Mus musculus Protein: Lpin1
Summary
InnateDB Protein IDBP-129217.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol Lpin1
Protein Name lipin 1
Synonyms 4631420P06; fld; Kiaa0188; Lipin1; mKIAA0188;
Species Mus musculus
Ensembl Protein ENSMUSP00000070583
InnateDB Gene IDBG-129213 (Lpin1)
Protein Structure
UniProt Annotation
Function Plays important roles in controlling the metabolism of fatty acids at differents levels. Acts as a magnesium-dependent phosphatidate phosphatase enzyme which catalyzes the conversion of phosphatidic acid to diacylglycerol during triglyceride, phosphatidylcholine and phosphatidylethanolamine biosynthesis. Acts also as nuclear transcriptional coactivator for PPARGC1A/PPARA regulatory pathway to modulate lipid metabolism gene expression. Is involved in adipocyte differentiation. Isoform 1 is recruited at the mitochondrion outer membrane and is involved in mitochondrial fission by converting phosphatidic acid to diacylglycerol. {ECO:0000269PubMed:16950137}.
Subcellular Localization Isoform 1: Mitochondrion outer membrane {ECO:0000269PubMed:21397848}. Cytoplasm {ECO:0000269PubMed:21397848}. Nucleus membrane {ECO:0000269PubMed:21397848}. Note=Recruited at the mitochondrion outer membrane following phosphatidic acid formation mediated by PLD6. In neuronals cells, isoform 1 is exclusively cytoplasmic. In 3T3-L1 pre-adipocytes, it primarily located in the cytoplasm.Isoform 2: Nucleus. Cytoplasm. Endoplasmic reticulum membrane. Note=Nuclear localization requires both CNEP1R1 and CTDNEP1. In neuronals cells, localized in both the cytoplasm and the nucleus. In 3T3-L1 pre-adipocytes, it is predominantly nuclear.
Disease Associations Note=Defects in Lpin1 are the cause of the fatty liver dystrophy phenotype (fld). Fld mutant mices are characterized by neonatal fatty liver and hypertriglyceridemia that resolve at weaning, and neuropathy affecting peripheral nerve in adulthood. Adipose tissue deficiency, glucose intolerance and increased susceptibility to atherosclerosis are associated with this mutation too. Two independent mutant alleles are characterized in this phenotype, fld and fld2j.
Tissue Specificity Specifically expressed in skeletal muscle. Also expressed prominently in adipose tissue, and testis. Lower expression also detected in kidney, lung, brain and liver. Isoform 1 is the predominant isoform in the liver. Isoform 2 is the major form in the brain. {ECO:0000269PubMed:16049017, ECO:0000269PubMed:17158099, ECO:0000269PubMed:19753306, ECO:0000269PubMed:22134922}.
Comments
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 7 experimentally validated interaction(s) in this database.
They are also associated with 4 interaction(s) predicted by orthology.
Experimentally validated
Total 7 [view]
Protein-Protein 7 [view]
Protein-DNA 0
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Predicted by orthology
Total 4 [view]
Gene Ontology

Molecular Function
Accession GO Term
GO:0001085 RNA polymerase II transcription factor binding
GO:0003713 transcription coactivator activity
GO:0005515 protein binding
GO:0008195 phosphatidate phosphatase activity
GO:0042826 histone deacetylase binding
GO:0042975 peroxisome proliferator activated receptor binding
Biological Process
GO:0000122 negative regulation of transcription from RNA polymerase II promoter
GO:0000266 mitochondrial fission
GO:0006351 transcription, DNA-templated
GO:0006629 lipid metabolic process
GO:0006642 triglyceride mobilization
GO:0009062 fatty acid catabolic process
GO:0016311 dephosphorylation
GO:0019432 triglyceride biosynthetic process
GO:0031065 positive regulation of histone deacetylation
GO:0031100 organ regeneration
GO:0031529 ruffle organization
GO:0031532 actin cytoskeleton reorganization
GO:0032869 cellular response to insulin stimulus
GO:0045444 fat cell differentiation
GO:0045598 regulation of fat cell differentiation
GO:0045944 positive regulation of transcription from RNA polymerase II promoter
GO:2001141 regulation of RNA biosynthetic process
Cellular Component
GO:0005634 nucleus
GO:0005667 transcription factor complex
GO:0005737 cytoplasm
GO:0005741 mitochondrial outer membrane
GO:0005789 endoplasmic reticulum membrane
GO:0031965 nuclear membrane
Protein Structure and Domains
PDB ID MGI:1891340
InterPro IPR007651 Lipin, N-terminal
IPR013209 LNS2, Lipin/Ned1/Smp2
IPR017986 WD40-repeat-containing domain
IPR023214 HAD-like domain
PFAM PF04571
PF08235
PF00702
PF08282
PF13419
PRINTS
PIRSF
SMART SM00775
TIGRFAMs
Post-translational Modifications
Modification
Cross-References
SwissProt Q91ZP3
PhosphoSite PhosphoSite-Q91ZP3
TrEMBL
UniProt Splice Variant
Entrez Gene 14245
UniGene Mm.470809
RefSeq NP_056578
MGI ID
MGI Symbol Lpin1
OMIM
CCDS CCDS25822
HPRD
IMGT
EMBL AF180471 AF412811 AK014526 AK019539
GenPept AAF44296 AAL07798 BAB29412 BAB31786