Subtelomeric chromatin is subject to evolutionarily conserved complex epigenetic regulation and is implicated in numerous aspects of cellular function including formation of heterochromatin, regulation of stress response pathways and control of lifespan. Subtelomeric DNA is characterized by the presence of specific repeated segments that serve to propagate silencing or to protect chromosomal regions from spreading epigenetic control. In this study, analysis of genome‐wide chromatin immunoprecipitation and expression data, suggests that several yeast transcription factors regulate subtelomeric silencing in response to various environmental stimuli through conditional association with proto‐silencing regions called X elements. In this context, Oaf1p, Rox1p, Gzf1p and Phd1p control the propagation of silencing toward centromeres in response to stimuli affecting stress responses and metabolism, whereas others, including Adr1p, Yap5p and Msn4p, appear to influence boundaries of silencing, regulating telomere‐proximal genes in Y′ elements. The factors implicated here are known to control adjacent genes at intrachromosomal positions, suggesting their dual functionality. This study reveals a path for the coordination of subtelomeric silencing with cellular environment, and with activities of other cellular processes.
It is well established that environmental conditions modulate gene expression through local binding of a variety of conditionally active transcription factors, each responsive to specific environmental cues. However, another prevalent mechanism of gene regulation in eukaryotic cells is the long‐range control of groups of genes by chromatin modifications or other position‐dependent mechanisms. One such phenomenon, gene silencing, is an important and evolutionarily conserved mode of regulation that controls expression of subtelomeric genes. These genes are enriched for stress response and metabolic genes and their regulation is controlled by the spreading of silencing molecules from chromosome ends (telomeres) into subtelomeric regions. Levels of subtelomeric silencing have been linked to cellular lifespan, and study of the regulation of silencing is fundamental to our understanding of human aging. The spread of silencing in subtelomeric regions is discontinuous, and is controlled by various genomic elements that can either relay and enhance silencing from telomeres (proto‐silencing) or create boundaries that protect some genomic regions from silencing. In yeast, every subtelomeric region contains an X element that proto‐silences centromere‐proximal genes, and also insulates telomere‐proximal genes from silencing.
In this paper, we identify a regulatory mechanism to control X element‐mediated proto‐silencing and insulating activities in response to environmental cues. The mechanism was identified using chromosome position analysis of microarray‐based chromatin immunoprecipitation (ChIP‐chip) data for environment‐responsive TFs and genome‐wide gene expression data under the same conditions. The mechanism involves the conditional association of environment‐responsive transcription factors to X elements. The binding at X elements results in regulation of proto‐silencing of centromere‐proximal genes, or insulation of telomere‐proximal genes (depending on the factor) in response to environmental stimuli related to stress response and metabolism. One example is shown below (Figure 4B). Transcription factor, Oaf1p, conditionally binds X elements in the presence of fatty acids and enhances proto‐silencing specifically under this condition. Oaf1p and several other factors implicated here are known to control adjacent genes at intrachromosomal positions, suggesting their dual functionality in both gene‐specific transcriptional regulation, and long‐range position‐dependent mechanism. Investigation of this mechanism during the response to fatty acid exposure showed that conditional proto‐silencing activity is dependent on Sir2p, a molecule known to be involved in subtelomeric silencing related to aging. This study reveals a path cells can use to coordinate subtelomeric silencing related to aging with cellular environment, and with the activities of other cellular processes.
Chromosome position analysis of ChIP‐chip data revealed that several carbon source and stress‐responsive yeast transcription factors conditionally bind subtelomeric X elements.
Integration of several microarray gene expression data sets showed that, in this context, the factors conditionally control the boundaries and strength of subtelomeric silencing.
Regulation of silencing by a fatty acid‐responsive factor was found to be dependent on Sir2p and independent of Hda1p.
These findings provide a critical link for establishing the mechanisms by which telomere biology is coordinated with other cellular processes including responses to environmental stimuli, aging and adaptation.
It is well established that environmental conditions modulate gene expression through local binding of a variety of conditionally active transcription factors (TFs), each responsive to specific environmental cues. However, another prevalent mechanism of gene regulation in eukaryotic cells is the long‐range control of groups of genes by chromatin modifications or other position‐dependent mechanisms. One such phenomenon, subtelomeric silencing, is an important and evolutionarily conserved mode of regulation that has been linked to cellular lifespan (Dang et al, 2009; Mak et al, 2009). Silencing factors, Sir2p, Sir3p and Sir4p bind to telomere repeat regions at chromosomal ends through interactions with the telomere‐binding protein Rap1p (Rusche et al, 2003). Cooperative binding leads to a spread of silencing activity toward the centromere, silencing the expression of nearby subtelomeric genes. Silencing is further augmented through the clustering and tethering of telomeres to the nuclear envelope, increasing the local concentration of silencing molecules near subtelomeric regions (Buhler and Gasser, 2009). However, additional anti‐ and proto‐silencing mechanisms exist to exert complex control of genes positioned within these subtelomeric regions (Fourel et al, 2002). Elucidation of how subtelomeric silencing and other telomere‐related processes are coordinated with both cellular environment and the activities of other cellular processes is fundamental to our understanding of human conditions including aging and cancer.
Nuclear chromosomes of Saccharomyces cerevisiae terminate with telomeric repeats characterized by stretches of the sequence TG1–3 (Shampay et al, 1984). Regions proximal to these repeats contain two different kinds of subtelomeric repeat regions (STRs) called X and Y′ elements (Pryde and Louis, 1997). X elements are short repetitive regions found on every telomere and are either adjacent to telomeric repeats, or are separated from telomeres by one or more Y′ elements. All X elements contain a 473‐bp core sequence containing an ARS consensus sequence and usually a binding site for the general regulatory factor (GRF), Abf1p. Many X elements also contain repeat regions on their telomeric side that contain a binding site for the GRF, Tbf1p (Louis et al, 1994; Pryde et al, 1995). Y′ elements are highly polymorphic repetitive elements of ∼5–7 kb that are found between terminal telomeric repeats and X elements on 17 of the 32 telomeres (Chan and Tye, 1983; Louis and Haber, 1990, 1992).
