Functional Complementation of Human Centromere Protein A (CENP-A) by Cse4p from Saccharomyces cerevisiae

REFERENCES

• Albertson, D. G., and Thomson J. N.. 1982. The kinetochores of Caenorhabditis elegans. Chromosoma 86:409–428.
   PubMed Web of Science ®Google Scholar
• Albertson, D. G., and Thomson J. N.. 1993. Segregation of holocentric chromosomes at meiosis in the nematode, Caenorhabditis elegans. Chromosome Res. 1:15–26.
   PubMedGoogle Scholar
• Amon, A. 1999. The spindle checkpoint. Curr. Opin. Genet. Dev. 9:69–75.
   PubMed Web of Science ®Google Scholar
• Arents, G., Burlingame R. W., Wang B. C., Love W. E., and Moudrianakis E. N.. 1991. The nucleosomal core histone octamer at 3.1 A resolution: a tripartite protein assembly and a left-handed superhelix. Proc. Natl. Acad. Sci. USA 88:10148–10152.
   PubMed Web of Science ®Google Scholar
• Biggins, S., and Murray A. W.. 1999. Sister chromatid cohesion in mitosis. Curr. Opin. Genet. Dev. 9:230–236.
   PubMedGoogle Scholar
• Brown, K. D., Wood K. W., and Cleveland D. W.. 1996. The kinesin-like protein CENP-E is kinetochore-associated throughout poleward chromosome segregation during anaphase-A. J. Cell Sci. 109:961–969.
   PubMed Web of Science ®Google Scholar
• Buchwitz, B. J., Ahmad K., Moore L. L., Roth M. B., and Henikoff S.. 1999. A histone-H3-like protein in C. elegans. Nature 401:547–548.
   PubMedGoogle Scholar
• Cheeseman, I. M., Drubin D. G., and Barnes G.. 2002. Simple centromere, complex kinetochore: linking spindle microtubules and centromeric DNA in budding yeast. J. Cell Biol. 157:199–203.
   PubMedGoogle Scholar
• Chen, Y., Baker R. E., Keith K. C., Harris K., Stoler S., and Fitzgerald-Hayes M.. 2000. The N terminus of the centromere H3-like protein Cse4p performs an essential function distinct from that of the histone fold domain. Mol. Cell. Biol. 20:7037–7048.
   PubMedGoogle Scholar
• Choi, J. H., Bertram P. G., Drenan R., Carvalho J., Zhou H. H., and Zheng X. F.. 2002. The FKBP12-rapamycin-associated protein (FRAP) is a CLIP-170 kinase. EMBO Rep. 3:988–994.
   PubMedGoogle Scholar
• Choo, K. H. 1997. Centromere DNA dynamics: latent centromeres and neocentromere formation. Am. J. Hum. Genet. 61:1225–1233.
   PubMedGoogle Scholar
• Choo, K. H. 2000. Centromerization. Trends Cell Biol. 10:182–188.
   PubMedGoogle Scholar
• Choo, K. H. 2001. Domain organization at the centromere and neocentromere. Dev. Cell 1:165–177.
   PubMedGoogle Scholar
• Cleveland, D. W., Mao Y., and Sullivan K. F.. 2003. Centromeres and kinetochores: from epigenetics to mitotic checkpoint signaling. Cell 112:407–421.
   PubMed Web of Science ®Google Scholar
• Cooke, C. A., Bernat R. L., and Earnshaw W. C.. 1990. CENP-B: a major human centromere protein located beneath the kinetochore. J. Cell Biol. 110:1475–1488.
   PubMed Web of Science ®Google Scholar
• Coquelle, F. M., Caspi M., Cordelieres F. P., Dompierre J. P., Dujardin D. L., Koifman C., Martin P., Hoogenraad C. C., Akhmanova A., Galjart N., De Mey J. R., and Reiner O.. 2002. LIS1, CLIP-170's key to the dynein/dynactin pathway. Mol. Cell. Biol. 22:3089–3102.
