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Reliable, easy-to-read patient information on common medical conditions β written in plain language, free of jargon, and grounded in current evidence. Browse the most frequent diagnoses, understand what they mean for everyday life, and learn which steps and questions help you have a focused conversation with your doctor.
PCSK6
Introduction
Proprotein convertase subtilisin/kexin type 6 is an enzyme that in humans is encoded by the PCSK6 gene.[1][2] PCSK6 is a protease that cleaves NODAL into an active form to help trigger the development of left/right (LR) asymmetry.[3] It may also be involved in left and right handedness in humans.[4][5][6]
Function
Function
The protein encoded by this gene belongs to the subtilisin-like proprotein convertase family. The members of this family are proprotein convertases that process latent precursor proteins into their biologically active products. This encoded protein is a calcium-dependent serine endoprotease that can cleave precursor protein at their paired basic amino acid processing sites. Some of its substrates are – transforming growth factor beta related proteins, proalbumin, and von Willebrand factor. Alternatively spliced transcript variants encoding different isoforms have been identified.[2]
PCSK6 also cleaves and activates corin, a serine protease that regulates sodium homeostasis and blood pressure.[7]
Clinical significance
Clinical significance
This gene is thought to play a role in tumor progression.[2]
PCSK6 deficiency causes salt-sensitive hypertension in mice.[7]
References
References
- β Kiefer MC, Tucker JE, Joh R, Landsberg KE, Saltman D, Barr PJ (Jan 1992). “Identification of a second human subtilisin-like protease gene in the fes/fps region of chromosome 15”. DNA Cell Biol. 10 (10): 757β69. doi:10.1089/dna.1991.10.757. PMIDΒ 1741956.
- β 2.0 2.1 2.2 “Entrez Gene: PCSK6 proprotein convertase subtilisin/kexin type 6”.
- β Constam DB, Robertson EJ (May 1, 2000). “SPC4/PACE4 regulates a TGFbeta signaling network during axis formation”. Genes & Development. 14 (9): 1146β55. doi:10.1101/gad.14.9.1146. PMCΒ 316583. PMIDΒ 10809672.
- β Scerri TS, Brandler WM, Paracchini S, Morris AP, Ring SM, Richardson AJ, Talcott JB, Stein J, Monaco AP (Feb 1, 2011). “PCSK6 is associated with handedness in individuals with dyslexia”. Human Molecular Genetics. 20 (3): 608β14. doi:10.1093/hmg/ddq475. PMCΒ 3016905. PMIDΒ 21051773.
- β Brandler WM, Morris AP, Evans DM, Scerri TS, Kemp JP, Timpson NJ, St Pourcain B, Smith GD, Ring SM, Stein J, Monaco AP, Talcott JB, Fisher SE, Webber C, Paracchini S (September 2013). “Common variants in left/right asymmetry genes and pathways are associated with relative hand skill”. PLOS Genetics. 9 (9): e1003751. doi:10.1371/journal.pgen.1003751. PMCΒ 3772043. PMIDΒ 24068947.
- β Shore R, Covill L, Pettigrew KA, Brandler WM, Diaz R, Xu Y, Tello JA, Talcott JB, Newbury DF, Stein J, Monaco AP, Paracchini S (March 16, 2016). “The handedness-associated PCSK6 locus spans an intronic promoter regulating novel transcripts”. Human Molecular Genetics. 25 (6): 1771β1779. doi:10.1093/hmg/ddw047. PMCΒ 4986331. PMIDΒ 26908617.
- β 7.0 7.1 Chen S, Cao P, Dong N, Peng J, Zhang C, Wang H, Zhou T, Yang J, Zhang Y, Martelli EE, Naga Prasad SV, Miller RE, Malfait AM, Zhou Y, Wu Q (Sep 2015). “PCSK6-mediated corin activation is essential for normal blood pressure”. Nature Medicine. 21 (9): 1048β53. doi:10.1038/nm.3920. PMCΒ 4710517. PMIDΒ 26259032.
Further reading
Further reading
- Shore R, Covill L, Pettigrew KA, Diaz R, Xu Y, Tello J, Talcott J, Newbury D, Stein J, Monaco A (2016). “The handedness-associated PCSK6 locus spans an intronic promoter regulating novel transcripts”. Hum Mol Gen. 25 (9): 1771β1779. doi:10.1093/hmg/ddw047. PMIDΒ 26604689.
- Bassi DE, Mahloogi H, Klein-Szanto AJ (2000). “The proprotein convertases furin and PACE4 play a significant role in tumor progression”. Mol. Carcinog. 28 (2): 63β9. doi:10.1002/1098-2744(200006)28:2<63::AID-MC1>3.0.CO;2-C. PMIDΒ 10900462.
- Moulard M, Decroly E (2001). “Maturation of HIV envelope glycoprotein precursors by cellular endoproteases”. Biochim. Biophys. Acta. 1469 (3): 121β32. doi:10.1016/S0304-4157(00)00014-9. PMIDΒ 11063880.
- Seidah NG, Prat A (2003). “Precursor convertases in the secretory pathway, cytosol and extracellular milieu”. Essays Biochem. 38: 79β94. PMIDΒ 12463163.
