Nucleic acids research · 2017
The adenovirus L4-22K protein regulates transcription and RNA splicing via a sequence-specific single-stranded RNA binding.
СтатьяПоддержка исследования: вне правительства СШАНазвание и аннотация: Перевод в очереди
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Lan Susan, Kamel Wael, Punga Tanel, Akusjärvi Göran
Аннотация
The adenovirus L4-22K protein both activates and suppresses transcription from the adenovirus major late promoter (MLP) by binding to DNA elements located downstream of the MLP transcriptional start site: the so-called DE element (positive) and the R1 region (negative). Here we show that L4-22K preferentially binds to the RNA form of the R1 region, both to the double-stranded RNA and the single-stranded RNA of the same polarity as the nascent MLP transcript. Further, L4-22K binds to a 5΄-CAAA-3΄ motif in the single-stranded RNA, which is identical to the sequence motif characterized for L4-22K DNA binding. L4-22K binding to single-stranded RNA results in an enhancement of U1 snRNA recruitment to the major late first leader 5΄ splice site. This increase in U1 snRNA binding results in a suppression of MLP transcription and a concurrent stimulation of major late first intron splicing.
Предметные рубрики MeSH
Adenoviruses, HumanBase SequenceBinding SitesDNA, Single-StrandedGene Expression RegulationGene Expression Regulation, ViralGene OrderHumansIntronsModels, BiologicalNucleotide MotifsProtein BindingRNA Splice SitesRNA SplicingRNA-Binding ProteinsRibonucleoprotein, U1 Small NuclearTranscription, GeneticViral Nonstructural Proteins