nuclear translation
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2021 ◽  
Vol 18 (9) ◽  
pp. 2008-2016
Author(s):  
Jia-Liang Liu ◽  
Yuan-He You ◽  
Zhuo-Wei Tian ◽  
Meng Xiao ◽  
Jia-Wei Zheng ◽  
...  


Author(s):  
Alexandre David ◽  
Jonathan W. Yewdell
Keyword(s):  


2014 ◽  
Vol 42 (4) ◽  
pp. 1224-1228 ◽  
Author(s):  
Tina McLeod ◽  
Akilu Abdullahi ◽  
Min Li ◽  
Saverio Brogna

The nucleolus is the most prominent morphological feature within the nucleus of eukaryotic cells and is best known for its role in ribosome biogenesis. It forms around highly transcribed ribosomal RNA gene repeats which yield precursor rRNAs that are co-transcriptionally processed, folded and, while still within the nucleolus, associate with most of the ribosomal proteins. The nucleolus is therefore often thought of as a factory for making ribosomal subunits, which are exported as inactive precursors to the cytoplasm where late maturation makes them capable of mRNA binding and translation initiation. However, recent studies have shown substantial evidence for the presence of functional, translation competent ribosomal subunits within the nucleus, particularly in the nucleolus. These observations raise the intriguing possibility that the nucleolus, as well as being a ribosome factory, is also an important nuclear protein-synthesis plant.



2013 ◽  
Vol 9 (12) ◽  
pp. 759-760
Author(s):  
Petra Van Damme ◽  
Gerben Menschaert
Keyword(s):  


2013 ◽  
Vol 110 (44) ◽  
pp. 17612-17613 ◽  
Author(s):  
J. W. Yewdell ◽  
A. David
Keyword(s):  


Nucleus ◽  
2012 ◽  
Vol 3 (4) ◽  
pp. 320-321 ◽  
Author(s):  
James Dahlberg ◽  
Elsebet Lund


2012 ◽  
Vol 197 (1) ◽  
pp. 45-57 ◽  
Author(s):  
Alexandre David ◽  
Brian P. Dolan ◽  
Heather D. Hickman ◽  
Jonathan J. Knowlton ◽  
Giovanna Clavarino ◽  
...  

Whether protein translation occurs in the nucleus is contentious. To address this question, we developed the ribopuromycylation method (RPM), which visualizes translation in cells via standard immunofluorescence microscopy. The RPM is based on ribosome-catalyzed puromycylation of nascent chains immobilized on ribosomes by antibiotic chain elongation inhibitors followed by detection of puromycylated ribosome-bound nascent chains with a puromycin (PMY)-specific monoclonal antibody in fixed and permeabilized cells. The RPM correlates localized translation with myriad processes in cells and can be applied to any cell whose translation is sensitive to PMY. In this paper, we use the RPM to provide evidence for translation in the nucleoplasm and nucleolus, which is regulated by infectious and chemical stress.



2012 ◽  
Vol 197 (1) ◽  
pp. 7-9 ◽  
Author(s):  
David W. Reid ◽  
Christopher V. Nicchitta

Although the physical separation of transcription in the nucleus and translation in the cytoplasm has presided as a fundamental tenet of cell biology for decades, it has not done so without recurring challenges and contentious debate. In this issue, David et al. (2012. J. Cell Biol. http://dx.doi.org/10.1083/jcb.201112145) rekindle the controversy by providing convincing experimental evidence for nuclear translation.





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