Literature DB >> 8524291

Translational efficiency is regulated by the length of the 3' untranslated region.

R L Tanguay1, D R Gallie.   

Abstract

All polyadenylated mRNAs contain sequence of variable length between the coding region and the poly(A) tail. Little has been done to establish what role the length of the 3' untranslated region (3'UTR) plays in posttranscriptional regulation. Using firefly luciferase (luc) reporter mRNA in transiently transfected Chinese hamster ovary (CHO) cells, we observed that the addition of a poly(A) tail increased expression 97-fold when the length of the 3'UTR was 19 bases but that its stimulatory effect was only 2.3-fold when the length of the 3'UTR was increased to 156 bases. The effect of the luc 3'UTR on poly(A) tail function was orientation independent, suggesting that its length and not its primary sequence was the important factor. Increasing the length of the 3'UTR increased expression from poly(A)- mRNA but had little effect on poly(A)+ mRNA. To examine the effect of length on translational efficiency and mRNA stability, a 20-base sequence was introduced and reiterated downstream of the luc stop codon to generate a nested set of constructs in which the length of the 3'UTR increased from 4 to 104 bases. For poly(A)- reporter mRNA, translational efficiency in CHO cells increased 38-fold as the length of the 3'UTR increased from 4 to 104 bases. Increasing the length of the 3'UTR beyond 104 bases increased expression even further. Increasing the length of the 3'UTR also resulted in a 2.5-fold stabilization of the reporter mRNA. For poly(A)+ mRNA, the translational efficiency and mRNA half-life increased only marginally as the length of the 3'UTR increased from 27 to 161 bases. However, positioning the poly(A) tail only 7 bases downstream of the stop codon resulted in a 39-fold reduction in the rate of translation relative to a construct with a 27-base 3'UTR, which may be a consequence of the poly(A) tail-poly(A)-binding protein complex functioning as a steric block to translocating ribosomes as they approached the termination codon. The optimal length of the 3' noncoding region for maximal poly(A) tail-mediated stimulation of translation is approximately 27 bases. These data suggest that the length of the 3'UTR plays an important role in determining both the translational efficiency and the stability of an mRNA.

Entities:  

Mesh:

Substances:

Year:  1996        PMID: 8524291      PMCID: PMC230988          DOI: 10.1128/MCB.16.1.146

Source DB:  PubMed          Journal:  Mol Cell Biol        ISSN: 0270-7306            Impact factor:   4.272


  46 in total

1.  Multiple cis-acting elements modulate the translational efficiency of GCN4 mRNA in yeast.

Authors:  D Tzamarias; D Alexandraki; G Thireos
Journal:  Proc Natl Acad Sci U S A       Date:  1986-07       Impact factor: 11.205

2.  Single-step method of RNA isolation by acid guanidinium thiocyanate-phenol-chloroform extraction.

Authors:  P Chomczynski; N Sacchi
Journal:  Anal Biochem       Date:  1987-04       Impact factor: 3.365

3.  The stem-loop structure at the 3' end of histone mRNA is necessary and sufficient for regulation of histone mRNA stability.

Authors:  N B Pandey; W F Marzluff
Journal:  Mol Cell Biol       Date:  1987-12       Impact factor: 4.272

4.  A conserved AU sequence from the 3' untranslated region of GM-CSF mRNA mediates selective mRNA degradation.

Authors:  G Shaw; R Kamen
Journal:  Cell       Date:  1986-08-29       Impact factor: 41.582

5.  Effects of intercistronic length on the efficiency of reinitiation by eucaryotic ribosomes.

Authors:  M Kozak
Journal:  Mol Cell Biol       Date:  1987-10       Impact factor: 4.272

6.  Multiple upstream AUG codons mediate translational control of GCN4.

Authors:  P P Mueller; A G Hinnebusch
Journal:  Cell       Date:  1986-04-25       Impact factor: 41.582

7.  Rapid and efficient site-specific mutagenesis without phenotypic selection.

Authors:  T A Kunkel; J D Roberts; R A Zakour
Journal:  Methods Enzymol       Date:  1987       Impact factor: 1.600

8.  Efficient in vitro synthesis of biologically active RNA and RNA hybridization probes from plasmids containing a bacteriophage SP6 promoter.

