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J Biol Chem, Vol. 274, Issue 38, 26962-26967, September 17, 1999

The Yeast Transcription Factor Mac1 Binds to DNA in a Modular Fashion^*

Celeste P. Jamison McDaniels^§, Laran T. Jensen^¶, Chandra Srinivasan^¶, Dennis R. Winge^¶, and Thomas D. Tullius^**

From the  Department of Chemistry, The Johns Hopkins University, Baltimore, Maryland 21218, the ^¶ Department of Biochemistry, University of Utah Health Sciences Center, Salt Lake City, Utah 84132, and the  Department of Chemistry, Boston University, Boston, Massachusetts 02215

	ABSTRACT

TOP ABSTRACT INTRODUCTION EXPERIMENTAL PROCEDURES RESULTS DISCUSSION REFERENCES

Mac1 is a metalloregulatory protein that regulates expression of the high affinity copper transport system in the yeast Saccharomyces cerevisiae. Under conditions of high copper concentration, Mac1 represses transcription of genes coding for copper transport proteins. Mac1 binds to DNA sequences called copper response elements (CuREs), which have the consensus sequence 5'-TTTGC(T/G)C(A/G)-3'. Mac1 contains two zinc binding sites, a copper binding site, and the sequence motif RGRP, which has been found in other proteins to mediate binding to the minor groove of A/T-rich sequences in DNA. We have used hydroxyl radical footprinting, missing nucleoside, and methylation interference experiments to investigate the structure of the complex of the DNA binding domain of Mac1 (called here Mac1_t) with the two CuRE sites found in the yeast CTR1 promoter. We conclude from these experiments that Mac1_t binds in a modular fashion to DNA, with its RGRP AT-hook motif interacting with the TTT sequence at the 5' end of the CTR1 CuRE site, and with another DNA-binding module(s) binding in the adjacent major groove in the GCTCA sequence.

	INTRODUCTION

TOP ABSTRACT INTRODUCTION EXPERIMENTAL PROCEDURES RESULTS DISCUSSION REFERENCES

Transcription of genes encoding the high affinity copper transport system in Saccharomyces cerevisiae is subject to copper-dependent repression. These genes include the plasma membrane permeases CTR1 and CTR3, the cell surface metalloreductase FRE1, and a FRE1 homolog of unknown function designated FRE7 (1-5). These genes are maximally expressed in copper-deficient yeast, but are repressed in copper-replete cells.

Copper-dependent expression of CTR1, CTR3, FRE1, and FRE7 is regulated by the transcriptional activator Mac1 (4, 6, 7). Binding sites for Mac1 exist in the 5' promoter sequences of each of the four genes (4, 7, 8). These sites, designated copper-response elements (CuREs),¹ have the consensus sequence 5'-TTTGC(T/G)C(A/G)-3'. Binding of Mac1 to CuREs is required for transcriptional activation of the target genes (4, 7). The CuRE is present in at least two copies in each of the four genes. The CuREs are oriented as either direct or inverted repeats. The spacing between CuRE sites is variable, and changes in spacing have a limited effect on expression (8). The apparent requirement for the presence of at least two CuRE sites likely lies in the need for synergism for proper copper-dependent gene regulation (8, 9).

The Mac1 protein consists of 417 amino acids (Fig. 1). The distribution of charged amino acid residues in Mac1 is not uniform; the N-terminal segment (residues 1-201) is strongly basic, while the C-terminal segment (residues 202-417) is mostly acidic (6). The DNA-binding domain of Mac1 maps to the N-terminal 159 residues. Two Zn(II) ions are coordinated by the protein in the DNA-binding domain (8). Part of the Mac1 DNA-binding domain (residues 1-40) is homologous to the conserved zinc-binding module found in the copper-activated transcription factors Ace1 and Amt1 from S. cerevisiae and Candida glabrata, respectively (6-8, 10-12). This zinc-binding subdomain has been implicated in making direct interactions with DNA in the minor groove of an A/T-rich sequence (13).

