Histone Acetylation at Promoters Is Differentially Affected by Specific Activators and Repressors

ABSTRACT We analyzed the relationship between histone acetylation and transcriptional regulation at 40 Saccharomyces cerevisiaepromoters that respond to specific activators and repressors. In accord with the general correlation between histone acetylation and transcriptional activity, Gcn4 and the general stress activators (Msn2 and Msn4) cause increased acetylation of histones H3 and H4. Surprisingly, Gal4-dependent activation is associated with a dramatic decrease in histone H4 acetylation, whereas acetylation of histone H3 is unaffected. A specific decrease in H4 acetylation is also observed, to a lesser extent, at promoters activated by Hap4, Adr1, Met4, and Ace1. Activation by heat shock factor has multiple effects; H4 acetylation increases at some promoters, whereas other promoters show an apparent decrease in H3 and H4 acetylation that probably reflects nucleosome loss or gross alteration of chromatin structure. Repression by targeted recruitment of the Sin3-Rpd3 histone deacetylase is associated with decreased H3 and H4 acetylation, whereas repression by Cyc8-Tup1 is associated with decreased H3 acetylation but variable effects on H4 acetylation; this suggests that Cyc8-Tup1 uses multiple mechanisms to reduce histone acetylation at promoters. Thus, individual activators confer distinct patterns of histone acetylation on target promoters, and transcriptional activation is not necessarily associated with increased acetylation. We speculate that the activator-specific decrease in histone H4 acetylation is due to blocking the access or function of an H4-specific histone acetylase such as Esa1.

[1]  A. Mirsky,et al.  ACETYLATION AND METHYLATION OF HISTONES AND THEIR POSSIBLE ROLE IN THE REGULATION OF RNA SYNTHESIS. , 1964, Proceedings of the National Academy of Sciences of the United States of America.

[2]  A. Mirsky,et al.  RNA synthesis and histone acetylation during the course of gene activation in lymphocytes. , 1966, Proceedings of the National Academy of Sciences of the United States of America.

[3]  Nancy Kleckner,et al.  A Method for Gene Disruption That Allows Repeated Use of URA3 Selection in the Construction of Multiply Disrupted Yeast Strains , 1987, Genetics.

[4]  T. R. Hebbes,et al.  A direct link between core histone acetylation and transcriptionally active chromatin. , 1988, The EMBO journal.

[5]  D. Hamer,et al.  Copper activates metallothionein gene transcription by altering the conformation of a specific DNA binding protein , 1988, Cell.

[6]  A. Eisen,et al.  The yeast regulatory protein ADR1 binds in a zinc-dependent manner to the upstream activating sequence of ADH2 , 1988, Molecular and cellular biology.

[7]  G. Hager,et al.  Glucocorticoid receptor-dependent disruption of a specific nucleosome on the mouse mammary tumor virus promoter is prevented by sodium butyrate. , 1990, Proceedings of the National Academy of Sciences of the United States of America.

[8]  L. Guarente,et al.  The HAP2 subunit of yeast CCAAT transcriptional activator contains adjacent domains for subunit association and DNA recognition: model for the HAP2/3/4 complex. , 1990, Genes & development.

[9]  M. Grunstein,et al.  Yeast histone H4 N-terminal sequence is required for promoter activation in vivo , 1991, Cell.

[10]  G. Hager,et al.  Histone hyperacetylation does not alter the positioning or stability of phased nucleosomes on the mouse mammary tumor virus long terminal repeat. , 1991, Biochemistry.

[11]  B. Turner,et al.  Histone H4 isoforms acetylated at specific lysine residues define individual chromosomes and chromatin domains in Drosophila polytene nuclei , 1992, Cell.

[12]  M. Grunstein,et al.  Histone H3 N‐terminal mutations allow hyperactivation of the yeast GAL1 gene in vivo. , 1992, The EMBO journal.

[13]  D. S. Gross,et al.  A critical role for heat shock transcription factor in establishing a nucleosome‐free region over the TATA‐initiation site of the yeast HSP82 heat shock gene. , 1993, The EMBO journal.

[14]  J. Broach,et al.  Transcriptional silencing in yeast is associated with reduced nucleosome acetylation. , 1993, Genes & development.

[15]  B. Turner,et al.  The inactive X chromosome in female mammals is distinguished by a lack of histone H4 acetylation, a cytogenetic marker for gene expression , 1993, Cell.

[16]  G. Schroth,et al.  Studies of the DNA binding properties of histone H4 amino terminus. Thermal denaturation studies reveal that acetylation markedly reduces the binding constant of the H4 "tail" to DNA. , 1993, The Journal of biological chemistry.

