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Proenkephalin

From Wikipedia, the free encyclopedia
Protein-coding gene in the species Homo sapiens

PENK
Available structures
PDBOrtholog search:PDBeRCSB
List of PDB id codes

1PLW,1PLX,2LWC,5E33,5E3A

Identifiers
AliasesPENK, proenkephalin, PE, PENK-A
External IDsOMIM:131330;MGI:104629;HomoloGene:4528;GeneCards:PENK;OMA:PENK - orthologs
Gene location (Human)
Chromosome 8 (human)
Chr.Chromosome 8 (human)[1]
Chromosome 8 (human)
Genomic location for PENK
Genomic location for PENK
Band8q12.1Start56,436,674bp[1]
End56,446,671bp[1]
Gene location (Mouse)
Chromosome 4 (mouse)
Chr.Chromosome 4 (mouse)[2]
Chromosome 4 (mouse)
Genomic location for PENK
Genomic location for PENK
Band4 A1|4 2.31 cMStart4,133,531bp[2]
End4,138,819bp[2]
RNA expression pattern
Bgee
HumanMouse (ortholog)
Top expressed in
  • nucleus accumbens

  • putamen

  • right testis

  • left testis

  • cartilage tissue

  • caudate nucleus

  • ganglionic eminence

  • middle frontal gyrus

  • external globus pallidus

  • urethra
Top expressed in
  • ciliary body

  • olfactory tubercle

  • nucleus accumbens

  • globus pallidus

  • superior frontal gyrus

  • efferent ductule

  • entorhinal cortex

  • calvaria

  • skin of external ear

  • iris
More reference expression data
BioGPS
n/a
Gene ontology
Molecular function
Cellular component
Biological process
Sources:Amigo /QuickGO
Orthologs
SpeciesHumanMouse
Entrez

5179

18619

Ensembl

ENSG00000181195

ENSMUSG00000045573

UniProt

P01210

P22005

RefSeq (mRNA)

NM_006211
NM_001135690

NM_001002927
NM_001348209

RefSeq (protein)

NP_001129162

NP_001002927
NP_001335138

Location (UCSC)Chr 8: 56.44 – 56.45 MbChr 4: 4.13 – 4.14 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Proenkephalin (PENK), formerly known asproenkephalin A (sinceproenkephalin B was renamedprodynorphin), is anendogenousopioidpolypeptidehormone which, viaproteolyiccleavage, produces theenkephalinpeptidesmet-enkephalin, and to a lesser extent,leu-enkephalin.[5] Upon cleavage, each proenkephalin peptide results in the generation of four copies of Met-enkephalin, two extended copies of met-enkephalin, and one copy of leu-enkephalin.[5] Contrarily, Leu-enkephalin is predominantly synthesized from prodynorphin, which produces three copies of it per cleavage, and no copies of Met-enkephalin. Other endogenous opioid peptides produced by proenkephalin includeadrenorphin,[6]amidorphin,[7]BAM-18,[8]BAM-20P,[9]BAM-22P,[9]peptide B,[10]peptide E,[11] andpeptide F.[12]

The following table lists the peptides that are derived from cleavage of the proenkephalin protein.[13]

PeptideAlternative NamesAmino acid positions
Met-enkephalinOpioid growth factor (OGF)107–111
PENK(114–133)Neuropeptide E; ENK-20114–133
Leu-enkephalin150–154
Met-enkephalin-Arg-PheMERF; Neuropeptide AF186–191
Met-enkephalin-Arg-Gly-LeuMERGL; Neuropeptide AM218–223
PENK(237–258)Neuropeptide F237–258

Clinical significance

[edit]

Proenkephalin is produced by themedium spiny neurons of thestriatum which undergo neurodegeneration in early stages ofHuntington's disease (HD). PENK[14] and related peptides[15][16] measured incerebrospinal fluid are proposed as potentialbiomarkers of disease progression in HD. Furthermore, PENK has been found associated with acute kidney injury[17] and glomerular filtration rate in steady-state and critically ill patients.[18][19]

See also

[edit]

