Abstract
We have constructed a fluorescent alpha-satellite DNA-binding protein to explore the motile and mechanical properties of human centromeres. A fusion protein consisting of human CENP-B coupled to the green fluorescent protein (GFP) of A. victoria specifically targets to centromeres when expressed in human cells. Morphometric analysis revealed that the alpha-satellite DNA domain bound by CENPB-GFP becomes elongated in mitosis in a microtubule-dependent fashion. Time lapse confocal microscopy in live mitotic cells revealed apparent elastic deformations of the central domain of the centromere that occurred during metaphase chromosome oscillations. These observations demonstrate that the interior region of the centromere behaves as an elastic element that could play a role in the mechanoregulatory mechanisms recently identified at centromeres. Fluorescent labeling of centromeres revealed that they disperse throughout the nucleus in a nearly isometric expansion during chromosome decondensation in telophase and early G1. During interphase, centromeres were primarily stationary, although motility of individual or small groups of centromeres was occasionally observed at very slow rates of 7-10 microns/h.
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- Ault J. G., Nicklas R. B. Tension, microtubule rearrangements, and the proper distribution of chromosomes in mitosis. Chromosoma. 1989 Jun;98(1):33–39. doi: 10.1007/BF00293332. [DOI] [PubMed] [Google Scholar]
- Bartholdi M. F. Nuclear distribution of centromeres during the cell cycle of human diploid fibroblasts. J Cell Sci. 1991 Jun;99(Pt 2):255–263. doi: 10.1242/jcs.99.2.255. [DOI] [PubMed] [Google Scholar]
- Blennow E., Telenius H., de Vos D., Larsson C., Henriksson P., Johansson O., Carter N. P., Nordenskjöld M. Tetrasomy 15q: two marker chromosomes with no detectable alpha-satellite DNA. Am J Hum Genet. 1994 May;54(5):877–883. [PMC free article] [PubMed] [Google Scholar]
- Bloom K. S., Amaya E., Carbon J., Clarke L., Hill A., Yeh E. Chromatin conformation of yeast centromeres. J Cell Biol. 1984 Nov;99(5):1559–1568. doi: 10.1083/jcb.99.5.1559. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Brenner S., Pepper D., Berns M. W., Tan E., Brinkley B. R. Kinetochore structure, duplication, and distribution in mammalian cells: analysis by human autoantibodies from scleroderma patients. J Cell Biol. 1981 Oct;91(1):95–102. doi: 10.1083/jcb.91.1.95. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Chalfie M., Tu Y., Euskirchen G., Ward W. W., Prasher D. C. Green fluorescent protein as a marker for gene expression. Science. 1994 Feb 11;263(5148):802–805. doi: 10.1126/science.8303295. [DOI] [PubMed] [Google Scholar]
- Clarke L., Carbon J. Isolation of a yeast centromere and construction of functional small circular chromosomes. Nature. 1980 Oct 9;287(5782):504–509. doi: 10.1038/287504a0. [DOI] [PubMed] [Google Scholar]
- Compton D. A., Yen T. J., Cleveland D. W. Identification of novel centromere/kinetochore-associated proteins using monoclonal antibodies generated against human mitotic chromosome scaffolds. J Cell Biol. 1991 Mar;112(6):1083–1097. doi: 10.1083/jcb.112.6.1083. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Cooke C. A., Bernat R. L., Earnshaw W. C. CENP-B: a major human centromere protein located beneath the kinetochore. J Cell Biol. 1990 May;110(5):1475–1488. doi: 10.1083/jcb.110.5.1475. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Cremer T., Kurz A., Zirbel R., Dietzel S., Rinke B., Schröck E., Speicher M. R., Mathieu U., Jauch A., Emmerich P. Role of chromosome territories in the functional compartmentalization of the cell nucleus. Cold Spring Harb Symp Quant Biol. 1993;58:777–792. doi: 10.1101/sqb.1993.058.01.085. [DOI] [PubMed] [Google Scholar]
- Cyert M. S., Scherson T., Kirschner M. W. Monoclonal antibodies specific for thiophosphorylated proteins recognize Xenopus MPF. Dev Biol. 1988 Sep;129(1):209–216. doi: 10.1016/0012-1606(88)90175-3. [DOI] [PubMed] [Google Scholar]
