#METABOLOMICS WORKBENCH amroilaiwy_20160325_083511 DATATRACK_ID:670
VERSION             	1
CREATED_ON             	September 20, 2017, 1:19 pm
#PROJECT
PR:PROJECT_TITLE                 	The ubiquitin ligase MuRF1 regulates PPARa activity in the heart by enhancing
PR:PROJECT_TITLE                 	nuclear export via monoubiquitination
PR:PROJECT_TYPE                  	Targeted Metabolomics
PR:PROJECT_SUMMARY               	The transcriptional regulation of peroxisome proliferator-activated receptor
PR:PROJECT_SUMMARY               	(PPAR) a by post-translational modification, such as ubiquitin, has not been
PR:PROJECT_SUMMARY               	described. We report here for the first time an ubiquitin ligase (muscle ring
PR:PROJECT_SUMMARY               	finger-1/MuRF1) that inhibits fatty acid oxidation by inhibiting PPARa, but not
PR:PROJECT_SUMMARY               	PPARß/d or PPAR? in cardiomyocytes in vitro. Similarly, MuRF1 Tg+ hearts
PR:PROJECT_SUMMARY               	showed significant decreases in nuclear PPARa activity and acyl-carnitine
PR:PROJECT_SUMMARY               	intermediates, while MuRF1-/- hearts exhibited increased PPARa activity and
PR:PROJECT_SUMMARY               	acyl-carnitine intermediates. MuRF1 directly interacts with PPARa,
PR:PROJECT_SUMMARY               	mono-ubiquitinates it, and targets it for nuclear export to inhibit fatty acid
PR:PROJECT_SUMMARY               	oxidation in a proteasome independent manner. We then identified a previously
PR:PROJECT_SUMMARY               	undescribed nuclear export sequence in PPARa, along with three specific lysines
PR:PROJECT_SUMMARY               	(292, 310, 388) required for MuRF1's targeting of nuclear export. These studies
PR:PROJECT_SUMMARY               	identify the role of ubiquitination in regulating cardiac PPARa, including the
PR:PROJECT_SUMMARY               	ubiquitin ligase that may be responsible for this critical regulation of cardiac
PR:PROJECT_SUMMARY               	metabolism in heart failure.
PR:INSTITUTE                     	University of North Carolina
PR:DEPARTMENT                    	McAllister Heart Institute, Department of Internal Medicine
PR:LABORATORY                    	Multiple Centers
PR:LAST_NAME                     	Willis
PR:FIRST_NAME                    	Monte
PR:ADDRESS                       	111 Mason Farm road, Chapel Hill, North Carolina, 27599-7126, USA
PR:EMAIL                         	monte_willis@med.unc.edu
PR:PHONE                         	919-360-7599
PR:FUNDING_SOURCE                	NIH, Fondation Leducq, AHA mid-Atlantic affiliate, AHA scientist development
PR:FUNDING_SOURCE                	grant, Jefferson-Pilot Corporation Fellowship in Academic Medicine
#STUDY
ST:STUDY_TITLE                   	Targeted metabolomics of MuRF1 overexpressing cardiomyocytes compared to their
ST:STUDY_TITLE                   	wildtype controls (part I)
ST:STUDY_TYPE                    	Targeted metabolomic analysis
ST:STUDY_SUMMARY                 	The transcriptional regulation of peroxisome proliferator-activated receptor
ST:STUDY_SUMMARY                 	(PPAR) a by post-translational modification, such as ubiquitin, has not been
ST:STUDY_SUMMARY                 	described. We report here for the first time an ubiquitin ligase (muscle ring
ST:STUDY_SUMMARY                 	finger-1/MuRF1) that inhibits fatty acid oxidation by inhibiting PPARa, but not
ST:STUDY_SUMMARY                 	PPARß/d or PPAR? in cardiomyocytes in vitro. Similarly, MuRF1 Tg+ hearts
ST:STUDY_SUMMARY                 	showed significant decreases in nuclear PPARa activity and acyl-carnitine
ST:STUDY_SUMMARY                 	intermediates, while MuRF1-/- hearts exhibited increased PPARa activity and
ST:STUDY_SUMMARY                 	acyl-carnitine intermediates. MuRF1 directly interacts with PPARa,
ST:STUDY_SUMMARY                 	mono-ubiquitinates it, and targets it for nuclear export to inhibit fatty acid
ST:STUDY_SUMMARY                 	oxidation in a proteasome independent manner. We then identified a previously
ST:STUDY_SUMMARY                 	undescribed nuclear export sequence in PPARa, along with three specific lysines
ST:STUDY_SUMMARY                 	(292, 310, 388) required for MuRF1's targeting of nuclear export. These studies
ST:STUDY_SUMMARY                 	identify the role of ubiquitination in regulating cardiac PPARa, including the
ST:STUDY_SUMMARY                 	ubiquitin ligase that may be responsible for this critical regulation of cardiac
ST:STUDY_SUMMARY                 	metabolism in heart failure.
