The adenovirus L4-22K protein regulates transcription and RNA splicing via a sequence-specific single-stranded RNA binding

Nucleic Acids Res. 2017 Feb 28;45(4):1731-1742. doi: 10.1093/nar/gkw1145.

Abstract

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.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenoviruses, Human / genetics
  • Adenoviruses, Human / metabolism
  • Base Sequence
  • Binding Sites
  • DNA, Single-Stranded / genetics
  • DNA, Single-Stranded / metabolism
  • Gene Expression Regulation*
  • Gene Expression Regulation, Viral
  • Gene Order
  • Humans
  • Introns
  • Models, Biological
  • Nucleotide Motifs
  • Protein Binding
  • RNA Splice Sites
  • RNA Splicing*
  • RNA-Binding Proteins / metabolism*
  • Ribonucleoprotein, U1 Small Nuclear / metabolism
  • Transcription, Genetic*
  • Viral Nonstructural Proteins / metabolism*

Substances

  • DNA, Single-Stranded
  • L4-22K protein, adenovirus
  • RNA Splice Sites
  • RNA-Binding Proteins
  • Ribonucleoprotein, U1 Small Nuclear
  • Viral Nonstructural Proteins