- Earnshaw W. C., Ratrie H., 3rd, Stetten G. Visualization of centromere proteins CENP-B and CENP-C on a stable dicentric chromosome in cytological spreads. Chromosoma. 1989 Jun;98(1):1–12. doi: 10.1007/BF00293329. [DOI] [PubMed] [Google Scholar]
- Earnshaw W. C., Sullivan K. F., Machlin P. S., Cooke C. A., Kaiser D. A., Pollard T. D., Rothfield N. F., Cleveland D. W. Molecular cloning of cDNA for CENP-B, the major human centromere autoantigen. J Cell Biol. 1987 Apr;104(4):817–829. doi: 10.1083/jcb.104.4.817. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Ferguson M., Ward D. C. Cell cycle dependent chromosomal movement in pre-mitotic human T-lymphocyte nuclei. Chromosoma. 1992 Aug;101(9):557–565. doi: 10.1007/BF00660315. [DOI] [PubMed] [Google Scholar]
- Funabiki H., Hagan I., Uzawa S., Yanagida M. Cell cycle-dependent specific positioning and clustering of centromeres and telomeres in fission yeast. J Cell Biol. 1993 Jun;121(5):961–976. doi: 10.1083/jcb.121.5.961. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Giménez-Abián J. F., Clarke D. J., Mullinger A. M., Downes C. S., Johnson R. T. A postprophase topoisomerase II-dependent chromatid core separation step in the formation of metaphase chromosomes. J Cell Biol. 1995 Oct;131(1):7–17. doi: 10.1083/jcb.131.1.7. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Gorbsky G. J., Ricketts W. A. Differential expression of a phosphoepitope at the kinetochores of moving chromosomes. J Cell Biol. 1993 Sep;122(6):1311–1321. doi: 10.1083/jcb.122.6.1311. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Haaf T., Schmid M. Chromosome topology in mammalian interphase nuclei. Exp Cell Res. 1991 Feb;192(2):325–332. doi: 10.1016/0014-4827(91)90048-y. [DOI] [PubMed] [Google Scholar]
- Haaf T., Warburton P. E., Willard H. F. Integration of human alpha-satellite DNA into simian chromosomes: centromere protein binding and disruption of normal chromosome segregation. Cell. 1992 Aug 21;70(4):681–696. doi: 10.1016/0092-8674(92)90436-g. [DOI] [PubMed] [Google Scholar]
- Haaf T., Ward D. C. Structural analysis of alpha-satellite DNA and centromere proteins using extended chromatin and chromosomes. Hum Mol Genet. 1994 May;3(5):697–709. doi: 10.1093/hmg/3.5.697. [DOI] [PubMed] [Google Scholar]
- Hirano T., Mitchison T. J. A heterodimeric coiled-coil protein required for mitotic chromosome condensation in vitro. Cell. 1994 Nov 4;79(3):449–458. doi: 10.1016/0092-8674(94)90254-2. [DOI] [PubMed] [Google Scholar]
- Hirano T., Mitchison T. J., Swedlow J. R. The SMC family: from chromosome condensation to dosage compensation. Curr Opin Cell Biol. 1995 Jun;7(3):329–336. doi: 10.1016/0955-0674(95)80087-5. [DOI] [PubMed] [Google Scholar]
- Hiraoka Y., Minden J. S., Swedlow J. R., Sedat J. W., Agard D. A. Focal points for chromosome condensation and decondensation revealed by three-dimensional in vivo time-lapse microscopy. Nature. 1989 Nov 16;342(6247):293–296. doi: 10.1038/342293a0. [DOI] [PubMed] [Google Scholar]
- Hiraoka Y., Sedat J. W., Agard D. A. Determination of three-dimensional imaging properties of a light microscope system. Partial confocal behavior in epifluorescence microscopy. Biophys J. 1990 Feb;57(2):325–333. doi: 10.1016/S0006-3495(90)82534-0. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Holloway S. L., Glotzer M., King R. W., Murray A. W. Anaphase is initiated by proteolysis rather than by the inactivation of maturation-promoting factor. Cell. 1993 Jul 2;73(7):1393–1402. doi: 10.1016/0092-8674(93)90364-v. [DOI] [PubMed] [Google Scholar]
- Hyman A. A., Mitchison T. J. Modulation of microtubule stability by kinetochores in vitro. J Cell Biol. 1990 May;110(5):1607–1616. doi: 10.1083/jcb.110.5.1607. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hyman A. A., Mitchison T. J. Two different microtubule-based motor activities with opposite polarities in kinetochores. Nature. 1991 May 16;351(6323):206–211. doi: 10.1038/351206a0. [DOI] [PubMed] [Google Scholar]
