Literature DB >> 15929942

mRNA with a <20-nt poly(A) tail imparted by the poly(A)-limiting element is translated as efficiently in vivo as long poly(A) mRNA.

Jing Peng1, Daniel R Schoenberg.   

Abstract

The poly(A)-limiting element (PLE) is a conserved sequence that restricts the length of the poly(A) tail to <20 nt. This study compared the translation of PLE-containing short poly(A) mRNA expressed in cells with translation in vitro of mRNAs with varying length poly(A) tails. In transfected cells, PLE-containing mRNA had a <20-nt poly(A) and accumulated to a level 20% higher than a matching control without a PLE. It was translated as well as the matching control mRNA with long poly(A) and showed equivalent binding to polysomes. Translation in a HeLa cell cytoplasmic extract was used to examine the impact of the PLE in the context of varying length poly(A) tails. Here the overall translation of +PLE mRNA was less than control mRNA with the same length poly(A), and the PLE did not overcome the effect of a short poly(A) tail. Because poly(A)-binding protein (PABP) is a dominant effector of poly(A)-dependent translation we reasoned excess PABP in our extract might overwhelm PLE regulation of translation. This was confirmed by experiments where PABP was inactivated with poly(rA) or Paip2, and the effect of both treatments was reversed by addition of recombinant PABP. These data indicate that the PLE functionally substitutes for bound PABP to stimulate translation of short poly(A) mRNA.

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Year:  2005        PMID: 15929942      PMCID: PMC1237109          DOI: 10.1261/rna.2470905

Source DB:  PubMed          Journal:  RNA        ISSN: 1355-8382            Impact factor:   4.942


  35 in total

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Journal:  RNA       Date:  2001-07       Impact factor: 4.942

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9.  Translational repression by a novel partner of human poly(A) binding protein, Paip2.

Authors:  K Khaleghpour; Y V Svitkin; A W Craig; C T DeMaria; R C Deo; S K Burley; N Sonenberg
Journal:  Mol Cell       Date:  2001-01       Impact factor: 17.970

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  19 in total

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Authors:  Jing Peng; Elizabeth L Murray; Daniel R Schoenberg
Journal:  RNA       Date:  2005-05-04       Impact factor: 4.942

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Review 4.  Developing mRNA-vaccine technologies.

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6.  Novel 3' ends that support translation.

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7.  Identification of cytoplasmic capping targets reveals a role for cap homeostasis in translation and mRNA stability.

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8.  Target specificity among canonical nuclear poly(A) polymerases in plants modulates organ growth and pathogen response.

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9.  Separate cis-trans pathways post-transcriptionally regulate murine CD154 (CD40 ligand) expression: a novel function for CA repeats in the 3'-untranslated region.

Authors:  B JoNell Hamilton; Xiao-Wei Wang; Jane Collins; Donald Bloch; Alan Bergeron; Brian Henry; Benjamin M Terry; Moe Zan; Andrew J Mouland; William F C Rigby
Journal:  J Biol Chem       Date:  2008-07-18       Impact factor: 5.157

10.  ENCODE tiling array analysis identifies differentially expressed annotated and novel 5' capped RNAs in hepatitis C infected liver.

Authors:  Milan E Folkers; Don A Delker; Christopher I Maxwell; Cassie A Nelson; Jason J Schwartz; David A Nix; Curt H Hagedorn
Journal:  PLoS One       Date:  2011-02-16       Impact factor: 3.240

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