// Workers AI · dad joke modeWhy did CDC14B go to therapy? It had a cell-ebration issue.

CDC14B
Identifiers
Aliases	CDC14B, CDC14B3, Cdc14B1, Cdc14B2, hcell division cycle 14B
External IDs	OMIM: 603505; MGI: 2441808; HomoloGene: 104197; GeneCards: CDC14B; OMA:CDC14B - orthologs
Available structures PDB Ortholog search: PDBe RCSB List of PDB id codes 1OHC, 1OHD, 1OHE
Enzyme activity EC # BRENDA ExPASy KEGG MetaCyc 3.1.3.16 ↗ ↗ ↗ ↗ 3.1.3.48 ↗ ↗ ↗ ↗
Gene location (Human) Chr. Chromosome 9 (human) Band 9q22.32-q22.33 Start 96,490,241 bp End 96,619,843 bp
Gene location (Mouse) Chr. Chromosome 13 (mouse) Band 13|13 B3 Start 64,189,268 bp End 64,275,290 bp
RNA expression pattern Bgee Human Mouse (ortholog) Top expressed in corpus callosum tendon of biceps brachii internal globus pallidus optic nerve retinal pigment epithelium C1 segment gonad inferior ganglion of vagus nerve bronchial epithelial cell seminal vesicula Top expressed in hand Epithelium of choroid plexus spermatid primitive streak gastrula maxillary prominence left lobe of liver mandibular prominence tail of embryo atrium More reference expression data BioGPS n/a
Gene ontology Molecular function protein tyrosine phosphatase activity phosphoprotein phosphatase activity hydrolase activity protein tyrosine/serine/threonine phosphatase activity phosphatase activity protein binding protein serine/threonine phosphatase activity Cellular component nucleus nucleolus cytoplasm nucleoplasm spindle pole centrosome mitotic spindle Biological process DNA repair cellular response to DNA damage stimulus dephosphorylation protein dephosphorylation peptidyl-tyrosine dephosphorylation positive regulation of ubiquitin protein ligase activity regulation of exit from mitosis mitotic spindle midzone assembly cilium assembly mitotic G2 DNA damage checkpoint signaling microtubule cytoskeleton organization mitotic cell cycle positive regulation of cytokinesis Sources:Amigo / QuickGO
Orthologs Species Human Mouse Entrez 8555 218294 Ensembl ENSG00000081377 ENSMUSG00000033102 UniProt O60729 Q6PFY9 RefSeq (mRNA) NM_001077181 NM_003671 NM_033331 NM_033332 NM_001351567 NM_001351568 NM_001351569 NM_001351570 NM_001122989 NM_172587 RefSeq (protein) NP_001070649 NP_003662 NP_201588 NP_001338496 NP_001338497 NP_001338498 NP_001338499 NP_001116461 NP_766175 Location (UCSC) Chr 9: 96.49 – 96.62 Mb Chr 13: 64.19 – 64.28 Mb PubMed search
Wikidata
View/Edit Human View/Edit Mouse

Dual specificity protein phosphatase CDC14B is an enzyme that in humans is encoded by the CDC14B gene.

The protein encoded by this gene is a member of the dual specificity protein tyrosine phosphatase family. This protein is highly similar to Saccharomyces cerevisiae Cdc14, a protein tyrosine phosphatase involved in the exit of cell mitosis and initiation of DNA replication, which suggests the role in cell cycle control. Specifically, it is thought to fulfil this role by bundling and stabilising microtubules. This protein has been shown to interact with and dephosphorylates tumor suppressor protein p53, and is thought to regulate the function of p53. Alternative splicing of this gene results in 3 transcript variants encoding distinct isoforms.

Interactions and Functions

CDC14B has been shown to interact with p53, de-phosphorylate p53 at Serine 315 and potentially modulate p53 stability. At the patho-physiological level, mice with CDC14B deletion were shown to exhibit early-onset ageing phenotypes.

Further reading

• Maruyama K, Sugano S (January 1994). "Oligo-capping: a simple method to replace the cap structure of eukaryotic mRNAs with oligoribonucleotides". Gene. 138 (1–2): 171–174. doi:10.1016/0378-1119(94)90802-8. PMID 8125298.
• Suzuki Y, Yoshitomo-Nakagawa K, Maruyama K, Suyama A, Sugano S (October 1997). "Construction and characterization of a full length-enriched and a 5'-end-enriched cDNA library". Gene. 200 (1–2): 149–156. doi:10.1016/S0378-1119(97)00411-3. PMID 9373149.
• Li L, Ljungman M, Dixon JE (January 2000). "The human Cdc14 phosphatases interact with and dephosphorylate the tumor suppressor protein p53". The Journal of Biological Chemistry. 275 (4): 2410–2414. doi:10.1074/jbc.275.4.2410. PMID 10644693.
• Mailand N, Lukas C, Kaiser BK, Jackson PK, Bartek J, Lukas J (April 2002). "Deregulated human Cdc14A phosphatase disrupts centrosome separation and chromosome segregation". Nature Cell Biology. 4 (4): 317–322. doi:10.1038/ncb777. PMID 11901424. S2CID 28955777.
• Kaiser BK, Zimmerman ZA, Charbonneau H, Jackson PK (July 2002). "Disruption of centrosome structure, chromosome segregation, and cytokinesis by misexpression of human Cdc14A phosphatase". Molecular Biology of the Cell. 13 (7): 2289–2300. doi:10.1091/mbc.01-11-0535. PMC 117313. PMID 12134069.
• Dryden SC, Nahhas FA, Nowak JE, Goustin AS, Tainsky MA (May 2003). "Role for human SIRT2 NAD-dependent deacetylase activity in control of mitotic exit in the cell cycle". Molecular and Cellular Biology. 23 (9): 3173–3185. doi:10.1128/MCB.23.9.3173-3185.2003. PMC 153197. PMID 12697818.
• Gray CH, Good VM, Tonks NK, Barford D (July 2003). "The structure of the cell cycle protein Cdc14 reveals a proline-directed protein phosphatase". The EMBO Journal. 22 (14): 3524–3535. doi:10.1093/emboj/cdg348. PMC 165618. PMID 12853468.
• Nalepa G, Harper JW (October 2004). "Visualization of a highly organized intranuclear network of filaments in living mammalian cells". Cell Motility and the Cytoskeleton. 59 (2): 94–108. doi:10.1002/cm.20023. PMID 15362113.
• Cho HP, Liu Y, Gomez M, Dunlap J, Tyers M, Wang Y (June 2005). "The dual-specificity phosphatase CDC14B bundles and stabilizes microtubules". Molecular and Cellular Biology. 25 (11): 4541–4551. doi:10.1128/MCB.25.11.4541-4551.2005. PMC 1140622. PMID 15899858.
• Vázquez-Novelle MD, Esteban V, Bueno A, Sacristán MP (August 2005). "Functional homology among human and fission yeast Cdc14 phosphatases". The Journal of Biological Chemistry. 280 (32): 29144–29150. doi:10.1074/jbc.M413328200. hdl:10366/157107. PMID 15911625.

External links

• Human CDC14B genome location and CDC14B gene details page in the UCSC Genome Browser.