X elements are proto‐silencers that both relay and enhance silencing from telomeres. In subtelomeric regions, maximal gene silencing and Sir2p, Sir3p and Rap1p binding occur at X elements and diminish toward centromeres (Fourel et al, 1999; Pryde and Louis, 1999; Zhu and Gustafsson, 2009). Proto‐silencing by X elements is dependent on Sir2, ‐3 and ‐4, and yKu70, a protein involved in tethering telomeres to the nuclear envelope (Pryde and Louis, 1999). X elements are also involved in establishing chromatin domain boundaries that protect Y′ element genes from silencing. In this case, GRFs facilitate interactions between X elements and Rap1p–Sir complexes, resulting in highly repressed heterochromatin, which spreads toward centromeres, bypassing Y′ elements (Fourel et al, 1999, 2002; Pryde and Louis, 1999; Zhu and Gustafsson, 2009). It has been proposed that this discontinuous spread of silencing is facilitated by telomeres folding onto themselves resulting in contact between telomeres and subtelomeres, and looping out of Y′ elements (Strahl‐Bolsinger et al, 1997; Pryde and Louis, 1999).
Subtelomeric regions (within 25 kb of telomeres) contain many uncharacterized genes, but are also enriched for genes encoding helicases implicated in telomere maintenance (present in Y′ elements) (Yamada et al, 1998), as well as genes involved in carbon source utilization (Pryde and Louis, 1997) and stress responses (Wyrick et al, 1999; Ai et al, 2002; Robyr et al, 2002). Subtelomeric gene expression and silencing can be dynamically regulated by environmental cues (Ai et al, 2002); however, the mechanisms controlling these activities remain to be understood. One study identified enrichment of TFs in subtelomeric regions in response to stress, and suggested that conditional binding of TFs upstream of genes in this region conditionally controlled their expression in a manner linked to histone deacetylase Hda1p (Mak et al, 2009).
In this study, we reveal a novel and fundamental mechanism for the regulation of subtelomeric silencing in response to environmental stimuli including stress and carbon source. Using chromosome position analysis of microarray‐based chromatin immunoprecipitation (ChIP‐chip) data for environment‐responsive TFs and genome‐wide gene expression data under the same conditions, we show that several environment‐responsive TFs interact with subtelomeric X elements and conditionally regulate their proto‐ and anti‐silencing activities in response to environmental stimuli. Investigation of this mechanism during the response to fatty acid exposure showed that conditional proto‐silencing activity is dependent on Sir2p and independent of Hda1p. TFs implicated in this process have previously been shown to modulate the expression of adjacent genes in response to the same stimuli, and have not previously been implicated in the regulation of silencing. The potential of this mechanism to coordinate telomere biology with environmental stimuli and other cellular processes is discussed.
Oaf1p conditionally binds subtelomeric X elements
Through network analysis of protein–DNA interactions from ChIP‐chip data, we have previously shown that four TFs, Oaf1p, Pip2p, Oaf3p and Adr1p, dynamically cooperate in the presence of fatty acids (Smith et al, 2007; Ratushny et al, 2008). These factors control two distinct classes of genes: those conditionally targeted by Oaf1p, Oaf3p and Adr1p, which enrich for general stress response genes downregulated by the stimulus, and those conditionally targeted by all four factors, which enrich for genes involved in fatty acid metabolism and are upregulated by the stimulus. Oaf1p is both a repressor and an activator, providing specificity and coordination of the two responses; it heterodimerizes with Pip2p and directly upregulates genes involved in fatty acid metabolism, and it binds independently of Pip2p to negatively regulate the class of genes involved in general stress response.
We sought to characterize the repressive activity of Oaf1p. Chromosome position analysis revealed that targets of Oaf1p in the context of negative regulation (those conditionally targeted by Oaf1p, Adr1p and Oaf3p, but not Pip2p) are enriched at regions within 10 kb of telomeres (Figure 1A). We did not detect a regional preference for the subclass of genes positively regulated by Oaf1p and none of these intergenic regions were within 10 kb of telomeres (data not shown). A higher resolution analysis of subtelomeric regions revealed striking enrichment of the targets between 5 and 7 kb from telomeres (Figure 1B; blue bars). In all, 25–30% of probes in these regions were bound by the three factors, considerably more than the 1% was expected if targets had no positional preference (green vector).
The positional enrichment of Oaf1p binding prompted us to test whether subtelomeric targets of Oaf1p coincided with X elements, which are found either at the telomeric ends of subtelomeric regions or centromere‐proximal to one or two 5–7 kb Y′ elements (Supplementary Figure S4) (Table I). Remarkably, 14 of the 15 X elements represented on the intergenic arrays were bound by Oaf1p, 79% of which had a binding pattern consistent with Oaf1p‐negative regulation (bound by Adr1p, Oaf1p, Oaf3p in the presence of fatty acid) and none had a binding pattern consistent with Oaf1p activation (bound by Oaf1p and Pip2p). These data suggest that Oaf1p conditionally binds X elements, and functions as a negative regulator in this context.