   PubMedGoogle Scholar
• Diamantopoulos, G. S., Perez F., Goodson H. V., Batelier G., Melki R., Kreis T. E., and Rickard J. E.. 1999. Dynamic localization of CLIP-170 to microtubule plus ends is coupled to microtubule assembly. J. Cell Biol. 144:99–112.
   PubMedGoogle Scholar
• Dobie, K. W., Hari K. L., Maggert K. A., and Karpen G. H.. 1999. Centromere proteins and chromosome inheritance: a complex affair. Curr. Opin. Genet. Dev. 9:206–217.
   PubMedGoogle Scholar
• Dujardin, D., Wacker U. I., Moreau A., Schroer T. A., Rickard J. E., and De Mey J. R.. 1998. Evidence for a role of CLIP-170 in the establishment of metaphase chromosome alignment. J. Cell Biol. 141:849–862.
   PubMedGoogle Scholar
• Elbashir, S. M., Harborth J., Lendeckel W., Yalcin A., Weber K., and Tuschl T.. 2001. Duplexes of 21-nucleotide RNAs mediate RNA interference in cultured mammalian cells. Nature 411:494–498.
   PubMed Web of Science ®Google Scholar
• El-Sheraby, A. M., and Hinchliffe J. R.. 1974. Apoptotic cells exhibit membrane phenotypes. J. Embryol. Exp. Morphol. 31:643–654.
   PubMedGoogle Scholar
• Figueroa, J., Saffrich R., Ansorge W., and Valdivia M.. 1998. Microinjection of antibodies to centromere protein CENP-A arrests cells in interphase but does not prevent mitosis. Chromosoma 107:397–405.
   PubMedGoogle Scholar
• Fritzler, M. J., and Kinsella T. D.. 1980. The CREST syndrome: a distinct serologic entity with anticentromere antibodies. Am. J. Med. 69:520–526.
   PubMed Web of Science ®Google Scholar
• Glowczewski, L., Yang P., Kalashnikova T., Santisteban M. S., and Smith M. M.. 2000. Histone-histone interactions and centromere function. Mol. Cell. Biol. 20:5700–5711.
   PubMed Web of Science ®Google Scholar
• Goshima, G., Kiyomitsu T., Yoda K., and Yanagida M.. 2003. Human centromere chromatin protein hMis12, essential for equal segregation, is independent of CENP-A loading pathway. J. Cell Biol. 160:25–39.
   PubMed Web of Science ®Google Scholar
• He, X., Rines D. R., Espelin C. W., and Sorger P. K.. 2001. Molecular analysis of kinetochore-microtubule attachment in budding yeast. Cell 106:195–206.
   PubMedGoogle Scholar
• Henikoff, S., Ahmad K., and Malik H. S.. 2001. The centromere paradox: stable inheritance with rapidly evolving DNA. Science 293:1098–1102.
   PubMed Web of Science ®Google Scholar
• Henikoff, S., Ahmad K., Platero J. S., and van Steensel B.. 2000. Heterochromatic deposition of centromeric histone H3-like proteins. Proc. Natl. Acad. Sci. USA 97:716–721.
   PubMedGoogle Scholar
• Howman, E. V., Fowler K. J., Newson A. J., Redward S., MacDonald A. C., Kalitsis P., and Choo K. H.. 2000. Early disruption of centromeric chromatin organization in centromere protein A (Cenpa) null mice. Proc. Natl. Acad. Sci. USA 97:1148–1153.
   PubMed Web of Science ®Google Scholar
• Hyland, K. M., Kingsbury J., Koshland D., and Hieter P.. 1999. Ctf19p: a novel kinetochore protein in Saccharomyces cerevisiae and a potential link between the kinetochore and mitotic spindle. J. Cell Biol. 145:15–28.
   PubMedGoogle Scholar
• Jackson, V. 1988. Deposition of newly synthesized histones: hybrid nucleosomes are not tandemly arranged on daughter DNA strands. Biochemistry 27:2109–2121.
   PubMedGoogle Scholar
• Janke, C., Ortiz J., Tanaka T. U., Lechner J., and Schiebel E.. 2002. Four new subunits of the Dam1-Duo1 complex reveal novel functions in sister kinetochore biorientation. EMBO J. 21:181–193.
