TY - JOUR
T1 - Divergent transcription is associated with promoters of transcriptional regulators
AU - Lepoivre, Cyrille
AU - Belhocine, Mohamed
AU - Bergon, Aurélie
AU - Griffon, Aurélien
AU - Yammine, Miriam
AU - Vanhille, Laurent
AU - Zacarias-Cabeza, Joaquin
AU - Garibal, Marc Antoine
AU - Koch, Frederic
AU - Maqbool, Muhammad A.
AU - Fenouil, Romain
AU - Loriod, Beatrice
AU - Holota, Hélène
AU - Gut, Marta
AU - Gut, Ivo
AU - Imbert, Jean
AU - Andrau, Jean Christophe
AU - Puthier, Denis
AU - Spicuglia, Salvatore
N1 - Funding Information:
Research in SS laboratory was supported by recurrent funding from the Inserm and Aix-Marseille University, and by specific grants from the European Union’s FP7 Program (agreement n° 282510-BLUEPRINT), the ARC (project n° SFI20111203756) and the A*MIDEX project (n° ANR-11-IDEX-0001-02) funded by the « Investissements d’Avenir » French Government program. The work was also granted for sequencing costs by an ESGI Consortium grant of the EU (to JCA, program T-DynRegSeq) from the Seventh Framework Program (FP7/2007-2013) under grant agreement no. 262055. The TGML sequencing platform is supported by grants from GIS IBiSA and France Génomique ANR Investissements d'Avenir (to JI).
PY - 2013/12/23
Y1 - 2013/12/23
N2 - Background: Divergent transcription is a wide-spread phenomenon in mammals. For instance, short bidirectional transcripts are a hallmark of active promoters, while longer transcripts can be detected antisense from active genes in conditions where the RNA degradation machinery is inhibited. Moreover, many described long non-coding RNAs (lncRNAs) are transcribed antisense from coding gene promoters. However, the general significance of divergent lncRNA/mRNA gene pair transcription is still poorly understood. Here, we used strand-specific RNA-seq with high sequencing depth to thoroughly identify antisense transcripts from coding gene promoters in primary mouse tissues.Results: We found that a substantial fraction of coding-gene promoters sustain divergent transcription of long non-coding RNA (lncRNA)/mRNA gene pairs. Strikingly, upstream antisense transcription is significantly associated with genes related to transcriptional regulation and development. Their promoters share several characteristics with those of transcriptional developmental genes, including very large CpG islands, high degree of conservation and epigenetic regulation in ES cells. In-depth analysis revealed a unique GC skew profile at these promoter regions, while the associated coding genes were found to have large first exons, two genomic features that might enforce bidirectional transcription. Finally, genes associated with antisense transcription harbor specific H3K79me2 epigenetic marking and RNA polymerase II enrichment profiles linked to an intensified rate of early transcriptional elongation.Conclusions: We concluded that promoters of a class of transcription regulators are characterized by a specialized transcriptional control mechanism, which is directly coupled to relaxed bidirectional transcription.
AB - Background: Divergent transcription is a wide-spread phenomenon in mammals. For instance, short bidirectional transcripts are a hallmark of active promoters, while longer transcripts can be detected antisense from active genes in conditions where the RNA degradation machinery is inhibited. Moreover, many described long non-coding RNAs (lncRNAs) are transcribed antisense from coding gene promoters. However, the general significance of divergent lncRNA/mRNA gene pair transcription is still poorly understood. Here, we used strand-specific RNA-seq with high sequencing depth to thoroughly identify antisense transcripts from coding gene promoters in primary mouse tissues.Results: We found that a substantial fraction of coding-gene promoters sustain divergent transcription of long non-coding RNA (lncRNA)/mRNA gene pairs. Strikingly, upstream antisense transcription is significantly associated with genes related to transcriptional regulation and development. Their promoters share several characteristics with those of transcriptional developmental genes, including very large CpG islands, high degree of conservation and epigenetic regulation in ES cells. In-depth analysis revealed a unique GC skew profile at these promoter regions, while the associated coding genes were found to have large first exons, two genomic features that might enforce bidirectional transcription. Finally, genes associated with antisense transcription harbor specific H3K79me2 epigenetic marking and RNA polymerase II enrichment profiles linked to an intensified rate of early transcriptional elongation.Conclusions: We concluded that promoters of a class of transcription regulators are characterized by a specialized transcriptional control mechanism, which is directly coupled to relaxed bidirectional transcription.
KW - Bidirectional promoter
KW - Developmental transcription factor
KW - Divergent transcription
KW - GC skew
KW - lncRNA
UR - http://www.scopus.com/inward/record.url?scp=84890772287&partnerID=8YFLogxK
U2 - 10.1186/1471-2164-14-914
DO - 10.1186/1471-2164-14-914
M3 - Article
C2 - 24365181
AN - SCOPUS:84890772287
SN - 1471-2164
VL - 14
JO - BMC Genomics
JF - BMC Genomics
IS - 1
M1 - 914
ER -