Authors:  D A Melton; P A Krieg; M R Rebagliati; T Maniatis; K Zinn; M R Green
Journal:  Nucleic Acids Res       Date:  1984-09-25       Impact factor: 16.971

9.  A single domain of yeast poly(A)-binding protein is necessary and sufficient for RNA binding and cell viability.

Authors:  A B Sachs; R W Davis; R D Kornberg
Journal:  Mol Cell Biol       Date:  1987-09       Impact factor: 4.272

Review 10.  Comparison of initiation of protein synthesis in procaryotes, eucaryotes, and organelles.

Authors:  M Kozak
Journal:  Microbiol Rev       Date:  1983-03
View more
  77 in total

1.  The length of the combined 3' untranslated region and poly(A) tail does not control rates of glyceraldehyde-3-phosphate dehydrogenase mRNA translation in three species of parasitic protists.

Authors:  B H ter Kuile; F J Sallés
Journal:  J Bacteriol       Date:  2000-06       Impact factor: 3.490

Review 2.  The mammary gland as a bioreactor: expression, processing, and production of recombinant proteins.

Authors:  A J Clark
Journal:  J Mammary Gland Biol Neoplasia       Date:  1998-07       Impact factor: 2.673

3.  Cap-independent translational enhancement of turnip crinkle virus genomic and subgenomic RNAs.

Authors:  F Qu; T J Morris
Journal:  J Virol       Date:  2000-02       Impact factor: 5.103

4.  A cis-acting element known to block 3' mRNA degradation enhances expression of polyA-minus mRNA in wild-type yeast cells and phenocopies a ski mutant.

Authors:  J T Brown; A W Johnson
Journal:  RNA       Date:  2001-11       Impact factor: 4.942

5.  A dynamic competition between release factor 2 and the tRNA(Sec) decoding UGA at the recoding site of Escherichia coli formate dehydrogenase H.

Authors:  J B Mansell; D Guévremont; E S Poole; W P Tate
Journal:  EMBO J       Date:  2001-12-17       Impact factor: 11.598

6.  Fending off decay: a combinatorial approach in intact cells for identifying mRNA stability elements.

Authors:  Z Chrzanowska-Lightowlers; R N Lightowlers
Journal:  RNA       Date:  2001-03       Impact factor: 4.942

7.  3'-UTR-located inverted Alu repeats facilitate mRNA translational repression and stress granule accumulation.

Authors:  Terry Fitzpatrick; Sui Huang
Journal:  Nucleus       Date:  2012-06-12       Impact factor: 4.197

8.  Competitive translation efficiency at the picornavirus type 1 internal ribosome entry site facilitated by viral cis and trans factors.

Authors:  Elena Y Dobrikova; Rachel N Grisham; Constanze Kaiser; Jennifer Lin; Matthias Gromeier
Journal:  J Virol       Date:  2006-04       Impact factor: 5.103

9.  Regulatory sequences in the 3' untranslated region of the human cGMP-phosphodiesterase beta-subunit gene.

Authors:  Mark R Verardo; Andrea Viczian; Natik Piri; Novrouz B Akhmedov; Barry E Knox; Debora B Farber
Journal:  Invest Ophthalmol Vis Sci       Date:  2009-02-14       Impact factor: 4.799

10.  A homogeneous cell-based bicistronic fluorescence assay for high-throughput identification of drugs that perturb viral gene recoding and read-through of nonsense stop codons.

Authors:  Tony S Cardno; Elizabeth S Poole; Suneeth F Mathew; Ryan Graves; Warren P Tate
Journal:  RNA       Date:  2009-06-17       Impact factor: 4.942

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.