   PubMedGoogle Scholar
• Keith, K. C., Baker R. E., Chen Y., Harris K., Stoler S., and Fitzgerald-Hayes M.. 1999. Analysis of primary structural determinants that distinguish the centromere-specific function of histone variant Cse4p from histone H3. Mol. Cell. Biol. 19:6130–6139.
   PubMedGoogle Scholar
• Keith, K. C., and Fitzgerald-Hayes M.. 2000. CSE4 genetically interacts with the Saccharomyces cerevisiae centromere DNA elements CDE I and CDE II but not CDE III. Implications for the path of the centromere DNA around a Cse4p variant nucleosome. Genetics 156:973–981.
   PubMed Web of Science ®Google Scholar
• Kiesslich, A., von Mikecz A., and Hemmerich P.. 2002. Cell cycle-dependent association of PML bodies with sites of active transcription in nuclei of mammalian cells. J. Struct. Biol. 140:167–179.
   PubMedGoogle Scholar
• Kitagawa, K., and Hieter P.. 2001. Evolutionary conservation between budding yeast and human kinetochores. Nat. Rev. Mol. Cell. Biol. 2:678–687.
   PubMedGoogle Scholar
• Kunitoku, N., Sasayama T., Marumoto T., Zhang D., Honda S., Kobayashi O., Hatakeyama K., Ushio Y., Saya H., and Hirota T.. 2003. CENP-A phosphorylation by Aurora-A in prophase is required for enrichment of Aurora-B at inner centromeres and for kinetochore function. Dev. Cell 5:853–864.
   PubMed Web of Science ®Google Scholar
• Lechner, J., and Carbon J.. 1991. A 240 kd multisubunit protein complex, CBF3, is a major component of the budding yeast centromere. Cell 64:717–725.
   PubMed Web of Science ®Google Scholar
• Lechner, J., and Ortiz J.. 1996. The Saccharomyces cerevisiae kinetochore. FEBS Lett. 389:70–74.
   PubMed Web of Science ®Google Scholar
• Li, Y., Bachant J., Alcasabas A. A., Wang Y., Qin J., and Elledge S. J.. 2002. The mitotic spindle is required for loading of the DASH complex onto the kinetochore. Genes Dev. 16:183–197.
   PubMedGoogle Scholar
• Lin, H., de Carvalho P., Kho D., Tai C. Y., Pierre P., Fink G. R., and Pellman D.. 2001. Polyploids require Bik1 for kinetochore-microtubule attachment. J. Cell Biol. 155:1173–1184.
   PubMed Web of Science ®Google Scholar
• Liu, S. T., Hittle J. C., Jablonski S. A., Campbell M. S., Yoda K., and Yen T. J.. 2003. Human CENP-I specifies localization of CENP-F, MAD1 and MAD2 to kinetochores and is essential for mitosis. Nat. Cell Biol. 5:341–345.
   PubMed Web of Science ®Google Scholar
• Lo, A. W., Magliano D. J., Sibson M. C., Kalitsis P., Craig J. M., and Choo K. H.. 2001. A novel chromatin immunoprecipitation and array (CIA) analysis identifies a 460-kb CENP-A-binding neocentromere DNA. Genome Res. 11:448–457.
   PubMedGoogle Scholar
• Malik, H. S., and Henikoff S.. 2001. Adaptive evolution of Cid, a centromere-specific histone in Drosophila. Genetics 157:1293–1298.
   PubMedGoogle Scholar
• Maney, T., Ginkel L. M., Hunter A. W., and Wordeman L.. 2000. The kinetochore of higher eucaryotes: a molecular view. Int. Rev. Cytol. 194:67–131.
   PubMedGoogle Scholar
• Mann, R. K., and Grunstein M.. 1992. Histone H3 N-terminal mutations allow hyperactivation of the yeast GAL1 gene in vivo. EMBO J. 11:3297–3306.
