Multiple protein-DNA interactions over the yeast HSC82 heat shock gene promoter.
Abstract
We have utilized DNase I and micrococcal nuclease (MNase) to map the chromatin structure of the HSC82 heat shock gene of Saccharomyces cerevisiae. The gene is expressed at a high basal level which is enhanced 2-3-fold by thermal stress. A single, heat-shock invariant DNase I hypersensitive domain is found within the HSC82 chromosomal locus; it maps to the gene's 5' end and spans 250 bp of promoter sequence. DNase I genomic footprinting reveals that within this hypersensitive region are four constitutive protein-DNA interactions. These map to the transcription initiation site, the TATA box, the promoter-distal heat shock element (HSE1) and a consensus GRF2 (REB1/Factor Y) sequence. However, two other potential regulatory sites, the promoter-proximal heat shock element (HSE0) and a consensus upstream repressor sequence (URS1), are not detectably occupied under either transcriptional state. In contrast to its sensitivity to DNAase I, the nucleosome-free promoter region is relatively protected from MNase; the enzyme excises a stable nucleoprotein fragment of approximately 210 bp. As detected by MNase, there are at least two sequence-positioned nucleosomes arrayed 5' of the promoter; regularly spaced nucleosomes exhibiting an average repeat length of 160-170 bp span several kilobases of both upstream and downstream regions. Similarly, the body of the gene, which exhibits heightened sensitivity to DNase I, displays a nucleosomal organization under both basal and induced states, but these nucleosomes are not detectably positioned with respect to the underlying DNA sequence and may be irregularly spaced and/or structurally altered. We present a model of the chromatin structure of HSC82 and compare it to one previously derived for the closely related, but differentially regulated, HSP82 heat shock gene.
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- Weintraub H, Groudine M. Chromosomal subunits in active genes have an altered conformation. Science. 1976 Sep 3;193(4256):848–856. [PubMed] [Google Scholar]
- Garel A, Axel R. Selective digestion of transcriptionally active ovalbumin genes from oviduct nuclei. Proc Natl Acad Sci U S A. 1976 Nov;73(11):3966–3970. [PMC free article] [PubMed] [Google Scholar]
- Nasmyth KA. The regulation of yeast mating-type chromatin structure by SIR: an action at a distance affecting both transcription and transposition. Cell. 1982 Sep;30(2):567–578. [PubMed] [Google Scholar]
- Sledziewski A, Young ET. Chromatin conformational changes accompany transcriptional activation of a glucose-repressed gene in Saccharomyces cerevisiae. Proc Natl Acad Sci U S A. 1982 Jan;79(2):253–256. [PMC free article] [PubMed] [Google Scholar]
- Lohr D. The chromatin structure of an actively expressed, single copy yeast gene. Nucleic Acids Res. 1983 Oct 11;11(19):6755–6773. [PMC free article] [PubMed] [Google Scholar]
- Lohr D. Chromatin structure and regulation of the eukaryotic regulatory gene GAL80. Proc Natl Acad Sci U S A. 1993 Nov 15;90(22):10628–10632. [PMC free article] [PubMed] [Google Scholar]
- Fedor MJ, Kornberg RD. Upstream activation sequence-dependent alteration of chromatin structure and transcription activation of the yeast GAL1-GAL10 genes. Mol Cell Biol. 1989 Apr;9(4):1721–1732. [PMC free article] [PubMed] [Google Scholar]
- Cavalli G, Thoma F. Chromatin transitions during activation and repression of galactose-regulated genes in yeast. EMBO J. 1993 Dec;12(12):4603–4613. [PMC free article] [PubMed] [Google Scholar]