References

[edit]
  1. ^abcGRCh38: Ensembl release 89: ENSG00000181195Ensembl, May 2017
  2. ^abcGRCm38: Ensembl release 89: ENSMUSG00000045573Ensembl, May 2017
  3. ^"Human PubMed Reference:".National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. ^"Mouse PubMed Reference:".National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. ^abDonald W. Pfaff (2002).Hormones, brain, and behavior. Elsevier. p. 173.ISBN 978-0-12-532109-9. Retrieved25 November 2011.
  6. ^Matsuo H, Miyata A, Mizuno K (1983). "Novel C-terminally amidated opioid peptide in human phaeochromocytoma tumour".Nature.305 (5936):721–723.Bibcode:1983Natur.305..721M.doi:10.1038/305721a0.PMID 6633641.S2CID 4320171.
  7. ^Seizinger BR, Liebisch DC, Gramsch C, Herz A, Weber E, Evans CJ, et al. (1985). "Isolation and structure of a novel C-terminally amidated opioid peptide, amidorphin, from bovine adrenal medulla".Nature.313 (5997):57–59.Bibcode:1985Natur.313...57S.doi:10.1038/313057a0.PMID 3965972.S2CID 4363051.
  8. ^Hurlbut DE, Evans CJ, Barchas JD, Leslie FM (June 1987). "Pharmacological properties of a proenkephalin A-derived opioid peptide: BAM 18".European Journal of Pharmacology.138 (3):359–366.doi:10.1016/0014-2999(87)90474-2.PMID 3040439.
  9. ^abMizuno K, Minamino N, Kangawa K, Matsuo H (December 1980). "A new family of endogenous "big" Met-enkephalins from bovine adrenal medulla: purification and structure of docosa- (BAM-22P) and eicosapeptide (BAM-20P) with very potent opiate activity".Biochemical and Biophysical Research Communications.97 (4):1283–1290.doi:10.1016/S0006-291X(80)80005-2.PMID 7213356.
  10. ^Micanovic R, Kruggel W, Ray P, Lewis RV (1984). "Purification and sequence of a non-opioid peptide derived from ovine proenkephalin: implications for possible species specific processing".Peptides.5 (5):853–856.doi:10.1016/0196-9781(84)90105-0.PMID 6504720.S2CID 3869685.
  11. ^Boarder MR, Evans C, Adams M, Erdelyi E, Barchas JD (December 1987). "Peptide E and its products, BAM 18 and Leu-enkephalin, in bovine adrenal medulla and cultured chromaffin cells: release in response to stimulation".Journal of Neurochemistry.49 (6):1824–1832.doi:10.1111/j.1471-4159.1987.tb02443.x.PMID 3681299.S2CID 19919675.
  12. ^Jones BN, Stern AS, Lewis RV, Kimura S, Stein S, Udenfriend S, et al. (October 1980). "Structure of two adrenal polypeptides containing multiple enkephalin sequences".Archives of Biochemistry and Biophysics.204 (1):392–395.doi:10.1016/0003-9861(80)90048-X.PMID 7425644.
  13. ^Salzet M, Tasiemski A (April 2001). "Involvement of pro-enkephalin-derived peptides in immunity".Developmental and Comparative Immunology.25 (3):177–85.doi:10.1016/s0145-305x(00)00047-1.PMID 11164883.
  14. ^Niemela V, Landtblom AM, Nyholm D, Kneider M, Constantinescu R, Paucar M, et al. (February 2021)."Proenkephalin Decreases in Cerebrospinal Fluid with Symptom Progression of Huntington's Disease".Movement Disorders.36 (2):481–491.doi:10.1002/mds.28391.PMC 7984171.PMID 33247616.
  15. ^Iadarola MJ, Mouradian MM (February 1989). "Decrease in a proenkephalin peptide in cerebrospinal fluid in Huntington's disease and progressive supranuclear palsy".Brain Research.479 (2):397–401.doi:10.1016/0006-8993(89)91648-X.PMID 2522341.S2CID 11033749.
  16. ^Barschke P, Abu-Rumeileh S, Al Shweiki MH, Barba L, Paolini Paoletti F, Oeckl P, et al. (September 2022)."Cerebrospinal fluid levels of proenkephalin and prodynorphin are differentially altered in Huntington's and Parkinson's disease".Journal of Neurology.269 (9):5136–5143.doi:10.1007/s00415-022-11187-8.PMC 9363351.PMID 35737109.S2CID 249930318.
  17. ^Lin LC, Chuan MH, Liu JH, Liao HW, Ng LL, Magnusson M, et al. (December 2023)."Proenkephalin as a biomarker correlates with acute kidney injury: a systematic review with meta-analysis and trial sequential analysis".Critical Care.27 (1): 481.doi:10.1186/s13054-023-04747-5.PMC 10702091.PMID 38057904.
  18. ^Beunders R, Donato LJ, van Groenendael R, Arlt B, Carvalho-Wodarz C, Schulte J, et al. (November 2023)."Assessing GFR With Proenkephalin".Kidney International Reports.8 (11):2345–2355.doi:10.1016/j.ekir.2023.08.006.PMC 10658254.PMID 38025210.
  19. ^Beunders R, van Groenendael R, Leijte GP, Kox M, Pickkers P (September 2020)."Proenkephalin Compared to Conventional Methods to Assess Kidney Function in Critically Ill Sepsis Patients".Shock.54 (3):308–314.doi:10.1097/SHK.0000000000001510.PMC 7458088.PMID 31977957.

External links

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