Abstract
Nek2 is a cell-cycle-regulated protein kinase that localizes to the centrosome and is likely to be involved in regulating centrosome structure at the G(2)/M transition. Here, we localize the functional human Nek2 gene to chromosome 1 and show that alternative polyadenylation signals provide a mechanism for generating two distinct isoforms. Sequencing of products generated by reverse transcriptase PCR, immunoblotting of cell extracts and transfection of antisense oligonucleotides together demonstrate that human Nek2 is expressed as two splice variants. These isoforms, designated Nek2A and Nek2B, are detected in primary blood lymphocytes as well as adult transformed cells. Nek2A and Nek2B, which can form homo- and hetero-dimers, both localize to the centrosome, although only Nek2A can induce centrosome splitting upon overexpression. Importantly, Nek2A and Nek2B exhibit distinct patterns of cell-cycle-dependent expression. Both are present in low amounts in the G(1) phase and exhibit increased abundance in the S and G(2) phases. However, Nek2A disappears in prometaphase-arrested cells, whereas Nek2B remains elevated. These results demonstrate that two alternative splice variants of the human centrosomal kinase Nek2 exist that differ in their expression patterns during mitosis. This has important implications for our understanding of both Nek2 protein kinase regulation and the control of centrosome structure during mitosis.
Full Text
The Full Text of this article is available as a PDF (309.0 KB).
Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Andersen S. S. Molecular characteristics of the centrosome. Int Rev Cytol. 1999;187:51–109. doi: 10.1016/s0074-7696(08)62416-x. [DOI] [PubMed] [Google Scholar]
- Andreassen P. R., Lacroix F. B., Villa-Moruzzi E., Margolis R. L. Differential subcellular localization of protein phosphatase-1 alpha, gamma1, and delta isoforms during both interphase and mitosis in mammalian cells. J Cell Biol. 1998 Jun 1;141(5):1207–1215. doi: 10.1083/jcb.141.5.1207. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Arama E., Yanai A., Kilfin G., Bernstein A., Motro B. Murine NIMA-related kinases are expressed in patterns suggesting distinct functions in gametogenesis and a role in the nervous system. Oncogene. 1998 Apr 9;16(14):1813–1823. doi: 10.1038/sj.onc.1201710. [DOI] [PubMed] [Google Scholar]
- Bornens M., Paintrand M., Berges J., Marty M. C., Karsenti E. Structural and chemical characterization of isolated centrosomes. Cell Motil Cytoskeleton. 1987;8(3):238–249. doi: 10.1002/cm.970080305. [DOI] [PubMed] [Google Scholar]
- Brinkley B. R. Managing the centrosome numbers game: from chaos to stability in cancer cell division. Trends Cell Biol. 2001 Jan;11(1):18–21. doi: 10.1016/s0962-8924(00)01872-9. [DOI] [PubMed] [Google Scholar]
- Calarco-Gillam P. D., Siebert M. C., Hubble R., Mitchison T., Kirschner M. Centrosome development in early mouse embryos as defined by an autoantibody against pericentriolar material. Cell. 1983 Dec;35(3 Pt 2):621–629. doi: 10.1016/0092-8674(83)90094-6. [DOI] [PubMed] [Google Scholar]
- Churcher Y., Moss S. E. Modulation of protein tyrosine phosphorylation during G1/S transition in activated human T-lymphoblasts. J Biol Chem. 1993 Dec 15;268(35):26144–26149. [PubMed] [Google Scholar]
- Doxsey S. The centrosome--a tiny organelle with big potential. Nat Genet. 1998 Oct;20(2):104–106. doi: 10.1038/2392. [DOI] [PubMed] [Google Scholar]