- Almer A, Rudolph H, Hinnen A, Hörz W. Removal of positioned nucleosomes from the yeast PHO5 promoter upon PHO5 induction releases additional upstream activating DNA elements. EMBO J. 1986 Oct;5(10):2689–2696. [PMC free article] [PubMed] [Google Scholar]
- Martínez-García JF, Estruch F, Pérez-Ortín JE. Chromatin structure of the 5' flanking region of the yeast LEU2 gene. Mol Gen Genet. 1989 Jun;217(2-3):464–470. [PubMed] [Google Scholar]
- Szent-Györgyi C, Finkelstein DB, Garrard WT. Sharp boundaries demarcate the chromatin structure of a yeast heat-shock gene. J Mol Biol. 1987 Jan 5;193(1):71–80. [PubMed] [Google Scholar]
- Elgin SC. The formation and function of DNase I hypersensitive sites in the process of gene activation. J Biol Chem. 1988 Dec 25;263(36):19259–19262. [PubMed] [Google Scholar]
- Gross DS, Garrard WT. Nuclease hypersensitive sites in chromatin. Annu Rev Biochem. 1988;57:159–197. [PubMed] [Google Scholar]
- Fascher KD, Schmitz J, Hörz W. Role of trans-activating proteins in the generation of active chromatin at the PHO5 promoter in S. cerevisiae. EMBO J. 1990 Aug;9(8):2523–2528. [PMC free article] [PubMed] [Google Scholar]
- Piña B, Brüggemeier U, Beato M. Nucleosome positioning modulates accessibility of regulatory proteins to the mouse mammary tumor virus promoter. Cell. 1990 Mar 9;60(5):719–731. [PubMed] [Google Scholar]
- Archer TK, Cordingley MG, Wolford RG, Hager GL. Transcription factor access is mediated by accurately positioned nucleosomes on the mouse mammary tumor virus promoter. Mol Cell Biol. 1991 Feb;11(2):688–698. [PMC free article] [PubMed] [Google Scholar]
- Morse RH. Nucleosome disruption by transcription factor binding in yeast. Science. 1993 Dec 3;262(5139):1563–1566. [PubMed] [Google Scholar]
- Gross DS, Adams CC, Lee S, Stentz B. 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. EMBO J. 1993 Oct;12(10):3931–3945. [PMC free article] [PubMed] [Google Scholar]
- Workman JL, Buchman AR. Multiple functions of nucleosomes and regulatory factors in transcription. Trends Biochem Sci. 1993 Mar;18(3):90–95. [PubMed] [Google Scholar]
- Wolffe AP. Transcription: in tune with the histones. Cell. 1994 Apr 8;77(1):13–16. [PubMed] [Google Scholar]
- Svaren J, Chalkley R. The structure and assembly of active chromatin. Trends Genet. 1990 Feb;6(2):52–56. [PubMed] [Google Scholar]
- Liu LF, Wang JC. Supercoiling of the DNA template during transcription. Proc Natl Acad Sci U S A. 1987 Oct;84(20):7024–7027. [PMC free article] [PubMed] [Google Scholar]
- Lee MS, Garrard WT. Transcription-induced nucleosome 'splitting': an underlying structure for DNase I sensitive chromatin. EMBO J. 1991 Mar;10(3):607–615. [PMC free article] [PubMed] [Google Scholar]
- Lee MS, Garrard WT. Positive DNA supercoiling generates a chromatin conformation characteristic of highly active genes. Proc Natl Acad Sci U S A. 1991 Nov 1;88(21):9675–9679. [PMC free article] [PubMed] [Google Scholar]
- van Holde KE, Lohr DE, Robert C. What happens to nucleosomes during transcription? J Biol Chem. 1992 Feb 15;267(5):2837–2840. [PubMed] [Google Scholar]
- Fedor MJ, Lue NF, Kornberg RD. Statistical positioning of nucleosomes by specific protein-binding to an upstream activating sequence in yeast. J Mol Biol. 1988 Nov 5;204(1):109–127. [PubMed] [Google Scholar]
- Thoma F, Simpson RT. Local protein-DNA interactions may determine nucleosome positions on yeast plasmids. Nature. 1985 May 16;315(6016):250–252. [PubMed] [Google Scholar]