[17]  K. Struhl,et al.  Functional dissection of the yeast Cyc8–Tupl transcriptional co-repressor complex , 1994, Nature.

[18]  B. Turner,et al.  Histone H4 acetylation distinguishes coding regions of the human genome from heterochromatin in a differentiation‐dependent but transcription‐independent manner. , 1995, The EMBO journal.

[19]  B. M. Jackson,et al.  The transcriptional activator GCN4 contains multiple activation domains that are critically dependent on hydrophobic amino acids , 1995, Molecular and cellular biology.

[20]  K. Struhl,et al.  Distinct TPR motifs of Cyc8 are involved in recruiting the Cyc8-Tup1 corepressor complex to differentially regulated promoters. , 1995, Genes & development.

[21]  V. Iyer,et al.  Mechanism of differential utilization of the his3 TR and TC TATA elements , 1995, Molecular and cellular biology.

[22]  D. Edmondson,et al.  Repression domain of the yeast global repressor Tup1 interacts directly with histones H3 and H4. , 1996, Genes & development.

[23]  D. Thomas,et al.  A heteromeric complex containing the centromere binding factor 1 and two basic leucine zipper factors, Met4 and Met28, mediates the transcription activation of yeast sulfur metabolism. , 1996, The EMBO journal.

[24]  M. Grunstein,et al.  HDA1 and RPD3 are members of distinct yeast histone deacetylase complexes that regulate silencing and transcription. , 1996, Proceedings of the National Academy of Sciences of the United States of America.

[25]  B M Turner,et al.  Efficient transcriptional silencing in Saccharomyces cerevisiae requires a heterochromatin histone acetylation pattern , 1996, Molecular and cellular biology.

[26]  T. Richmond,et al.  Crystal structure of the nucleosome core particle at 2.8 Å resolution , 1997, Nature.

[27]  K. Luo,et al.  SIR2 and SIR4 interactions differ in core and extended telomeric heterochromatin in yeast. , 1997, Genes & development.

[28]  D. Eide,et al.  Zap1p, a metalloregulatory protein involved in zinc-responsive transcriptional regulation in Saccharomyces cerevisiae , 1997, Molecular and cellular biology.

[29]  T. R. Hebbes,et al.  Chromosomal mapping of core histone acetylation by immunoselection. , 1997, Methods.

[30]  R Ohba,et al.  Yeast Gcn5 functions in two multisubunit complexes to acetylate nucleosomal histones: characterization of an Ada complex and the SAGA (Spt/Ada) complex. , 1997, Genes & development.

[31]  M. Grunstein Histone acetylation in chromatin structure and transcription , 1997, Nature.

[32]  K. Struhl,et al.  Histone deacetylase activity of Rpd3 is important for transcriptional repression in vivo. , 1998, Genes & development.

[33]  J. Lucchesi,et al.  Targeting of MOF, a putative histone acetyl transferase, to the X chromosome of Drosophila melanogaster. , 1998, Developmental genetics.

[34]  B. M. Jackson,et al.  The Gcn4p Activation Domain Interacts Specifically In Vitro with RNA Polymerase II Holoenzyme, TFIID, and the Adap-Gcn5p Coactivator Complex , 1998, Molecular and Cellular Biology.

[35]  D. Stillman,et al.  In vivo functions of histone acetylation/deacetylation in Tup1p repression and Gcn5p activation. , 1998, Cold Spring Harbor symposia on quantitative biology.

[36]  J. Lucchesi,et al.  Dosage compensation in flies and worms: the ups and downs of X-chromosome regulation. , 1998, Current opinion in genetics & development.

[37]  M. Grunstein,et al.  Transcriptional repression by UME6 involves deacetylation of lysine 5 of histone H4 by RPD3 , 1998, Nature.

[38]  B. Turner,et al.  Essential and redundant functions of histone acetylation revealed by mutation of target lysines and loss of the Gcn5p acetyltransferase , 1998, The EMBO journal.

[39]  M. Bissell,et al.  Characterization of BCE-1, a Transcriptional Enhancer Regulated by Prolactin and Extracellular Matrix and Modulated by the State of Histone Acetylation , 1998, Molecular and Cellular Biology.

[40]  S. Berger,et al.  Critical residues for histone acetylation by Gcn5, functioning in Ada and SAGA complexes, are also required for transcriptional function in vivo. , 1998, Genes & development.

[41]  K. Struhl,et al.  Targeted Recruitment of the Sin3-Rpd3 Histone Deacetylase Complex Generates a Highly Localized Domain of Repressed Chromatin In Vivo , 1998, Molecular and Cellular Biology.

[42]  K. Struhl Histone acetylation and transcriptional regulatory mechanisms. , 1998, Genes & development.

