JBC INTERFERin siRNA transfection reagent

HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Lee, C. C.
Right arrow Articles by Tate, W. P.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Lee, C. C.
Right arrow Articles by Tate, W. P.
Social Bookmarking
 Add to CiteULike   Add to Complore   Add to Connotea   Add to Del.icio.us   Add to Digg   Add to Reddit   Add to Technorati  
What's this?

J. Biol. Chem., Vol. 262, Issue 8, 3548-3552, Mar, 1987

Isolation of a rat mitochondrial release factor. Accommodation of the changed genetic code for termination

CC Lee, KM Timms, CN Trotman and WP Tate

A single release factor has been isolated and partially purified from rat mitochondria. It requires ethanol in addition to the specific termination codon when assayed in a heterologous system with Escherichia coli ribosomes. The factor recognizes the codons UAA and UAG but not UGA, and therefore it has been designated mtRF-1. A factor of the bacterial RF-2 type, which in E. coli recognizes UGA, or of the mammalian type, which recognizes all three termination codons, has not been detected in mitochondria. The absence of a factor responding to UGA accommodates the use of this codon as a signal for tryptophan in the rat mitochondrial genetic code. The mtRF-1 could translate all of the known termination codons in the rat mitochondrial genome. It does not respond to AGG and AGA which in bovine and human mitochondrial DNA code for termination but which in rat mitochondria may not code for either an amino acid or for termination.
Add to CiteULike CiteULike   Add to Complore Complore   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us   Add to Digg Digg   Add to Reddit Reddit   Add to Technorati Technorati    What's this?


This article has been cited by other articles:


Home page
Mol Biol EvolHome page
A. J. Heidel and G. Glockner
Mitochondrial Genome Evolution in the Social Amoebae
Mol. Biol. Evol., July 1, 2008; 25(7): 1440 - 1450.
[Abstract] [Full Text] [PDF]


Home page
GENES CELLSHome page
Y. Nozaki, N. Matsunaga, T. Ishizawa, T. Ueda, and N. Takeuchi
HMRF1L is a human mitochondrial translation release factor involved in the decoding of the termination codons UAA and UAG.
Genes Cells, May 1, 2008; 13(5): 429 - 438.
[Abstract] [Full Text] [PDF]


Home page
Hum Mol GenetHome page
R. J. Temperley, S. H. Seneca, K. Tonska, E. Bartnik, L. A. Bindoff, R. N. Lightowlers, and Z. M.A. Chrzanowska-Lightowlers
Investigation of a pathogenic mtDNA microdeletion reveals a translation-dependent deadenylation decay pathway in human mitochondria
Hum. Mol. Genet., September 15, 2003; 12(18): 2341 - 2348.
[Abstract] [Full Text] [PDF]


Home page
Microbiol. Mol. Biol. Rev.Home page
M. C. Ganoza, M. C. Kiel, and H. Aoki
Evolutionary Conservation of Reactions in Translation
Microbiol. Mol. Biol. Rev., September 1, 2002; 66(3): 460 - 485.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
M. E. Askarian-Amiri, H. J. Pel, D. Guevremont, K. K. McCaughan, E. S. Poole, V. G. Sumpter, and W. P. Tate
Functional Characterization of Yeast Mitochondrial Release Factor 1
J. Biol. Chem., June 2, 2000; 275(23): 17241 - 17248.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 All ASBMB Journals   Molecular and Cellular Proteomics 
 Journal of Lipid Research   ASBMB Today 
Copyright © 1987 by the American Society for Biochemistry and Molecular Biology.