Copper at concentrations above 1 nM represses Mac1 function in vivo by attenuating DNA binding activity. Footprinting experiments in vivo revealed that Mac1 binds to the CuREs upstream of the CTR3 gene in copper-starved but not copper-replete cells (4). Further studies have shown, however, that copper-dependent inactivation of Mac1 is more complex than this simple picture might suggest. First, DNA binding in vitro either by the minimal DNA binding domain of Mac1 or by full-length Mac1 prepared by in vitro transcription/translation is not copper-dependent (7, 8). Second, the transactivation activity of Mac1 is repressed in copper-supplemented cells (14, 15). Transactivation activity maps to two cysteine-rich sequences (residues 264-337) in the C-terminal region of Mac1 (15). Eight Cu(I) ions bind within this domain (16). Binding of Cu(I) to the Cys-rich motif induces an intramolecular interaction with the N-terminal DNA-binding domain (16).

The CuRE sequences bound by Mac1 resemble the DNA binding sites for Ace1 and Amt1 in having an A/T-rich sequence upstream of a related core element (4, 7). This observation suggests that Ace1 and Mac1 may interact with DNA in a similar manner, even though Ace1 activates the copper sequestration machinery of the cell, while Mac1 activates the copper acquisition machinery (7, 17).

To investigate the interaction of Mac1 with its DNA binding site, we performed hydroxyl radical footprinting, missing nucleoside, and methylation interference experiments. For these experiments we used a truncated version of Mac1, which we call Mac1_t. This protein contains the minimal DNA-binding domain of Mac1, and consists of residues 1-159 of Mac1 (see Fig. 1) plus a C-terminal His tag. We studied the binding of Mac1_t to a fragment of the CTR1 promoter in order to establish the contacts that Mac1 makes with a CuRE site.

View larger version (40K): [in this window] [in a new window]   Fig. 1.   Amino acid sequence of Mac1. The 159 amino acids that make up Mac1t are boxed.

	EXPERIMENTAL PROCEDURES

TOP ABSTRACT INTRODUCTION EXPERIMENTAL PROCEDURES RESULTS DISCUSSION REFERENCES

DNA Preparation-- A DNA molecule containing a segment of the CTR1 promoter, spanning positions 361 to 299 upstream of the transcription start site, was inserted into the BamHI-XbaI site of plasmid pBluescript SK+. This plasmid was amplified in Escherichia coli DH5 cells and isolated using the Qiagen Plasmid Kit. Purified plasmid DNA was stored at 20 °C in Tris·EDTA buffer (10 mM Tris, 0.2 mM EDTA, pH 8.0).

The CTR1-containing plasmid was digested with restriction endonucleases NotI and EcoRI (New England Biolabs, Beverly, MA). The resulting 96-bp restriction fragment was singly end-labeled at either the NotI terminus using [-³²P]dGTP or at the EcoRI terminus using [-³²P]dATP (Amersham Pharmacia Biotech) with the Klenow large fragment of DNA polymerase (New England Biolabs).

Protein Preparation-- The truncated version of Mac1 that we studied, Mac1_t, was prepared as described previously (8). Mac1_t was stored in 20 mM sodium phosphate buffer (pH 7.5), 0.3 M NaCl, 5 mM dithiothreitol, and 50% glycerol, at 20 °C.

