PPP1R14A
| PPP1R14A | |||
|---|---|---|---|
| Identifiers | |||
Gene ontology | |||
| Molecular function | |||
| Cellular component | |||
| Biological process | |||
| Sources:Amigo / QuickGO | |||
Ensembl |
| ||||||||
|---|---|---|---|---|---|---|---|---|---|
| UniProt | |||||||||
| RefSeq (mRNA) | |||||||||
| RefSeq (protein) | |||||||||
| Location (UCSC) | n/a | Chr 7: 28.99 – 28.99 Mb | |||||||
| PubMed search | [2] | [3] | |||||||
| View/Edit Human | View/Edit Mouse |
Protein phosphatase 1 regulatory subunit 14A also known as CPI-17 (C-kinase potentiated Protein phosphatase-1 Inhibitor Mr = 17 kDa) is a protein that in humans is encoded by the PPP1R14A gene.[4][5][6]
Function
CPI-17 is a
PAK
. Agonist stimulation of smooth muscle enhances CPI-17 phosphorylation mainly through PKC and ROCK. Myosin phosphatase inhibition increases myosin phosphorylation and smooth muscle contraction in the absence of increased intracellular Ca2+ concentration. This phenomenon is known as Ca2+ sensitization, which occurs in response to agonist stimulation of smooth muscle. In Purkinje neuron, CPI-17 is involved in long-term synaptic depression.
There are three homologues of CPI-17:
- Phosphatase Holoenzyme Inhibitor (PHI: PPP1R14B),
- Kinase Enhanced Phosphatase Inhibitor (KEPI: PPP1R14C), and
- Gastric-Brain Phosphatase Inhibitor (GBPI: PPP1R14D).
Clinical significance
CPI-17 is up-regulated some cancer cells, and causes hyperphosphorylation of tumor suppressor merlin/NF2.[7][6] In prostate cancer, CPI-17 expressions are reported to be associated with GWAS risk SNP rs7247241 T allele and increase cell proliferation. [8]
References
- ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000037166 – Ensembl, May 2017
- ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
- ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
- PMID 8720121.
- PMID 11467857.
- ^ a b "Entrez Gene: PPP1R14A protein phosphatase 1, regulatory (inhibitor) subunit 14A".
- PMID 19846560.
- PMID 34849858.
Further reading
- Eto M, Ohmori T, Suzuki M, Furuya K, Morita F (December 1995). "A novel protein phosphatase-1 inhibitory protein potentiated by protein kinase C. Isolation from porcine aorta media and characterization". Journal of Biochemistry. 118 (6): 1104–1107. PMID 8720121.
- Eto M, Senba S, Morita F, Yazawa M (June 1997). "Molecular cloning of a novel phosphorylation-dependent inhibitory protein of protein phosphatase-1 (CPI17) in smooth muscle: its specific localization in smooth muscle". FEBS Letters. 410 (2–3): 356–360. S2CID 83782622.
- Koyama M, Ito M, Feng J, Seko T, Shiraki K, Takase K, et al. (June 2000). "Phosphorylation of CPI-17, an inhibitory phosphoprotein of smooth muscle myosin phosphatase, by Rho-kinase". FEBS Letters. 475 (3): 197–200. S2CID 24077777.
- Hamaguchi T, Ito M, Feng J, Seko T, Koyama M, Machida H, et al. (August 2000). "Phosphorylation of CPI-17, an inhibitor of myosin phosphatase, by protein kinase N". Biochemical and Biophysical Research Communications. 274 (3): 825–830. PMID 10924361.
- Li Z, Yu L, Zhang Y, Gao J, Zhang P, Wan B, et al. (2002). "Identification of human, mouse and rat PPP1R14A, protein phosphatase-1 inhibitor subunit 14A, & mapping human PPP1R14A to chromosome 19q13.13-q13.2". Molecular Biology Reports. 28 (2): 91–101. S2CID 37230257.
- Dubois T, Howell S, Zemlickova E, Aitken A (April 2002). "Identification of casein kinase Ialpha interacting protein partners". FEBS Letters. 517 (1–3): 167–171. S2CID 84792445.
- Liu QR, Zhang PW, Lin Z, Li QF, Woods AS, Troncoso J, Uhl GR (January 2004). "GBPI, a novel gastrointestinal- and brain-specific PP1-inhibitory protein, is activated by PKC and inactivated by PKA". The Biochemical Journal. 377 (Pt 1): 171–181. PMID 12974676.
- Eto M, Kitazawa T, Brautigan DL (June 2004). "Phosphoprotein inhibitor CPI-17 specificity depends on allosteric regulation of protein phosphatase-1 by regulatory subunits". Proceedings of the National Academy of Sciences of the United States of America. 101 (24): 8888–8893. PMID 15184667.
- Zemlickova E, Johannes FJ, Aitken A, Dubois T (March 2004). "Association of CPI-17 with protein kinase C and casein kinase I". Biochemical and Biophysical Research Communications. 316 (1): 39–47. PMID 15003508.
- Kolosova IA, Ma SF, Adyshev DM, Wang P, Ohba M, Natarajan V, et al. (November 2004). "Role of CPI-17 in the regulation of endothelial cytoskeleton". American Journal of Physiology. Lung Cellular and Molecular Physiology. 287 (5): L970–L980. PMID 15234908.
- Jin H, Sperka T, Herrlich P, Morrison H (August 2006). "Tumorigenic transformation by CPI-17 through inhibition of a merlin phosphatase". Nature. 442 (7102): 576–579. PMID 16885985.
- Morin C, Sirois M, Echave V, Gomes MM, Rousseau E (May 2007). "Epoxyeicosatrienoic acid relaxing effects involve Ca2+-activated K+ channel activation and CPI-17 dephosphorylation in human bronchi". American Journal of Respiratory Cell and Molecular Biology. 36 (5): 633–641. PMID 17237191.
- Lartey J, Smith M, Pawade J, Strachan B, Mellor H, López Bernal A (June 2007). "Up-regulation of myometrial RHO effector proteins (PKN1 and DIAPH1) and CPI-17 (PPP1R14A) phosphorylation in human pregnancy is associated with increased GTP-RHOA in spontaneous preterm labor". Biology of Reproduction. 76 (6): 971–982. PMID 17301291.
- Eto M, Kitazawa T, Matsuzawa F, Aikawa S, Kirkbride JA, Isozumi N, et al. (December 2007). "Phosphorylation-induced conformational switching of CPI-17 produces a potent myosin phosphatase inhibitor". Structure. 15 (12): 1591–1602. PMID 18073109.
- Dimopoulos GJ, Semba S, Kitazawa K, Eto M, Kitazawa T (January 2007). "Ca2+-dependent rapid Ca2+ sensitization of contraction in arterial smooth muscle". Circulation Research. 100 (1): 121–129. PMID 17158339.
- Kim JI, Young GD, Jin L, Somlyo AV, Eto M (August 2009). "Expression of CPI-17 in smooth muscle during embryonic development and in neointimal lesion formation". Histochemistry and Cell Biology. 132 (2): 191–198. PMID 19437030.
- Kitazawa T, Semba S, Huh YH, Kitazawa K, Eto M (July 2009). "Nitric oxide-induced biphasic mechanism of vascular relaxation via dephosphorylation of CPI-17 and MYPT1". The Journal of Physiology. 587 (Pt 14): 3587–3603. PMID 19470783.
 | This article on a gene on human chromosome 19 is a stub. You can help Wikipedia by expanding it. |