   PubMed Web of Science ®Google Scholar
• McEwen, B. F., Ding Y., and Heagle A. B.. 1998. Relevance of kinetochore size and microtubule-binding capacity for stable chromosome attachment during mitosis in PtK1 cells. Chromosome Res. 6:123–132.
   PubMedGoogle Scholar
• McEwen, B. F., Hsieh C. E., Mattheyses A. L., and Rieder C. L.. 1998. A new look at kinetochore structure in vertebrate somatic cells using high-pressure freezing and freeze substitution. Chromosoma 107:366–375.
   PubMedGoogle Scholar
• Measday, V., Hailey D. W., Pot I., Givan S. A., Hyland K. M., Cagney G., Fields S., Davis T. N., and Hieter P.. 2002. Ctf3p, the Mis6 budding yeast homolog, interacts with Mcm22p and Mcm16p at the yeast outer kinetochore. Genes Dev. 16:101–113.
   PubMedGoogle Scholar
• Mellor, J., Jiang W., Funk M., Rathjen J., Barnes C. A., Hinz T., Hegemann J. H., and Philippsen P.. 1990. CPF1, a yeast protein which functions in centromeres and promoters. EMBO J. 9:4017–4026.
   PubMedGoogle Scholar
• Meluh, P. B., and Koshland D.. 1997. Budding yeast centromere composition and assembly as revealed by in vivo cross-linking. Genes Dev. 11:3401–3412.
   PubMedGoogle Scholar
• Meluh, P. B., and Koshland D.. 1995. Evidence that the MIF2 gene of Saccharomyces cerevisiae encodes a centromere protein with homology to the mammalian centromere protein CENP-C. Mol. Biol. Cell 6:793–807.
   PubMed Web of Science ®Google Scholar
• Meluh, P. B., Yang P., Glowczewski L., Koshland D., and Smith M. M.. 1998. Cse4p is a component of the core centromere of Saccharomyces cerevisiae. Cell 94:607–613.
   PubMed Web of Science ®Google Scholar
• Muro, Y., Masumoto H., Yoda K., Nozaki N., Ohashi M., and Okazaki T.. 1992. Centromere protein B assembles human centromeric alpha-satellite DNA at the 17-bp sequence, CENP-B box. J. Cell Biol. 116:585–596.
   PubMedGoogle Scholar
• Nekrasov, V. S., Smith M. A., Peak-Chew S., and Kilmartin J. V.. 2003. Interactions between centromere complexes in Saccharomyces cerevisiae. Mol. Biol. Cell 14:4931–4946.
   PubMedGoogle Scholar
• Nishihashi, A., Haraguchi T., Hiraoka Y., Ikemura T., Regnier V., Dodson H., Earnshaw W. C., and Fukagawa T.. 2002. CENP-I is essential for centromere function in vertebrate cells. Dev. Cell 2:463–476.
   PubMedGoogle Scholar
• Ortiz, J., Stemmann O., Rank S., and Lechner J.. 1999. A putative protein complex consisting of Ctf19, Mcm21, and Okp1 represents a missing link in the budding yeast kinetochore. Genes Dev. 13:1140–1155.
   PubMedGoogle Scholar
• Palmer, D. K., O'Day K., Trong H. L., Charbonneau H., and Margolis R. L.. 1991. Purification of the centromere-specific protein CENP-A and demonstration that it is a distinctive histone. Proc. Natl. Acad. Sci. USA 88:3734–3738.
   PubMedGoogle Scholar
• Palmer, D. K., O'Day K., Wener M. H., Andrews B. S., and Margolis R. L.. 1987. A 17-kD centromere protein (CENP-A) copurifies with nucleosome core particles and with histones. J. Cell Biol. 104:805–815.
   PubMed Web of Science ®Google Scholar
• Perez, F., Diamantopoulos G. S., Stalder R., and Kreis T. E.. 1999. CLIP-170 highlights growing microtubule ends in vivo. Cell 96:517–527.
   PubMed Web of Science ®Google Scholar
• Pidoux, A. L., and Allshire R. C.. 2000. Centromeres: getting a grip of chromosomes. Curr. Opin. Cell Biol. 12:308–319.
