Literature DB >> 7198941

Differential capacity for translation and lack of competition between mRNAs that segregate to free and membrane-bound polysomes.

J D Richter, L D Smith.   

Abstract

The Xenopus oocyte was used to study translation, stability and subcellular compartmentation of injected heterologous mRNAs. The capacity of the oocyte to translate a membrane-free mRNA, globin, was not saturable by amounts up to 100 ng injected. In contrast, the ability of the oocyte to translate a membrane-associated mRNA, zein, saturated at 20 ng or less of injected mRNA. The hybridization of RNA from message-injected oocytes to cDNA probes revealed that approximately the same amount of globin and zein mRNAs remained stable and that this fraction was as little as 2.1% at the highest amount injected (80 ng). However, while almost all of the globin mRNA at all concentrations injected was found in a polysome pellet, most of the zein mRNA at saturating concentrations was found in a post-polysomal supernatant. The reason for the limited translation of zein mRNA appears to be due to a paucity of oocyte rough endoplasmic reticulum since the injection of dog pancreas rough endoplasmic reticulum into oocytes previously injected with zein mRNA stimulates zein synthesis. Displacement and competition experiments between four different mRNAs indicate that injected messages are distributed to two translational compartments, membrane-bound and free, and that this occurs either prior to the initiation of translation or involves message-specific factors.

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Year:  1981        PMID: 7198941     DOI: 10.1016/0092-8674(81)90372-x

Source DB:  PubMed          Journal:  Cell        ISSN: 0092-8674            Impact factor:   41.582


  27 in total

1.  Variable ratio of permeability to gating charge of rBIIA sodium channels and sodium influx in Xenopus oocytes.

Authors:  N G Greeff; F J Kühn
Journal:  Biophys J       Date:  2000-11       Impact factor: 4.033

2.  Tandem linkage of Shaker K+ channel subunits does not ensure the stoichiometry of expressed channels.

Authors:  K McCormack; L Lin; L E Iverson; M A Tanouye; F J Sigworth
Journal:  Biophys J       Date:  1992-11       Impact factor: 4.033

3.  Modifications of the 5' cap of mRNAs during Xenopus oocyte maturation: independence from changes in poly(A) length and impact on translation.

Authors:  D L Gillian-Daniel; N K Gray; J Aström; A Barkoff; M Wickens
Journal:  Mol Cell Biol       Date:  1998-10       Impact factor: 4.272

4.  Cap-independent translation initiation in Xenopus oocytes.

Authors:  B D Keiper; R E Rhoads
Journal:  Nucleic Acids Res       Date:  1997-01-15       Impact factor: 16.971

5.  The extracellular domain of p75NTR is necessary to inhibit neurotrophin-3 signaling through TrkA.

Authors:  P S Mischel; S G Smith; E R Vining; J S Valletta; W C Mobley; L F Reichardt
Journal:  J Biol Chem       Date:  2001-01-09       Impact factor: 5.157

6.  Stimulation of Xenopus oocyte protein synthesis by microinjected adenovirus RNA.

Authors:  J D Richter; N C Jones; L D Smith
Journal:  Proc Natl Acad Sci U S A       Date:  1982-06       Impact factor: 11.205

7.  The stem-loop binding protein is required for efficient translation of histone mRNA in vivo and in vitro.

Authors:  Ricardo Sànchez; William F Marzluff
Journal:  Mol Cell Biol       Date:  2002-10       Impact factor: 4.272

8.  Competitive and non-competitive regulation of calcium-dependent inactivation in CaV1.2 L-type Ca2+ channels by calmodulin and Ca2+-binding protein 1.

Authors:  Shimrit Oz; Adva Benmocha; Yehezkel Sasson; Dana Sachyani; Lior Almagor; Amy Lee; Joel A Hirsch; Nathan Dascal
Journal:  J Biol Chem       Date:  2013-03-25       Impact factor: 5.157

9.  Cap ribose methylation of c-mos mRNA stimulates translation and oocyte maturation in Xenopus laevis.

Authors:  H Kuge; G G Brownlee; P D Gershon; J D Richter
Journal:  Nucleic Acids Res       Date:  1998-07-01       Impact factor: 16.971

10.  Determination of KA values by controlled receptor expression in Xenopus oocytes.

Authors:  H Murakoshi; K Nunoki; K Ishii; N Taira
Journal:  Br J Pharmacol       Date:  1995-10       Impact factor: 8.739

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