Other environment‐responsive TFs conditionally bind X elements
To determine whether this X element‐binding property of Oaf1p is shared with other environment‐responsive factors, a comprehensive ChIP‐chip data set of 203 yeast TFs (Harbison et al, 2004) was analyzed. Factors that were found to interact with at least one X element‐containing probe on the microarrays are shown in Figure 2. The top two graphs (Figure 2A and B) show factors that were analyzed in the absence and presence of a stress stimulus, while the bottom graph (Figure 2C) shows factors tested only in the absence of stress. Bars marked with asterisks correspond to factors that significantly enriched at X elements. This analysis identified 19 factors that appeared to (conditionally) concentrate at X elements, including known X element‐binding proteins Rap1p (Zhu and Gustafsson, 2009) and Reb1p (Chasman et al, 1990).
Some of the TFs that enriched at X elements have previously been shown to enrich in promoter regions of genes within subtelomeres (marked with a white circle on or above the bar) (Mak et al, 2009). Therefore, we determined the subtelomeric‐binding profiles of the factors to determine whether they specifically enrich at X elements compared with the rest of the subtelomeric region (Figure 3). Binding profiles correlated with the position of X elements with Pearson's correlation coefficients >0.8 and P‐values <1 × 10−6, with the exception of Phd1p, which had a coefficient of 0.51 and P=0.0045. This correlation of TF binding with X elements was not detected by a previous analysis (Mak et al, 2009) possibly because of the lower resolution of the previous study (which tested genomic fragments of ∼390 kb compared with 10 kb used here). In addition, the previous study analyzed the positions of all X elements for correlation, whereas here, X elements that were not present on the microarrays were excluded from the analysis.
Analysis of X element binding with high resolution tiled arrays
To further characterize the interaction of TFs with X elements, an in depth analysis of Oaf1p binding was conducted by repeating the ChIP of Oaf1p in the absence or presence of medium containing fatty acids, and analyzing the targets on tiled microarrays of the entire yeast genome (see Materials and methods). Subtelomeric‐binding profiles under each condition were determined and are shown as histograms of the mean number of peaks per chromosome arm (Figure 4A, top two panels). These data revealed that Oaf1p targets in the presence of fatty acids were not only enriched 5–7 kb from telomeres, but were also enriched within 1 kb of telomeres, whereas in the absence of fatty acids the profile was similar to background (compare blue bars to red vector of mean binding frequency per kb in the entire genome). The Oaf1p‐binding profile was strongly correlated with the positions of X elements (Figure 4A, third panel) in the presence of fatty acids, with a Pearson's correlation coefficient (ρ) of 0.98 (P<0.01), but not in the absence of fatty acids (ρ= −0.15). This strong correlation is supported by the fact that Oaf1p targeted almost all X elements in the genome with a false discovery rate (FDR) <0.001 in the presence of fatty acids (Figure 4B).
The high‐resolution ChIP‐chip data set enabled analysis of specificity of Oaf1p binding at individual X elements (Supplementary Figure S1), which revealed that Oaf1p specifically binds to unique probes in most X elements in response to fatty acids. The data set also enabled identification of a putative DNA‐recognition sequence for Oaf1p in the context of negative regulation (see Materials and methods). This sequence (G[not A]AGGGTAANNNNN[not C][not C]) is similar to the predicted binding motif of GRF, Reb1p (RTTACCCK) (Badis et al, 2008) and for the reasons outlined below, was termed subtelomeric Reb1‐binding (SRB) motif. This motif occurs 238 times in the entire genome, and 65% of the motifs are within 100 bp of an Oaf1p‐binding position (e.g., see Figure 6A). CPA analysis of the motif showed that it strongly enriches in subtelomeric regions at a frequency of >1 per arm, and colocalizes with X elements (Supplementary Figure S2). To characterize the interaction of Oaf1p with the SRB motif, an electromobility shift assay (EMSA) was performed (Supplementary Figure S2). Whereas the DNA‐biding domain (DBD) of Reb1p bound the SRB motif, the DBD of Oaf1p did not, suggesting that Oaf1p does not interact directly with X elements and that this interaction might be mediated by Reb1p.
X element‐binding TFs conditionally regulate proto‐silencing
Conditional binding of Oaf1p to X elements in the presence of fatty acids appeared to correlate with an overall repression of subtelomeric gene expression (compare ratio of down versus upregulated genes (blue versus red bars) in Figure 4B). This led us to hypothesize that X element‐binding TFs regulate X element‐mediated proto‐silencing in response to environmental stimuli. To test this, expression profiles of subtelomeric genes centromere‐proximal to X elements (within 20 kb) were analyzed during three responses that correspond to dynamic repositioning of factors at X elements in Figures 2 and 4 (Figure 5). The region was enriched for genes that significantly decreased in expression in response to fatty acid stress, but increased in expression in response to H2O2 or butanol stress (compared with the percentage of significantly up and downregulated genes in the entire genome, represented as green and red shading, respectively). Expression profiles that were determined to be significantly different from the global responses using a Student's t‐test are marked with asterisks. Y′ element genes that are telomere‐proximal to X elements were analyzed in the same way, and their responses were not significantly different from the global responses to the stimuli, except for a subtle enrichment of upregulated genes at 2 h of H2O2 exposure (3 versus 2.5% in the genome) (data not shown). These data suggest environmental regulation of X element‐mediated proto‐silencing.
