A conserved motif of vertebrate Y RNAs essential for chromosomal DNA replication

  1. Timothy J. Gardiner,
  2. Christo P. Christov,
  3. Alexander R. Langley and
  4. Torsten Krude
  1. Department of Zoology, University of Cambridge, Cambridge CB2 3EJ, United Kingdom

    Abstract

    Noncoding Y RNAs are required for the reconstitution of chromosomal DNA replication in late G1 phase template nuclei in a human cell-free system. Y RNA genes are present in all vertebrates and in some isolated nonvertebrates, but the conservation of Y RNA function and key determinants for its function are unknown. Here, we identify a determinant of Y RNA function in DNA replication, which is conserved throughout vertebrate evolution. Vertebrate Y RNAs are able to reconstitute chromosomal DNA replication in the human cell-free DNA replication system, but nonvertebrate Y RNAs are not. A conserved nucleotide sequence motif in the double-stranded stem of vertebrate Y RNAs correlates with Y RNA function. A functional screen of human Y1 RNA mutants identified this conserved motif as an essential determinant for reconstituting DNA replication in vitro. Double-stranded RNA oligonucleotides comprising this RNA motif are sufficient to reconstitute DNA replication, but corresponding DNA or random sequence RNA oligonucleotides are not. In intact cells, wild-type hY1 or the conserved RNA duplex can rescue an inhibition of DNA replication after RNA interference against hY3 RNA. Therefore, we have identified a new RNA motif that is conserved in vertebrate Y RNA evolution, and essential and sufficient for Y RNA function in human chromosomal DNA replication.

    Keywords

    Footnotes

    • Reprint requests to: Torsten Krude, Department of Zoology, University of Cambridge, Downing Street, Cambridge CB2 3EJ, United Kingdom; e-mail: tk1{at}mole.bio.cam.ac.uk; fax: +44 (0)1223 336676.

    • Article published online ahead of print. Article and publication date are at http://www.rnajournal.org/cgi/doi/10.1261/rna.1472009.

      • Received November 19, 2008.
      • Accepted April 2, 2009.
    | Table of Contents