Báo cáo khoa học: Activator-binding domains of the SWI ⁄ SNF chromatin remodeling complex characterized in vitro are required for its recruitment to promoters in vivo pot

Activator-binding domains of the SWI
⁄
SNF chromatin
remodeling complex characterized in vitro are required
for its recruitment to promoters in vivo
Monica E. Ferreira
1,2
, Philippe Prochasson
3,
*, Kurt D. Berndt
1,2
, Jerry L. Workman
3
and Anthony
P. H. Wright
1,2
1 School of Life Sciences, So
¨
derto
¨
rns Ho
¨
gskola, Huddinge, Sweden
2 Department of Biosciences and Medical Nutrition, Karolinska Institutet, Huddinge, Sweden
3 Stowers Institute for Medical Research, Kansas City, MO, USA
ATP-dependent chromatin remodeling complexes are a
group of enzymes that modulate transcriptional activa-
tion, as well as other chromosomal processes, by con-
trolling the accessibility of specific DNA sequences
within chromatin. A large number of remodeling com-
plexes have been identified based on similarities

between their ATPase subunits. The SWI ⁄ SNF com-
plex was the first remodeling complex to be discovered
by studies in yeast but it is conserved in eukaryotes
and has been intensively studied. The yeast SWI ⁄ SNF
complex has an estimated molecular weight of just
over 1 MDa and is composed of twelve different
subunits, one of which is the single ATPase of the
complex, Swi2 ⁄ Snf2 [1–6]. The SWI ⁄ SNF complex
interacts nonspecifically with DNA through multiple
interaction surfaces, using the energy of ATP-hydroly-
sis to remodel chromatin both in cis by sliding histone
octamers along the DNA molecule and in trans by
nucleosome disassembly, evicting H2A ⁄ H2B dimers or
entire histone octamers [7–13].
The inherent ability of SWI ⁄ SNF to influence accessi-
bility of important target sequences is manifested by the
subset of yeast genes that depend on SWI ⁄ SNF for
normal expression during standard growth conditions
on rich media [14,15]. Early functional studies indicated
that SWI ⁄ SNF facilitates DNA binding of transcrip-
Keywords
chromatin remodeling; coactivator
recruitment; SWI ⁄ SNF complex;
transcriptional activation; yeast
Correspondence
A. P. H. Wright, School of Life Sciences,
So
¨
derto
¨

rns Ho
¨
gskola, S-141 89 Huddinge,
Sweden
Fax: +46 8 6084510
Tel: +46 8 6084708
E-mail:
*Present address
Department of Pathology and Laboratory
Medicine, University of Kansas Medical
Center, KS, USA
(Received 15 December 2008, revised 20
February 2009, accepted 23 February 2009)
doi:10.1111/j.1742-4658.2009.06979.x
Interaction between acidic activation domains and the activator-binding
domains of Swi1 and Snf5 of the yeast SWI ⁄ SNF chromatin remodeling
complex has previously been characterized in vitro. Although deletion of
both activator-binding domains leads to phenotypes that differ from the
wild-type, their relative importance for SWI ⁄ SNF recruitment to target
genes has not been investigated. In the present study, we used chromatin
immunoprecipitation assays to investigate the individual and collective
importance of the activator-binding domains for SWI ⁄ SNF recruitment to
genes within the GAL regulon in vivo. We also investigated the conse-
quences of defective SWI ⁄ SNF recruitment for target gene activation. We
demonstrate that deletion of both activator-binding domains essentially
abolishes galactose-induced SWI ⁄ SNF recruitment and causes a reduction
in transcriptional activation similar in magnitude to that associated with a
complete loss of SWI ⁄ SNF activity. The activator-binding domains in Swi1
and Snf5 make approximately equal contributions to the recruitment of
SWI ⁄ SNF to each of the genes studied. The requirement for SWI ⁄ SNF