Next, the roles of TFs in proto‐silencing were investigated by analyzing microarray expression profiles of subtelomeric genes in TF deletion strains (Figure 5). Growth in the presence of fatty acids resulted in decreased expression of subtelomeric genes centromere‐proximal to X elements. Under the same condition, deletion of OAF1 resulted in increased expression of these genes compared with the wild‐type strain, suggesting that Oaf1p is an enhancer of X element‐mediated proto‐silencing during this response. However, deletion of ROX1 or PHD1 resulted in enrichment of genes with significantly decreased expression in the presence of H2O2 or butanol, respectively, suggesting that Rox1p and Phd1p conditionally antagonize proto‐silencing. To evaluate whether these activities were due to direct activation or repression by the TFs rather than regulation of proto‐silencing at X elements, the analyses were repeated with direct targets of factors implicated in the responses excluded, and the results were very similar (Supplementary Figure S3). Together, these data suggest that conditional interaction of TFs with X elements regulate proto‐silencing activity in response to the environment with long‐range effects on genes that are not immediately adjacent to X elements.
To investigate these effects on distal genes, we analyzed the impact of Oaf1p regulation on specific subtelomeric genes (Figure 6). Panel A shows the binding patterns of Oaf1p in subtelomeric regions on chromosome arms 13 and 14 L. On both arms, X elements were detected (top row), bound by Oaf1p in the presence of fatty acids (second and third rows), and overlapped with SRB motifs, but not oleate response elements (OREs), which bind Oaf1p–Pip2p heterodimers that activate transcription (Rottensteiner et al, 2003) (fourth row). GFP fusion proteins encoded by genes not adjacent to X elements (open reading frames; ORFs marked with asterisks in fifth row) were monitored by fluorescence‐activated cell sorting (FACS) in the absence or presence of fatty acids in wild‐type and Δoaf1 cells (panel B). With the notable exception of Pex6–GFP (see below) the majority of proteins tested had reduced levels in the presence of fatty acid compared with glycerol (left), and this effect was dependent on the presence of Oaf1p (right). Negative regulation by Oaf1p was specific to the fatty acid response and was not apparent in glycerol‐grown cells (data not shown). Altogether, 10 genes centromere‐proximal to X elements were analyzed by FACS, 3 of which had significant decreases in expression in an OAF1 deletion strain by microarray analysis. In all, 7 of the 10 corresponding fusion proteins had significantly decreased abundance in fatty acid medium, and 6 had significant fatty acid‐specific negative regulation by OAF1. These data support our interpretation that the binding of Oaf1p to X elements has a conditional role in controlling subtelomeric silencing.
A notable exception to the trend is PEX6 (shown in Panels A and B), which had increased protein levels in response to oleate and positive regulation by Oaf1p. A possible mechanism of upregulation is that, although Oaf1p is a proto‐silencer at the X element on this chromosome arm, it also directly activates PEX6 by binding the upstream ORE as a heterodimer with Pip2p (Smith et al, 2007) (Figure 6A). These results are consistent with previous studies showing that PEX6 is upregulated by fatty acid exposure (Smith et al, 2002), and that transcriptional activators have access to promoters within otherwise silent chromatin (Xu et al, 2006; Mak et al, 2009). This phenomenon offers an explanation for why not all subtelomeric genes centromere‐proximal to X elements were observed to be affected by Oaf1p‐mediated silencing.
Oaf1p‐mediated silencing is dependent on SIR2
To support the conclusion that Oaf1p interacts with X elements and mediates its effect on subtelomeric silencing from this position, we analyzed the expression of a reporter gene of subtelomeric silencing in the strains FEP318‐23 and FEP318‐19 (Loney et al, 2009). In these strains, a gene encoding Ura3–GFP is positioned in a subtelomeric region of chromosome end III‐R or XI‐L adjacent and centromere‐proximal to the endogenous X element (Figure 7). The effects of fatty acid exposure and OAF1 deletion on this reporter were analyzed by FACS (Figure 7A). The data suggest that Oaf1p conditionally enhances silencing of the reporter gene in the presence of fatty acids. The reporter gene was also used to elucidate which histone deacetylase is involved in Oaf1p‐mediated regulation of silencing. We tested for genetic interactions between OAF1 and two genes encoding histone deacetylases, SIR2, which is known to be required for X element‐mediated proto‐silencing (Pryde and Louis, 1999), and HDA1, which is involved in another subtelomeric silencing mechanism (Robyr et al, 2002) (Figure 7B). FACS analysis of reporter gene output in various genetic backgrounds suggests that Oaf1p‐mediated silencing is dependent on Sir2p and not Hda1p. These data support the contention that environment‐responsive TFs conditionally regulate Sir‐mediated silencing from X elements and that this function is distinct from their roles linked to Hda1p at other subtelomeric loci (Mak et al, 2009).
The reporter gene used here can also be used in a 5FOA viability assay that can measure levels of silencing of a subtelomeric URA3 gene, which directly correlates with cell viability in the presence of 5FOA. This assay was used to test the effects of five TFs on the expression of Ura3–GFP under conditions of X element binding as determined by chromosome position analysis (Figure 2) using previously published ChIP‐chip data (Harbison et al, 2004). The results of this approach suggest a role for Gzf3p in reducing X element‐mediated proto‐silencing in the presence of rapamycin (Supplementary Figure S4). This positive influence on transcription is in contrast to its known role as a negative regulator of nitrogen catabolic genes (Soussi‐Boudekou et al, 1997). No effect on silencing was detected for the other four factors tested in the assay (Xbp1p, Yap6p, Rox1p and Cha4p) (data not shown) possibly because of the sensitivity of the assay, or the fact that the assay requires modification of the growth conditions used for chromosome position analysis in Figure 2.