- Ikeno M., Masumoto H., Okazaki T. Distribution of CENP-B boxes reflected in CREST centromere antigenic sites on long-range alpha-satellite DNA arrays of human chromosome 21. Hum Mol Genet. 1994 Aug;3(8):1245–1257. doi: 10.1093/hmg/3.8.1245. [DOI] [PubMed] [Google Scholar]
- Inoué S., Salmon E. D. Force generation by microtubule assembly/disassembly in mitosis and related movements. Mol Biol Cell. 1995 Dec;6(12):1619–1640. doi: 10.1091/mbc.6.12.1619. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Janevski J., Park P. C., De Boni U. Organization of centromeric domains in hepatocyte nuclei: rearrangement associated with de novo activation of the vitellogenin gene family in Xenopus laevis. Exp Cell Res. 1995 Apr;217(2):227–239. doi: 10.1006/excr.1995.1082. [DOI] [PubMed] [Google Scholar]
- Jordan M. A., Thrower D., Wilson L. Effects of vinblastine, podophyllotoxin and nocodazole on mitotic spindles. Implications for the role of microtubule dynamics in mitosis. J Cell Sci. 1992 Jul;102(Pt 3):401–416. doi: 10.1242/jcs.102.3.401. [DOI] [PubMed] [Google Scholar]
- LaSalle J. M., Lalande M. Homologous association of oppositely imprinted chromosomal domains. Science. 1996 May 3;272(5262):725–728. doi: 10.1126/science.272.5262.725. [DOI] [PubMed] [Google Scholar]
- Larin Z., Fricker M. D., Tyler-Smith C. De novo formation of several features of a centromere following introduction of a Y alphoid YAC into mammalian cells. Hum Mol Genet. 1994 May;3(5):689–695. doi: 10.1093/hmg/3.5.689. [DOI] [PubMed] [Google Scholar]
- Le M. H., Duricka D., Karpen G. H. Islands of complex DNA are widespread in Drosophila centric heterochromatin. Genetics. 1995 Sep;141(1):283–303. doi: 10.1093/genetics/141.1.283. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Li X., Nicklas R. B. Mitotic forces control a cell-cycle checkpoint. Nature. 1995 Feb 16;373(6515):630–632. doi: 10.1038/373630a0. [DOI] [PubMed] [Google Scholar]
- Liao H., Winkfein R. J., Mack G., Rattner J. B., Yen T. J. CENP-F is a protein of the nuclear matrix that assembles onto kinetochores at late G2 and is rapidly degraded after mitosis. J Cell Biol. 1995 Aug;130(3):507–518. doi: 10.1083/jcb.130.3.507. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Lichter P., Cremer T., Borden J., Manuelidis L., Ward D. C. Delineation of individual human chromosomes in metaphase and interphase cells by in situ suppression hybridization using recombinant DNA libraries. Hum Genet. 1988 Nov;80(3):224–234. doi: 10.1007/BF01790090. [DOI] [PubMed] [Google Scholar]
- Lombillo V. A., Stewart R. J., McIntosh J. R. Minus-end-directed motion of kinesin-coated microspheres driven by microtubule depolymerization. Nature. 1995 Jan 12;373(6510):161–164. doi: 10.1038/373161a0. [DOI] [PubMed] [Google Scholar]
- Manuelidis L. Different central nervous system cell types display distinct and nonrandom arrangements of satellite DNA sequences. Proc Natl Acad Sci U S A. 1984 May;81(10):3123–3127. doi: 10.1073/pnas.81.10.3123. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Manuelidis L. Indications of centromere movement during interphase and differentiation. Ann N Y Acad Sci. 1985;450:205–221. doi: 10.1111/j.1749-6632.1985.tb21494.x. [DOI] [PubMed] [Google Scholar]
- Marschall L. G., Clarke L. A novel cis-acting centromeric DNA element affects S. pombe centromeric chromatin structure at a distance. J Cell Biol. 1995 Feb;128(4):445–454. doi: 10.1083/jcb.128.4.445. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Masumoto H., Masukata H., Muro Y., Nozaki N., Okazaki T. A human centromere antigen (CENP-B) interacts with a short specific sequence in alphoid DNA, a human centromeric satellite. J Cell Biol. 1989 Nov;109(5):1963–1973. doi: 10.1083/jcb.109.5.1963. [DOI] [PMC free article] [PubMed] [Google Scholar]
- McIntosh J. R., Cande W. Z., Snyder J. A. Structure and physiology of the mammalian mitotic spindle. Soc Gen Physiol Ser. 1975;30:31–76. [PubMed] [Google Scholar]