recruitment correlates with GAL genes that are highly and rapidly induced
by galactose.
Abbreviation
FRET, fluorescence resonance energy transfer.
FEBS Journal 276 (2009) 2557–2565 ª 2009 The Authors Journal compilation ª 2009 FEBS 2557
tional activators and general transcription factors to
target genes [1,16–18]. However, the abundance of the
SWI ⁄ SNF complex was found to be low [1], suggesting
that remodeling of target promoters in vivo requires
recruitment of SWI ⁄ SNF by interaction with specific
transcription factors. Consistently, many activator-
bound sequences in the yeast genome are located within
nucleosome-free regions, such as linker regions, nucleo-
some excluding sequences or regions where maintenance
of the nucleosome-free state depends at least in part on
chromatin binding factors [19–23]. By contrast, TATA
boxes and transcription initiation sites are commonly
found within positioned nucleosomes. Taken together,
these findings suggest that the predominant coactivating
role of SWI ⁄ SNF may be at steps downstream of activa-
tor binding rather than as a facilitator of activator bind-
ing, although these roles are not mutually exclusive, as
exemplified by a recent in vivo study on activation of the
PHO5 gene by the Pho4 activator [24]. Further support
for activator-dependent recruitment of SWI ⁄ SNF comes
from a number of studies demonstrating that the activa-
tion domain of activators is required for SWI ⁄ SNF
recruitment [12,25–29].
Although activator dependence of coactivator recruit-
ment has been well established, fewer studies have

provided evidence for a direct interaction between acti-
vators and coactivators in vivo. Two main approaches
have been adopted to identify direct targets. Using fluo-
rescence resonance energy transfer (FRET) to measure
in vivo interactions between proteins fused to derivatives
of the green fluorescent protein, the activation domain
of the transcriptional activator Gal4 was reported to
interact directly with the Tra1 subunit of the histone
acetyl transferase complex SAGA [30]. A photo-cross-
linking strategy has independently identified Tra1 as a
direct target of Gal4, and several other acidic activators
[31]. Thus, the FRET and cross-linking approaches
appear to cross-validate each other. A photo-cross-
linking approach has identified the Swi1, Snf5 and
Swi2 ⁄ Snf2 subunits of the SWI ⁄ SNF complex as direct
targets bound by several acidic activators [32]. Subse-
quently, two partially redundant regions of Swi1 and
Snf5, respectively, were shown to mediate interaction
with transcriptional activators in vitro [33]. Recombi-
nant activator interaction domains interact with
activation domains in vitro using a two-step mechanism,
where rapid ionic interaction with an unfolded activa-
tion domain is followed by a slow entropy-driven step
during which the activation domain folds [34]. A similar
mechanism has been reported in another activator target
interaction context and it has been suggested that the
intrinsic conformational flexibility of the interaction
mechanism may facilitate activator interactions with
different coactivator targets [35]. Deletion of both acti-
vator-binding domains does not disrupt the composi-

tion, stability or catalytic properties of the SWI ⁄ SNF
complex, but the phenotype of a mutant lacking both
domains differs from the wild-type [33]. Thus, it is
possible that the phenotypic defects are a result of the
inability of this mutant SWI ⁄ SNF complex to interact
with- and be recruited by- activator proteins in vivo.
This conclusion would support the importance of acti-
vator-dependent recruitment of SWI ⁄ SNF in relation to
other possible recruitment mechanisms mediated via the
nonspecific DNA binding domains in the complex, the
acetyl-histone binding bromo-domain of Swi2⁄ Snf2 or
protein interactions mediated by accessory subunits that
could also potentially contribute to SWI ⁄ SNF recruit-
ment in vivo [7,13,36,37].
The present study aimed to determine whether the
activator-binding domains of the SWI ⁄ SNF complex
are important for its recruitment to target genes
in vivo, as well as for their transcriptional activation.
We also investigated the relative significance of the
two activator-binding domains for recruitment of
SWI ⁄ SNF to different target genes.
Results
A subset of GAL genes require SWI/SNF activity
for efficient activation by galactose
To determine whether the activator-binding domains
of the SWI ⁄ SNF complex are important for its recruit-
ment to promoters in vivo and to determine whether
the Swi1 and Snf5 domains are differentially important
on different promoters, we required a group of genes
that are activated by the same activator. We chose to

