• Title of article

    Activation-Induced Cytidine Deaminase Targets DNA at Sites of RNA Polymerase II Stalling by Interaction with Spt5

  • Author/Authors

    Rushad Pavri، نويسنده , , Anna Gazumyan، نويسنده , , Mila Jankovic، نويسنده , , Michela Di Virgilio، نويسنده , , Isaac Klein، نويسنده , , Camilo Ansarah-Sobrinho، نويسنده , , Wolfgang Resch، نويسنده , , Arito Yamane، نويسنده , , Bernardo Reina-San-Martin، نويسنده , , Vasco Barreto، نويسنده , , Thomas J. Nieland، نويسنده , , David E. Root، نويسنده , , Rafael Casellas، نويسنده , , Michel C. Nussenzweig، نويسنده ,

  • Issue Information
    هفته نامه با شماره پیاپی سال 2010
  • Pages
    12
  • From page
    122
  • To page
    133
  • Abstract
    Activation-induced cytidine deaminase (AID) initiates antibody gene diversification by creating U:G mismatches. However, AID is not specific for antibody genes; Off-target lesions can activate oncogenes or cause chromosome translocations. Despite its importance in these transactions little is known about how AID finds its targets. We performed an shRNA screen to identify factors required for class switch recombination (CSR) of antibody loci. We found that Spt5, a factor associated with stalled RNA polymerase II (Pol II) and single stranded DNA (ssDNA), is required for CSR. Spt5 interacts with AID, it facilitates association between AID and Pol II, and AID recruitment to its Ig and non-Ig targets. ChIP-seq experiments reveal that Spt5 colocalizes with AID and stalled Pol II. Further, Spt5 accumulation at sites of Pol II stalling is predictive of AID-induced mutation. We propose that AID is targeted to sites of Pol II stalling in part via its association with Spt5.
  • Journal title
    CELL
  • Serial Year
    2010
  • Journal title
    CELL
  • Record number

    1020449