H2A.Z Functions To Regulate Progression through the Cell Cycle

REFERENCES

• Adam, M., F. Robert, M. Larochelle, and L. Gaudreau. 2001. H2A.Z is required for global chromatin integrity and for recruitment of RNA polymerase II under specific conditions. Mol. Cell. Biol. 21:6270–6279.
   PubMed Web of Science ®Google Scholar
• Alcasabas, A. A., A. J. Osborn, J. Bachant, F. Hu, P. J. Werler, K. Bousset, K. Furuya, J. F. Diffley, A. M. Carr, and S. J. Elledge. 2001. Mrc1 transduces signals of DNA replication stress to activate Rad53. Nat. Cell Biol. 3:958–965.
   PubMed Web of Science ®Google Scholar
• Andrews, B., and V. Measday. 1998. The cyclin family of budding yeast: abundant use of a good idea. Trends Genet. 14:66–72.
   PubMedGoogle Scholar
• Aparicio, O. M., A. M. Stout, and S. P. Bell. 1999. Differential assembly of Cdc45p and DNA polymerases at early and late origins of DNA replication. Proc. Natl. Acad. Sci. USA 96:9130–9135.
   PubMed Web of Science ®Google Scholar
• Aparicio, O. M., D. M. Weinstein, and S. P. Bell. 1997. Components and dynamics of DNA replication complexes in S. cerevisiae: redistribution of MCM proteins and Cdc45p during S phase. Cell 91:59–69.
   PubMed Web of Science ®Google Scholar
• Araki, H., P. A. Ropp, A. L. Johnson, L. H. Johnston, A. Morrison, and A. Sugino. 1992. DNA polymerase II, the probable homolog of mammalian DNA polymerase epsilon, replicates chromosomal DNA in the yeast Saccharomyces cerevisiae. EMBO J. 11:733–740.
   PubMedGoogle Scholar
• Bell, S. P., and B. Stillman. 1992. ATP-dependent recognition of eukaryotic origins of DNA replication by a multiprotein complex. Nature 357:128–134.
   PubMed Web of Science ®Google Scholar
• Brewer, B. J., and W. L. Fangman. 1991. Mapping replication origins in yeast chromosomes. Bioessays 13:317–322.
   PubMedGoogle Scholar
• Chanet, R., and M. Heude. 2003. Characterization of mutations that are synthetic lethal with pol3-13, a mutated allele of DNA polymerase delta in Saccharomyces cerevisiae. Curr. Genet. 43:337–350.
   PubMedGoogle Scholar
• Choy, J. S., and S. J. Kron. 2002. NuA4 subunit Yng2 function in intra-S-phase DNA damage response. Mol. Cell. Biol. 22:8215–8225.
   PubMed Web of Science ®Google Scholar
• Clarkson, M. J., J. R. Wells, F. Gibson, R. Saint, and D. J. Tremethick. 1999. Regions of variant histone His2AvD required for Drosophila development. Nature 399:694–697.
   PubMedGoogle Scholar
• Cosgrove, A. J., C. A. Nieduszynski, and A. D. Donaldson. 2002. Ku complex controls the replication time of DNA in telomere regions. Genes Dev. 16:2485–2490.
   PubMed Web of Science ®Google Scholar
• Cosma, M. P. 2002. Ordered recruitment: gene-specific mechanism of transcription activation. Mol. Cell 10:227–236.
   PubMedGoogle Scholar
• Cosma, M. P., S. Panizza, and K. Nasmyth. 2001. Cdk1 triggers association of RNA polymerase to cell cycle promoters only after recruitment of the mediator by SBF. Mol. Cell 7:1213–1220.
   PubMed Web of Science ®Google Scholar
• Cosma, M. P., T. Tanaka, and K. Nasmyth. 1999. Ordered recruitment of transcription and chromatin remodeling factors to a cell cycle- and developmentally regulated promoter. Cell 97:299–311.
   PubMed Web of Science ®Google Scholar
• Cross, F. R., and M. D. Jacobson. 2000. Conservation and function of a potential substrate-binding domain in the yeast Clb5 B-type cyclin. Mol. Cell. Biol. 20:4782–4790.
   PubMedGoogle Scholar
• Dhillon, N., and R. T. Kamakaka. 2000. A histone variant, Htz1p, and a Sir1p-like protein, Esc2p, mediate silencing at HMR. Mol. Cell 6:769–780.