- Mitchison T. J., Kirschner M. W. Properties of the kinetochore in vitro. II. Microtubule capture and ATP-dependent translocation. J Cell Biol. 1985 Sep;101(3):766–777. doi: 10.1083/jcb.101.3.766. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Murphy T. D., Karpen G. H. Localization of centromere function in a Drosophila minichromosome. Cell. 1995 Aug 25;82(4):599–609. doi: 10.1016/0092-8674(95)90032-2. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Nicklas R. B. Measurements of the force produced by the mitotic spindle in anaphase. J Cell Biol. 1983 Aug;97(2):542–548. doi: 10.1083/jcb.97.2.542. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Nicklas R. B. The forces that move chromosomes in mitosis. Annu Rev Biophys Biophys Chem. 1988;17:431–449. doi: 10.1146/annurev.bb.17.060188.002243. [DOI] [PubMed] [Google Scholar]
- Nicklas R. B., Ward S. C. Elements of error correction in mitosis: microtubule capture, release, and tension. J Cell Biol. 1994 Sep;126(5):1241–1253. doi: 10.1083/jcb.126.5.1241. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Nicklas R. B., Ward S. C., Gorbsky G. J. Kinetochore chemistry is sensitive to tension and may link mitotic forces to a cell cycle checkpoint. J Cell Biol. 1995 Aug;130(4):929–939. doi: 10.1083/jcb.130.4.929. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Pluta A. F., Mackay A. M., Ainsztein A. M., Goldberg I. G., Earnshaw W. C. The centromere: hub of chromosomal activities. Science. 1995 Dec 8;270(5242):1591–1594. doi: 10.1126/science.270.5242.1591. [DOI] [PubMed] [Google Scholar]
- Pluta A. F., Saitoh N., Goldberg I., Earnshaw W. C. Identification of a subdomain of CENP-B that is necessary and sufficient for localization to the human centromere. J Cell Biol. 1992 Mar;116(5):1081–1093. doi: 10.1083/jcb.116.5.1081. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Polizzi C., Clarke L. The chromatin structure of centromeres from fission yeast: differentiation of the central core that correlates with function. J Cell Biol. 1991 Jan;112(2):191–201. doi: 10.1083/jcb.112.2.191. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Prasher D. C., Eckenrode V. K., Ward W. W., Prendergast F. G., Cormier M. J. Primary structure of the Aequorea victoria green-fluorescent protein. Gene. 1992 Feb 15;111(2):229–233. doi: 10.1016/0378-1119(92)90691-h. [DOI] [PubMed] [Google Scholar]
- Rieder C. L., Borisy G. G. The attachment of kinetochores to the pro-metaphase spindle in PtK1 cells. Recovery from low temperature treatment. Chromosoma. 1981;82(5):693–716. doi: 10.1007/BF00285776. [DOI] [PubMed] [Google Scholar]
- Rieder C. L., Cole R. W., Khodjakov A., Sluder G. The checkpoint delaying anaphase in response to chromosome monoorientation is mediated by an inhibitory signal produced by unattached kinetochores. J Cell Biol. 1995 Aug;130(4):941–948. doi: 10.1083/jcb.130.4.941. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Rieder C. L., Schultz A., Cole R., Sluder G. Anaphase onset in vertebrate somatic cells is controlled by a checkpoint that monitors sister kinetochore attachment to the spindle. J Cell Biol. 1994 Dec;127(5):1301–1310. doi: 10.1083/jcb.127.5.1301. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Roos U. P. Light and electron microscopy of rat kangaroo cells in mitosis. II. Kinetochore structure and function. Chromosoma. 1973;41(2):195–220. doi: 10.1007/BF00319696. [DOI] [PubMed] [Google Scholar]
- Skibbens R. V., Rieder C. L., Salmon E. D. Kinetochore motility after severing between sister centromeres using laser microsurgery: evidence that kinetochore directional instability and position is regulated by tension. J Cell Sci. 1995 Jul;108(Pt 7):2537–2548. doi: 10.1242/jcs.108.7.2537. [DOI] [PubMed] [Google Scholar]
- Skibbens R. V., Skeen V. P., Salmon E. D. Directional instability of kinetochore motility during chromosome congression and segregation in mitotic newt lung cells: a push-pull mechanism. J Cell Biol. 1993 Aug;122(4):859–875. doi: 10.1083/jcb.122.4.859. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Steiner N. C., Clarke L. A novel epigenetic effect can alter centromere function in fission yeast. Cell. 1994 Dec 2;79(5):865–874. doi: 10.1016/0092-8674(94)90075-2. [DOI] [PubMed] [Google Scholar]
