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Human Gene Promoters Are Intrinsically Bidirectional

2015; Elsevier BV; Volume: 60; Issue: 3 Linguagem: Inglês

10.1016/j.molcel.2015.10.015

1097-4164

Robin Andersson, Yun Chen, Leighton J. Core, John T. Lis, Albin Sandelin, Torben Heick Jensen,

Gene Regulatory Network Analysis

A recent Molecular Cell paper by Duttke et al. concluded that "human promoters are intrinsically directional" (Duttke et al., 2015Duttke S.H.C. Lacadie S.A. Ibrahim M.M. Glass C.K. Corcoran D.L. Benner C. Heinz S. Kadonaga J.T. Ohler U. Mol. Cell. 2015; 57: 674-684Abstract Full Text Full Text PDF PubMed Scopus (81) Google Scholar). This, at least on the surface, contradicts earlier observations (Almada et al., 2013Almada A.E. Wu X. Kriz A.J. Burge C.B. Sharp P.A. Nature. 2013; 499: 360-363Crossref PubMed Scopus (276) Google Scholar, Core et al., 2008Core L.J. Waterfall J.J. Lis J.T. Science. 2008; 322: 1845-1848Crossref PubMed Scopus (1416) Google Scholar, Ntini et al., 2013Ntini E. Järvelin A.I. Bornholdt J. Chen Y. Boyd M. Jørgensen M. Andersson R. Hoof I. Schein A. Andersen P.R. et al.Nat. Struct. Mol. Biol. 2013; 20: 923-928Crossref PubMed Scopus (193) Google Scholar, Seila et al., 2008Seila A.C. Calabrese J.M. Levine S.S. Yeo G.W. Rahl P.B. Flynn R.A. Young R.A. Sharp P.A. Science. 2008; 322: 1849-1851Crossref PubMed Scopus (689) Google Scholar). As part of the disagreement could be based on a different usage of scientific terms, we find it important to contribute our perspective, hoping to reach common definitions. In addition, we present a reconsideration of an important question asked by Duttke et al., namely whether divergent transcription is a generic feature of human promoters. A core promoter has been classically defined by biochemical studies as the minimal region of DNA required to support assembly of a general transcription complex and initiate transcription. This activity is often encompassed by the ± 50 bp surrounding the transcription start site (TSS) (Kadonaga, 2012Kadonaga J.T. Wiley Interdiscip. Rev. Dev. Biol. 2012; 1: 40-51Crossref PubMed Scopus (154) Google Scholar). Core promoters rarely act alone in vivo, requiring nearby transcription factor binding to regulate their activity. Therefore, the term "promoter" often includes more extended upstream regions that contribute to regulation of initiation at the core promoter. The terms "core promoter," "TSS," and "promoter" have at times been used interchangeably in the literature, which in light of current genomic data is likely to cause confusion. Although well described in vitro, core promoters can be difficult to define in vivo, making high-throughput mapping of TSSs paramount for promoter identification. Systematic genomic studies have demonstrated that mammalian mRNA TSSs are typically accompanied by upstream TSSs firing in the opposite direction to produce so-called promoter upstream transcripts (PROMPTs) or upstream antisense RNAs (uaRNAs), which are most often unstable and non-coding (Almada et al., 2013Almada A.E. Wu X. Kriz A.J. Burge C.B. Sharp P.A. Nature. 2013; 499: 360-363Crossref PubMed Scopus (276) Google Scholar, Andersson et al., 2014Andersson R. Refsing Andersen P. Valen E. Core L.J. Bornholdt J. Boyd M. Heick Jensen T. Sandelin A. Nat. Commun. 2014; 5: 5336Crossref PubMed Scopus (110) Google Scholar, Core et al., 2008Core L.J. Waterfall J.J. Lis J.T. Science. 2008; 322: 1845-1848Crossref PubMed Scopus (1416) Google Scholar, Core et al., 2014Core L.J. Martins A.L. Danko C.G. Waters C.T. Siepel A. Lis J.T. Nat. Genet. 2014; 46: 1311-1320Crossref PubMed Scopus (373) Google Scholar, Flynn et al., 2011Flynn R.A. Almada A.E. Zamudio J.R. Sharp P.A. Proc. Natl. Acad. Sci. USA. 2011; 108: 10460-10465Crossref PubMed Scopus (135) Google Scholar, Ntini et al., 2013Ntini E. Järvelin A.I. Bornholdt J. Chen Y. Boyd M. Jørgensen M. Andersson R. Hoof I. Schein A. Andersen P.R. et al.Nat. Struct. Mol. Biol. 2013; 20: 923-928Crossref PubMed Scopus (193) Google Scholar, Preker et al., 2008Preker P. Nielsen J. Kammler S. Lykke-Andersen S. Christensen M.S. Mapendano C.K. Schierup M.H. Jensen T.H. Science. 2008; 322: 1851-1854Crossref PubMed Scopus (565) Google Scholar, Seila et al., 2008Seila A.C. Calabrese J.M. Levine S.S. Yeo G.W. Rahl P.B. Flynn R.A. Young R.A. Sharp P.A. Science. 