ST:INSTITUTE                     	University of North Carolina
ST:DEPARTMENT                    	McAllister Heart Institute, Department of Internal Medicine
ST:LABORATORY                    	Multiple Centers
ST:LAST_NAME                     	Willis
ST:FIRST_NAME                    	Monte
ST:ADDRESS                       	111 Mason Farm road, Chapel Hill, North Carolina, 27599-7126, USA
ST:EMAIL                         	monte_willis@med.unc.edu
ST:PHONE                         	919-360-7599
#SUBJECT
SU:SUBJECT_TYPE                  	Animal
SU:SUBJECT_SPECIES               	Mus musculus
SU:TAXONOMY_ID                   	10090
#SUBJECT_SAMPLE_FACTORS:         	SUBJECT(optional)[tab]SAMPLE[tab]FACTORS(NAME:VALUE pairs separated by |)[tab]Additional sample data
SUBJECT_SAMPLE_FACTORS           	-	Heart 1	Genotype:WT-MuRF1 tg+	
SUBJECT_SAMPLE_FACTORS           	-	Heart 2	Genotype:WT-MuRF1 tg+	
SUBJECT_SAMPLE_FACTORS           	-	Heart 3	Genotype:WT-MuRF1 tg+	
SUBJECT_SAMPLE_FACTORS           	-	Heart 4	Genotype:MuRF1 tg+	
SUBJECT_SAMPLE_FACTORS           	-	Heart 5	Genotype:MuRF1 tg+	
SUBJECT_SAMPLE_FACTORS           	-	Heart 6	Genotype:MuRF1 tg+	
#COLLECTION
CO:COLLECTION_SUMMARY            	COS7 and H9C2 cells were transfected with PPRE-luc, pcDNA 3.1, ß-galactosidase,
CO:COLLECTION_SUMMARY            	and the corresponding PPAR isoform (PPARa, PPARß/d or PPAR?) as indicated.
CO:COLLECTION_SUMMARY            	24 hours followings transfection cells were transduced with Ad.GFP-Myc-MuRF1.
CO:COLLECTION_SUMMARY            	Cells were harvested 24hours later following observation of GFP by light
CO:COLLECTION_SUMMARY            	microscopy
#TREATMENT
TR:TREATMENT_SUMMARY             	N/A
#SAMPLEPREP
SP:SAMPLEPREP_SUMMARY            	Acyl-carnitines were analyzed using stable isotope dilution techniques. Amino
SP:SAMPLEPREP_SUMMARY            	acids and acyl-carnitine measurements were made by flow injection tandem mass
SP:SAMPLEPREP_SUMMARY            	spectrometry
#CHROMATOGRAPHY
CH:CHROMATOGRAPHY_TYPE           	GC
CH:INSTRUMENT_NAME               	Waters Acquity
CH:COLUMN_NAME                   	ACQUITY UPLC 1.7 µm column
#ANALYSIS
AN:ANALYSIS_TYPE                 	MS
#MS
MS:MS_COMMENTS                   	-
MS:INSTRUMENT_NAME               	Agilent 5975
MS:INSTRUMENT_TYPE               	Single quadrupole
MS:MS_TYPE                       	EI
MS:ION_MODE                      	POSITIVE
#MS_METABOLITE_DATA
MS_METABOLITE_DATA:UNITS         	uM
MS_METABOLITE_DATA_START
Samples	Heart 1	Heart 2	Heart 3	Heart 4	Heart 5	Heart 6
Factors	Genotype:WT-MuRF1 tg+	Genotype:WT-MuRF1 tg+	Genotype:WT-MuRF1 tg+	Genotype:MuRF1 tg+	Genotype:MuRF1 tg+	Genotype:MuRF1 tg+
