HPGD

HPGD
Available structures PDB Ortholog search: PDBe RCSB List of PDB id codes 2GDZ
Identifiers
Aliases	HPGD, 15-PGDH, PGDH, PGDH1, PHOAR1, SDR36C1, hydroxyprostaglandin dehydrogenase 15-(NAD), 15-hydroxyprostaglandin dehydrogenase
External IDs	OMIM: 601688; MGI: 108085; HomoloGene: 68095; GeneCards: HPGD; OMA:HPGD - orthologs
Gene location (Human) Chr. Chromosome 4 (human) Band 4q34.1 Start 174,490,175 bp End 174,523,154 bp
Gene location (Mouse) Chr. Chromosome 8 (mouse) Band 8|8 B2 Start 56,747,620 bp End 56,774,078 bp
RNA expression pattern Bgee Human Mouse (ortholog) Top expressed in jejunal mucosa rectum mucosa of colon placenta metanephric glomerulus right lung lower lobe of lung mucosa of sigmoid colon mucosa of transverse colon mucosa of ileum Top expressed in right lung lobe seminal vesicula wall of urinary bladder mucosa of urinary bladder transitional epithelium of urinary bladder pyloric antrum epithelium of stomach left colon body of femur duodenum More reference expression data BioGPS More reference expression data
Gene ontology Molecular function NAD binding 15-hydroxyprostaglandin dehydrogenase (NAD+) activity catalytic activity prostaglandin E receptor activity NAD+ binding oxidoreductase activity protein homodimerization activity Cellular component nucleoplasm basolateral plasma membrane extracellular exosome cytoplasm cytosol extracellular space Biological process prostaglandin metabolic process thrombin-activated receptor signaling pathway lipid metabolism negative regulation of cell cycle fatty acid metabolic process lipoxygenase pathway birth lipoxin metabolic process transforming growth factor beta receptor signaling pathway ovulation ductus arteriosus closure response to lipopolysaccharide kidney development female pregnancy response to estradiol positive regulation of apoptotic process response to ethanol positive regulation of vascular associated smooth muscle cell proliferation long-chain fatty acid biosynthetic process lipoxin biosynthetic process Sources:Amigo / QuickGO
Orthologs Species Human Mouse Entrez 3248 15446 Ensembl ENSG00000164120 ENSMUSG00000031613 UniProt P15428 Q8VCC1 RefSeq (mRNA) NM_000860 NM_001145816 NM_001256301 NM_001256305 NM_001256306 NM_001256307 NM_001363574 NM_008278 RefSeq (protein) NP_000851 NP_001139288 NP_001243230 NP_001243234 NP_001243235 NP_001243236 NP_001350503 NP_032304 Location (UCSC) Chr 4: 174.49 – 174.52 Mb Chr 8: 56.75 – 56.77 Mb PubMed search
Wikidata
View/Edit Human View/Edit Mouse

Hydroxyprostaglandin dehydrogenase 15-(NAD) (the HUGO-approved official symbol = HPGD; HGNC ID, HGNC:5154), also called 15-hydroxyprostaglandin dehydrogenase [NAD+], is an enzyme that in humans is encoded by the HPGD gene.

In melanocytic cells HPGD gene expression may be regulated by MITF.