Hydroxyl Radical Footprinting Experiments-- A singly end-labeled DNA restriction fragment (0.1 pmol) in a buffer containing 20 mM Tris (pH 7.8), 65 mM KCl, 5 mM MgCl₂, 2.5 mM dithiothreitol, and 0.1 mg/ml bovine serum albumin was incubated for 15 min on ice with 25 nM Mac1_t. The hydroxyl radical footprinting reaction was carried out by the addition of 2 mM Fe(II), 4 mM EDTA, 0.03% hydrogen peroxide, and 20 mM sodium ascorbate (final concentrations) (18, 19). The reaction was allowed to proceed for 2 min and was stopped by the addition of 26 mM thiourea. The DNA was precipitated by the addition of 0.3 M sodium acetate and ethanol. The DNA pellet was rinsed with 85% ethanol and lyophilized. The DNA was resuspended in 90% formamide-containing tracking dyes, heated at 90 °C for 4 min, and electrophoresed on a 10% polyacrylamide-8 M urea denaturing gel (19:1 acrylamide:bisacrylamide, 1× Tris·borate·EDTA buffer) at 70 watts constant power. The dried gel was imaged by exposure of an imaging phosphor plate (Molecular Dynamics, Sunnyvale, CA). The phosphor plate was scanned on a Molecular Dynamics model 400E PhosphorImager using ImageQuant software.

Missing Nucleoside Experiments-- A 3' end-labeled DNA restriction fragment in Tris·EDTA buffer was treated with the hydroxyl radical by adding 2 mM Fe(II), 4 mM EDTA, 0.03% H₂O₂, and 20 mM sodium ascorbate (final concentrations), as described previously (20). The reaction was allowed to proceed for 2 min, and was stopped by the addition of 26 mM thiourea. The DNA was precipitated by the addition of 0.3 M sodium acetate and ethanol. The DNA pellet was rinsed with 70% ethanol and lyophilized. The hydroxyl radical-treated DNA was resuspended in the protein binding buffer described above for the footprinting experiments. Mac1_t was added to the hydroxyl radical-treated DNA at a concentration of 25 nM. Binding was allowed to proceed for 15 min on ice. After the addition of glycerol (4% final concentration), the sample was immediately loaded on a 7.5% polyacrylamide native electrophoresis gel (37.5:1 acrylamide:bisacrylamide, 1× Tris·borate·EDTA buffer). The gel was run at 25 V/cm at 4 °C. To locate the bands containing DNA, the gel was exposed to Kodak XAR-5 x-ray film for 30 min at room temperature. Bands containing protein-bound and unbound DNA were excised from the gel matrix and eluted by the crush and soak procedure (21). DNA was isolated, precipitated, and electrophoresed on a 10% denaturing polyacrylamide gel as described above. Gel composition, running conditions, imaging, and analysis were the same as for the footprinting experiments.

Methylation Interference Experiments-- DNA radiolabeled at the 3' end, in a buffer consisting of 200 µl of 50 mM sodium cacodylate (pH 8.0), 1 mM EDTA, was treated with 0.5 µl of dimethyl sulfate for 15 s. The reaction was stopped by addition of 300 mM sodium acetate and 100 mM 2-mercaptoethanol. DNA was precipitated by addition of ethanol. The DNA pellet was rinsed with 70% ethanol and lyophilized (21). Methylated DNA was resuspended in protein binding buffer. Mac1_t was added to a concentration of 25 nM, and binding was allowed to proceed for 15 min on ice. After the addition of glycerol (4% final concentration), the sample was loaded on a native polyacrylamide gel with composition, buffer, and running conditions as described above for the missing nucleoside experiment. Bands containing protein-bound and unbound DNA were excised from the gel. DNA was extracted from the gel and precipitated by addition of ethanol. The DNA pellet was rinsed with 70% ethanol and lyophilized. The DNA pellet was suspended in 100 µl of 1 M piperidine and heated at 90 °C for 20 min. DNA was precipitated by addition of 300 mM sodium acetate and ethanol. The DNA pellet was rinsed with 85% ethanol, lyophilized, dissolved in formamide buffer, and loaded on a 10% denaturing polyacrylamide sequencing gel. Gel composition, running conditions, and imaging were the same as described above for the footprinting experiments.

Quantitative Analysis of Gel Images-- We used the image analysis program GelExplorer (22) to integrate the intensities of the bands in the gel images from the footprinting and missing nucleoside experiments. Normalization of data from one lane to another was achieved by summing the whole-band integrals of at least five bands above and below the protein binding site, and then multiplying by a factor such that the summed integral for the normalizing bands had the same value as the similar sum measured for the reference lane. Based on studies we performed during the development of the GelExplorer method (22), we estimate that the experimental error in a band integral determined by GelExplorer analysis is ±5%.