- Freed E., Lacey K. R., Huie P., Lyapina S. A., Deshaies R. J., Stearns T., Jackson P. K. Components of an SCF ubiquitin ligase localize to the centrosome and regulate the centrosome duplication cycle. Genes Dev. 1999 Sep 1;13(17):2242–2257. doi: 10.1101/gad.13.17.2242. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Fry A. M., Arnaud L., Nigg E. A. Activity of the human centrosomal kinase, Nek2, depends on an unusual leucine zipper dimerization motif. J Biol Chem. 1999 Jun 4;274(23):16304–16310. doi: 10.1074/jbc.274.23.16304. [DOI] [PubMed] [Google Scholar]
- Fry A. M., Descombes P., Twomey C., Bacchieri R., Nigg E. A. The NIMA-related kinase X-Nek2B is required for efficient assembly of the zygotic centrosome in Xenopus laevis. J Cell Sci. 2000 Jun;113(Pt 11):1973–1984. doi: 10.1242/jcs.113.11.1973. [DOI] [PubMed] [Google Scholar]
- Fry A. M., Faragher A. J. Identification of centrosome kinases. Methods Cell Biol. 2001;67:305–323. doi: 10.1016/s0091-679x(01)67021-3. [DOI] [PubMed] [Google Scholar]
- Fry A. M., Mayor T., Meraldi P., Stierhof Y. D., Tanaka K., Nigg E. A. C-Nap1, a novel centrosomal coiled-coil protein and candidate substrate of the cell cycle-regulated protein kinase Nek2. J Cell Biol. 1998 Jun 29;141(7):1563–1574. doi: 10.1083/jcb.141.7.1563. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Fry A. M., Mayor T., Nigg E. A. Regulating centrosomes by protein phosphorylation. Curr Top Dev Biol. 2000;49:291–312. doi: 10.1016/s0070-2153(99)49014-3. [DOI] [PubMed] [Google Scholar]
- Fry A. M., Meraldi P., Nigg E. A. A centrosomal function for the human Nek2 protein kinase, a member of the NIMA family of cell cycle regulators. EMBO J. 1998 Jan 15;17(2):470–481. doi: 10.1093/emboj/17.2.470. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Fry A. M., Nigg E. A. Characterization of mammalian NIMA-related kinases. Methods Enzymol. 1997;283:270–282. doi: 10.1016/s0076-6879(97)83022-4. [DOI] [PubMed] [Google Scholar]
- Fry A. M., Schultz S. J., Bartek J., Nigg E. A. Substrate specificity and cell cycle regulation of the Nek2 protein kinase, a potential human homolog of the mitotic regulator NIMA of Aspergillus nidulans. J Biol Chem. 1995 May 26;270(21):12899–12905. doi: 10.1074/jbc.270.21.12899. [DOI] [PubMed] [Google Scholar]
- Graf J. D., Kobel H. R. Genetics of Xenopus laevis. Methods Cell Biol. 1991;36:19–34. doi: 10.1016/s0091-679x(08)60270-8. [DOI] [PubMed] [Google Scholar]
- Heald R. Motor function in the mitotic spindle. Cell. 2000 Aug 18;102(4):399–402. doi: 10.1016/s0092-8674(00)00044-1. [DOI] [PubMed] [Google Scholar]
- Heald R., Tournebize R., Blank T., Sandaltzopoulos R., Becker P., Hyman A., Karsenti E. Self-organization of microtubules into bipolar spindles around artificial chromosomes in Xenopus egg extracts. Nature. 1996 Aug 1;382(6590):420–425. doi: 10.1038/382420a0. [DOI] [PubMed] [Google Scholar]
- Heald R., Tournebize R., Habermann A., Karsenti E., Hyman A. Spindle assembly in Xenopus egg extracts: respective roles of centrosomes and microtubule self-organization. J Cell Biol. 1997 Aug 11;138(3):615–628. doi: 10.1083/jcb.138.3.615. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Helps N. R., Luo X., Barker H. M., Cohen P. T. NIMA-related kinase 2 (Nek2), a cell-cycle-regulated protein kinase localized to centrosomes, is complexed to protein phosphatase 1. Biochem J. 2000 Jul 15;349(Pt 2):509–518. doi: 10.1042/0264-6021:3490509. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Kellogg D. R., Moritz M., Alberts B. M. The centrosome and cellular organization. Annu Rev Biochem. 1994;63:639–674. doi: 10.1146/annurev.bi.63.070194.003231. [DOI] [PubMed] [Google Scholar]
