Article

  • The EMBO Journal (2005) 24, 1831 - 1841
  • doi:10.1038/sj.emboj.7600662

Published online: 28 April 2005

  • Subject Category:

A Kaposi's sarcoma virus RNA element that increases the nuclear abundance of intronless transcripts

Nicholas K Conrad1 and Joan A Steitz1

  1. Department of Molecular Biophysics and Biochemistry, Howard Hughes Medical Institute, Yale University, New Haven, CT, USA

Correspondence to:

Joan A Steitz, Department of Molecular Biophysics and Biochemistry, Howard Hughes Medical Institute, Yale University, New Haven, CT 06536, USA. Tel.: +1 203 737 4418; Fax: +1 203 624 8213; E-mail: joan.steitz@yale.edu

Received 14 January 2005; Accepted 6 April 2005


The Kaposi's sarcoma-associated herpesvirus produces a 1077 nucleotide noncoding, polyadenylated, exclusively nuclear RNA called PAN that is highly expressed in lytically infected cells. We report that PAN contains a novel post-transcriptional element essential for its abundant accumulation. The element, PAN–ENE (PAN RNA expression and nuclear retention element), increases the efficiency of 3'-end formation in vivo and is sufficient to enhance RNA abundance from an otherwise inefficiently expressed intronless beta-globin construct. The PAN–ENE does not concomitantly increase the production of encoded protein. Rather, it retains the unspliced beta-globin mRNA in the nucleus. Tethering of export factors can override the nuclear retention of the PAN–ENE, supporting a mechanism whereby the PAN–ENE blocks assembly of an export-competent mRNP. The activities of the PAN–ENE are specific to intronless constructs, since inserting the PAN–ENE into a spliced beta-globin construct has no effect on mRNA abundance and does not affect localization. This is the first characterization of a cis-acting element that increases RNA abundance of intronless transcripts but inhibits assembly of an export-competent mRNP.

  • Keywords:

    • 3'-end formation,
    • KSHV,
    • nuclear retention,
    • PAN,
    • RNA export
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