	RESULTS

TOP ABSTRACT INTRODUCTION EXPERIMENTAL PROCEDURES RESULTS DISCUSSION REFERENCES

The minimal DNA-binding domain of Mac1 consists of the N-terminal 159 residues (8). For our experiments we used a His-tagged derivative of this 159-residue truncated version of Mac1, which we call Mac1_t. Mac1_t binds to the CuRE sequence with an apparent affinity of 5 nM (8). Mac1-(1-194) fused to glutathione S-transferase gave similar results to Mac1_t in DNA binding experiments, demonstrating that the His tag of Mac1_t does not affect DNA binding. We carried out footprinting, missing nucleoside, and methylation interference experiments with Mac1_t bound to the 96-bp CTR1 DNA molecule, which contains two CuRE sites separated by 14 bp. In the CTR1 promoter the two CuRE sites are arranged as an inverted repeat.

Hydroxyl Radical Footprints of Mac1_t Bound to the CTR1 Promoter-- We see a single strong hydroxyl radical footprint for Mac1_t on only one DNA strand in each of the two CuRE sites in the CTR1 promoter (Fig. 2). The region most strongly protected is found at positions 336 to 331 on the coding strand and at 304 to 308 on the noncoding strand. The most protected nucleotides are T(334) on the coding strand and the symmetry-related T(305) on the noncoding strand. The strong footprint is centered on the 5'-TTTG-3' sequence in each CuRE inverted repeat. One or two nucleotides to the 5' side of each CuRE consensus sequence also are protected.

View larger version (47K): [in this window] [in a new window]   Fig. 2.   Hydroxyl radical footprints of Mac1t bound to the CTR1 promoter. A, phosphorimages of denaturing gels from a hydroxyl radical footprinting experiment. Lane G, products of a Maxam-Gilbert guanine-specific sequencing reaction; lane 1, DNA treated with hydroxyl radical; lane 2, Mac1t-DNA complex treated with hydroxyl radical. Brackets to the right of each autoradiograph mark the two CuRE sites present in CTR1. B, densitometer scans of lanes from one of the phosphorimages shown in panel A. Data for the coding strand are shown. Solid line, DNA treated with the hydroxyl radical in the absence of protein. Dashed line, DNA treated with the hydroxyl radical with Mac1t present. C, GelExplorer-derived footprints for Mac1t bound to the CTR1 promoter. Note that the y axes of the two plots are oriented in opposite directions. Positive values in these plots represent nucleotides protected from hydroxyl radical cleavage; negative values represent nucleotides for which cleavage is enhanced in the presence of protein.

Besides the strong single-strand footprint we see in each of the two CuRE sites, much weaker footprints are found on both strands in the 14 bp that separate the CuRE sites (Fig. 2, B and C). The four nucleotides that make up the 3'-half of each CuRE site (5'-CTCA-3') are not protected (in fact, are slightly enhanced in cleavage in the presence of protein). The next 15 nucleotides are protected to a slight but noticeable extent from hydroxyl radical cleavage by bound Mac1_t.

Missing Nucleoside Analysis of Mac1_t Binding to the CTR1 Promoter-- We used the missing nucleoside interference assay to obtain information about specific nucleosides that are important for DNA binding by Mac1_t. In this experiment (20), a protein is allowed to bind to a sample of DNA that has first been randomly gapped by reaction with the hydroxyl radical. Each individual DNA molecule in the sample has at most one gap in its backbone. Certain gaps in the DNA backbone (missing nucleosides) interfere with protein binding, while other gaps have no effect on binding. To determine which missing nucleosides fall into which category, the mixture of gapped DNA and protein is electrophoresed on a native polyacrylamide gel, which separates free DNA from DNA-protein complexes. DNA extracted from the bound and free fractions is subjected to denaturing gel electrophoresis to reveal which missing nucleosides interfered with protein binding, and which had no effect.

