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n3:pmcid

PMC0

bibo:doi

10.1038%2Fnature09033

n6:contains

_:vb7489784 _:vb7489788 _:vb7489770 _:vb7489773 _:vb7489797

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_:vb7489770

rdf:type

n6:Section

dc:title

discussion

n6:contains

_:vb7489772 _:vb7489771

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_:vb7489771

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Previous studies of a few individual enhancer loci have proposed several models for delivery of RNAPII from an enhancer to a promoter, including tracking of RNAPII along DNA and direct transfer of RNAPII via DNA looping>>20<<. Our observation that eRNAs are produced only within 2 kb enhancer domains and not along the entire distance between enhancers and promoters suggests that transcription-dependent RNAPII tracking is not likely to be a widespread mechanism

n3:mentions

n2:18467100

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_:vb7489772

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For example, RNAPII has previously been shown to recruit chromatin-modifying enzymes such histone methyltransferases>>26<<. In this regard, it is noteworthy that eRNAs are observed only within the H3K4me1-modified enhancer domain, and the level of the H3K4me1 modification and the level of eRNA synthesis are tightly correlated (compare Figs. 1b top and 4c).

n3:mentions

n2:12764140

Subject Item

_:vb7489773

rdf:type

n6:Section

dc:title

defining activity-regulated enhancers

n6:contains

_:vb7489776 _:vb7489777 _:vb7489778 _:vb7489779 _:vb7489780 _:vb7489781 _:vb7489782 _:vb7489783 _:vb7489774 _:vb7489775

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_:vb7489774

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Recent genome-wide studies have established that enhancers can be defined as DNA sequences that bind the transcriptional co-activator p300/CBP, that bind H3K4me1, and that are located distally from known transcription start sites (TSSs)>>3<<-5. We applied these criteria to define neuronal activity-regulated enhancers.

n3:mentions

n2:17708682 n2:17277777 n2:19212405

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_:vb7489775

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Using ChIP-Seq>>6<<, we first identified CBP binding sites throughout the mouse genome using two different antibodies against CBP and selected only those CBP-bound genomic loci detected by both antibodies (Methods).

n3:mentions

n2:19736561

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_:vb7489776

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n3:Context

rdf:value

To specifically identify CBP binding sites at enhancers, we asked which of the distal CBP sites are also bound by H3K4me1-modified histones, which mark active chromatin regions including enhancers>>3<<,7,8. About 13,000 distal CBP sites are located within 2 kb of H3K4me1-modified regions (Figs. 1, 2b, and Supplementary Figs. 1c, 3). We removed from this enhancer list a subset (7%) of enhancers that in addition to binding H3K4me1 also

n3:mentions

n2:17277777

Subject Item

_:vb7489777

rdf:type

n3:Context

rdf:value

To specifically identify CBP binding sites at enhancers, we asked which of the distal CBP sites are also bound by H3K4me1-modified histones, which mark active chromatin regions including enhancers3,>>7<<,8. About 13,000 distal CBP sites are located within 2 kb of H3K4me1-modified regions (Figs. 1, 2b, and Supplementary Figs. 1c, 3). We removed from this enhancer list a subset (7%) of enhancers that in addition to binding H3K4me1 also bind

n3:mentions

n2:17512414

Subject Item

_:vb7489778

rdf:type

n3:Context

rdf:value

To specifically identify CBP binding sites at enhancers, we asked which of the distal CBP sites are also bound by H3K4me1-modified histones, which mark active chromatin regions including enhancers3,7,>>8<<. About 13,000 distal CBP sites are located within 2 kb of H3K4me1-modified regions (Figs. 1, 2b, and Supplementary Figs. 1c, 3). We removed from this enhancer list a subset (7%) of enhancers that in addition to binding H3K4me1 also bind

n3:mentions

n2:18787082

Subject Item

_:vb7489779

rdf:type

n3:Context

rdf:value

We removed from this enhancer list a subset (7%) of enhancers that in addition to binding H3K4me1 also bind the transcription initiation site-associated histone mark H3K4me>>37<<,8 and therefore may represent uncharacterized promoters (Figs.

n3:mentions

n2:17512414

Subject Item

_:vb7489780

rdf:type

n3:Context

rdf:value

We removed from this enhancer list a subset (7%) of enhancers that in addition to binding H3K4me1 also bind the transcription initiation site-associated histone mark H3K4me37,>>8<< and therefore may represent uncharacterized promoters (Figs.

n3:mentions

n2:18787082

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_:vb7489781

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rdf:value

One activity-regulated neuronal enhancer was independently identified as an enhancer that drives the activity-regulated transcription of arc/arg3.1, a gene that regulates synaptic function>>9<<-12. This arc enhancer, which is located 7 kb upstream of the arc TSS, is necessary to drive activity-regulated arc transcription13,14. To determine if the activity-regulated enhancers we identified have the ability to induce transcription

n3:mentions

n2:11466419 n2:17088211 n2:17088213 n2:17088210

Subject Item

_:vb7489782

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This arc enhancer, which is located 7 kb upstream of the arc TSS, is necessary to drive activity-regulated arc transcription>>13<<,14. To determine if the activity-regulated enhancers we identified have the ability to induce transcription at a promoter in an activity-dependent manner, we tested seven of the enhancers in a luciferase reporter assay (Fig. 3). We found