   PubMedGoogle Scholar
• Diffley, J. F. 2004. Regulation of early events in chromosome replication. Curr. Biol. 14:R778—R786.
   Google Scholar
• Dirick, L., T. Bohm, and K. Nasmyth. 1995. Roles and regulation of Cln-Cdc28 kinases at the start of the cell cycle of Saccharomyces cerevisiae. EMBO J. 14:4803–4813.
   PubMed Web of Science ®Google Scholar
• Donaldson, A. D., M. K. Raghuraman, K. L. Friedman, F. R. Cross, B. J. Brewer, and W. L. Fangman. 1998. CLB5-dependent activation of late replication origins in S. cerevisiae. Mol. Cell 2:173–182.
   PubMed Web of Science ®Google Scholar
• Early, A., L. S. Drury, and J. F. Diffley. 2004. Mechanisms involved in regulating DNA replication origins during the cell cycle and in response to DNA damage. Philos. Trans. R Soc. Lond. B. Biol. Sci. 359:31–38.
   PubMedGoogle Scholar
• Ehrenhofer-Murray, A. E. 2004. Chromatin dynamics at DNA replication, transcription and repair. Eur. J. Biochem. 271:2335–2349.
   PubMedGoogle Scholar
• Ehrenhofer-Murray, A. E., R. T. Kamakaka, and J. Rine. 1999. A role for the replication proteins PCNA, RF-C, polymerase epsilon and Cdc45 in transcriptional silencing in Saccharomyces cerevisiae. Genetics 153:1171–1182.
   PubMedGoogle Scholar
• Ehrenhofer-Murray, A. E., D. H. Rivier, and J. Rine. 1997. The role of Sas2, an acetyltransferase homologue of Saccharomyces cerevisiae, in silencing and ORC function. Genetics 145:923–934.
   PubMedGoogle Scholar
• Friedman, K. L., B. J. Brewer, and W. L. Fangman. 1997. Replication profile of Saccharomyces cerevisiae chromosome VI. Genes Cells 2:667–678.
   PubMed Web of Science ®Google Scholar
• Friedman, K. L., J. D. Diller, B. M. Ferguson, S. V. Nyland, B. J. Brewer, and W. L. Fangman. 1996. Multiple determinants controlling activation of yeast replication origins late in S phase. Genes Dev. 10:1595–1607.
   PubMedGoogle Scholar
• Friedman, K. L., M. K. Raghuraman, W. L. Fangman, and B. J. Brewer. 1995. Analysis of the temporal program of replication initiation in yeast chromosomes. J. Cell Sci. Suppl. 19:51–58.
   PubMedGoogle Scholar
• Futcher, B. 1996. Cyclins and the wiring of the yeast cell cycle. Yeast 12:1635–1646.
   PubMed Web of Science ®Google Scholar
• Garber, P. M., and J. Rine. 2002. Overlapping roles of the spindle assembly and DNA damage checkpoints in the cell-cycle response to altered chromosomes in Saccharomyces cerevisiae. Genetics 161:521–534.
   PubMedGoogle Scholar
• Ghidelli, S., D. Donze, N. Dhillon, and R. T. Kamakaka. 2001. Sir2p exists in two nucleosome-binding complexes with distinct deacetylase activities. EMBO J. 20:4522–4535.
   PubMedGoogle Scholar
• Gibson, D. G., J. G. Aparicio, F. Hu, and O. M. Aparicio. 2004. Diminished S-phase cyclin-dependent kinase function elicits vital Rad53-dependent checkpoint responses in Saccharomyces cerevisiae. Mol. Cell. Biol. 24:10208–10222.
   PubMedGoogle Scholar
• Grunstein, M. 1990. Histone function in transcription. Annu. Rev. Cell Biol. 6:643–678.
   PubMedGoogle Scholar
• Hanawalt, P. C. 1994. Transcription-coupled repair and human disease. Science 266:1957–1958.
   PubMed Web of Science ®Google Scholar
• Horak, C. E., N. M. Luscombe, J. Qian, P. Bertone, S. Piccirrillo, M. Gerstein, and M. Snyder. 2002. Complex transcriptional circuitry at the G1/S transition in Saccharomyces cerevisiae. Genes Dev. 16:3017–3033.