The missing nucleoside pattern for the coding strand shows that loss of any of the nucleosides from positions 335 to 328 and 312 to 307 interferes with protein binding (Fig. 3). The pattern for the non-coding strand shows that nucleosides at positions 332 to 324 and 313 to 305 are important for protein binding.

View larger version (33K): [in this window] [in a new window]   Fig. 3.   Missing nucleoside analysis of Mac1t binding to the CTR1 promoter. A, phosphorimages of denaturing gels from a missing nucleoside experiment. Lane G, products of a Maxam-Gilbert guanine-specific sequencing reaction; lane F, hydroxyl radical-treated DNA (the input DNA for the experiment); lane U, gapped DNA that did not bind to Mac1t (unbound DNA); lane B, gapped DNA that bound to Mac1t (bound DNA). The brackets to the right of each autoradiograph mark the two CuRE sites present in CTR1. B, GelExplorer-derived missing nucleoside patterns for Mac1t binding to the CTR1. Integrals of bands in phosphorimages were determined using GelExplorer (22). Plotted is the ratio of the integral of a band in the free DNA lane (F) to the integral of the corresponding band in the bound DNA lane (B), minus 1. Positive values in this plot represent nucleosides whose loss interferes with binding of Mac1t.

Methylation Interference Analysis of Mac1_t Binding to the CTR1 Promoter-- Methylation of any of the guanines in the two CuRE sequences interferes with protein binding (Fig. 4). These results confirm that Mac1_t makes specific interactions in the major groove of the CuRE site.

View larger version (75K): [in this window] [in a new window]   Fig. 4.   Methylation interference analysis of Mac1t binding to the CTR1 promoter. Lane G, products of a Maxam-Gilbert guanine-specific sequencing reaction; lane B, methylated DNA that bound to Mac1t; lane U, methylated DNA that was unable to bind to Mac1t; lane F, input methylated DNA. DNA in each lane was treated with piperidine before denaturing gel electrophoresis to reveal positions of methylated guanines. Guanine residues critical for Mac1t binding are indicated to the right of each autoradiograph. The brackets to the left of each autoradiograph mark the two CuRE sites present in CTR1.

The results of our footprinting, missing nucleoside, and methylation interference experiments are summarized on a helical representation of DNA in Fig. 5.

View larger version (235K): [in this window] [in a new window]   Fig. 5.   DNA binding data for Mac1t superimposed on a double-helical representation of the CTR1 promoter. The strong hydroxyl radical protections observed in the CuRE sites are indicated by green coloring of the sugar-phosphate backbone. The much weaker footprints at the center of the CTR1 promoter (see Fig. 2, B and C) are indicated by yellow coloring of the backbone. The DNA backbone is colored blue where no footprint is observed. Missing nucleoside signals are indicated by red coloring of the bases. Guanine bases at which methylation interference signals are observed are marked by black filled circles. Vertical bars and sequences adjacent to the DNA model mark the positions of the CuRE sites in the CTR1 promoter. The arrow at the top right points to the additional protection seen in the TA CuRE site (see text for details).

	DISCUSSION

TOP ABSTRACT INTRODUCTION EXPERIMENTAL PROCEDURES RESULTS DISCUSSION REFERENCES

Major Groove Interactions-- Both methylation interference and missing nucleoside experiments show that Mac1_t interacts with the major groove of DNA in the CuRE sequence (Fig. 5). Methylation of any of the three guanines in either copy of the CuRE in the CTR1 promoter interferes with binding (Fig. 4). A set of strong missing nucleoside signals (Fig. 3) is found in the same region of the CuRE, supporting this conclusion.