Conditional insulation of Y′ element genes
The effects of conditional TF binding to X elements on Y′ element gene expression were also tested. First, analysis of two other microarray gene expression data sets (Smith et al, 2002, 2007) suggested that Y′ element genes are upregulated in response to two non‐fermentative carbon sources (oleate and glycerol) and that this is mediated by the conditional binding of Adr1p to X elements (Figure 8B). Next, microarray data of TF deletion strains grown in rich medium (Hu et al, 2007) were analyzed for expression of Y′ element genes (Figure 2). The analysis suggested that six of the factors that bind X elements in rich medium are involved in anti‐silencing of Y′ element genes under this condition, whereas little or no influence was detected for genes centromere‐proximal to X elements under this condition (Figure 8A). It should be noted that Y′ elements share a very high degree of sequence homology with each other; therefore, it is not possible to address expression of individual Y′ element genes by this analysis. However, all ORFs in Y′ elements are thought to encode similar protein sequences with putative helicase motifs, and helicase activity of a Y′ element encoded protein has been characterized (Yamada et al, 1998). In addition, the negative effects of the six TF deletions on Y′ element gene expression identified in Figure 8A are dramatic as the mean expression values of Y′ element genes were at least sixfold lower than in wild‐type strains. These data indicate that there is a dramatic influence of X element‐bound TFs on Y′ element gene expression as a class of genes, suggesting that they are involved in functional regulation of Y′ element processes.
Subtelomeric gene expression has long been implicated in cellular responses to the environment and control of lifespan; however, the mechanisms underlying these links are only now being established. Subtelomeric chromatin silencing is mediated by the activity of the Sirtuin family of proteins (Michan and Sinclair, 2007). Sir2p establishes chromatin silencing in subtelomeric regions by histone H4 deacetylation and by recruiting other silencing proteins. A decline of Sir2p activity corresponds to compromised subtelomeric transcriptional silencing, which apparently leads to decreased longevity (Dang et al, 2009). Additionally, caloric restriction extends lifespan, and this activity is linked to both the TOR pathway and Sirtuin activities (Medvedik et al, 2007). Moreover, activation of the TOR pathway by rapamycin exposure, stimulates Sir3p phosphorylation and subtelomeric silencing (Ai et al, 2002).
In addition to Sir‐mediated silencing, a second subtelomeric silencing mechanism involving the histone deacetylase Hda1p is active in yeast (Robyr et al, 2002). A recent study showed that environment‐responsive TFs conditionally enrich in subtelomeric regions, and suggested that they bind upstream of target genes and regulate their expression in an Hda1p‐linked manner (Mak et al, 2009). In this study, we show that control of subtelomeric gene expression is also mediated by a novel mechanism involving environment‐responsive TF binding to subtelomeric X‐elements, which leads to both control of proto‐silencing at distally located sites and boundary activity (Figure 9).
Proto‐silencing activities of stress‐responsive TFs
The spread of silencing in yeast subtelomeres is not continuous. Subtelomeric X elements interact with telomeric silencing molecules and relay Sir2p‐mediated silencing to centromere‐proximal genes. This proto‐silencing activity is known to be mediated by the GRF, Abf1p (Pryde and Louis, 1999). The data presented here suggest that proto‐silencing mediated by X elements is regulated in response to the cellular environment by multiple TFs that conditionally interact with X elements. In particular, Oaf1p binds X elements and enhances this silencing in response to fatty acid exposure, and Rox1p, Gzf3p and Phd1p bind and conditionally antagonize silencing in response to exposure to H2O2, rapamycin and butanol, respectively (Figure 5 and Supplementary Figure S4). Analysis of conditional Oaf1p‐mediated silencing showed that it is dependent on SIR2 but not HDA1, consistent with a novel role for TFs in X element‐mediated silencing that is distinct from their roles related to Hda1p at other subtelomeric loci (Mak et al, 2009).
Although the coregulatory mechanism identified here conditionally regulates a group of positionally and functionally related genes in subtelomeric regions that make up ∼5% of the yeast genome, the consequences of this regulation remain elusive. This is consistent with our previous study showing that genes that transcriptionally respond to fatty acid exposure are largely not (measurably) required for fitness when grown on this carbon source (Smith et al, 2006). Some of these responses likely reflect the many fundamental and complex relationships between cells and their environment that enable long‐term survival of the species that are not easily measurable in the laboratory. These responses might result in a subtle growth advantage or other desirable property, which can influence the evolution of the organism. It will be interesting to learn to what extent this regulatory mechanism impacts aging, evolution and other ‘broad‐scale’ cellular processes.
Anti‐silencing activities of stress‐responsive TFs
Y′ elements are known to be protected from silencing by telomere‐directed anti‐silencing activity mediated by GRFs bound to X elements including Tbf1p (Fourel et al, 1999, 2001), Rap1p and Abf1p (Fourel et al, 2002). Y′ element gene expression is responsive to meiosis (Burns et al, 1994), but little is known about the regulation of Y′ element gene expression in response to environmental cues. In this study, we show that a large number of TFs interact with X elements (Figure 2) and appear to positively regulate Y′ element genes in rich medium (Figure 8A). These genes are further upregulated after the cells are switched from glucose (a fermentative carbon source that does not require the Kreb's cycle for metabolism) to non‐fermentative growth conditions (with higher metabolic oxidation from active respiration) (Schuller, 2003) (Figure 8B). Our data suggest that Adr1p conditionally binds X elements (Figure 1) and is involved in activating these genes during non‐fermentative growth (Figure 8B). Importantly, these data are consistent with a previous study showing that transcriptional activation domains of several TFs, when tethered to tandem DNA sites in X elements, can act as insulators of telomere‐proximal genes and that this mechanism of regulation is distinct from transcriptional activation (Fourel et al, 2001). Therefore, we propose that X element‐bound TFs regulate Y′ element gene expression by increasing insulation from silencing propagating from X elements.