- Kornberg RD, Stryer L. Statistical distributions of nucleosomes: nonrandom locations by a stochastic mechanism. Nucleic Acids Res. 1988 Jul 25;16(14A):6677–6690. [PMC free article] [PubMed] [Google Scholar]
- Gross DS, English KE, Collins KW, Lee SW. Genomic footprinting of the yeast HSP82 promoter reveals marked distortion of the DNA helix and constitutive occupancy of heat shock and TATA elements. J Mol Biol. 1990 Dec 5;216(3):611–631. [PubMed] [Google Scholar]
- Borkovich KA, Farrelly FW, Finkelstein DB, Taulien J, Lindquist S. hsp82 is an essential protein that is required in higher concentrations for growth of cells at higher temperatures. Mol Cell Biol. 1989 Sep;9(9):3919–3930. [PMC free article] [PubMed] [Google Scholar]
- McDaniel D, Caplan AJ, Lee MS, Adams CC, Fishel BR, Gross DS, Garrard WT. Basal-level expression of the yeast HSP82 gene requires a heat shock regulatory element. Mol Cell Biol. 1989 Nov;9(11):4789–4798. [PMC free article] [PubMed] [Google Scholar]
- Reed KC, Mann DA. Rapid transfer of DNA from agarose gels to nylon membranes. Nucleic Acids Res. 1985 Oct 25;13(20):7207–7221. [PMC free article] [PubMed] [Google Scholar]
- Nedospasov SA, Georgiev GP. Non-random cleavage of SV40 DNA in the compact minichromosome and free in solution by micrococcal nuclease. Biochem Biophys Res Commun. 1980 Jan 29;92(2):532–539. [PubMed] [Google Scholar]
- Wu C. The 5' ends of Drosophila heat shock genes in chromatin are hypersensitive to DNase I. Nature. 1980 Aug 28;286(5776):854–860. [PubMed] [Google Scholar]
- Adams CC, Gross DS. The yeast heat shock response is induced by conversion of cells to spheroplasts and by potent transcriptional inhibitors. J Bacteriol. 1991 Dec;173(23):7429–7435. [PMC free article] [PubMed] [Google Scholar]
- Galas DJ, Schmitz A. DNAse footprinting: a simple method for the detection of protein-DNA binding specificity. Nucleic Acids Res. 1978 Sep;5(9):3157–3170. [PMC free article] [PubMed] [Google Scholar]
- Huibregtse JM, Engelke DR. Direct sequence and footprint analysis of yeast DNA by primer extension. Methods Enzymol. 1991;194:550–562. [PubMed] [Google Scholar]
- Wiederrecht G, Shuey DJ, Kibbe WA, Parker CS. The Saccharomyces and Drosophila heat shock transcription factors are identical in size and DNA binding properties. Cell. 1987 Feb 13;48(3):507–515. [PubMed] [Google Scholar]
- Sorger PK, Lewis MJ, Pelham HR. Heat shock factor is regulated differently in yeast and HeLa cells. Nature. 1987 Sep 3;329(6134):81–84. [PubMed] [Google Scholar]
- Jakobsen BK, Pelham HR. Constitutive binding of yeast heat shock factor to DNA in vivo. Mol Cell Biol. 1988 Nov;8(11):5040–5042. [PMC free article] [PubMed] [Google Scholar]
- Kim Y, Geiger JH, Hahn S, Sigler PB. Crystal structure of a yeast TBP/TATA-box complex. Nature. 1993 Oct 7;365(6446):512–520. [PubMed] [Google Scholar]
- Kim JL, Nikolov DB, Burley SK. Co-crystal structure of TBP recognizing the minor groove of a TATA element. Nature. 1993 Oct 7;365(6446):520–527. [PubMed] [Google Scholar]
- Lohr D, Kovacic RT, Van Holde KE. Quantitative analysis of the digestion of yeast chromatin by staphylococcal nuclease. Biochemistry. 1977 Feb 8;16(3):463–471. [PubMed] [Google Scholar]
- Szent-Gyorgyi C, Isenberg I. The organization of oligonucleosomes in yeast. Nucleic Acids Res. 1983 Jun 11;11(11):3717–3736. [PMC free article] [PubMed] [Google Scholar]