2008; 322: 1849-1851Crossref PubMed Scopus (689) Google Scholar). Transcription initiation of mRNA and PROMPT/uaRNA is characteristically tightly spaced (110–250 bp between TSSs), centered around a high density of transcription factor binding, and encompassed by positioned nucleosomes that define a nucleosome depleted region (NDR). Based on this, and on data discussed below, we therefore suggest that a mammalian gene promoter is generally demarcated by an NDR that contains two oppositely oriented core promoters (Figure S1A). Because of this property, such promoters were called divergent or bidirectional. Although language used in some of the early reports on divergent promoters could be interpreted to support a model where a single core promoter supports both mRNA and PROMPT/uaRNA transcription, this was, to our knowledge, not the intention. Nor is such a notion supported by high-resolution TSS mapping in mammals (Almada et al., 2013Almada A.E. Wu X. Kriz A.J. Burge C.B. Sharp P.A. Nature. 2013; 499: 360-363Crossref PubMed Scopus (276) Google Scholar, Andersson et al., 2014Andersson R. Refsing Andersen P. Valen E. Core L.J. Bornholdt J. Boyd M. Heick Jensen T. Sandelin A. Nat. Commun. 2014; 5: 5336Crossref PubMed Scopus (110) Google Scholar, Core et al., 2014Core L.J. Martins A.L. Danko C.G. Waters C.T. Siepel A. Lis J.T. Nat. Genet. 2014; 46: 1311-1320Crossref PubMed Scopus (373) Google Scholar, Ntini et al., 2013Ntini E. Järvelin A.I. Bornholdt J. Chen Y. Boyd M. Jørgensen M. Andersson R. Hoof I. Schein A. Andersen P.R. et al.Nat. Struct. Mol. Biol. 2013; 20: 923-928Crossref PubMed Scopus (193) Google Scholar) or ChIP-exo data from yeast (Rhee and Pugh, 2012Rhee H.S. Pugh B.F. Nature. 2012; 483: 295-301Crossref PubMed Scopus (347) Google Scholar). The model depicted in Figure S1A is also used by Duttke et al. and by others (e.g., Scruggs et al., 2015Scruggs B.S. Gilchrist D.A. Nechaev S. Muse G.W. Burkholder A. Fargo D.C. Adelman K. Mol. Cell. 2015; 58: 1101-1112Abstract Full Text Full Text PDF PubMed Scopus (139) Google Scholar). An important question arising from these observations is whether divergent transcription is an inherent feature of human gene promoters. Duttke et al. set out to answer this by using a 5′-GRO-seq protocol to obtain nascent RNA 5′ ends from HeLa-S3 cell nuclei. These 5′ ends were used to classify NDR-defined promoters (detected by DNase I hypersensitivity) to UCSC gene TSSs as either unidirectional or divergent, and they found 56% (2,237/3,978) and 44% (1,741/3,978), respectively, in each class (Duttke et al., 2015Duttke S.H.C. Lacadie S.A. Ibrahim M.M. Glass C.K. Corcoran D.L. Benner C. Heinz S. Kadonaga J.T. Ohler U. Mol. Cell. 2015; 57: 674-684Abstract Full Text Full Text PDF PubMed Scopus (81) Google Scholar). It was further argued that unidirectional transcription was caused by a lack of core promoter signals in the reverse direction of the respective gene TSSs. Distinguishing whether a promoter is divergently transcribed will critically depend on the method used and its sensitivity. To visualize this, we sorted unidirectionally and divergently classified promoters by the widths of their DNase I hypersensitive sites (DHSs) and plotted around DHS midpoints the frequencies of mapped reads of previously published datasets, including CAGE and RNA-seq data from control and exosome (hRRP40)-depleted HeLa-S3 cells as well as GRO-seq (HeLa-S3) and GRO-cap (similar to 5′-GRO-seq) data from K562 and GM12878 cells. It is evident that the clear majority of claimed unidirectional promoters also support transcription initiation from the reverse DNA strand (Figure S1B). The 5′-GRO-seq assay by Duttke et al. does not detect these transcription events. Consistently, a substantially lower fraction of 5′-GRO-seq reads map within 500 bp of uniform ENCODE DHS midpoints compared to the CAGE and GRO-cap data (Figure S1C). We suggest that this decreased ability to detect promoter-proximal RNAs is due to differences in the published GRO-seq protocols (see Supplemental Experimental Procedures), rather than because of differently used thresholds. What then is the degree of divergent transcription initiation from human gene promoters? To address this, we assessed which fraction of transcribed gene promoters analyzed by Duttke et al. also display detectable reverse-strand