The role of metabolic control of Y′ element gene expression is not known. Y′ elements have been implicated in an alternative lengthening of telomeres (ALT) mechanism that is active in the absence of functional telomerase, as survivors of telomerase mutants have been found to have amplification of these repeats, which may physically buffer chromatin degradation (Lundblad and Blackburn, 1993). This amplification coincides with increased expression of Y′ element genes, which encode helicases (Yamada et al, 1998) and involves active Ty1 transposable elements which also lead to gene duplications elsewhere in the genome. Therefore, it has been suggested that survivors of telomerase mutants with Y′ element amplification, likely also have increased genetic variation and are more suited to the stressful environment (Maxwell et al, 2004). This mechanism may be evolutionarily conserved, as recent data suggest that some cancer cells use a similar survival strategy to amplify subtelomeric repeat elements to lengthen telomeres (Marciniak et al, 2005). Considering these data, it will be interesting to determine whether conditional regulation of Y′ element gene expression by X element‐binding TFs is linked to adaptation.
Coordination of telomere biology with other cellular responses
It is noteworthy that Oaf1p (Smith et al, 2007) and other X element‐binding TFs, including Yap5p, Yap6p (Tan et al, 2008) and Pdr1p (MacPherson et al, 2006) are implicated as dual function activator/repressor proteins, which are also properties of X element‐binding GRFs (Rap1p, Abf1p and Tbf1p) and GRFs known to nucleate heterochromatin formation in other systems such as ikaros in mouse and Cft1p in human cells (Gasser, 2001). Bifunctionality enables X element‐binding TFs to coordinate subtelomeric silencing with other cellular responses. One way to accomplish this is through context‐specific cooperation amongst factors, which has been suggested for many of the X element‐binding TFs (MacPherson et al, 2006; Smith et al, 2007; Tan et al, 2008). For example, Oaf1p heterodimerizes with Pip2p to activate genes involved in fatty acid metabolism; however, Pip2p does not appear to be involved in regulation of X element‐mediated proto‐silencing. Thus, the distinct roles of Oaf1p can be coordinated by controlling the abundance of Pip2p (Smith et al, 2007). Similarly, other X element‐binding factors appear to have context‐specific binding partners: Pdr1p and Msn4p each conditionally binds to X elements, but X element interactions were not detected with their other known protein partners, (Pdr3p/Stb5p and Msn2p, respectively) (Mamnun et al, 2002; MacPherson et al, 2006). It will be interesting to determine whether dual functionality of these and other factors have similar roles in coordinating silencing with other cellular processes.
It is also possible that X element‐association of at least some of the TFs may significantly impact the activity of the factor, regardless of the impact on subtelomeric silencing. For example, the interaction may serve to keep the factors positioned at the nuclear periphery to sequester the factor from intrachromosomal targets, or to receive signals transduction across the nuclear membrane, roles which have recently been attributed to the nuclear lamina underlying the inner nuclear membrane in metazoans, which is not present in yeast (Andres and Gonzalez, 2009).
Repression of subtelomeric genes through the spreading of silencing molecules from telomeres toward the centromere is an evolutionarily conserved phenomenon. In this study, we show using chromosome position analysis of genome‐wide ChIP‐chip and expression data, that silencing is regulated in response to stress and metabolism by a group of TFs that also modulate intrachromosomal gene expression in response to the same stimuli. These findings provide a critical link in establishing the mechanisms by which telomere biology is coordinated with other cellular processes including responses to environmental stimuli, aging and adaptation.
Materials and methods
Strains and cell culture
GFP fusion strains are from the BY4741 (S65T) GFP collection, and deletion strains are from the BY4742 deletion library available from Invitrogen (Carlsbad, CA) except for Δoaf1, which has previously been described (Smith et al, 2007). Haploid tagged strains with OAF1 deletions were generated by mating, sporulation and tetrad dissection. Strains were grown in 1% yeast extract, 2% peptone and 2% glucose (YPD), SCIM (1.7 g yeast nitrogen base without amino acids and ammonium sulfate (YNB‐aa‐as)/l, 0.5% yeast extract, 0.5% peptone, 0.79 g complete supplement mixture/l, 5 g ammonium sulfate/l) containing either 0.1% glucose (SCIM‐O) or 0.5% Tween 40 (w/v) and 0.15% (w/v) oleate (SCIM‐D), or YPB (0.3% yeast extract, 0.5% potassium phosphate (pH 6.0), 0.5% peptone) with either 2% glucose (YPBD), 3% glycerol (YPBG) or 0.5% Tween 40 (w/v) and 0.15% (w/v) oleate (YPBO).
Chromosome position analysis (CPA)
Unless otherwise stated, all mapping of features to chromosome positions was done using Map Peak tool of NimbleScan software version 2.4. (Roche NimbleGen, Madison, WI). Chromosome ends were the first and last base pair of each chromosome sequence, which does not include telomeric repeats (from the Saccharomyces genome database (SGD) website (www.yeastgenome.org) on 9 September 2008). The positions of ORFs and start sites were from the S. cerevisiae annotation file from NimbleGen (created on 2 February 2007). The positions of X and Y′ elements and other genomic features were from SGD (31 December 2008). For generation of CPA histograms, features spanning more than one bin were counted only once and placed in the bin closest to the telomere. When CPA profiles were compared, Pearson's product moment correlation function of R 2.3.0 was used.