study the GAL regulon, which is known to be regu-
lated by the Gal4 activator protein. We first tested a
group of known Gal4 target genes [38] to identify a
group of genes showing robust induction under our
conditions. Table 1 shows that several GAL genes are
activated shortly after addition of galactose to cultures
grown with raffinose as carbon source. Induction of
PGM2, FUR4, MTH1 and PCL10 was not detected
under our conditions. It is likely that these genes are
induced at a later time after galactose addition. Using
the identified set of galactose-induced genes, we next
screened for those genes that require the SWI ⁄ SNF
complex for induction by galactose. For this purpose,
we used strain YPP33, in which the entire ORFs of
SWI1 and SNF5 are both deleted, because deletion of
these genes has been shown to disrupt the integrity
of the SWI ⁄ SNF complex [39,40]. The most appropriate
time for revealing SWI ⁄ SNF dependence was found to
Mechanism of SWI ⁄ SNF recruitment to promoters M. E. Ferreira et al.
2558 FEBS Journal 276 (2009) 2557–2565 ª 2009 The Authors Journal compilation ª 2009 FEBS
be 30 min after galactose addition to the cultures.
Under these conditions GAL1, GAL10, GCY1, GAL2
and GAL7 showed a high degree of SWI ⁄ SNF depen-
dence for induction by galactose (Fig. 1). GAL80 and
GAL3 did not show significant SWI ⁄ SNF dependence,
nor did PGM2, which was included as a control to
represent those genes that were not induced at this
time-point. We conclude that a subset of Gal4-induc-
ible genes were induced under our conditions, and that
a further subset of these genes were SWI ⁄ SNF depen-

dent. The SWI⁄ SNF-dependent set of galactose-
induced genes was studied further.
Identification of galactose-induced genes that are
direct targets of SWI
⁄
SNF
Before we could test the significance of the Swi1 and
Snf5 activator interaction domains, it was necessary to
investigate whether the selected genes were direct tar-
gets of the SWI ⁄ SNF complex. We therefore used a
chromatin immunoprecipitation assay to determine
whether the SWI ⁄ SNF complex is associated with the
promoters of the selected genes under identical galac-
tose induction conditions. A schematic of the investi-
gated GAL promoter regions is shown in Fig. 2A.
Figure 2B shows that SWI ⁄ SNF is recruited to the
GAL1-10, GAL2 and GAL7 promoters within 30 min
of galactose induction. It is noteworthy that the GAL1
and GAL10 genes are divergent genes regulated by a
common regulatory region. SWI ⁄ SNF recruitment to
GCY1 did not differ significantly from the ILS1 gene
that is not regulated by SWI ⁄ SNF. The specificity of
the Snf2 antibody used in this assay was demonstrated
by the observation that only background levels of
precipitation were observed using chromatin extracts
lacking the Snf2 protein (Fig. 2C). Based on these
observations, we conclude that GAL1, GAL10, GAL2
and GAL7 are direct targets bound by SWI ⁄ SNF
under our experimental conditions.
The activator-binding domains of Swi1 and Snf5

are required for promoter recruitment of the
SWI
⁄
SNF complex
We next studied the level of SWI ⁄ SNF recruitment to
the GAL1-10, GAL2 and GAL7 regulatory regions in
strains lacking either or both the Swi1 (residues 329–
655) and Snf5 (residues 2–327) activator-binding
domains, 30 min after galactose induction. Quantifying
recruitment in relation to background binding to the
promoter of the SWI ⁄ SNF-independent ILS1 gene, we
found that SWI ⁄ SNF recruitment to GAL1-10 and
GAL2 is reduced by approximately 50% in strains
lacking either the Swi1 or the Snf5 activator-binding
domains (Fig. 3). In the strain lacking both activator-
binding domains, the level of SWI ⁄ SNF recruitment is
reduced to background levels. We have consistently
observed that the activation domains are required for
the recruitment of SWI ⁄ SNF to the GAL7 gene, but
technical problems have thus far prevented acquisition
of quantitative data. We conclude that the activator-
binding domains identified in vitro are essential for
SWI ⁄ SNF recruitment in vivo and that Swi1 and Snf5
Table 1. Wild-type induction 30 min post galactose addition:
screening by real-time RT-PCR.
Gene Fold induction
GAL2 522
GAL1 > 1000
GAL7 > 1000
GAL10 197