   PubMedGoogle Scholar
• Pierre, P., Pepperkok R., and Kreis T. E.. 1994. Molecular characterization of two functional domains of CLIP-170 in vivo. J. Cell Sci. 107:1909–1920.
   PubMedGoogle Scholar
• Pierre, P., Scheel J., Rickard J. E., and Kreis T. E.. 1992. CLIP-170 links endocytic vesicles to microtubules. Cell 70:887–900.
   PubMed Web of Science ®Google Scholar
• Prasher, D. C., Eckenrode V. K., Ward W. W., Prendergast F. G., and Cormier M. J.. 1992. Primary structure of the Aequorea victoria green-fluorescent protein. Gene 111:229–233.
   PubMed Web of Science ®Google Scholar
• Remboutsika, E., Lutz Y., Gansmuller A., Vonesch J. L., Losson R., and Chambon P.. 1999. The putative nuclear receptor mediator TIF1alpha is tightly associated with euchromatin. J. Cell Sci. 112:1671–1683.
   PubMed Web of Science ®Google Scholar
• Rickard, J. E., and Kreis T. E.. 1990. Identification of a novel nucleotide-sensitive microtubule-binding protein in HeLa cells. J. Cell Biol. 110:1623–1633.
   PubMedGoogle Scholar
• Rieder, C. L., and Salmon E. D.. 1998. The vertebrate cell kinetochore and its roles during mitosis. Trends Cell Biol. 8:310–318.
   PubMed Web of Science ®Google Scholar
• Rose, S. M., and Garrard W. T.. 1984. Differentiation-dependent chromatin alterations precede and accompany transcription of immunoglobulin light chain genes. J. Biol. Chem. 259:8534–8544.
   PubMed Web of Science ®Google Scholar
• Schroer, T. A. 2000. Motors, clutches and brakes for membrane traffic: a commemorative review in honor of Thomas Kreis. Traffic 1:3–10.
   PubMedGoogle Scholar
• Schuyler, S. C., and Pellman D.. 2001. Microtubule “plus-end-tracking proteins”: the end is just the beginning. Cell 105:421–424.
   PubMed Web of Science ®Google Scholar
• Shelby, R. D., Monier K., and Sullivan K. F.. 2000. Chromatin assembly at kinetochores is uncoupled from DNA replication. J. Cell Biol. 151:1113–1118.
   PubMed Web of Science ®Google Scholar
• Shelby, R. D., Vafa O., and Sullivan K. F.. 1997. Assembly of CENP-A into centromeric chromatin requires a cooperative array of nucleosomal DNA contact sites. J. Cell Biol. 136:501–513.
   PubMed Web of Science ®Google Scholar
• Smith, M. M. 2002. Centromeres and variant histones: what, where, when and why? Curr. Opin. Cell Biol. 14:279–285.
   PubMed Web of Science ®Google Scholar
• Smith, M. M. 2002. Histone variants and nucleosome deposition pathways. Mol. Cell 9:1158–1160.
   PubMedGoogle Scholar
• Smith, M. M., Yang P., Santisteban M. S., Boone P. W., Goldstein A. T., and Megee P. C.. 1996. A novel histone H4 mutant defective in nuclear division and mitotic chromosome transmission. Mol. Cell. Biol. 16:1017–1026.
   PubMedGoogle Scholar
• Spector, D. L., Goldman R. D., and Leinwand L. A.. 1997. Cells, a laboratory manual, vol. 1 to 3. Cold Spring Harbor Laboratory Press, New York, N.Y.
   Google Scholar
• Stoler, S., Keith K. C., Curnick K. E., and Fitzgerald-Hayes M.. 1995. A mutation in CSE4, an essential gene encoding a novel chromatin-associated protein in yeast, causes chromosome nondisjunction and cell cycle arrest at mitosis. Genes Dev. 9:573–586.
   PubMed Web of Science ®Google Scholar
• Sugata, N., Li S., Earnshaw W. C., Yen T. J., Yoda K., Masumoto H., Munekata E., Warburton P. E., and Todokoro K.. 2000. Human CENP-H multimers colocalize with CENP-A and CENP-C at active centromere-kinetochore complexes. Hum. Mol. Genet. 9:2919–2926.
