Standing out in the field of IgY Immunotechnology

  • Home
    Home A full collection of all the Research Archive entries.
  • Years
    Years Sort entries by year.
  • Tags
    Tags Displays a list of tags that have been used in the blog.
  • Archives
    Archives Contains a list of research entries that were created previously.

Poly(A) Binding Protein C1 Is Essential for Efficient L1 Retrotransposition and Affects L1 RNP Formation*

Posted by on in 2012
  • Font size: Larger Smaller
  • Hits: 2382
  • Print
corresponding authorLixin Dai,a,b Martin S. Taylor,a,c Kathryn A. O'Donnell,a,b,* and Jef D. Boekecorresponding authora,b   2012.  Mol Cell Biol 32:4323-4336. doi:  10.1128/MCB.06785-11 
Corresponding author.
Address correspondence to Jef D. Boeke, ude.imhj@ekeobj.
*Present address: Kathryn A. O'Donnell, Department of Molecular Biology, University of Texas Southwestern Medical Center, Dallas, Texas, USA.


Poly(A) binding proteins (PABPs) specifically bind the polyadenosine tail of mRNA and have been shown to be important for RNA polyadenylation, translation initiation, and mRNA stability. Using a modified L1 retrotransposition vector, we examined the effects of two PABPs (encoded by PABPN1 and PABPC1) on the retrotransposition activity of the L1 non-long-terminal-repeat (non-LTR) retrotransposon in both HeLa and HEK293T cells. We demonstrated that knockdown of these two genes by RNA interference (RNAi) effectively reduced L1 retrotransposition by 70 to 80% without significantly changing L1 transcription or translation or the status of the poly(A) tail. We identified that both poly(A) binding proteins were associated with the L1 ribonucleoprotein complex, presumably through L1 mRNA. Depletion of PABPC1caused a defect in L1 RNP formation. Knockdown of the PABPC1 inhibitor PAIP2 increased L1 retrotransposition up to 2-fold. Low levels of exogenous overexpression of PABPN1 and PABPC1 increased L1 retrotransposition, whereas unregulated overexpression of these two proteins caused pleiotropic effects, such as hypersensitivity to puromycin and decreased L1 activity. Our data suggest that PABPC1 is essential for the formation of L1 RNA-protein complexes and may play a role in L1 RNP translocation in the host cell.

*Custom Chicken IgY and the Affinity Purified Donkey anti-Chicken IgY agarose precipitation reagent used in this publication were manufactured by Gallus Immunotech Inc. 



See the whole paper here:

Last modified on