transcription as a function of thresholds on the number of mapped 5′ ends per million library reads (TPMs). We estimated library-specific noise level distributions and used these to derive thresholds (dashed vertical lines in Figure S1D, see Supplemental Experimental Procedures) to call promoter-associated transcription initiation events distinguishable from noise. CAGE-hRRP40 data found 69% (1,433/2,089) of unidirectionally classified transcribed gene promoters and 82% (3,400/4,157) of all classified transcribed gene promoters to be divergently transcribed (Figure S1D). GRO-cap data yielded comparable numbers; 78% (1,491/1,919) and 88% (3,472/3,966) for GM12878 and 83% (1,594/1,929) and 90% (3,591/3,971) for K562 cells, respectively. The union of calls suggests 93% (3,974/4,285) of all Duttke et al. classified transcribed promoters to be divergent. These estimates are lower boundaries, since the sensitivity of any of the employed methods will improve with greater sequencing depth. Although the fraction of promoter reads in either orientation varies considerably for different genes, reverse-strand reads constituted on average 46.5% and 25.5% of total GRO-cap reads associated with classified divergent and unidirectional promoters, respectively (see Supplemental Experimental Procedures and Figure S1B, last two panels). Thus, we conclude that the vast majority of human gene promoters are intrinsically bidirectional, and that their amount of reverse-strand transcription is not negligible. The identification of reverse-strand TSSs at classified unidirectional promoters enabled improved core promoter analysis at well-defined focus points. Consequently, we detected TATA- and Inr-sequences ∼30 bp upstream of and at CAGE-defined reverse-strand TSSs, respectively (Figure S1E). In support of PIC formation at these sites, TBP and TFIIB recruitment was observed by ChIP-exo in K562 cells, and RNAPII was found downstream at the pause site (Figure S1F, data from Short Read Archive SRP019209). It thus appears that PICs form at NDR edges for most, if not all, transcriptionally active loci, and that PIC positioning is influenced by core promoter elements at either edge. Although the mechanistic significance of reverse-oriented transcription remains to be delineated, a near-universal existence of gene promoter-associated divergent transcription initiation is important to note. We are presently in a flux in the definitions of transcription regulatory elements in general, driven by insights from new technologies. Here, our understanding of any roles and causes of divergent promoter transcription may be vital for comprehending basic properties of promoters and core promoters and how they interact with the surrounding transcription factors and chromatin architecture. Such knowledge might be crucial to appreciate how these genetic elements have evolved to maintain their activity and receptiveness to regulation. R.A., Y.C., and L.C. analyzed data. R.A., Y.C., L.C., J.T.L., A.S., and T.H.J. interpreted results and wrote the letter. Download .pdf (6.85 MB) Help with pdf files Document S1. Supplemental Experimental Procedures and Figure S1 Human Promoters Are Intrinsically DirectionalDuttke et al.Molecular CellJanuary 29, 2015In BriefDuttke et al. show that the human basal RNA polymerase II machinery and core promoter are unidirectional and that reverse-oriented transcripts originate from separate reverse-directed core promoters. About half of active HeLa promoters are found as unidirectional, depleted at their upstream edges of core promoter sequences and associated chromatin features. Full-Text PDF Open ArchivePerspectives on Unidirectional versus Divergent TranscriptionDuttke et al.Molecular CellNovember 05, 2015In BriefIn their Letter to the Editor, Andersson et al. (2015) examined divergent and unidirectional human promoter regions reported in our February 2015 Molecular Cell paper (Duttke et al., 2015) and compared our results with data from their concurrent studies (Andersson et al., 2014; Core et al., 2014). They concluded that the nature of our transcription start site (TSS) data generated by the 5′-GRO-seq method (Lam et al., 2013) led to an inflation of the percentage of unidirectional promoter regions, and further suggested that unidirectional promoter regions may not exist. Full-Text PDF Open Archive