   PubMedGoogle Scholar
• Sugata, N., Munekata E., and Todokoro K.. 1999. Characterization of a novel kinetochore protein, CENP-H. J. Biol. Chem. 274:27343–27346.
   PubMedGoogle Scholar
• Sugimoto, K., Fukuda R., and Himeno M.. 2000. Centromere/kinetochore localization of human centromere protein A (CENP-A) exogenously expressed as a fusion to green fluorescent protein. Cell Struct. Funct. 25:253–261.
   PubMedGoogle Scholar
• Sullivan, K. F. 2001. A solid foundation: functional specialization of centromeric chromatin. Curr. Opin. Genet. Dev. 11:182–188.
   PubMed Web of Science ®Google Scholar
• Sullivan, K. F., Hechenberger M., and Masri K.. 1994. Human CENP-A contains a histone H3 related histone fold domain that is required for targeting to the centromere. J. Cell Biol. 127:581–592.
   PubMedGoogle Scholar
• Tai, C. Y., Dujardin D. L., Faulkner N. E., and Vallee R. B.. 2002. Role of dynein, dynactin, and CLIP-170 interactions in LIS1 kinetochore function. J. Cell Biol. 156:959–968.
   PubMedGoogle Scholar
• Takahashi, K., Chen E. S., and Yanagida M.. 2000. Requirement of Mis6 centromere connector for localizing a CENP-A-like protein in fission yeast. Science 288:2215–2219.
   PubMedGoogle Scholar
• Tyler-Smith, C., and Floridia G.. 2000. Many paths to the top of the mountain: diverse evolutionary solutions to centromere structure. Cell 102:5–8.
   PubMedGoogle Scholar
• Vafa, O., and Sullivan K. F.. 1997. Chromatin containing CENP-A and alpha-satellite DNA is a major component of the inner kinetochore plate. Curr. Biol. 7:897–900.
   PubMed Web of Science ®Google Scholar
• von Mikecz, A., Zhang S., Montminy M., Tan E. M., and Hemmerich P.. 2000. CREB-binding protein (CBP)/p300 and RNA polymerase II colocalize in transcriptionally active domains in the nucleus. J. Cell Biol. 150:265–273.
   PubMedGoogle Scholar
• Warburton, P. E., Cooke C. A., Bourassa S., Vafa O., Sullivan B. A., Stetten G., Gimelli G., Warburton D., Tyler-Smith C., Sullivan K. F., Poirier G. G., and Earnshaw W. C.. 1997. Immunolocalization of CENP-A suggests a distinct nucleosome structure at the inner kinetochore plate of active centromeres. Curr. Biol. 7:901–904.
   PubMedGoogle Scholar
• Westermann, S., Cheeseman I. M., Anderson S., Yates III J. R., Drubin D. G., and Barnes G.. 2003. Architecture of the budding yeast kinetochore reveals a conserved molecular core. J. Cell Biol. 163:215–222.
   PubMed Web of Science ®Google Scholar
• Wiens, G. R., and Sorger P. K.. 1998. Centromeric chromatin and epigenetic effects in kinetochore assembly. Cell 93:313–316.
   PubMedGoogle Scholar
• Wigge, P. A., and Kilmartin J. V.. 2001. The Ndc80p complex from Saccharomyces cerevisiae contains conserved centromere components and has a function in chromosome segregation. J. Cell Biol. 152:349–360.
   PubMed Web of Science ®Google Scholar
• Yoda, K., Ando S., Morishita S., Houmura K., Hashimoto K., Takeyasu K., and Okazaki T.. 2000. Human centromere protein A (CENP-A) can replace histone H3 in nucleosome reconstitution in vitro. Proc. Natl. Acad. Sci. USA 97:7266–7271.
   PubMedGoogle Scholar
• Yu, H. G., Hiatt E. N., Chan A., Sweeney M., and Dawe R. K.. 1997. Neocentromere-mediated chromosome movement in maize. J. Cell Biol. 139:831–840.
   PubMedGoogle Scholar