See also

• Primary hypertrophic osteoathropathy

Further reading

• Erwich JJ, Keirse MJ (1992). "Placental localization of 15-hydroxy-prostaglandin dehydrogenase in early and term human pregnancy". Placenta. 13 (3): 223–9. doi:10.1016/0143-4004(92)90037-T. PMID 1635910.
• Ensor CM, Yang JY, Okita RT, Tai HH (1990). "Cloning and sequence analysis of the cDNA for human placental NAD(+)-dependent 15-hydroxyprostaglandin dehydrogenase". J. Biol. Chem. 265 (25): 14888–91. PMID 1697582.
• Ensor CM, Tai HH (1991). "Site-directed mutagenesis of the conserved tyrosine 151 of human placental NAD(+)-dependent 15-hydroxyprostaglandin dehydrogenase yields a catalytically inactive enzyme". Biochem. Biophys. Res. Commun. 176 (2): 840–5. doi:10.1016/S0006-291X(05)80262-1. PMID 2025296.
• Krook M, Marekov L, Jörnvall H (1990). "Purification and structural characterization of placental NAD(+)-linked 15-hydroxyprostaglandin dehydrogenase. The primary structure reveals the enzyme to belong to the short-chain alcohol dehydrogenase family". Biochemistry. 29 (3): 738–43. doi:10.1021/bi00455a021. PMID 2337593.
• Pichaud F, Frendo JL, Delage-Mourroux R, et al. (1995). "Sequence of a novel mRNA coding for a C-terminal-truncated form of human NAD(+)-dependent 15-hydroxyprostaglandin dehydrogenase". Gene. 162 (2): 319–22. doi:10.1016/0378-1119(95)00319-2. PMID 7557451.
• Sangha RK, Walton JC, Ensor CM, et al. (1994). "Immunohistochemical localization, messenger ribonucleic acid abundance, and activity of 15-hydroxyprostaglandin dehydrogenase in placenta and fetal membranes during term and preterm labor". J. Clin. Endocrinol. Metab. 78 (4): 982–9. doi:10.1210/jc.78.4.982. PMID 8157731.
• Krook M, Ghosh D, Duax W, Jörnvall H (1993). "Three-dimensional model of NAD(+)-dependent 15-hydroxyprostaglandin dehydrogenase and relationships to the NADP(+)-dependent enzyme (carbonyl reductase)". FEBS Lett. 322 (2): 139–42. doi:10.1016/0014-5793(93)81554-D. PMID 8482380.
• Pichaud F, Delage-Mourroux R, Pidoux E, et al. (1997). "Chromosomal localization of the type-I 15-PGDH gene to 4q34-q35". Hum. Genet. 99 (2): 279–81. doi:10.1007/s004390050354. PMID 9048936.
• Delage-Mourroux R, Pichaud F, Frendo JL, et al. (1997). "Cloning and sequencing of a new 15-hydroxyprostaglandin dehydrogenase related mRNA". Gene. 188 (1): 143–8. doi:10.1016/S0378-1119(96)00800-1. PMID 9099873.
• Patel FA, Clifton VL, Chwalisz K, Challis JR (1999). "Steroid regulation of prostaglandin dehydrogenase activity and expression in human term placenta and chorio-decidua in relation to labor". J. Clin. Endocrinol. Metab. 84 (1): 291–9. doi:10.1210/jc.84.1.291. PMID 9920098.
• Zhou H, Tai HH (1999). "Threonine 188 is critical for interaction with NAD+ in human NAD+-dependent 15-hydroxyprostaglandin dehydrogenase". Biochem. Biophys. Res. Commun. 257 (2): 414–7. doi:10.1006/bbrc.1999.0356. PMID 10198228.
• Greenland KJ, Jantke I, Jenatschke S, et al. (2000). "The human NAD+-dependent 15-hydroxyprostaglandin dehydrogenase gene promoter is controlled by Ets and activating protein-1 transcription factors and progesterone". Endocrinology. 141 (2): 581–97. doi:10.1210/en.141.2.581. PMID 10650939.
• Conner CE, Kelly RW, Hume R (2001). "Regulation of prostaglandin availability in human fetal lung by differential localisation of prostaglandin H synthase-1 and prostaglandin dehydrogenase". Histochem. Cell Biol. 116 (4): 313–9. doi:10.1007/s004180100323. PMID 11702189.
• Giannoulias D, Patel FA, Holloway AC, et al. (2002). "Differential changes in 15-hydroxyprostaglandin dehydrogenase and prostaglandin H synthase (types I and II) in human pregnant myometrium". J. Clin. Endocrinol. Metab. 87 (3): 1345–52. doi:10.1210/jc.87.3.1345. PMID 11889207.
• Cho H, Tai HH (2003). "Threonine 11 of human NAD(+)-dependent 15-hydroxyprostaglandin dehydrogenase may interact with NAD(+) during catalysis". Prostaglandins Leukot. Essent. Fatty Acids. 66 (5–6): 505–9. doi:10.1054/plef.2002.0391. PMID 12144871.
• Strausberg RL, Feingold EA, Grouse LH, et al. (2003). "Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences". Proc. Natl. Acad. Sci. U.S.A. 99 (26): 16899–903. doi:10.1073/pnas.242603899. PMC 139241. PMID 12477932.
• Tai HH, Ensor CM, Zhou H, Yan F (2003). Structure and function of human NAD(+)-linked 15-hydroxyprostaglandin dehydrogenase. Advances in Experimental Medicine and Biology. Vol. 507. pp. 245–50. doi:10.1007/978-1-4615-0193-0_37. ISBN 978-1-4613-4960-0. PMID 12664592. {{cite book}}: |journal= ignored (help)
• McKeown KJ, Challis JR (2003). "Regulation of 15-hydroxy prostaglandin dehydrogenase by corticotrophin-releasing hormone through a calcium-dependent pathway in human chorion trophoblast cells". J. Clin. Endocrinol. Metab. 88 (4): 1737–41. doi:10.1210/jc.2002-021369. PMID 12679466.
• Patel FA, Funder JW, Challis JR (2003). "Mechanism of cortisol/progesterone antagonism in the regulation of 15-hydroxyprostaglandin dehydrogenase activity and messenger ribonucleic acid levels in human chorion and placental trophoblast cells at term". J. Clin. Endocrinol. Metab. 88 (6): 2922–33. doi:10.1210/jc.2002-021710. PMID 12788907.
• Nandy A, Jenatschke S, Hartung B, et al. (2004). "Genomic structure and transcriptional regulation of the human NAD+-dependent 15-hydroxyprostaglandin dehydrogenase gene". J. Mol. Endocrinol. 31 (1): 105–21. doi:10.1677/jme.0.0310105. PMID 12914529.