PGM2 1.2
GAL80 4.6
GAL3 51
GCY1 1.8
FUR4 1.5
a
MTH1 0.7
PCL10 2.4
a
a
Large clonal variation.
Fig. 1. Identification of SWI ⁄ SNF dependent GAL genes. Normal-
ized expression of galactose-induced genes 30 min after galactose
addition in strain YPP33 (grey bars, swi1D, snf5D), in which the
entire ORFs of SWI1 and SNF5 are deleted, relative to normalized
expression in the wild-type strain (arbitrarily set to 1, black bars,
Wt). PGM2 was included as a non-induced control. The expression
levels of Gal4 target genes, quantified by real-time PCR after cDNA
synthesis, were normalized against expression of a control gene,
ILS1, and normalized expression levels were scaled to give a wild-
type value of 1 for all tested genes. Error bars indicate the SD of
mean values from three independent cultures.
M. E. Ferreira et al. Mechanism of SWI ⁄ SNF recruitment to promoters
FEBS Journal 276 (2009) 2557–2565 ª 2009 The Authors Journal compilation ª 2009 FEBS 2559
contribute similarly to its recruitment to GAL1-10 and
GAL2.
The activator-binding domains of Swi1 and Snf5
are required for galactose-induced expression of
SWI
⁄

SNF-dependent genes
It was next necessary to determine whether the defect
in SWI ⁄ SNF recruitment resulting from the deletion of
one or both activator-binding domains would lead to
reduced galactose-induced expression of target genes.
Figure 4 shows that induction of GAL1, GAL10,
GAL2 and GAL7 is severely reduced in a strain lacking
both the Swi1 and Snf5 activator-binding domains.
Recruitment of the SWI ⁄ SNF complex via activator
interactions with these activator-binding domains is
thus critical for normal galactose induction of the
tested genes. Interestingly, the strains lacking either the
Fig. 3. The activator-binding domains of the SWI ⁄ SNF complex are
required for its recruitment to promoters. Enrichment of the immu-
noprecipitated GAL1-10 and GAL2 promoters under inducing condi-
tions (galactose, 30 min) in the wild-type strain (black bars, Wt),
strain YPP310 (light grey bars, DDABDswi1 + snf5) lacking both
activator-binding domains (SWI1D329-655, SNF5D2-327), strain
YPP211 (white bars, DABDsnf5) lacking the Snf5 activator-binding
domain (SNF5D2-327) and strain YPP247 (dark grey bars, DAB-
Dswi1) lacking the Swi1 activator-binding domain (SWI1D329-655).
The level of SWI ⁄ SNF enrichment on the promoters is relative to
the negative control promoter, ILS1. Error bars indicate the values
obtained from two independent experiments.
A
B
C
Fig. 2. SWI ⁄ SNF is recruited to the GAL1-10, GAL7 and GAL2 pro-
moters within 30 min of galactose induction. (A) Schematic of the
investigated GAL promoter regions. Solid black lines indicate the

promoter regions that were used as the input sequence for primer
design using
PRIMER3 software. The positions of primers used for
detection in chromatin immunoprecipitation experiments are
indicated by arrows. (B) Amount of promoter DNA, detected by
real-time PCR, for different genes in wild-type cells grown under
non-inducing conditions (grey bars, Raf) and inducing conditions
(galactose 30 min, black bars, Gal) precipitated by anti-Snf2 serum,
shown as a percentage of input (% IP). ILS1 is included as a
SWI ⁄ SNF-independent control. The asterisk indicates the level of
background with beads only. Error bars indicate the values obtained
from two independent cultures. (C) Enrichment of the GAL1-10
promoter relative to a region of the ILS1 coding sequence under
inducing conditions, using different amounts of Snf2 antibody on
extracts from the SNF2 deletion strain 11586 (grey bars, snf2D)
and the wild-type strain (black bars, Wt).
Mechanism of SWI ⁄ SNF recruitment to promoters M. E. Ferreira et al.
2560 FEBS Journal 276 (2009) 2557–2565 ª 2009 The Authors Journal compilation ª 2009 FEBS
Swi1 or Snf5 activator-binding domains showed little,
if any, reduction in the level of galacose induction of
the same genes. Thus, the small reduction in SWI ⁄ SNF
recruitment observed in these mutants is not sufficient
to cause a reduction in induced gene expression under
the conditions studied.
Discussion
The galactose regulon in Saccharomyces cerevisiae is
an appropriate system for studying the components of
coactivators that are required for their recruitment.
During growth on nonrepressing, non-inducing sugars
such as raffinose, the Gal4 activator is bound to its