   PubMed Web of Science ®Google Scholar
• Howe, L., D. Auston, P. Grant, S. John, R. G. Cook, J. L. Workman, and L. Pillus. 2001. Histone H3 specific acetyltransferases are essential for cell cycle progression. Genes Dev. 15:3144–3154.
   PubMed Web of Science ®Google Scholar
• Iizuka, M., and B. Stillman. 1999. Histone acetyltransferase HBO1 interacts with the ORC1 subunit of the human initiator protein. J. Biol. Chem. 274:23027–23034.
   PubMed Web of Science ®Google Scholar
• Kamakaka, R. T., and S. Biggins. 2005. Histone variants: deviants? Genes Dev. 19:295–310.
   PubMed Web of Science ®Google Scholar
• Kobor, M. S., S. Venkatasubrahmanyam, M. D. Meneghini, J. W. Gin, J. L. Jennings, A. J. Link, H. D. Madhani, and J. Rine. 2004. A protein complex Containing the conserved Swi2/Snf2-Related ATPase Swr1p deposits histone variant H2A.Z into euchromatin. PLoS Biol. 2:E131.
   PubMed Web of Science ®Google Scholar
• Krebs, J. E., C. J. Fry, M. L. Samuels, and C. L. Peterson. 2000. Global role for chromatin remodeling enzymes in mitotic gene expression. Cell 102:587–598.
   PubMed Web of Science ®Google Scholar
• Krebs, J. E., M. H. Kuo, C. D. Allis, and C. L. Peterson. 1999. Cell cycle-regulated histone acetylation required for expression of the yeast HO gene. Genes Dev. 13:1412–1421.
   PubMed Web of Science ®Google Scholar
• Krogan, N. J., K. Baetz, M. C. Keogh, N. Datta, C. Sawa, T. C. Kwok, N. J. Thompson, M. G. Davey, J. Pootoolal, T. R. Hughes, A. Emili, S. Buratowski, P. Hieter, and J. F. Greenblatt. 2004. Regulation of chromosome stability by the histone H2A variant Htz1, the Swr1 chromatin remodeling complex, and the histone acetyltransferase NuA4. Proc. Natl. Acad. Sci. USA 101:13513–13518.
   PubMedGoogle Scholar
• Krogan, N. J., M. C. Keogh, N. Datta, C. Sawa, O. W. Ryan, H. Ding, R. A. Haw, J. Pootoolal, A. Tong, V. Canadien, D. P. Richards, X. Wu, A. Emili, T. R. Hughes, S. Buratowski, and J. F. Greenblatt. 2003. A Snf2 family ATPase complex required for recruitment of the histone H2A variant Htz1. Mol. Cell 12:1565–1576.
   PubMed Web of Science ®Google Scholar
• Kusch, T., L. Florens, W. H. Macdonald, S. K. Swanson, R. L. Glaser, J. R. Yates III, S. M. Abmayr, M. P. Washburn, and J. L. Workman. 2004. Acetylation by Tip60 is required for selective histone variant exchange at DNA lesions. Science 306:2084–2087.
   PubMed Web of Science ®Google Scholar
• Larochelle, M., and L. Gaudreau. 2003. H2A.Z has a function reminiscent of an activator required for preferential binding to intergenic DNA. EMBO J. 22:4512–4522.
   PubMed Web of Science ®Google Scholar
• Le Masson, I., D. Y. Yu, K. Jensen, A. Chevalier, R. Courbeyrette, Y. Boulard, M. M. Smith, and C. Mann. 2003. Yaf9, a novel NuA4 histone acetyltransferase subunit, is required for the cellular response to spindle stress in yeast. Mol. Cell. Biol. 23:6086–6102.
   PubMed Web of Science ®Google Scholar
• Leach, T. J., M. Mazzeo, H. L. Chotkowski, J. P. Madigan, M. G. Wotring, and R. L. Glaser. 2000. Histone H2A.Z is widely but nonrandomly distributed in chromosomes of Drosophila melanogaster. J. Biol. Chem. 275:23267–23272.
   PubMed Web of Science ®Google Scholar
• Lengronne, A., and E. Schwob. 2002. The yeast CDK inhibitor Sic1 prevents genomic instability by promoting replication origin licensing in late G(1). Mol. Cell 9:1067–1078.
   PubMed Web of Science ®Google Scholar
• Lipford, J. R., and S. P. Bell. 2001. Nucleosomes positioned by ORC facilitate the initiation of DNA replication. Mol. Cell 7:21–30.