- Pederson DS, Morse RH. Effect of transcription of yeast chromatin on DNA topology in vivo. EMBO J. 1990 Jun;9(6):1873–1881. [PMC free article] [PubMed] [Google Scholar]
- Cartwright IL, Elgin SC. Nucleosomal instability and induction of new upstream protein-DNA associations accompany activation of four small heat shock protein genes in Drosophila melanogaster. Mol Cell Biol. 1986 Mar;6(3):779–791. [PMC free article] [PubMed] [Google Scholar]
- Costlow NA, Simon JA, Lis JT. A hypersensitive site in hsp70 chromatin requires adjacent not internal DNA sequence. Nature. 1985 Jan 10;313(5998):147–149. [PubMed] [Google Scholar]
- Brown ME, Amin J, Schiller P, Voellmy R, Scott WA. Determinants for the DNase I-hypersensitive chromatin structure 5' to a human HSP70 gene. J Mol Biol. 1988 Sep 5;203(1):107–117. [PubMed] [Google Scholar]
- Lee MS, Garrard WT. Uncoupling gene activity from chromatin structure: promoter mutations can inactivate transcription of the yeast HSP82 gene without eliminating nucleosome-free regions. Proc Natl Acad Sci U S A. 1992 Oct 1;89(19):9166–9170. [PMC free article] [PubMed] [Google Scholar]
- Johnston M, Davis RW. Sequences that regulate the divergent GAL1-GAL10 promoter in Saccharomyces cerevisiae. Mol Cell Biol. 1984 Aug;4(8):1440–1448. [PMC free article] [PubMed] [Google Scholar]
- Thoma F. Structural changes in nucleosomes during transcription: strip, split or flip? Trends Genet. 1991 Jun;7(6):175–177. [PubMed] [Google Scholar]
- Xiao H, Lis JT. Germline transformation used to define key features of heat-shock response elements. Science. 1988 Mar 4;239(4844):1139–1142. [PubMed] [Google Scholar]
- Amin J, Ananthan J, Voellmy R. Key features of heat shock regulatory elements. Mol Cell Biol. 1988 Sep;8(9):3761–3769. [PMC free article] [PubMed] [Google Scholar]
- Fernandes M, Xiao H, Lis JT. Fine structure analyses of the Drosophila and Saccharomyces heat shock factor--heat shock element interactions. Nucleic Acids Res. 1994 Jan 25;22(2):167–173. [PMC free article] [PubMed] [Google Scholar]
- Tuite MF, Bossier P, Fitch IT. A highly conserved sequence in yeast heat shock gene promoters. Nucleic Acids Res. 1988 Dec 23;16(24):11845–11845. [PMC free article] [PubMed] [Google Scholar]
- Chasman DI, Lue NF, Buchman AR, LaPointe JW, Lorch Y, Kornberg RD. A yeast protein that influences the chromatin structure of UASG and functions as a powerful auxiliary gene activator. Genes Dev. 1990 Apr;4(4):503–514. [PubMed] [Google Scholar]
- Carmen AA, Holland MJ. The upstream repression sequence from the yeast enolase gene ENO1 is a complex regulatory element that binds multiple trans-acting factors including REB1. J Biol Chem. 1994 Apr 1;269(13):9790–9797. [PubMed] [Google Scholar]
- Luche RM, Sumrada R, Cooper TG. A cis-acting element present in multiple genes serves as a repressor protein binding site for the yeast CAR1 gene. Mol Cell Biol. 1990 Aug;10(8):3884–3895. [PMC free article] [PubMed] [Google Scholar]
- Farrelly FW, Finkelstein DB. Complete sequence of the heat shock-inducible HSP90 gene of Saccharomyces cerevisiae. J Biol Chem. 1984 May 10;259(9):5745–5751. [PubMed] [Google Scholar]
- Furter-Graves EM, Hall BD. DNA sequence elements required for transcription initiation of the Schizosaccharomyces pombe ADH gene in Saccharomyces cerevisiae. Mol Gen Genet. 1990 Sep;223(3):407–416. [PubMed] [Google Scholar]
- Giardina C, Lis JT. DNA melting on yeast RNA polymerase II promoters. Science. 1993 Aug 6;261(5122):759–762. [PubMed] [Google Scholar]