DNA binding sites in target genes but its activity is
repressed by its association with the Gal80 repressor
protein. Upon addition of galactose to such cultures,
the Gal3 protein antagonizes Gal80-mediated repres-
sion and Gal4 is immediately able to recruit necessary
factors to its target genes [41]. As shown in the present
study, the SWI ⁄ SNF complex is rapidly recruited to a
subset of Gal4 target genes within 30 min of galactose
addition, and defects affecting the SWI ⁄ SNF complex
caused reduced activation of these genes within the
same time window. The activator-binding domains in
the Swi1 and Snf5 subunits of the SWI ⁄ SNF complex
are essential for recruitment of the SWI ⁄ SNF complex
to these genes, as well for their subsequent activation.
Our observation thus strongly supports the model pro-
posing that the activator-binding domains, largely
defined and characterized in vitro, are necessary for
SWI ⁄ SNF recruitment in vivo. This is crucial for
understanding the roles played by the different
SWI ⁄ SNF subunits and, from the results obtained in
the present study, we can now add that other regions
of SWI ⁄ SNF cannot replace the recruiting function of
the Swi1 and Snf5 activator-binding domains. The
in vivo validation of the Swi1 and Snf5 activator-bind-
ing domains is also of interest in relation to the two-
step binding mechanism between Gal4 and Swi1 that
has been characterized in vitro [34], and our results
suggest that the coupled binding and folding mecha-
nism is likely to be relevant in vivo. This binding mech-
anism is assumed to be generally important for

transcription factor interactions with other proteins
and may be important for the function of the increas-
ingly large group of proteins that have been shown to
contain intrinsically unstructured regions. The intrinsic
conformation flexibility that is inherent in this binding
mechanism would help to explain how activator
proteins are able to form specific interactions with the
large range of structurally distinct factors that they
recruit to target genes.
The Swi1 and Snf5 activator-binding domains
appear to work additively because deletion of one or
the other domain individually reduces SWI ⁄ SNF
recruitment to approximately 50% of that seen in
wild-type cells. The existence of two activator-binding
domains might be an adaptation to the fact that acti-
vators generally bind DNA as dimers, with the result
that two activation domains are available to recruit
target factors via two independent interactions. Alter-
natively, a larger number of activator-binding domains
could contribute to recruitment by increasing the prob-
ability of contact between activator and coactivator,
leading to a faster on-rate during recruitment. The
Fig. 4. The activator-binding domains of the SWI ⁄ SNF complex are
required for activation of target promoters. Normalized expression
of the GAL1, GAL10, GAL2 and GAL7 genes under inducing
conditions (galactose, 30 min), in strain YPP310 (light grey bars,
DDABDswi1 + snf5) lacking both activator-binding domains
(SWI1D329-655, SNF5D2-327), strain YPP211 (white bars, DAB-
Dsnf5) lacking the Snf5 activator-binding domain (SNF5D2-327) and
strain YPP247 (dark grey bars, DABDswi1) lacking the Swi1 activa-

tor-binding domain (SWI1D329-655), relative to the wild-type tested
in parallel (black bars, Wt, level arbitrarily set to 1). GAL transcript
levels were quantified by real-time PCR after cDNA synthesis and
normalized against transcript levels of a control (ILS1) to obtain nor-
malized GAL expression. Normalized GAL expression levels were
subsequently scaled to give a wild-type value of 1 for all tested
genes. Error bars indicate the SD of means obtained from three
independent cultures.
M. E. Ferreira et al. Mechanism of SWI ⁄ SNF recruitment to promoters
FEBS Journal 276 (2009) 2557–2565 ª 2009 The Authors Journal compilation ª 2009 FEBS 2561
latter alternative is consistent with measurements
showing rapid dynamics of activator and coactivator
association and disassociation with chromatin in vivo
[42,43]. For the genes investigated in the present study,
we have not observed differences in the relative impor-
tance of the Swi1 and Snf5 activator interaction
domains during SWI ⁄ SNF recruitment to different
genes. It remains possible that the two interaction
domains play differential roles on other SWI ⁄ SNF-
dependent genes or under different physiological
conditions; for example, during mitosis when a larger
number of genes become SWI ⁄ SNF dependent [44].
We have previously shown that such differences can
exist as demonstrated by the observation that different
subunits of the Tup-Ssn6 corepressor complex are
differentially important for the repression of different
target genes in fission yeast [45,46].
Swi1 and Snf5 are known to be required for the
structural integrity of the SWI ⁄ SNF complex [39,40].
The defect in transcriptional activation of GAL genes