   PubMed Web of Science ®Google Scholar
• Lopes, M., C. Cotta-Ramusino, A. Pellicioli, G. Liberi, P. Plevani, M. Muzi-Falconi, C. S. Newlon, and M. Foiani. 2001. The DNA replication checkpoint response stabilizes stalled replication forks. Nature 412:557–561.
   PubMed Web of Science ®Google Scholar
• Madigan, J. P., H. L. Chotkowski, and R. L. Glaser. 2002. DNA double-strand break-induced phosphorylation of Drosophila histone variant H2Av helps prevent radiation-induced apoptosis. Nucleic Acids Res. 30:3698–3705.
   PubMed Web of Science ®Google Scholar
• Malone, E. A., C. D. Clark, A. Chiang, and F. Winston. 1991. Mutations in SPT16/CDC68 suppress cis- and trans-acting mutations that affect promoter function in Saccharomyces cerevisiae. Mol. Cell. Biol. 11:5710–5717.
   PubMed Web of Science ®Google Scholar
• McCarroll, R. M., and W. L. Fangman. 1988. Time of replication of yeast centromeres and telomeres. Cell 54:505–513.
   PubMedGoogle Scholar
• Megee, P. C., B. A. Morgan, and M. M. Smith. 1995. Histone H4 and the maintenance of genome integrity. Genes Dev. 9:1716–1727.
   PubMed Web of Science ®Google Scholar
• Melo, J., and D. Toczyski. 2002. A unified view of the DNA-damage checkpoint. Curr. Opin. Cell Biol. 14:237–245.
   PubMed Web of Science ®Google Scholar
• Meneghini, M. D., M. Wu, and H. D. Madhani. 2003. Conserved histone variant H2A.Z protects euchromatin from the ectopic spread of silent heterochromatin. Cell 112:725–736.
   PubMed Web of Science ®Google Scholar
• Mizuguchi, G., X. Shen, J. Landry, W. H. Wu, S. Sen, and C. Wu. 2004. ATP-driven exchange of histone H2A.Z variant catalyzed by SWR1 chromatin remodeling complex. Science 303:343–348.
   PubMed Web of Science ®Google Scholar
• Nash, P., X. Tang, S. Orlicky, Q. Chen, F. B. Gertler, M. D. Mendenhall, F. Sicheri, T. Pawson, and M. Tyers. 2001. Multisite phosphorylation of a CDK inhibitor sets a threshold for the onset of DNA replication. Nature 414:514–521.
   PubMed Web of Science ®Google Scholar
• Nasmyth, K. 1993. Control of the yeast cell cycle by the Cdc28 protein kinase. Curr. Opin. Cell Biol. 5:166–179.
   PubMed Web of Science ®Google Scholar
• Navas, T. A., Z. Zhou, and S. J. Elledge. 1995. DNA polymerase epsilon links the DNA replication machinery to the S phase checkpoint. Cell 80:29–39.
   PubMed Web of Science ®Google Scholar
• Pasero, P., K. Shimada, and B. P. Duncker. 2003. Multiple roles of replication forks in S phase checkpoints: sensors, effectors and targets. Cell Cycle 2:568–572.
   PubMedGoogle Scholar
• Paulovich, A. G., and L. H. Hartwell. 1995. A checkpoint regulates the rate of progression through S phase in S. cerevisiae in response to DNA damage. Cell 82:841–847.
   PubMed Web of Science ®Google Scholar
• Peterson, C. L., and J. Cote. 2004. Cellular machineries for chromosomal DNA repair. Genes Dev. 18:602–616.
   PubMed Web of Science ®Google Scholar
• Raghuraman, M. K., E. A. Winzeler, D. Collingwood, S. Hunt, L. Wodicka, A. Conway, D. J. Lockhart, R. W. Davis, B. J. Brewer, and W. L. Fangman. 2001. Replication dynamics of the yeast genome. Science 294:115–121.
   PubMed Web of Science ®Google Scholar
• Rangasamy, D., L. Berven, P. Ridgway, and D. J. Tremethick. 2003. Pericentric heterochromatin becomes enriched with H2A.Z during early mammalian development. EMBO J. 22:1599–1607.
   PubMedGoogle Scholar
• Rowley, A., R. A. Singer, and G. C. Johnston. 1991. CDC68, a yeast gene that affects regulation of cell proliferation and transcription, encodes a protein with a highly acidic carboxyl terminus. Mol. Cell. Biol. 11:5718–5726.
