ATP is required for interactions between UAP56 and two conserved mRNA export proteins, Aly and CIP29, to assemble the TREX complex

Genes Dev. 2010 Sep 15;24(18):2043-53. doi: 10.1101/gad.1898610.

Abstract

The conserved TREX mRNA export complex is known to contain UAP56, Aly, Tex1, and the THO complex. Here, we carried out proteomic analysis of immunopurified human TREX complex and identified the protein CIP29 as the only new component with a clear yeast relative (known as Tho1). Tho1 is known to function in mRNA export, and we provide evidence that CIP29 likewise functions in this process. Like the known TREX components, a portion of CIP29 localizes in nuclear speckle domains, and its efficient recruitment to mRNA is both splicing- and cap-dependent. We show that UAP56 mediates an ATP-dependent interaction between the THO complex and both CIP29 and Aly, indicating that TREX assembly is ATP-dependent. Using recombinant proteins expressed in Escherichia coli, we show that UAP56, Aly, and CIP29 form an ATP-dependent trimeric complex, and UAP56 bridges the interaction between CIP29 and Aly. We conclude that the interaction of two conserved export proteins, CIP29 and Aly, with UAP56 is strictly regulated by ATP during assembly of the TREX complex.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenosine Triphosphate / metabolism*
  • Animals
  • COS Cells
  • Cell Cycle Proteins / metabolism
  • Chlorocebus aethiops
  • DEAD-box RNA Helicases / genetics
  • DEAD-box RNA Helicases / metabolism*
  • Exodeoxyribonucleases / metabolism
  • HeLa Cells
  • Humans
  • Nuclear Proteins / genetics
  • Nuclear Proteins / metabolism*
  • Nucleocytoplasmic Transport Proteins / metabolism*
  • RNA Processing, Post-Transcriptional / physiology
  • RNA Transport
  • RNA, Messenger / metabolism*
  • RNA-Binding Proteins / metabolism*
  • Transcription Factors / metabolism*

Substances

  • ALYREF protein, human
  • Cell Cycle Proteins
  • Nuclear Proteins
  • Nucleocytoplasmic Transport Proteins
  • RNA, Messenger
  • RNA-Binding Proteins
  • SARNP protein, human
  • Tex1 protein, human
  • Transcription Factors
  • Adenosine Triphosphate
  • Exodeoxyribonucleases
  • DDX39B protein, human
  • DEAD-box RNA Helicases