in the mutant lacking both the Swi1 and Snf5 activator
interaction domains is essentially the same as that
observed in the absence of both subunits. Therefore,
the two activation domains appear to be essential for
SWI ⁄ SNF activity, at least for the genes that we have
studied. This is expected if SWI ⁄ SNF recruitment by
activator proteins is required for its activity. However,
in mutants lacking only one of the activator-binding
domains, the transcriptional activation levels were not
affected under our conditions, despite the observed
50% reduction in SWI ⁄ SNF recruitment. One possible
explanation for the lack of an exact correlation
between the amount of recruited SWI ⁄ SNF and tran-
scriptional activation could be that the wild-type
SWI ⁄ SNF complex is recruited in excess, at least under
the conditions investigated. Another possibility is that
the reduced level of SWI ⁄ SNF recruitment does not
affect transcriptional activation as a result of the com-
pensatory action of some other factor. The SAGA
complex, another Gal4-associated co-activator
[30,47,48], is a potential candidate for such a factor
because partial redundancy between SWI ⁄ SNF and
Gcn5, the histone acetyl transferase of SAGA, has pre-
viously been demonstrated in relation to activation of
the SUC2 gene [49].
Among the collection of GAL genes screened in the
present study, we identified both SWI ⁄ SNF-dependent
genes as well as GAL genes that have little or no
requirement for SWI ⁄ SNF. SWI ⁄ SNF dependence was
associated with a class of highly inducible GAL genes

(GAL1, GAL10, GAL2 and GAL7), whereas genes
showing lower inducibility by galactose after 30 min
(GAL3, GAL80 and PGM2) were not significantly
dependent on SWI ⁄ SNF. Thus, the extent of
SWI ⁄ SNF dependence may depend on the extent
and ⁄ or rate of induction. GCY1 is an exception
because it was strongly dependent on SWI ⁄ SNF, even
though it is relatively mildly induced by galactose. The
results obtained in the present study suggest that
GCY1 is an indirect target of SWI ⁄ SNF because we
were unable to detect an association of SWI ⁄ SNF with
GCY1. However, other explanations are possible. For
example, SWI ⁄ SNF might interact with regions of
GCY1 that are not detected by the primers used.
Unlike the other SWI ⁄ SNF-dependent genes, basal
levels of GCY1 expression were also dependent on
SWI ⁄ SNF (data not shown). It is therefore likely that
a factor required for GCY1 expression in both unin-
duced and induced conditions is SWI ⁄ SNF dependent.
Although an association of SWI ⁄ SNF with the GAL1-
10 and GAL7 genes has been reported previously [50],
albeit under different conditions than those reported
here, SWI ⁄ SNF association with GAL2 is a novel find-
ing of the present study. Furthermore, we demonstrate
that SWI ⁄ SNF is important for the efficient activation
of a number of GAL genes upon galactose induction
of cultures grown with raffinose as carbon source,
which comprise conditions where SWI ⁄ SNF has previ-
ously been reported not to play a role [51]. This
discrepancy may be explained by differences in assay

conditions because the apparent dependence on
SWI ⁄ SNF is lower at later times after galactose induc-
tion under our conditions (data not shown). It is thus
possible that SWI ⁄ SNF is predominantly required for
the transition to induced expression levels rather than
their maintenance under prolonged growth on
galactose.
Experimental procedures
Yeast strains
The yeast strains used in the present study are listed in
Table 2. Genomic partial deletions of the SWI1 and SNF5
ORFs, corresponding to amino acid residues 329–655 of
Table 2. Strains used in the present study.
Strain Relevant genotype Reference
W303 1A Wild-type [55]
YPP33 swi1D::HIS, snf5D::HIS [33]
YPP247
a
SWI1D329-655 Present study
YPP211
a
SNF5D2-327 Present study
YPP310
a
SWI1D329-655, SNF5D2-327 Present study
11586 snf2D::KanMX4 [56]
a
Isogenic to W303 1A.
Mechanism of SWI ⁄ SNF recruitment to promoters M. E. Ferreira et al.
2562 FEBS Journal 276 (2009) 2557–2565 ª 2009 The Authors Journal compilation ª 2009 FEBS