C2	23.6000	22.5000	20.8000	18.5000	18.8000	26.9000
C3	0.3530	0.9490	0.6430	0.8450	0.6460	0.9690
C4/Ci4	0.0973	0.0727	0.0661	0.0837	0.0352	0.0502
C5:1	0.0137	0.0412	0.0505	0.0367	0.0443	0.0436
C5's	0.0294	0.0257	0.0447	0.0365	0.0279	0.0248
C4-OH	0.6950	0.5340	0.5530	0.4500	0.6190	0.5900
C6	0.1640	0.0910	0.0364	0.0438	0.0366	0.0117
C5-OH/C3-DC	0.5270	0.6480	0.9940	0.8870	0.5750	0.7230
Ci4-DC/C4-DC	0.3300	0.3780	0.3780	0.4070	0.2970	0.3600
C8:1	0.0041	0.0170	0.0105	0.0105	0.0111	0.0079
C8	0.0089	0.0073	0.0034	0.0039	0.0076	0.0068
C5-DC	0.0037	0.0054	0.0012	0.0076	0.0018	0.0095
C6:1-DC/C8:1-OH	0.0147	0.0065	0.0097	0.0030	0.0106	0.0084
C6-DC	0.0276	0.0434	0.0190	0.0873	0.0670	0.0354
C10:3	0.0012	0.0005		0.0013	0.0033	0.0016
C10:2	0.0033	0.0068	0.0013	0.0040	0.0054	0.0030
C10:1	0.0117	0.0115	0.0059	0.0070	0.0059	0.0069
C10	0.0081	0.0074	0.0028	0.0036		0.0014
C7-DC	0.0040	0.0048	0.0083	0.0057	0.0001	0.0040
C8:1-DC	0.0042		0.0025	0.0055	0.0067	0.0039
C10-OH/C8-DC	0.0765	0.1070	0.0580	0.0821	0.1100	0.0352
C12:1	0.0063	0.0068	0.0025	0.0035	0.0010	
C12	0.0081		0.0007	0.0006	0.0026	0.0011
C12-OH/C10-DC	0.0759	0.1140	0.0584	0.0765	0.1070	0.0331
C14:2	0.0058	0.0094	0.0065	0.0065	0.0027	0.0034
C14:1	0.0117	0.0098	0.0056	0.0098	0.0051	0.0033
C14	0.0250	0.0100	0.0064	0.0108	0.0089	0.0067
C14:1-OH/C12:1-DC	0.1070	0.1010	0.0514	0.0624	0.0669	0.0195
C14-OH/C12-DC	0.0963	0.0826	0.0515	0.0729	0.1000	0.0312
C16:2	0.0145	0.0058	0.0036	0.0052	0.0042	0.0029
C16:1	0.0188	0.0396	0.0175	0.0282	0.0224	0.0099
C16	0.0711	0.0295	0.0215	0.0189	0.0173	0.0125
C16:1-OH/C14:1-DC	0.0748	0.0839	0.0424	0.0351	0.0482	0.0109
C16-OH/C14-DC	0.1230	0.1020	0.0375	0.0457	0.0652	0.0198
C18:2	0.0357	0.0555	0.0391	0.0301	0.0403	0.0119
C18:1	0.0403	0.0456	0.0191	0.0330	0.0357	0.0224
C18	0.0431	0.0192	0.0154	0.0130	0.0071	0.0080
C18:2-OH	0.1010	0.0536	0.0235	0.0190	0.0318	0.0044
C18:1-OH/C16:1-DC	0.1340	0.0987	0.0484	0.0434	0.0625	0.0183
C18-OH/C16-DC	0.0606	0.0466	0.0249	0.0295	0.0386	0.0131
C20:4	0.0048	0.0104	0.0064	0.0154	0.0067	0.0047
C20	0.0138	0.0054	0.0025	0.0025	0.0042	0.0018
C20:1-OH/C18:1-DC	0.0169	0.0189	0.0080	0.0094	0.0170	0.0140
C20-OH/C18-DC	0.0067	0.0069	0.0033	0.0037	0.0048	0.0037
C22	0.0046			0.0027	0.0030	0.0011
MS_METABOLITE_DATA_END
#METABOLITES
METABOLITES_START
metabolite_name
C2
C3
C4/Ci4
C5:1
C5's
C4-OH
C6
C5-OH/C3-DC
Ci4-DC/C4-DC
C8:1
C8
C5-DC
C6:1-DC/C8:1-OH
C6-DC
C10:3
C10:2
C10:1
C10
C7-DC
C8:1-DC
C10-OH/C8-DC
C12:1
C12
C12-OH/C10-DC
C14:2
C14:1
C14
C14:1-OH/C12:1-DC
C14-OH/C12-DC
C16:2
C16:1
C16
C16:1-OH/C14:1-DC
C16-OH/C14-DC
C18:2
C18:1
C18
C18:2-OH
C18:1-OH/C16:1-DC
C18-OH/C16-DC
C20:4
C20
C20:1-OH/C18:1-DC
C20-OH/C18-DC
C22
METABOLITES_END
#END