LRP6
Available structures PDB Ortholog search: PDBe RCSB List of PDB id codes 3S2K, 3S8V, 3S8Z, 3S94, 3SOB, 3SOQ, 3SOV, 4A0P, 4DG6, 4NM5, 4NM7
Identifiers
Aliases	LRP6, ADCAD2, STHAG7, LDL receptor related protein 6
External IDs	OMIM: 603507 MGI: 1298218 HomoloGene: 1747 GeneCards: LRP6
Gene location (Human) Chr. Chromosome 12 (human)[1] Band 12p13.2 Start 12,116,025 bp[1] End 12,267,044 bp[1]
Gene location (Mouse) Chr. Chromosome 6 (mouse)[2] Band 6 G1|6 65.37 cM Start 134,423,439 bp[2] End 134,543,928 bp[2]
RNA expression pattern Bgee Human Mouse (ortholog) Top expressed in Achilles tendon corpus callosum liver stromal cell of endometrium ganglionic eminence placenta sural nerve skeletal muscle tissue right lobe of liver myometrium Top expressed in ascending aorta aortic valve cumulus cell secondary oocyte extraocular muscle extensor digitorum longus muscle stria vascularis left lung lobe plantaris muscle pineal gland More reference expression data BioGPS More reference expression data
Gene ontology Molecular function low-density lipoprotein particle receptor activity apolipoprotein binding protein homodimerization activity kinase inhibitor activity frizzled binding Wnt-protein binding toxin transmembrane transporter activity protein binding coreceptor activity involved in Wnt signaling pathway identical protein binding Wnt-activated receptor activity signaling receptor binding coreceptor activity involved in canonical Wnt signaling pathway Cellular component integral component of membrane Wnt-Frizzled-LRP5/6 complex Wnt signalosome Golgi apparatus early endosome membrane membrane receptor complex synapse extracellular region cell surface neuronal cell body early endosome endoplasmic reticulum caveola cytoplasmic vesicle plasma membrane membrane raft Biological process negative regulation of protein phosphorylation Wnt signaling pathway involved in somitogenesis cerebellum morphogenesis roof of mouth development dopaminergic neuron differentiation positive regulation of Wnt signaling pathway involved in dorsal/ventral axis specification regulation of transcription, DNA-templated endocytosis receptor-mediated endocytosis involved in cholesterol transport embryonic pattern specification convergent extension negative regulation of protein kinase activity thalamus development axis elongation involved in somitogenesis canonical Wnt signaling pathway involved in neural crest cell differentiation positive regulation of cytosolic calcium ion concentration response to peptide hormone canonical Wnt signaling pathway involved in regulation of cell proliferation neural crest cell differentiation positive regulation of DNA-binding transcription factor activity Wnt signaling pathway cellular response to cholesterol neural crest formation trachea cartilage morphogenesis positive regulation of transcription, DNA-templated odontogenesis of dentin-containing tooth multicellular organism development midbrain-hindbrain boundary development neural tube closure positive regulation of cell cycle external genitalia morphogenesis Wnt signaling pathway involved in dorsal/ventral axis specification pericardium morphogenesis cerebral cortex development embryonic retina morphogenesis in camera-type eye canonical Wnt signaling pathway negative regulation of protein serine/threonine kinase activity protein localization to plasma membrane negative regulation of canonical Wnt signaling pathway negative regulation of smooth muscle cell apoptotic process face morphogenesis primitive streak formation positive regulation of transcription by RNA polymerase II chemical synaptic transmission toxin transport Wnt signaling pathway involved in midbrain dopaminergic neuron differentiation positive regulation of canonical Wnt signaling pathway beta-catenin destruction complex disassembly midbrain dopaminergic neuron differentiation gastrulation with mouth forming second anterior/posterior pattern specification embryonic limb morphogenesis midbrain development bone remodeling embryonic camera-type eye morphogenesis bone morphogenesis branching involved in mammary gland duct morphogenesis cell-cell adhesion Sources:Amigo / QuickGO
Orthologs Species Human Mouse Entrez 4040 16974 Ensembl ENSG00000070018 ENSG00000281324 ENSMUSG00000030201 UniProt O75581 O88572 RefSeq (mRNA) NM_002336 NM_008514 RefSeq (protein) NP_002327 NP_032540 Location (UCSC) Chr 12: 12.12 – 12.27 Mb Chr 6: 134.42 – 134.54 Mb PubMed search [3] [4]
Wikidata
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Low-density lipoprotein receptor-related protein 6 is a protein that in humans is encoded by the LRP6 gene.^[5][6] LRP6 is a key component of the LRP5/LRP6/Frizzled co-receptor group that is involved in canonical Wnt pathway.

Structure

LRP6 is a transmembrane low-density lipoprotein receptor that shares a similar structure with LRP5. In each protein, about 85% of its 1600-amino-acid length is extracellular. Each has four β-propeller motifs at the amino terminal end that alternate with four epidermal growth factor (EGF)-like repeats. Most extracellular ligands bind to LRP5 and LRP6 at the β-propellers. Each protein has a single-pass, 22-amino-acid segment that crosses the cell membrane and a 207-amino-acid segment that is internal to the cell.^[7]

Function

LRP6 acts as a co-receptor with LRP5 and the Frizzled protein family members for transducing signals by Wnt proteins through the canonical Wnt pathway.^[7]

Interactions

Canonical WNT signals are transduced through Frizzled receptor and LRP5/LRP6 coreceptor to downregulate GSK3beta (GSK3B) activity not depending on Ser-9 phosphorylation.^[8] Reduction of canonical Wnt signals upon depletion of LRP5 and LRP6 results in p120-catenin degradation.^[9]

LRP6 is regulated by extracellular proteins in the Dickkopf (Dkk) family (like DKK1^[10]), sclerostin, R-spondins and members of the cysteine-knot-type protein family.^[7]

Clinical significance

Loss-of-function mutations or LRP6 in humans lead to increased plasma LDL and triglycerides, hypertension, diabetes and osteoporosis.^[7] Similarly, mice with a loss-of-function Lrp6 mutation have low bone mass.^[11] LRP6 is critical in bone's anabolic response to parathyroid hormone (PTH) treatment, whereas LRP5 is not involved.^[11] On the other hand, LRP6 does not appear active in mechanotransduction (bone's response to forces), while LRP5 is critical in that role.^[11] Sclerostin, one of the inhibitors of LRP6, is a promising osteocyte-specific Wnt antagonist in osteoporosis clinical trials.^[12][13]