Cyclin A2

Cyclin A2

PDB rendering based on 1e9h.
Available structures
PDB Ortholog search: PDBe, RCSB
Identifiers
Symbols CCNA2 ; CCN1; CCNA
External IDs OMIM: 123835 MGI: 108069 HomoloGene: 55562 ChEMBL: 2582 GeneCards: CCNA2 Gene
RNA expression pattern
More reference expression data
Orthologs
Species Human Mouse
Entrez 890 12428
Ensembl ENSG00000145386 ENSMUSG00000027715
UniProt P20248 P51943
RefSeq (mRNA) NM_001237 NM_009828
RefSeq (protein) NP_001228 NP_033958
Location (UCSC) Chr 4:
121.82 – 121.82 Mb		 Chr 3:
36.56 – 36.57 Mb
PubMed search

Cyclin-A2 is a protein that in humans is encoded by the CCNA2 gene.[1] It is one of the two types of cyclin A: cyclin A1 is expressed during meiosis and embryogenesis while cyclin A2 is expressed in dividing somatic cells.[2]

Function

Cyclin A2 belongs to the cyclin family, whose members regulate cell cycle progression by interacting with CDK kinases. Cyclin A2 is unique in that it can activate two different CDK kinases; it binds CDK2 during S phase, and CDK1 during the transition from G2 to M phase.[3]

Cyclin A2 is synthesized at the onset of S phase and localizes to the nucleus, where the cyclin A2-CDK2 complex is implicated in the initiation and progression of DNA synthesis. Phosphorylation of CDC6 and MCM4 by the cyclin A2-CDK2 complex prevents re-replication of DNA during the cell cycle.[2]

Cyclin A2 is involved in the G2/M transition but it cannot independently form a maturation promoting factor (MPF).[4] Recent studies have shown that the cyclin A2-CDK1 complex triggers cyclin B1-CDK1 activation which results in chromatin condensation and the breakdown of the nuclear envelope.[5]

Regulation

The levels of cyclin A2 are tightly synchronized with the progression of the cell cycle.[6] Transcription initiates in late G1, peaks and plateaus in mid-S, and declines in G2.[6][2]

Cyclin A2 transcription is mostly regulated by the transcription factor E2F and begins in G1, after the R point.[6][2] Absence of cyclin A2 before the R point is due to the E2F inhibition by hypophosphorylated retinoblastoma protein (pRb). After the R point, pRb is phosphorylated and can no longer bind E2F, leading to cyclin A2 transcription.[7][8] The cyclin A2-CDK2 complex eventually phosphorylates E2F, turning off cyclin A2 transcription.[6] E2F promotes cyclin A2 transcription by de-repressing the promoter.[6][7]

Interactions

Cyclin A2 has been shown to interact with:

Clinical significance

Cyclin A2 (Ccna2) is a key protein involved in the direction of mammalian cardiac myocytes to grow and divide, and has been shown to induce cardiac repair following myocardial infarction.[17] Normally, Ccna2 is silenced postnatally in mammalian cardiac myocytes. Because of this gene silencing, adult heart muscle cells cannot divide readily to repair and regenerate after a heart attack.[17]

Ccna2 has been found to induce cardiac repair in small-animal models following myocardial infarction.[17] Preclinical trials involving injections of adenovirus which contained the Ccna2 gene into infarcted porcine (pig) hearts has shown to be protective of MI in pig hearts.[17] Ccna2 mediated cardiac repair showed both a decrease in fibrosis in the peri-infarct tissue and a greater number of cardiomyocytes at the sites of injection.[17] Delivery of Ccna2 into cardiac tissue invokes a regenerative response and markedly enhances cardiac function.[17][18][19]

Cancer

Increased expression of cyclin A2 has been observed in many types of cancer such as breast, cervical, liver, and lung among others.[2][20][21][22][23] While it is not clear whether increased expression of cyclin A2 is a cause or result of tumorigenesis, it is indicative of prognostic values such as predictions of survival or relapse.[2]

Overexpression of cyclin A2 in mammalian cells can result in the delayed onset of metaphase and anaphase.[24] It is also possible that cyclin A2-CDK contributes to tumorigenesis by the phosphorylation of oncoproteins or tumor suppressors like p53.[25]

