A cross-eyed geneticist’s view V. How Sydney Brenner, Leslie Barnett, Eugene Katz, and Francis Crick inferred that UGA is a nonsense codon

2019 ◽  
Vol 44 (6) ◽  
Author(s):  
Durgadas P Kasbekar
Keyword(s):  
2004 ◽  
Vol 10 (4) ◽  
pp. 613
Author(s):  
Inder M. Verma

Science ◽  
2004 ◽  
Vol 305 (5687) ◽  
pp. 1118-1118 ◽  
Author(s):  
L. E. Orgel

1995 ◽  
Vol 15 (4) ◽  
pp. 2231-2244 ◽  
Author(s):  
S Zhang ◽  
M J Ruiz-Echevarria ◽  
Y Quan ◽  
S W Peltz

In both prokaryotes and eukaryotes, nonsense mutations in a gene can enhance the decay rate or reduce the abundance of the mRNA transcribed from that gene, and we call this process nonsense-mediated mRNA decay. We have been investigating the cis-acting sequences involved in this decay pathway. Previous experiments have demonstrated that, in addition to a nonsense codon, specific sequences 3' of a nonsense mutation, which have been defined as downstream elements, are required for mRNA destabilization. The results presented here identify a sequence motif (TGYYGATGYYYYY, where Y stands for either T or C) that can predict regions in genes that, when positioned 3' of a nonsense codon, promote rapid decay of its mRNA. Sequences harboring two copies of the motif from five regions in the PGK1, ADE3, and HIS4 genes were able to function as downstream elements. In addition, four copies of this motif can function as an independent downstream element. The sequences flanking the motif played a more significant role in modulating its activity when fewer copies of the sequence motif were present. Our results indicate the sequences 5' of the motif can modulate its activity by maintaining a certain distance between the sequence motif and the termination codon. We also suggest that the sequences 3' of the motif modulate the activity of the downstream element by forming RNA secondary structures. Consistent with this view, a stem-loop structure positioned 3' of the sequence motif can enhance the activity of the downstream element. This sequence motif is one of the few elements that have been identified that can predict regions in genes that can be involved in mRNA turnover. The role of these sequences in mRNA decay is discussed.


1994 ◽  
Vol 14 (12) ◽  
pp. 8219-8228
Author(s):  
P Belgrader ◽  
J Cheng ◽  
X Zhou ◽  
L S Stephenson ◽  
L E Maquat

Frameshift and nonsense mutations within the gene for human triosephosphate isomerase (TPI) that generate a nonsense codon within the first three-fourths of the protein coding region have been found to reduce the abundance of the product mRNA that copurifies with nuclei. The cellular process and location of the nonsense codon-mediated reduction have proven difficult to elucidate for technical reasons. We show here, using electron microscopy to judge the purity of isolated nuclei, that the previously established reduction to 25% of the normal mRNA level is evident for nuclei that are free of detectable cytoplasmic contamination. Therefore, the reduction is likely to be characteristic of bona fide nuclear RNA. Fully spliced nuclear mRNA is identified by Northern (RNA) blot hybridization and a reverse transcription-PCR assay as the species that undergoes decay in experiments that used the human c-fos promoter to elicit a burst and subsequent shutoff of TPI gene transcription upon the addition of serum to serum-deprived cells. Finally, the finding that deletion of a 5' splice site of the TPI gene results predominantly but not exclusively in the removal by splicing (i.e., skipping) of the upstream exon as a part of the flanking introns has been used to demonstrate that decay is specific to those mRNA products that maintain the nonsense codon. This result, together with our previous results that implicate translation by ribosomes and charged tRNAs in the decay mechanism, indicate that nonsense codon recognition takes place after splicing and triggers decay solely in cis. The possibility that decay takes place during the process of mRNA export from the nucleus to the cytoplasm is discussed.


Cell ◽  
1975 ◽  
Vol 6 (3) ◽  
pp. 269-277 ◽  
Author(s):  
M.R. Capecchi ◽  
S.H. Hughes ◽  
G.M. Wahl
Keyword(s):  

2004 ◽  
Vol 7 (10) ◽  
pp. 1027-1028 ◽  
Author(s):  
Nikos K Logothetis
Keyword(s):  

Biotempo ◽  
2017 ◽  
Vol 6 ◽  
pp. 51-55
Author(s):  
Lidia Cruz Neyra
Keyword(s):  

La estructura del ADN (ácido desoxirribonucleico), llamada molécula de la vida, pues ella contiene la información genética de los seres vivos fue descubierta por James Watson y Francis Crick en 1953, veinte años después, Stanley Cohen y Herbert Boyer, descubrieron que combinando genes, se puede obtener una nueva estructura, a través de la ingeniería genética. Los avances de la biotecnología e ingeniería genética han permitido la producción de alimentos derivados de Organismos Genéticamente Modificados (OGM) o transgénicos, los cuales han generado diferentes controversias sobre su uso. El presente trabajo es una pequeña revisión bibliográfica acerca de lo que es un alimento transgénico con ejemplos que permitan comprender sus ventajas y los riesgos que pudieran existir para la salud y medio ambiente


2004 ◽  
Vol 29 (4) ◽  
pp. 378-380
Author(s):  
Michel Morange
Keyword(s):  

2018 ◽  
Vol 28 (7) ◽  
pp. R305
Author(s):  
Bob Goldstein
Keyword(s):  

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