[43]  P. Grant,et al.  Transcriptional activators direct histone acetyltransferase complexes to nucleosomes , 1998, Nature.

[44]  C. Allis,et al.  Histone acetyltransferase activity of yeast Gcn5p is required for the activation of target genes in vivo. , 1998, Genes & development.

[45]  A. Schmitt,et al.  Transcriptional Factor Mutations Reveal Regulatory Complexities of Heat Shock and Newly Identified Stress Genes in Saccharomyces cerevisiae * , 1998, The Journal of Biological Chemistry.

[46]  K. Natarajan,et al.  Transcriptional activation by Gcn4p involves independent interactions with the SWI/SNF complex and the SRB/mediator. , 1999, Molecular cell.

[47]  C. Allis,et al.  Cell cycle-regulated histone acetylation required for expression of the yeast HO gene. , 1999, Genes & development.

[48]  J. Workman,et al.  Activation Domain-Specific and General Transcription Stimulation by Native Histone Acetyltransferase Complexes , 1999, Molecular and Cellular Biology.

[49]  T. Maniatis,et al.  Virus infection leads to localized hyperacetylation of histones H3 and H4 at the IFN-beta promoter. , 1999, Molecular cell.

[50]  Michael R. Green,et al.  Enhancement of TBP binding by activators and general transcription factors , 1999, Nature.

[51]  K. Nasmyth,et al.  Ordered Recruitment of Transcription and Chromatin Remodeling Factors to a Cell Cycle– and Developmentally Regulated Promoter , 2016, Cell.

[52]  John J. Wyrick,et al.  Chromosomal landscape of nucleosome-dependent gene expression and silencing in yeast , 1999, Nature.

[53]  L. Pillus,et al.  Esa1p Is an Essential Histone Acetyltransferase Required for Cell Cycle Progression , 1999, Molecular and Cellular Biology.

[54]  R. Evans,et al.  Regulation of Hormone-Induced Histone Hyperacetylation and Gene Activation via Acetylation of an Acetylase , 1999, Cell.

[55]  T. Kouzarides Histone acetylases and deacetylases in cell proliferation. , 1999, Current opinion in genetics & development.

[56]  S. Harashima,et al.  Conservation of Histone Binding and Transcriptional Repressor Functions in a Schizosaccharomyces pombeTup1p Homolog , 1999, Molecular and Cellular Biology.

[57]  K. Struhl,et al.  Binding of TBP to promoters in vivo is stimulated by activators and requires Pol II holoenzyme , 1999, Nature.

[58]  R. Kornberg,et al.  Chromatin-modifying and -remodeling complexes. , 1999, Current opinion in genetics & development.

[59]  P. Grant,et al.  NuA4, an essential transcription adaptor/histone H4 acetyltransferase complex containing Esa1p and the ATM‐related cofactor Tra1p , 1999, The EMBO journal.

[60]  R. Simpson,et al.  The organized chromatin domain of the repressed yeast a cell‐specific gene STE6 contains two molecules of the corepressor Tup1p per nucleosome , 2000, The EMBO journal.

[61]  Kevin Struhl,et al.  Preferential Accessibility of the Yeast his3 Promoter Is Determined by a General Property of the DNA Sequence, Not by Specific Elements , 2000, Molecular and Cellular Biology.

[62]  L. Guarente,et al.  Transcriptional silencing and longevity protein Sir2 is an NAD-dependent histone deacetylase , 2000, Nature.

[63]  C. Allis,et al.  The language of covalent histone modifications , 2000, Nature.

[64]  A. Johnson,et al.  Turning genes off by Ssn6-Tup1: a conserved system of transcriptional repression in eukaryotes. , 2000, Trends in biochemical sciences.

[65]  Michael Grunstein,et al.  Global histone acetylation and deacetylation in yeast , 2000, Nature.

[66]  C. Peterson,et al.  Global Role for Chromatin Remodeling Enzymes in Mitotic Gene Expression , 2000, Cell.

[67]  K. Struhl,et al.  Gcn4 activator targets Gcn5 histone acetyltransferase to specific promoters independently of transcription. , 2000, Molecular cell.

[68]  J. H. Waterborg,et al.  Steady-state Levels of Histone Acetylation in Saccharomyces cerevisiae * , 2000, The Journal of Biological Chemistry.

[69]  D. Stillman,et al.  Ssn6-Tup1 interacts with class I histone deacetylases required for repression. , 2000, Genes & development.

[70]  P. Brown,et al.  Coordinate regulation of yeast ribosomal protein genes is associated with targeted recruitment of Esa1 histone acetylase. , 2000, Molecular cell.