CPA of targets in a fatty acid‐responsive network in Figure 1
ChIP‐chip analysis of four TFs from cells grown in low glucose medium (SCIM‐O), or 5 h after transferring the cells to medium containing fatty acid (SCIM‐D) using intergenic microarrays has been described (Smith et al, 2007). Conditional protein–DNA interaction networks were clustered based on network topologies to identify groups of intergenic regions targeted by the same subset of TFs (Smith et al, 2007). For CPA, targets in each cluster were binned by their distance to closest telomere using the Dcount database function of Microsoft Excel. To obtain a background profile, the analysis was also done for all intergenic regions on the microarrays. The expected frequency of probes bound by Adr1p, Oaf1p and Oaf3p (but not Pip2p) was the total number of intergenic regions with this network topology/total number of intergenic regions on the array. To determine the representation of each subtelomeric region on the microarrays, individual 1 kb segments were scored as represented if there was any overlap with one or more intergenic region on the array. In all, 12.5% of chromosomes within 1 kb of telomeres were represented on the arrays; the number rose to ∼75% between 5 and 10 kb from telomeres.
ChIP‐chip data of 204 DNA‐binding factors (Harbison et al, 2004) was from the Pvalbyintergenic_9.2_forpaper file at http://jura.wi.mit.edu/young_public/regulatory_code/files_for_paper.zip. It was determined by CPA that 25 probes in the data set overlap with X elements. For each set of target probes (with interaction P‐values <0.01), the number of X element‐containing probes were determined. Significant enrichment of X element probes for each experiment was determined by calculating hypergeometric distribution P‐values using R and applying a Bonferroni's multiple test correction of 352, corresponding to the number of experiments in the study. The heat maps of the binding profiles and X‐element positions shown in Figure 3 were generated using MeV 4.5 (Saeed et al, 2006).
ChIP‐chip analysis using tiled microarrays
ChIP‐chip analysis of Oaf1p was performed in the presence (SCIM‐D) and absence of fatty acids (SCIM‐O) as previously described (Smith et al, 2007) with the changes described below. Three biological replicates of each experiment were performed. For each replicate, linkers were annealed to DNA ends in whole‐cell extract and IP fractions, and fragments were amplified by ligation‐mediated PCR with high‐fidelity Taq polymerase, and shipped to NimbleGen Systems of Iceland for labeling, hybridization, scanning and preliminary analysis as described below: Equal amounts of DNA in whole‐cell extracts and IP fraction were labeled with Cy3 and Cy5, respectively, combined and co‐hybridized at 42°C to microarrays of 50‐mer DNA probes that span both strands of the entire genome positioned every 64 bp (resulting in 14 bases of DNA between probes). Data was extracted using NimbleScan software and the log2 ratios of IP versus whole‐cell extract for each probe was determined. Log2 ratios of adjacent probes were analyzed together to find peak regions of TF binding along with FDR using Find Peaks function of NimbleScan software. The chromatin localization data have been submitted to Gene Expression Omnibus database under accession number GSE21852.
Analysis of experimental noise in ChIP‐chip data (Procedure for Supplementary Figure S1)
The sequences of all 50‐mer probes spotted on the tiled microarrays (NimbleGen Systems, Iceland) that were within both an X element and an Oaf1p‐binding peak (from one biological replicate in the presence of fatty acids) were compared with the sequence of the entire yeast genome using FASTA program (at SGD website). Microarray probes that shared less than 92% identity with any other 50 base sequences in the entire genome were considered to be sufficiently unique to have no significant background binding to other genomic fragments in the experiment. This cutoff was established empirically in previously published microarray control studies using the same 50‐mer probe length and hybridization temperature of 42°C (Deng et al, 2008).
CPA of tiling array ChIP‐chip data in Figure 4
CPA was performed on peak regions of TF binding (FDRs <0.001). Histograms were generated, showing the mean number of peaks per chromosome arm in 1 kb segments of subtelomeric regions. This was calculated by dividing the number of peaks per segment by the number of chromosome arms (32) and by the number of strands analyzed (2). For each experiment, three biological replicates were analyzed separately and used to determine average number of peaks at each position and s.e.
Gene expression microarrays
The time course data set comparing cells grown in glycerol medium (YPBG) to those switched to oleate medium (YPBO) (Figure 5A) have been described (Smith et al, 2002). Comparison of TF deletion strains to a wild‐type strain after 5 h of growth in medium containing fatty acids (SCIM‐D) (Figures 5A and 7B) have been described (Smith et al, 2007). The time course data set of 0.3 mM H2O2 exposure (Figure 5B) has been described (Gasch et al, 2000). Comparisons of TF deletion strains to a wild‐type strain during growth in rich medium (YPD) (Figure 8A) have been described (Hu et al, 2007). Comparisons of cells grown in glucose (YPBD), glycerol (YPBG), or oleate (YPBO) (Figure 8B) have been described (Smith et al, 2002).
For the TF deletion analyses in Figure 5B and C, TF deletion strains were compared with an isogenic wild‐type strain by microarray analysis under conditions used for ChIP‐chip analysis of the factors (Harbison et al, 2004). All mutant and wild‐type strains were grown in YPD to a density of 1 × 107 cells/ml, treated with stimulus, and compared. For Δrox1, Δxbp1 and Δphd1 analyses, cells were exposed to 4 mM H2O2 for 30 min, 0.4 mM H2O2 for 20 min, or 1% butanol for 90 min, respectively. To prepare samples for microarray analyses, total RNA was isolated by hot acid phenol extraction and then purified on Qiagen RNeasy columns according to the manufacturer's instructions. Next, cDNA was synthesized and labeled using a Superscript indirect cDNA labeling system (Invitrogen). Equal amounts of differently labeled cDNA samples were mixed and hybridized to S.cerevisiae oligonucleotide gene expression arrays (Agilent). All experiments were performed with duplicate biological and technical replicates of each condition, and included replicates in each labeling orientation. Replicates were merged and analyzed for significantly differentially expressed genes using maximum‐likelihood analysis (Ideker et al, 2000). Significantly differentially expressed genes were those with a lambda value above 20.74, which was determined empirically to correspond to a false positive rate of 0.001. These gene expression data have been submitted to Gene Expression Omnibus database under accession number GSE21926.