- Kelsell D. P., Rooke L., Warne D., Bouzyk M., Cullin L., Cox S., West L., Povey S., Spurr N. K. Development of a panel of monochromosomal somatic cell hybrids for rapid gene mapping. Ann Hum Genet. 1995 Apr;59(Pt 2):233–241. doi: 10.1111/j.1469-1809.1995.tb00743.x. [DOI] [PubMed] [Google Scholar]
- Khodjakov A., Cole R. W., Oakley B. R., Rieder C. L. Centrosome-independent mitotic spindle formation in vertebrates. Curr Biol. 2000 Jan 27;10(2):59–67. doi: 10.1016/s0960-9822(99)00276-6. [DOI] [PubMed] [Google Scholar]
- Khodjakov A., Rieder C. L. The sudden recruitment of gamma-tubulin to the centrosome at the onset of mitosis and its dynamic exchange throughout the cell cycle, do not require microtubules. J Cell Biol. 1999 Aug 9;146(3):585–596. doi: 10.1083/jcb.146.3.585. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Lu K. P., Hunter T. The NIMA kinase: a mitotic regulator in Aspergillus nidulans and vertebrate cells. Prog Cell Cycle Res. 1995;1:187–205. doi: 10.1007/978-1-4615-1809-9_15. [DOI] [PubMed] [Google Scholar]
- Mack G. J., Rees J., Sandblom O., Balczon R., Fritzler M. J., Rattner J. B. Autoantibodies to a group of centrosomal proteins in human autoimmune sera reactive with the centrosome. Arthritis Rheum. 1998 Mar;41(3):551–558. doi: 10.1002/1529-0131(199803)41:3<551::AID-ART22>3.0.CO;2-X. [DOI] [PubMed] [Google Scholar]
- Matthies H. J., McDonald H. B., Goldstein L. S., Theurkauf W. E. Anastral meiotic spindle morphogenesis: role of the non-claret disjunctional kinesin-like protein. J Cell Biol. 1996 Jul;134(2):455–464. doi: 10.1083/jcb.134.2.455. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Mayor T., Meraldi P., Stierhof Y. D., Nigg E. A., Fry A. M. Protein kinases in control of the centrosome cycle. FEBS Lett. 1999 Jun 4;452(1-2):92–95. doi: 10.1016/s0014-5793(99)00534-7. [DOI] [PubMed] [Google Scholar]
- Mayor T., Stierhof Y. D., Tanaka K., Fry A. M., Nigg E. A. The centrosomal protein C-Nap1 is required for cell cycle-regulated centrosome cohesion. J Cell Biol. 2000 Nov 13;151(4):837–846. doi: 10.1083/jcb.151.4.837. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Megraw T. L., Kao L. R., Kaufman T. C. Zygotic development without functional mitotic centrosomes. Curr Biol. 2001 Jan 23;11(2):116–120. doi: 10.1016/s0960-9822(01)00017-3. [DOI] [PubMed] [Google Scholar]
- Moritz M., Zheng Y., Alberts B. M., Oegema K. Recruitment of the gamma-tubulin ring complex to Drosophila salt-stripped centrosome scaffolds. J Cell Biol. 1998 Aug 10;142(3):775–786. doi: 10.1083/jcb.142.3.775. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Nigg E. A. Mitotic kinases as regulators of cell division and its checkpoints. Nat Rev Mol Cell Biol. 2001 Jan;2(1):21–32. doi: 10.1038/35048096. [DOI] [PubMed] [Google Scholar]
- Paintrand M., Moudjou M., Delacroix H., Bornens M. Centrosome organization and centriole architecture: their sensitivity to divalent cations. J Struct Biol. 1992 Mar-Apr;108(2):107–128. doi: 10.1016/1047-8477(92)90011-x. [DOI] [PubMed] [Google Scholar]
- Piel M., Meyer P., Khodjakov A., Rieder C. L., Bornens M. The respective contributions of the mother and daughter centrioles to centrosome activity and behavior in vertebrate cells. J Cell Biol. 2000 Apr 17;149(2):317–330. doi: 10.1083/jcb.149.2.317. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Puntoni F., Villa-Moruzzi E. Protein phosphatase-1 alpha, gamma 1, and delta: changes in phosphorylation and activity in mitotic HeLa cells and in cells released from the mitotic block. Arch Biochem Biophys. 1997 Apr 15;340(2):177–184. doi: 10.1006/abbi.1997.9889. [DOI] [PubMed] [Google Scholar]