Swi1 and 2–327 of Snf5, were made using the Cre-loxP
system [52] and verified by PCR.
Galactose induction experiments
Yeast were pre-cultured in yeast-peptone-dextrose medium
at 30 °C for approximately 24 h, washed and diluted in
sterile-filtered YP 2% raffinose, supplemented with adenine,
and grown for at least 16 h until a D
600
of approximately
0.4–0.7 was reached, at which point each culture was split
in two and induced for 30 min at 30 °C by the addition of
one-tenth of the culture volume of a 20% galactose solu-
tion, or mock induced using an equal volume of sterile
deionized water.
Preparation of RNA
Samples for total RNA extraction were harvested at room
temperature by centrifugation, immediately frozen in liquid
nitrogen and stored at )70 °C until purification. Total
RNA was extracted using hot phenol extraction, followed
by further purification using an RNA Easy mini kit (Qia-
gen, Solna, Sweden). Total RNA was treated with amplifi-
cation grade DNase I (Invitrogen, Lidingo
¨
, Sweden)
according to manufacturer’s instructions, followed by
another round of purification using an RNA Easy mini kit.
The quality of RNA was checked by electrophoresis of
total RNA, and by control RT-PCR, using 50 ng total
RNA per 25 lL of reaction, 200 nm each of ARN1 specific
primers and SuperScript III Platinum One-Step RT-PCR

System with Platinum Taq (Invitrogen), followed by elec-
trophoresis. RNA preparations were verified DNA-free by
control reactions without reverse transcriptase.
Chromatin immunoprecipitation
The chromatin immunoprecipitation protocol was adapted
from a previously described method [53], with several modi-
fications. Samples were cross-linked for 1 h. Lysis was
carried out using a bead-beater and lysis buffer contained
150 mm NaCl. Prior to immunoprecipitation, lysates were
pre-cleared by 1 h incubation at 4 °C with Protein A
Agarose ⁄ Salmon Sperm DNA (catalogue number 16-157;
Millipore, Solna, Sweden), and the total protein concentra-
tion of pre-cleared chromatin extracts determined using the
Bradford assay. Chromatin equivalent to 25 lg of total
protein was used in each IP reaction, incubated overnight
at 4 °C with 5 lg of a polyclonal rabbit Snf2 antibody
(catalogue number sc-33629; SDS Biosciences, Falkenberg,
Sweden), followed by Protein A Agarose ⁄ Salmon Sperm
DNA incubation for no more than 1 h. Beads were washed
twice for 15 min in lysis buffer containing 150 m m NaCl,
followed by a 15-min wash in lysis buffer containing
500 mm NaCl, two 15-min washes in deoxycholate buffer
and, finally, a 5-min wash in TE buffer. Chromatin was
eluted from washed beads by 1 h of incubation with elution
buffer at 65 °C, repeated once, and cross-links were sub-
sequently reversed by overnight incubation at 65 °C. After
proteinase K treatment, samples were treated with RNase
(Roche, Bromma, Sweden) and purified using PCR clean-
up columns (Qiagen). The specificity of the antibody was
tested with a non-isogenic Dsnf2 strain as a control, using

1, 5 and 10 lg of Snf2 antibody per reaction, and the
routinely-used beads only as a control.
Real-time PCR and RT-PCR
Quantitative PCR was performed in duplicate 25-lL reac-
tions using the MyiQ Single-Color Real-Time PCR Detec-
tion System (Bio-Rad, Sundbyberg, Sweden), 200 nm of
each primer and, unless otherwise stated, iQ SYBR Green
Supermix (Bio-Rad). One-step quantitative RT-PCR was
performed with SuperScript III Platinum SYBR Green One-
Step qRT-PCR kit (Invitrogen) supplemented with 10 n m
fluorescein (Invitrogen), using 50 ng of total RNA per reac-
tion, and expression of ARN1 was used for normalization.
For two-step qRT-PCR, cDNA was prepared using iScript
cDNA Synthesis kit (Bio-Rad), containing oligo-dT and
random primers. cDNA corresponding to 50 ng of input
total RNA was used for each subsequent quantitative PCR
reaction with specific primers, and expression of ILS1 was
used for normalization. Unless otherwise stated, the ILS1
promoter region was used for normalization in chromatin
immunoprecipitation experiments for comparison of wild-
type and mutant strains. Primers used for quantification of
transcripts and promoter regions were for the most part
designed using primer3 software [54]. Primer sequences are
available from the authors upon request.
Acknowledgements
We thank Professor Hans Ronne at Uppsala Univer-
sity for sharing the SNF2 deletion strain. This work
was supported by a grant to A.W. from the Swedish
Research Council, and by a Leukemia and Lymphoma
Society Special Fellowship to P.P.

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