See also

References

  1. ↑ Paterlini P, De Mitri MS, Martin C, Münnich A, Bréchot C (July 1991). "A TaqI polymorphism in the human cyclin A gene". Nucleic Acids Res. 19 (9): 2516. doi:10.1093/nar/19.9.2516. PMC 329485. PMID 1675006.
  2. 1 2 3 4 5 6 Yam CH, Fung TK, Poon RY (Aug 2002). "Cyclin A in cell cycle control and cancer". Cell. Mol. Life Sci. 59 (8): 1317–26. doi:10.1007/s00018-002-8510-y. PMID 12363035.
  3. ↑ Pagano M, Pepperkok R, Verde F, Ansorge W, Draetta G (March 1992). "Cyclin A is required at two points in the human cell cycle". EMBO J. 11 (3): 961–71. PMC 556537. PMID 1312467.
  4. ↑ Fung TK, Ma HT, Poon RY (Mar 2007). "Specialized roles of the two mitotic cyclins in somatic cells: cyclin A as an activator of M phase-promoting factor". Mol. Biol. Cell 18 (5): 1861–73. doi:10.1091/mbc.E06-12-1092. PMC 1855023. PMID 17344473.
  5. ↑ Gong D, Ferrell JE (Sep 2010). "The roles of cyclin A2, B1, and B2 in early and late mitotic events". Mol. Biol. Cell 21 (18): 3149–61. doi:10.1091/mbc.E10-05-0393. PMC 2938381. PMID 20660152.
  6. 1 2 3 4 5 Henglein B, Chenivesse X, Wang J, Eick D, Bréchot C (Jun 1994). "Structure and cell cycle-regulated transcription of the human cyclin A gene". Proc. Natl. Acad. Sci. U.S.A. 91 (12): 5490–4. doi:10.1073/pnas.91.12.5490. PMC 44021. PMID 8202514.
  7. 1 2 Woo RA, Poon RY (Jul–Aug 2003). "Cyclin-dependent kinases and S phase control in mammalian cells". Cell Cycle 2 (4): 316–24. doi:10.4161/cc.2.4.468. PMID 12851482.
  8. 1 2 Xu M, Sheppard KA, Peng CY, Yee AS, Piwnica-Worms H (1994). "Cyclin A/CDK2 binds directly to E2F-1 and inhibits the DNA-binding activity of E2F-1/DP-1 by phosphorylation". Mol. Cell. Biol. 14 (12): 8420–31. PMC 359381. PMID 7969176.
  9. ↑ Petersen BO, Lukas J, Sørensen CS, Bartek J, Helin K (January 1999). "Phosphorylation of mammalian CDC6 by cyclin A/CDK2 regulates its subcellular localization". EMBO J. 18 (2): 396–410. doi:10.1093/emboj/18.2.396. PMC 1171134. PMID 9889196.
  10. ↑ Saha P, Chen J, Thome KC, Lawlis SJ, Hou ZH, Hendricks M, Parvin JD, Dutta A (May 1998). "Human CDC6/Cdc18 associates with Orc1 and cyclin-cdk and is selectively eliminated from the nucleus at the onset of S phase". Mol. Cell. Biol. 18 (5): 2758–67. PMC 110655. PMID 9566895.
  11. ↑ Henneke G, Koundrioukoff S, Hübscher U (July 2003). "Phosphorylation of human Fen1 by cyclin-dependent kinase modulates its role in replication fork regulation". Oncogene 22 (28): 4301–13. doi:10.1038/sj.onc.1206606. PMID 12853968.
  12. ↑ Ohtoshi A, Maeda T, Higashi H, Ashizawa S, Yamada M, Hatakeyama M (January 2000). "beta3-endonexin as a novel inhibitor of cyclin A-associated kinase". Biochem. Biophys. Res. Commun. 267 (3): 947–52. doi:10.1006/bbrc.1999.2007. PMID 10673397.
  13. ↑ Dyson N, Dembski M, Fattaey A, Ngwu C, Ewen M, Helin K (December 1993). "Analysis of p107-associated proteins: p107 associates with a form of E2F that differs from pRB-associated E2F-1". J. Virol. 67 (12): 7641–7. PMC 238233. PMID 8230483.