- Rhee K., Wolgemuth D. J. The NIMA-related kinase 2, Nek2, is expressed in specific stages of the meiotic cell cycle and associates with meiotic chromosomes. Development. 1997 Jun;124(11):2167–2177. doi: 10.1242/dev.124.11.2167. [DOI] [PubMed] [Google Scholar]
- Richter J. D. Cytoplasmic polyadenylation in development and beyond. Microbiol Mol Biol Rev. 1999 Jun;63(2):446–456. doi: 10.1128/mmbr.63.2.446-456.1999. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Schnackenberg B. J., Khodjakov A., Rieder C. L., Palazzo R. E. The disassembly and reassembly of functional centrosomes in vitro. Proc Natl Acad Sci U S A. 1998 Aug 4;95(16):9295–9300. doi: 10.1073/pnas.95.16.9295. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Schultz S. J., Fry A. M., Sütterlin C., Ried T., Nigg E. A. Cell cycle-dependent expression of Nek2, a novel human protein kinase related to the NIMA mitotic regulator of Aspergillus nidulans. Cell Growth Differ. 1994 Jun;5(6):625–635. [PubMed] [Google Scholar]
- Sluder G., Hinchcliffe E. H. The coordination of centrosome reproduction with nuclear events during the cell cycle. Curr Top Dev Biol. 2000;49:267–289. doi: 10.1016/s0070-2153(99)49013-1. [DOI] [PubMed] [Google Scholar]
- Tanaka K., Parvinen M., Nigg E. A. The in vivo expression pattern of mouse Nek2, a NIMA-related kinase, indicates a role in both mitosis and meiosis. Exp Cell Res. 1997 Dec 15;237(2):264–274. doi: 10.1006/excr.1997.3788. [DOI] [PubMed] [Google Scholar]
- Tugendreich S., Tomkiel J., Earnshaw W., Hieter P. CDC27Hs colocalizes with CDC16Hs to the centrosome and mitotic spindle and is essential for the metaphase to anaphase transition. Cell. 1995 Apr 21;81(2):261–268. doi: 10.1016/0092-8674(95)90336-4. [DOI] [PubMed] [Google Scholar]
- Uto K., Nakajo N., Sagata N. Two structural variants of Nek2 kinase, termed Nek2A and Nek2B, are differentially expressed in Xenopus tissues and development. Dev Biol. 1999 Apr 15;208(2):456–464. doi: 10.1006/dbio.1999.9231. [DOI] [PubMed] [Google Scholar]
- Uto K., Sagata N. Nek2B, a novel maternal form of Nek2 kinase, is essential for the assembly or maintenance of centrosomes in early Xenopus embryos. EMBO J. 2000 Apr 17;19(8):1816–1826. doi: 10.1093/emboj/19.8.1816. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Wigley W. C., Fabunmi R. P., Lee M. G., Marino C. R., Muallem S., DeMartino G. N., Thomas P. J. Dynamic association of proteasomal machinery with the centrosome. J Cell Biol. 1999 May 3;145(3):481–490. doi: 10.1083/jcb.145.3.481. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Wittmann T., Hyman A., Desai A. The spindle: a dynamic assembly of microtubules and motors. Nat Cell Biol. 2001 Jan;3(1):E28–E34. doi: 10.1038/35050669. [DOI] [PubMed] [Google Scholar]
- Zimmerman W., Sparks C. A., Doxsey S. J. Amorphous no longer: the centrosome comes into focus. Curr Opin Cell Biol. 1999 Feb;11(1):122–128. doi: 10.1016/s0955-0674(99)80015-5. [DOI] [PubMed] [Google Scholar]
- de Saint Phalle B., Sullivan W. Spindle assembly and mitosis without centrosomes in parthenogenetic Sciara embryos. J Cell Biol. 1998 Jun 15;141(6):1383–1391. doi: 10.1083/jcb.141.6.1383. [DOI] [PMC free article] [PubMed] [Google Scholar]