   PubMed Web of Science ®Google Scholar
• Rupes, I. 2002. Checking cell size in yeast. Trends Genet. 18:479–485.
   PubMed Web of Science ®Google Scholar
• Sambrook J., and D. W. Russell. 2001. Molecular cloning: a laboratory manual, 3rd ed. Cold Spring Harbor Laboratory Press, Cold Spring Harbor, N.Y.
   Google Scholar
• Santisteban, M. S., T. Kalashnikova, and M. M. Smith. 2000. Histone H2A.Z regulates transcription and is partially redundant with nucleosome remodeling complexes. Cell 103:411–422.
   PubMedGoogle Scholar
• Santocanale, C., and J. F. Diffley. 1998. A Mec1- and Rad53-dependent checkpoint controls late-firing origins of DNA replication. Nature 395:615–618.
   PubMed Web of Science ®Google Scholar
• Schmitt, M. E., T. A. Brown, and B. L. Trumpower. 1990. A rapid and simple method for preparation of RNA from Saccharomyces cerevisiae. Nucleic Acids Res. 18:3091–3092.
   PubMed Web of Science ®Google Scholar
• Schwob, E., and K. Nasmyth. 1993. CLB5 and CLB6, a new pair of B cyclins involved in DNA replication in Saccharomyces cerevisiae. Genes Dev. 7:1160–1175.
   PubMed Web of Science ®Google Scholar
• Sherman, F. 1991. Getting started with yeast. Methods Enzymol. 194:3–21.
   PubMed Web of Science ®Google Scholar
• Shimada, K., P. Pasero, and S. M. Gasser. 2002. ORC and the intra-S-phase checkpoint: a threshold regulates Rad53p activation in S phase. Genes Dev. 16:3236–3252.
   PubMed Web of Science ®Google Scholar
• Simpson, R. T. 1990. Nucleosome positioning can affect the function of a cis-acting DNA element in vivo. Nature 343:387–389.
   PubMed Web of Science ®Google Scholar
• Stevenson, J. B., and D. E. Gottschling. 1999. Telomeric chromatin modulates replication timing near chromosome ends. Genes Dev. 13:146–151.
   PubMedGoogle Scholar
• Suter, B., A. Tong, M. Chang, L. Yu, G. W. Brown, C. Boone, and J. Rine. 2004. The origin recognition complex links replication, sister chromatid cohesion and transcriptional silencing in Saccharomyces cerevisiae. Genetics 167:579–591.
   PubMed Web of Science ®Google Scholar
• Svejstrup, J. Q. 2002. Mechanisms of transcription-coupled DNA repair. Nat. Rev. Mol. Cell. Biol. 3:21–29.
   PubMed Web of Science ®Google Scholar
• Swaminathan, J., E. M. Baxter, and V. G. Corces. 2005. The role of H2Av variant replacement and histone H4 acetylation in the establishment of Drosophila heterochromatin. Genes Dev., in press. 19:65–76.
   PubMedGoogle Scholar
• Takayama, Y., Y. Kamimura, M. Okawa, S. Muramatsu, A. Sugino, and H. Araki. 2003. GINS, a novel multiprotein complex required for chromosomal DNA replication in budding yeast. Genes Dev. 17:1153–1165.
   PubMed Web of Science ®Google Scholar
• Tanaka, S., and J. F. Diffley. 2002. Deregulated G1-cyclin expression induces genomic instability by preventing efficient pre-RC formation. Genes Dev. 16:2639–2649.
   PubMed Web of Science ®Google Scholar
• Tercero, J. A., and J. F. Diffley. 2001. Regulation of DNA replication fork progression through damaged DNA by the Mec1/Rad53 checkpoint. Nature 412:553–557.
   PubMed Web of Science ®Google Scholar
• Tercero, J. A., M. P. Longhese, and J. F. Diffley. 2003. A central role for DNA replication forks in checkpoint activation and response. Mol. Cell 11:1323–1336.