- Tsuji A, Higashine K, Hine C, Mori K, Tamai Y, Nagamune H, Matsuda Y (1994). “Identification of novel cDNAs encoding human kexin-like protease, PACE4 isoforms”. Biochem. Biophys. Res. Commun. 204 (3): 1381β2. doi:10.1006/bbrc.1994.2616. PMIDΒ 7980617.
- Tsuji A, Higashine K, Hine C, Mori K, Tamai Y, Nagamune H, Matsuda Y (1994). “Identification of novel cDNAs encoding human kexin-like protease, PACE4 isoforms”. Biochem. Biophys. Res. Commun. 200 (2): 943β50. doi:10.1006/bbrc.1994.1541. PMIDΒ 8179631.
- Vollenweider F, Benjannet S, Decroly E, Savaria D, Lazure C, Thomas G, ChrΓ©tien M, Seidah NG (1996). “Comparative cellular processing of the human immunodeficiency virus (HIV-1) envelope glycoprotein gp160 by the mammalian subtilisin/kexin-like convertases”. Biochem. J. 314 (Pt 2): 521β32. PMCΒ 1217081. PMIDΒ 8670066.
- Zhong M, Benjannet S, Lazure C, Munzer S, Seidah NG (1997). “Functional analysis of human PACE4-A and PACE4-C isoforms: identification of a new PACE4-CS isoform”. FEBS Lett. 396 (1): 31β6. doi:10.1016/0014-5793(96)01059-9. PMIDΒ 8906861.
- Decroly E, Wouters S, Di Bello C, Lazure C, Ruysschaert JM, Seidah NG (1997). “Identification of the paired basic convertases implicated in HIV gp160 processing based on in vitro assays and expression in CD4(+) cell lines”. J. Biol. Chem. 271 (48): 30442β50. doi:10.1074/jbc.271.48.30442. PMIDΒ 8940009.
- Inocencio NM, Sucic JF, Moehring JM, Spence MJ, Moehring TJ (1997). “Endoprotease activities other than furin and PACE4 with a role in processing of HIV-I gp160 glycoproteins in CHO-K1 cells”. J. Biol. Chem. 272 (2): 1344β8. doi:10.1074/jbc.272.2.1344. PMIDΒ 8995442.
- Mori K, Kii S, Tsuji A, Nagahama M, Imamaki A, Hayashi K, Akamatsu T, Nagamune H, Matsuda Y (1997). “A novel human PACE4 isoform, PACE4E is an active processing protease containing a hydrophobic cluster at the carboxy terminus”. J. Biochem. 121 (5): 941β8. doi:10.1093/oxfordjournals.jbchem.a021677. PMIDΒ 9192737.
- Tsuji A, Hine C, Tamai Y, Yonemoto K, Mori K, Yoshida S, Bando M, Sakai E, Mori K, Akamatsu T, Matsuda Y (1997). “Genomic organization and alternative splicing of human PACE4 (SPC4), kexin-like processing endoprotease”. J. Biochem. 122 (2): 438β52. doi:10.1093/oxfordjournals.jbchem.a021772. PMIDΒ 9378725.
- Moulard M, Chaloin L, Canarelli S, Mabrouk K, Darbon H, Challoin L (1998). “Retroviral envelope glycoprotein processing: structural investigation of the cleavage site”. Biochemistry. 37 (13): 4510β7. doi:10.1021/bi972662f. PMIDΒ 9521771.
- Nagahama M, Taniguchi T, Hashimoto E, Imamaki A, Mori K, Tsuji A, Matsuda Y (1998). “Biosynthetic processing and quaternary interactions of proprotein convertase SPC4 (PACE4)”. FEBS Lett. 434 (1β2): 155β9. doi:10.1016/S0014-5793(98)00970-3. PMIDΒ 9738469.
- Viale A, Ortola C, Hervieu G, Furuta M, Barbero P, Steiner DF, Seidah NG, Nahon JL (1999). “Cellular localization and role of prohormone convertases in the processing of pro-melanin concentrating hormone in mammals”. J. Biol. Chem. 274 (10): 6536β45. doi:10.1074/jbc.274.10.6536. PMIDΒ 10037747.
- Mori K, Imamaki A, Nagata K, Yonetomi Y, Kiyokage-Yoshimoto R, Martin TJ, Gillespie MT, Nagahama M, Tsuji A, Matsuda Y (1999). “Subtilisin-like proprotein convertases, PACE4 and PC8, as well as furin, are endogenous proalbumin convertases in HepG2 cells”. J. Biochem. 125 (3): 627β33. doi:10.1093/oxfordjournals.jbchem.a022329. PMIDΒ 10050053.
- Sucic JF, Moehring JM, Inocencio NM, Luchini JW, Moehring TJ (1999). “Endoprotease PACE4 is Ca2+-dependent and temperature-sensitive and can partly rescue the phenotype of a furin-deficient cell strain”. Biochem. J. 339 (3): 639β47. doi:10.1042/0264-6021:3390639. PMCΒ 1220200. PMIDΒ 10215603.
- Tsuji A, Yoshida S, Hasegawa S, Bando M, Yoshida I, Koide S, Mori K, Matsuda Y (2000). “Human subtilisin-like proprotein convertase, PACE4 (SPC4) gene expression is highly regulated through E-box elements in HepG2 and GH4C1 cells”. J. Biochem. 126 (3): 494β502. doi:10.1093/oxfordjournals.jbchem.a022478. PMIDΒ 10467164.