  14. ↑ Joaquin M, Bessa M, Saville MK, Watson RJ (November 2002). "B-Myb overcomes a p107-mediated cell proliferation block by interacting with an N-terminal domain of p107". Oncogene 21 (52): 7923–32. doi:10.1038/sj.onc.1206001. PMID 12439743.
  15. ↑ Rosner M, Hengstschläger M (November 2004). "Tuberin binds p27 and negatively regulates its interaction with the SCF component Skp2". J. Biol. Chem. 279 (47): 48707–15. doi:10.1074/jbc.M405528200. PMID 15355997.
  16. ↑ Marti A, Wirbelauer C, Scheffner M, Krek W (May 1999). "Interaction between ubiquitin-protein ligase SCFSKP2 and E2F-1 underlies the regulation of E2F-1 degradation". Nat. Cell Biol. 1 (1): 14–9. doi:10.1038/8984. PMID 10559858.
  17. 1 2 3 4 5 6 Shapiro SD, Ranjan AK, Kawase Y, Cheng RK, Kara RJ, Bhattacharya R, Guzman-Martinez G, Sanz J, Garcia MJ, Chaudhry HW (2014). "Cyclin A2 induces cardiac regeneration after myocardial infarction through cytokinesis of adult cardiomyocytes". Sci Transl Med 6 (224): 224ra27. doi:10.1126/scitranslmed.3007668. PMID 24553388.
  18. ↑ Woo YJ, Panlilio CM, Cheng RK, Liao GP, Suarez EE, Atluri P, Chaudhry HW (2007). "Myocardial regeneration therapy for ischemic cardiomyopathy with cyclin A2". J. Thorac. Cardiovasc. Surg. 133 (4): 927–33. doi:10.1016/j.jtcvs.2006.07.057. PMID 17382628.
  19. ↑ Laflamme MA, Murry CE (2011). "Heart regeneration". Nature 473 (7347): 326–35. doi:10.1038/nature10147. PMC 4091722. PMID 21593865.
  20. ↑ Bukholm IR, Bukholm G, Nesland JM (Jul 2001). "Over-expression of cyclin A is highly associated with early relapse and reduced survival in patients with primary breast carcinomas". Int. J. Cancer 93 (2): 283–7. doi:10.1002/ijc.1311. PMID 11410878.
  21. ↑ Kanai M, Shiozawa T, Xin L, Nikaido T, Fujii S (May 1998). "Immunohistochemical detection of sex steroid receptors, cyclins, and cyclin-dependent kinases in the normal and neoplastic squamous epithelia of the uterine cervix". Cancer 82 (9): 1709–19. doi:10.1002/(sici)1097-0142(19980501)82:9<1709::aid-cncr18>3.0.co;2-8. PMID 9576293.
  22. ↑ Ohashi R, Gao C, Miyazaki M, Hamazaki K, Tsuji T, Inoue Y, Uemura T, Hirai R, Shimizu N, Namba M (Jan–Feb 2001). "Enhanced expression of cyclin E and cyclin A in human hepatocellular carcinomas". Anticancer Res. 21 (1B): 657–62. PMID 11299822.
  23. ↑ Volm M, Koomägi R, Mattern J, Stammler G (1997). "Cyclin A is associated with an unfavourable outcome in patients with non-small-cell lung carcinomas". Br. J. Cancer 75 (12): 1774–8. doi:10.1038/bjc.1997.302. PMC 2223613. PMID 9192980.
  24. ↑ den Elzen N, Pines J (Apr 2001). "Cyclin A is destroyed in prometaphase and can delay chromosome alignment and anaphase". J. Cell Biol. 153 (1): 121–36. doi:10.1083/jcb.153.1.121. PMC 2185531. PMID 11285279.
  25. ↑ Wang Y, Prives C (Jul 1995). "Increased and altered DNA binding of human p53 by S and G2/M but not G1 cyclin-dependent kinases". Nature 376 (6535): 88–91. doi:10.1038/376088a0. PMID 7596441.

Further reading

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