–69°00 6–67°-02 HDAC4-TGFB3-RBL1-SIN3A

Ephrin Receptor Signaling

GRIN2B-GRIN2A-MAP2K2-PDGFA-CXCL12-GNAO1-ITGA2-GNAI1-ARPC3-CDC2-ACVR2A P = 1.E-03

1–26°00 3–64°-02 SOX9-GNAO1-RARB-TGFB3-SFRP5-ACVR2A

  1. The pathways sub-lined were found in at least two of the three analyses.1 Biological process GO terms obtained by the Gene Ontology Tree Machine software (GOTM). Are only indicated the enriched biological process GO terms with a significant level of pvalue < 0.01 (see Methods) and a minimum of 3 genes associated. 2 Kegg pathways: are only indicated those with a minimum of 3 genes associated and having a probability to be observed in the cluster 4-fold superior than the probability to obtain it by chance.3 Ingenuity pathways: are indicated the top five Canonical pathways associated to each cluster (pvalue < 0.01). Only canonical pathways with at least 3 genes affiliated were conserved.