- Stratmann R., Lehner C. F. Separation of sister chromatids in mitosis requires the Drosophila pimples product, a protein degraded after the metaphase/anaphase transition. Cell. 1996 Jan 12;84(1):25–35. doi: 10.1016/s0092-8674(00)80990-3. [DOI] [PubMed] [Google Scholar]
- Strunnikov A. V., Larionov V. L., Koshland D. SMC1: an essential yeast gene encoding a putative head-rod-tail protein is required for nuclear division and defines a new ubiquitous protein family. J Cell Biol. 1993 Dec;123(6 Pt 2):1635–1648. doi: 10.1083/jcb.123.6.1635. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Sullivan K. F., Glass C. A. CENP-B is a highly conserved mammalian centromere protein with homology to the helix-loop-helix family of proteins. Chromosoma. 1991 Jul;100(6):360–370. doi: 10.1007/BF00337514. [DOI] [PubMed] [Google Scholar]
- Sullivan K. F., Hechenberger M., Masri K. Human CENP-A contains a histone H3 related histone fold domain that is required for targeting to the centromere. J Cell Biol. 1994 Nov;127(3):581–592. doi: 10.1083/jcb.127.3.581. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Tippit D. H., Pickett-Heaps J. D., Leslie R. Cell division in two large pennate diatoms Hantzschia and Nitzschia III. A new proposal for kinetochore function during prometaphase. J Cell Biol. 1980 Aug;86(2):402–416. doi: 10.1083/jcb.86.2.402. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Tyler-Smith C., Brown W. R. Structure of the major block of alphoid satellite DNA on the human Y chromosome. J Mol Biol. 1987 Jun 5;195(3):457–470. doi: 10.1016/0022-2836(87)90175-6. [DOI] [PubMed] [Google Scholar]
- Tyler-Smith C., Oakey R. J., Larin Z., Fisher R. B., Crocker M., Affara N. A., Ferguson-Smith M. A., Muenke M., Zuffardi O., Jobling M. A. Localization of DNA sequences required for human centromere function through an analysis of rearranged Y chromosomes. Nat Genet. 1993 Dec;5(4):368–375. doi: 10.1038/ng1293-368. [DOI] [PubMed] [Google Scholar]
- Tyler-Smith C., Willard H. F. Mammalian chromosome structure. Curr Opin Genet Dev. 1993 Jun;3(3):390–397. doi: 10.1016/0959-437x(93)90110-b. [DOI] [PubMed] [Google Scholar]
- Voullaire L. E., Slater H. R., Petrovic V., Choo K. H. A functional marker centromere with no detectable alpha-satellite, satellite III, or CENP-B protein: activation of a latent centromere? Am J Hum Genet. 1993 Jun;52(6):1153–1163. [PMC free article] [PubMed] [Google Scholar]
- Wendell K. L., Wilson L., Jordan M. A. Mitotic block in HeLa cells by vinblastine: ultrastructural changes in kinetochore-microtubule attachment and in centrosomes. J Cell Sci. 1993 Feb;104(Pt 2):261–274. doi: 10.1242/jcs.104.2.261. [DOI] [PubMed] [Google Scholar]
- Wevrick R., Willard H. F. Long-range organization of tandem arrays of alpha satellite DNA at the centromeres of human chromosomes: high-frequency array-length polymorphism and meiotic stability. Proc Natl Acad Sci U S A. 1989 Dec;86(23):9394–9398. doi: 10.1073/pnas.86.23.9394. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Wevrick R., Willard V. P., Willard H. F. Structure of DNA near long tandem arrays of alpha satellite DNA at the centromere of human chromosome 7. Genomics. 1992 Dec;14(4):912–923. doi: 10.1016/s0888-7543(05)80112-0. [DOI] [PubMed] [Google Scholar]
- Willard H. F. Evolution of alpha satellite. Curr Opin Genet Dev. 1991 Dec;1(4):509–514. doi: 10.1016/s0959-437x(05)80200-x. [DOI] [PubMed] [Google Scholar]
- Yen T. J., Li G., Schaar B. T., Szilak I., Cleveland D. W. CENP-E is a putative kinetochore motor that accumulates just before mitosis. Nature. 1992 Oct 8;359(6395):536–539. doi: 10.1038/359536a0. [DOI] [PubMed] [Google Scholar]
- Yin H., Wang M. D., Svoboda K., Landick R., Block S. M., Gelles J. Transcription against an applied force. Science. 1995 Dec 8;270(5242):1653–1657. doi: 10.1126/science.270.5242.1653. [DOI] [PubMed] [Google Scholar]