Positional analysis of expression data in Figures 5 and 8, Supplementary Figure S3
Two groups of subtelomeric genes, those within Y′ element genes and those within 20 kb of X elements, were identified by CPA (described above). Significantly differentially expressed genes were those identified in the original publications except for the H2O2 time course data (Gasch et al, 2000) and the data set of TF deletions in rich medium (Hu et al, 2007); for these data sets, genes with expression ratios at least 2 s.d. values from the mean were considered to be significantly differentially expressed. For each experiment, the percentage of genes that significantly increased and decreased in expression were determined for each subtelomeric region and for the entire genome. Expression profiles of the subtelomeric gene groups were compared with those of all genes using a two‐tailed heteroscedastic Student's t‐test. Unless otherwise stated, statistically significant effects were those with Student's t‐test P‐values <0.001.
Cells were grown overnight in YPD, transferred to glycerol medium (YPBG), and grown overnight to a cell density of ∼3 × 106 cells/ml. Cells were harvested by centrifugation, resuspended in oleate (YPBO) or glycerol medium (YPBG) and grown for an additional 8–18 h. For each sample, fluorescence intensities of 10 000 cells were measured using a FACS Caliber flow cytometer (BD Biosciences, San Jose, CA) with a forward scatter threshold of 18. Data were analyzed with WinMDI 2.8 (at http://FACS.scripps.edu/) with smoothing of 20 units. Three or four biological replicates of each experiment were performed and used for Student's t‐tests of statistical significance.
Oaf1p‐binding motif analysis in Supplementary Figure S2
DNA sequences corresponding to Oaf1p‐binding peaks were identified using Nimblescan software with FDR threshold <0.001. Oaf1p peaks that overlapped with intergenic regions bound by Oaf1p in the context of negative regulation in the network (i.e., also bound by Adr1p and Oaf3p, but not Pip2p in the presence of fatty acid) were selected and used for motif finding with AlignACE (Roth et al, 1998) and MEME version 4.1.1 (Bailey and Elkan, 1994). Together, these analyses identified a putative Oaf1p recognition sequence (AGGGTAANGNNN[not C][not C]) that was termed SRB motif. The entire genome was searched for this motif using Fuzznuc of Emboss software (Rice et al, 2000). The overlap of the motif with Oaf1p‐binding peaks was determined with the Map Peaks tool of Nimblescan software.
EMSA was performed using LightShift Chemiluminescent EMSA Kit (Thermoscientific, Rockford, IL) with previously reported conditions for Reb1p binding (Chasman et al, 1990). DBDs of Oaf1p (227 aa) and Reb1p (483 aa) used in the analysis were generated as GST‐fusion proteins and purified using GST Gene Fusion system (GE Healthcare, Piscataway, NJ). To construct expression plasmids, Oaf1p and Reb1p DNA fragments were amplified from genomic DNA by PCR with oligonucleotides (AAGGGATCCGGAAATGATGATAATA and TTGCTCGAGGGTATCATCGTGTT) and (AAGGGATCCCTCAACAAATCTAG and TTGCTCGAGGGAATTAATTTTCTG), respectively, and ligated into pGEX‐4T1 with BamHI and XhoI. Double‐stranded target DNA in the EMSA was ACCTCCCCACTCGTTACCCTGCCCCACT, which is found in Oaf1p‐binding peak in X element on chromosome arm 14R and contains an SRB domain (underlined).
5‐FOA viability assay of subtelomeric silencing in Supplementary Figure S4
Strains for this assay were a kind gift of Dr Edward Louis and were described previously (Loney et al, 2009). Silencing assays were performed as described previously (Gottschling et al, 1990). Briefly, the ORF of GZF3 was disrupted with a KanMX cassette in strain FEP318‐19 (with subtelomeric URA3–GFP as shown in Supplementary Figure S4) by homologous recombination of a PCR fragment from ΔGZF3 (BY4742 deletion library; Invitrogen). FEP318‐19 and FEP318‐19 ΔGZF3 were grown in 5 ml YEPD overnight to saturation along with control strains with and without intrachromosomal URA–GFP (PIY125 and FYBL1‐8B, respectively). Tenfold serial dilutions of each strain were spotted (2 μl/spot) on YNBD rapamycin plates (1.7 g yeast nitrogen base without amino acids/l; 5 g ammonium sulfate/l, 2% dextrose, 20 mg uracil/l, 20 mg l‐histidine–HCl/l, 60 mg l‐leucine/l, 50 mg l‐lysine/l, 20 g agar/l, and 100 nM rapamycin) with and without 1 g/l 5‐FOA (Bio 101 Inc.). Images were taken after 72 h of growth at 30°C. The same assay was performed with deletion strains XPB1, YAP6 and ROX1 in the presence of 2 mM H2O2 and CHA4 in the presence of 0.2 mg sulfometuron methyl/l in place of rapamycin.
We thank Dr David Dilworth for insightful suggestions. We thank Dr Edward Louis for the kind gift of URA3–GFP reporter strains. This work was funded by grants NIH/NIGMS R01 GM075152, NIH P50 GM076547 and NIH U54 RR022220. We also thank the Luxembourg Centre for Systems Biomedicine and the University of Luxembourg for support. Author contributions:JS and JA conceived initial concepts and designed the research. JS, LM and LV conducted experiments. JS performed data analysis. YW contributed unpublished data. JS, RK and LM processed and displayed data for presentation. JS and JA wrote the paper.
Conflict of Interest
The authors declare that they have no conflict of interest.
Supplementary Information [msb2010110-sup-0001.pdf]
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