Minor Groove Interactions-- Hydroxyl radical footprinting, which shows how Mac1_t is positioned on the binding site, reveals an interesting structural result. The strongest protections are located exclusively at the 5'-TTTG-3' sequence of each CuRE, on one strand only. One or two adjacent nucleotides to the 5' side of each CuRE also are strongly protected. It is somewhat surprising, based on our experience in footprinting other proteins (19), that a corresponding strong footprint on the other strand is not observed. Instead, the DNA backbone is weakly protected on the other strand across the major groove from the strong footprint (Fig. 5), and no protection is found across the minor groove.

As shown in Fig. 5, the set of strong protections (green) defines the edge of the minor groove that is adjacent to the major groove in which contacts were detected by missing nucleoside and methylation interference experiments. Missing nucleoside signals also are observed at these strongly footprinted nucleotides, further evidence of the importance of these interactions to the binding of Mac1_t to DNA.

The RGRP DNA Binding Motif of Mac1_t-- Several DNA-binding proteins, such as Amt1, Ace1, HMG-I(Y), and Hin recombinase, make important interactions with the minor groove of DNA. A feature held in common by each of these proteins is the amino acid sequence motif GRP (G = glycine; R = arginine; P = proline) (7, 23-26). This sequence motif has been called the AT-hook (27), because it has been found to target A/T-rich sequences for binding. Mac1 has the related motif RGRP near its N terminus (residues 36-39, Fig. 1).

For HMG-I(Y) and Hin recombinase, how the GRP motif (and the related (and overlapping) RGRP motif) interacts with DNA has been determined by NMR (24) and x-ray (28) structural studies, respectively. The (R)GR motif forms a concave surface that is inserted in the minor groove of A/T-rich sequences. Analysis of the x-ray and NMR structures demonstrates that interactions made by arginine are instrumental in sequence-specific binding. The proline in the (R)GRP motif directs the peptide backbone away from the minor groove. Residues in the protein that surround the core (R)GR motif were found to bind to adjacent nucleotides.

We suggest that the RGRP motif of Mac1_t contributes to the strong footprint we see on the T-rich strand of the CuRE. By analogy to the NMR structure of the HMG-I(Y)-DNA complex (24), the two arginines (residues 36 and 38) of Mac1_t's RGRP sequence (Fig. 1) would be oriented so as to interact with thymines in the minor groove. It also is possible that the nearby basic residue Arg-34 interacts with the T·A base pair 5' to the TTT segment of the CTR1 CuRE. Similar to what is seen for other (R)GRP-containing proteins, Pro-39 would direct the peptide chain out of the DNA minor groove so that an adjacent domain of the protein is situated to make the base-specific contacts in the major groove that we observe.

Multiple DNA-binding Modules in Mac1_t-- Our methylation and missing nucleoside interference data show that Mac1_t makes important contacts with the CuRE at the 5'-TTTGCTC-3' sequence on the coding strand and with the 3'-ACGAGT-5' sequence on the noncoding strand, whereas our hydroxyl radical footprinting data show strong protection only of the coding-strand sequence 5'-t(t/a)TTTG-3'. Weak footprints are apparent in the center of the binding site, between the two CuRE repeats. Consideration of both the footprinting and missing nucleoside data suggests to us that there are two distinct DNA binding domains in Mac1_t, perhaps coincident with the two zinc-binding modules of this protein. The N-terminal zinc-binding module, which is thought to bind in the minor groove (4, 7, 15), would be associated with the RGRP motif, and thus participate in making the contacts observed at the TTT sequence at the 5' end of the CuRE. The second zinc module would then make the contacts we observe in the adjacent major groove.

Our model of a modular interaction of Mac1 with DNA recalls the mode of DNA binding of another GRP-containing protein, Hin recombinase. Structural studies on Hin recombinase revealed a helix-turn-helix motif, which binds in the major groove. Residues N-terminal to the helix-turn-helix extend across the phosphodiester backbone to the adjacent minor groove (28-30), where the GRP motif binds. A survey of AT-hook-containing proteins revealed several other examples of proteins with additional and distinct DNA-binding domains in addition to the AT-hook (27). Our hydroxyl radical footprinting and missing nucleoside interference data suggest to us that Mac1_t contacts the TTT sequence on one edge of the minor groove, adjacent to the major groove where methylation interference and missing nucleoside experiments show the protein binds (see Fig. 5).

