http://www.cnr.it/ontology/cnr/individuo/prodotto/ID26522
Genome-wide analysis of mammalian promoter architecture and evolution. (Articolo in rivista)
- Type
- Label
- Genome-wide analysis of mammalian promoter architecture and evolution. (Articolo in rivista) (literal)
- Anno
- 2006-01-01T00:00:00+01:00 (literal)
- Alternative label
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
- Carninci P, et al. (literal)
- Pagina inizio
- Pagina fine
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroVolume
- Rivista
- Note
- ISI Web of Science (WOS) (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
- 1 Genome Exploration Research Group, RIKEN Genomic Sciences Center (GSC), RIKEN Yokohama Institute, 1-7-22 Suehiro-cho, Tsurumi-ku, Yokohama, Kanagawa, 230-0045, Japan; 2 Genome Science Laboratory, Discovery Research Institute, RIKEN Wako Institute, 2-1 Hirosawa, Wako, Saitama, 351-0198, Japan; 3 Center for Genomics and Bioinformatics, Karolinska Institutet, Berzelius v. 35, S-171 77 Stockholm, Sweden; 13 Dulbecco Telethon Institute, Institute of Genetics and Biophysics, Consiglio Nazionale delle Ricerche (IGB CNR), Epigenetics and Genome Reprogramming Laboratory, Pietro Castellino Street 111, Napoli, 80131, Italy; et al. (literal)
- Titolo
- Genome-wide analysis of mammalian promoter architecture and evolution. (literal)
- Abstract
- Mammalian promoters can be separated into two classes, conserved TATA boxenriched promoters, which initiate at a well-defined site, and more plastic, broad and evolvable CpG-rich promoters. We have sequenced tags corresponding to several hundred thousand transcription start sites (TSSs) in the mouse and human genomes, allowing precise analysis of the sequence architecture and evolution of distinct promoter classes. Different tissues and families of genes differentially use distinct types of promoters. Our tagging methods allow quantitative analysis of promoter usage in different tissues and show that differentially regulated alternative TSSs are a common feature in protein-coding genes and commonly generate alternative N termini. Among the TSSs, we identified new start sites associated with the majority of exons and with 3' UTRs. These data permit genome-scale identification of tissue-specific promoters and analysis of the cis-acting elements associated with them. (literal)
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- Autore CNR
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