n3:mentions

n2:19116276

Subject Item

_:vb7489783

rdf:type

n3:Context

rdf:value

This arc enhancer, which is located 7 kb upstream of the arc TSS, is necessary to drive activity-regulated arc transcription13,>>14<<. To determine if the activity-regulated enhancers we identified have the ability to induce transcription at a promoter in an activity-dependent manner, we tested seven of the enhancers in a luciferase reporter assay (Fig. 3). We found

n3:mentions

n2:19193899

Subject Item

_:vb7489784

rdf:type

n6:Section

dc:title

characterization of enhancers

n6:contains

_:vb7489785 _:vb7489786 _:vb7489787

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_:vb7489785

rdf:type

n3:Context

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CREB, SRF, and NPAS4 are known activity-regulated TFs that play an important role in various aspects of brain development including neuronal survival, synapse development and synaptic plasticity>>15<<,16. We find in neurons that CREB, SRF, and NPAS4 bind to neuronal enhancers as well as promoters (Supplementary Table 3). Although both CREB and SRF bind enhancers before membrane depolarization, their binding at enhancers in some cases

n3:mentions

n2:18558867

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_:vb7489786

rdf:type

n3:Context

rdf:value

CREB, SRF, and NPAS4 are known activity-regulated TFs that play an important role in various aspects of brain development including neuronal survival, synapse development and synaptic plasticity15,>>16<<. We find in neurons that CREB, SRF, and NPAS4 bind to neuronal enhancers as well as promoters (Supplementary Table 3). Although both CREB and SRF bind enhancers before membrane depolarization, their binding at enhancers in some cases

n3:mentions

n2:18815592

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_:vb7489787

rdf:type

n3:Context

rdf:value

In contrast, the binding of NPAS4, which is not present in neurons at significant levels prior to membrane depolarization>>16<<, was not detected prior to stimulation but was found at ∼28,000 sites in membrane-depolarized neurons (Figs.

n3:mentions

n2:18815592

Subject Item

_:vb7489788

rdf:type

n6:Section

dc:title

transcription at enhancers

n6:contains

_:vb7489796 _:vb7489792 _:vb7489793 _:vb7489794 _:vb7489795 _:vb7489789 _:vb7489790 _:vb7489791

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At promoters, CBP recruits components of the basal transcription machinery, including RNAPII, thereby facilitating the assembly of functional transcription complexes that initiate mRNA synthesis>>17<<. Since CBP binds to enhancers in an activity-dependent manner, we asked if CBP also recruits RNAPII to these enhancers.

n3:mentions

n2:8576192

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_:vb7489790

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Consistent with previous studies>>18<<,19, a large number of RNAPII sites were found to be located near annotated TSSs (Figs.

n3:mentions

n2:16086846

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_:vb7489791

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Consistent with previous studies18,>>19<<, a large number of RNAPII sites were found to be located near annotated TSSs (Figs.

n3:mentions

n2:15988478

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_:vb7489792

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While RNAPII has previously been reported to be present at several enhancers, including the β-globin and MHC class II gene enhancers>>20<<,21, it has not been thought to play a widespread role in enhancer function.

n3:mentions

n2:18467100

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_:vb7489793

rdf:type

n3:Context

rdf:value

While RNAPII has previously been reported to be present at several enhancers, including the β-globin and MHC class II gene enhancers20,>>21<<, it has not been thought to play a widespread role in enhancer function.

n3:mentions

n2:16126390

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_:vb7489794

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Fourth, a promoter prediction algorithm (ProSOM)>>22<< revealed that fewer than 100 of ∼12,000 enhancer regions are predicted to be promoters compared to 8,494 out of 27,857 annotated TSSs.

n3:mentions

n2:18586720

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Finally, a few enhancers, including the well-characterized β-globin enhancer, have previously been shown to recruit RNAPII and drive transcription>>23<<,24. These findings argue against the possibility that RNAPII-bound enhancers that produce eRNAs are actually un-annotated promoters.

n3:mentions

n2:15465832

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_:vb7489796

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Finally, a few enhancers, including the well-characterized β-globin enhancer, have previously been shown to recruit RNAPII and drive transcription23,>>24<<. These findings argue against the possibility that RNAPII-bound enhancers that produce eRNAs are actually un-annotated promoters.

n3:mentions

n2:15371553

Subject Item

_:vb7489797

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n6:Section

dc:title

mechanism of erna synthesis

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_:vb7489798 _:vb7489799 _:vb7489800

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_:vb7489798

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The assumption in this analysis is that an enhancer is most likely to promote mRNA synthesis of the nearest gene>>3<<,25. We found that changes in eRNA expression levels that occur at enhancers upon membrane depolarization are strongly correlated with changes in mRNA expression levels at nearby genes. Changes in RNAPII levels at enhancers are also, to a

n3:mentions

n2:17277777

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_:vb7489799

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The assumption in this analysis is that an enhancer is most likely to promote mRNA synthesis of the nearest gene3,>>25<<. We found that changes in eRNA expression levels that occur at enhancers upon membrane depolarization are strongly correlated with changes in mRNA expression levels at nearby genes. Changes in RNAPII levels at enhancers are also, to a

n3:mentions

n2:19295514

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We tested this hypothesis in the specific case of the arc enhancer using arc knock-out neurons in which most of the arc gene, including the arc promoter is deleted but the arc enhancer remains intact>>10<<. To characterize the arc enhancer in arc knock-out neurons, we first performed ChIP experiments testing for the binding of SRF and RNAPII, two factors that we found by ChIP-Seq to be bound to the arc enhancer (Fig. 6a and b). In arc

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