The remarkable aspect of the Mac1_t footprint, that only one strand is strongly protected at the edge of each CuRE, can be accommodated by this model. We suggest that the RGRP AT-hook motif of Mac1_t is constrained to be located closer to one strand of the minor groove in which it is bound, because of its conjunction with other DNA-binding module(s) of the protein. Protection thus is observed only for the T-rich strand. This is in contrast to the structural results for HMG-I(Y) and Hin recombinase, in which the (R)GRP motif is seen to bind deep in the minor groove and interact with both strands.

Differences in the Interaction of Mac1_t with the Two CuRE Sequences of CTR1-- Kosman and co-workers (9) recently demonstrated that the identity of nucleotides adjacent to the CuRE consensus sequence can affect the DNA binding and transactivation activity of Mac1. The two CuRE sites of CTR1 have identical 8-base pair consensus sequences, but the base pairs to the 5' side of each site differ. In the upstream site the sequence is 5'-TATTTGCTCA-3', while in the downstream site the sequence is 5'-TTTTTGCTCA-3' (reading the other strand), where the 5'-flanking nucleotides are underlined. Kosman and co-workers (9) found that Mac1 binds preferentially to the former (TA) site. Constructs made to contain two TA CuRE sites were more effective at transcriptional activation, while a CuRE site with two TT sites had lower transcriptional activity than wild-type. Our results are consistent with these observations. We find that Mac1_t strongly protects two nucleotides immediately to the 5' side of the upstream (TA) CuRE site (Fig. 5, arrow), while at the downstream (TT) CuRE site only one nucleotide adjacent to the CuRE is protected, and not very strongly at that (see Fig. 2).

Summary and Conclusions-- The results of our chemical footprinting and interference experiments define in detail the interactions that the DNA binding domain of Mac1 makes with the two CuRE sites in the CTR1 promoter of S. cerevisae. Missing nucleoside and methylation interference experiments show clearly that Mac1 binds in the major groove of DNA at the conserved GCTC sequence of the CuRE site. We observe a single strong hydroxyl radical footprint that starts near the middle of each CuRE and extends to nucleotides that flank the 5' side of the site. This strong footprint defines the edge of the major groove in which the protein binds, and the minor groove of the TTT sequence at the 5' side of the CuRE site. We conclude that Mac1 binds in a modular fashion to the CuRE, with the RGRP AT-hook sequence of the protein binding in the T-rich minor groove, and other parts of the protein, likely including zinc-binding motif(s), interacting with the major groove.

	ACKNOWLEDGEMENTS

We gratefully acknowledge the use of densitometry instrumentation maintained by the Institute for Biophysical Research on Macromolecular Assemblies at Johns Hopkins University, which was supported by a National Science Foundation Biological Research Centers Award and by a grant from the W. M. Keck Foundation.

	FOOTNOTES

^* This work was supported in part by United States Public Health Service Grants GM41930 (to T. D. T.) and CA61286 (to D. R. W).The costs of publication of this article were defrayed in part by the payment of page charges. The article must therefore be hereby marked "advertisement" in accordance with 18 U.S.C. Section 1734 solely to indicate this fact.

^§ Recipient of National Research Service Award GM15503 from the United States Public Health Service.

^** To whom correspondence should be addressed. Tel.: 617-353-2482; Fax: 617-353-3535; E-mail: tullius@bu.edu.

	ABBREVIATIONS

The abbreviations used are: CuRE, copper response element; His tag, 6× histidine tag; bp, base pair(s).

	REFERENCES

TOP ABSTRACT INTRODUCTION EXPERIMENTAL PROCEDURES RESULTS DISCUSSION REFERENCES

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