   PubMed Web of Science ®Google Scholar
• Tong, A. H., G. Lesage, G. D. Bader, H. Ding, H. Xu, X. Xin, J. Young, G. F. Berriz, R. L. Brost, M. Chang, Y. Chen, X. Cheng, G. Chua, H. Friesen, D. S. Goldberg, J. Haynes, C. Humphries, G. He, S. Hussein, L. Ke, N. Krogan, Z. Li, J. N. Levinson, H. Lu, P. Menard, C. Munyana, A. B. Parsons, O. Ryan,R. Tonikian, T. Roberts, A. M. Sdicu, J. Shapiro, B. Sheikh, B. Suter, S. L. Wong, L. V. Zhang, H. Zhu, C. G. Burd, S. Munro, C. Sander, J. Rine, J. Greenblatt, M. Peter, A. Bretscher, G. Bell, F. P. Roth, G. W. Brown, B. Andrews, H. Bussey, and C. Boone. 2004. Global mapping of the yeast genetic interaction network. Science 303:808–813.
   PubMed Web of Science ®Google Scholar
• Tyers, M., G. Tokiwa, and B. Futcher. 1993. Comparison of the Saccharomyces cerevisiae G1 cyclins: Cln3 may be an upstream activator of Cln1, Cln2 and other cyclins. EMBO J. 12:1955–1968.
   PubMed Web of Science ®Google Scholar
• Verger, A., and M. Crossley. 2004. Chromatin modifiers in transcription and DNA repair. Cell Mol. Life Sci. 61:2154–2162.
   PubMedGoogle Scholar
• Verma, R., H. McDonald, J. R. Yates III, and R. J. Deshaies. 2001. Selective degradation of ubiquitinated Sic1 by purified 26S proteasome yields active S phase cyclin-Cdk. Mol. Cell 8:439–448.
   PubMedGoogle Scholar
• Vogelauer, M., L. Rubbi, I. Lucas, B. J. Brewer, and M. Grunstein. 2002. Histone acetylation regulates the time of replication origin firing. Mol. Cell 10:1223–1233.
   PubMed Web of Science ®Google Scholar
• Weinberger, M., P. A. Trabold, M. Lu, K. Sharma, J. A. Huberman, and W. C. Burhans. 1999. Induction by adozelesin and hydroxyurea of origin recognition complex-dependent DNA damage and DNA replication checkpoints in Saccharomyces cerevisiae. J. Biol. Chem. 274:35975–35984.
   PubMedGoogle Scholar
• Weinreich, M., M. A. Palacios DeBeer, and C. A. Fox. 2004. The activities of eukaryotic replication origins in chromatin. Biochim. Biophys. Acta 1677:142–157.
   PubMed Web of Science ®Google Scholar
• Wittenberg, C., and S. I. Reed. 2005. Cell cycle-dependent transcription in yeast: promoters, transcription factors, and transcriptomes. Oncogene 24:2746–2755.
   PubMed Web of Science ®Google Scholar
• Wittenberg, C., K. Sugimoto, and S. I. Reed. 1990. G1-specific cyclins of S. cerevisiae: cell cycle periodicity, regulation by mating pheromone, and association with the p34CDC28 protein kinase. Cell 62:225–237.
   PubMed Web of Science ®Google Scholar
• Wyrick, J. J., J. G. Aparicio, T. Chen, J. D. Barnett, E. G. Jennings, R. A. Young, S. P. Bell, and O. M. Aparicio. 2001. Genome-wide distribution of ORC and MCM proteins in S. cerevisiae: high-resolution mapping of replication origins. Science 294:2357–2360.
   PubMed Web of Science ®Google Scholar
• Yamashita, M., Y. Hori, T. Shinomiya, C. Obuse, T. Tsurimoto, H. Yoshikawa, and K. Shirahige. 1997. The efficiency and timing of initiation of replication of multiple replicons of Saccharomyces cerevisiae chromosome VI. Genes Cells 2:655–665.
   PubMedGoogle Scholar
• Yan, H., S. Gibson, and B. K. Tye. 1991. Mcm2 and Mcm3, two proteins important for ARS activity, are related in structure and function. Genes Dev. 5:944–957.
   PubMed Web of Science ®Google Scholar
• Zhang, W., J. R. Bone, D. G. Edmondson, B. M. Turner, and S. Y. Roth. 1998. Essential and redundant functions of histone acetylation revealed by mutation of target lysines and loss of the Gcn5p acetyltransferase. EMBO J. 17:3155–3167.
   PubMed Web of Science ®Google Scholar
• Zou, L., and B. Stillman. 1998. Formation of a preinitiation complex by S-phase cyclin CDK-dependent loading of Cdc45p onto chromatin. Science 280:593–596.
   PubMed Web of Science ®Google Scholar