Faculty Opinions recommendation of The bacterial enzyme RppH triggers messenger RNA degradation by 5' pyrophosphate removal.

Author(s):  
Stephen Busby
Nature ◽  
2008 ◽  
Vol 451 (7176) ◽  
pp. 355-358 ◽  
Author(s):  
Atilio Deana ◽  
Helena Celesnik ◽  
Joel G. Belasco

1982 ◽  
Vol 60 (5) ◽  
pp. 580-585 ◽  
Author(s):  
Réal Lemieux ◽  
Claude Godin

Rabbit reticulocyte membrane-bound ribosomes liberated by deoxycholate treatment contain degraded forms of ribosomal and messenger RNA. This degradation occurs after the liberation of the ribosomes from the membranes by the detergent because intact ribosomal and messenger RNA can be extracted from washed membranes by phenol treatment. Increasing the ionic strength of the detergent buffer prevents this RNA degradation and allows the recovery of membrane-bound ribosomes capable of protein synthesis. Comparison of the proteins synthesized in vitro by the polyribosomes shows that the main protein produced by both free and membrane-bound ribosomes is globin. However, the two types of polyribosomes could be distinguished by the nonglobin proteins they produce.


Neurology ◽  
2005 ◽  
Vol 65 (3) ◽  
pp. 420-425 ◽  
Author(s):  
S. Nakano ◽  
A. Shinde ◽  
H. Ito ◽  
H. Ito ◽  
H. Kusaka

2002 ◽  
Vol 12 (8) ◽  
pp. R285-R287 ◽  
Author(s):  
Ambro van Hoof ◽  
Roy Parker

2005 ◽  
Vol 52 (9) ◽  
pp. 2697-2707 ◽  
Author(s):  
Jun Fukae ◽  
Yoshiharu Amasaki ◽  
Yumi Yamashita ◽  
Toshiyuki Bohgaki ◽  
Shinsuke Yasuda ◽  
...  

Antibiotics ◽  
2019 ◽  
Vol 8 (2) ◽  
pp. 48 ◽  
Author(s):  
Jennifer M. Colquhoun ◽  
Lisha Ha ◽  
Andrew Beckley ◽  
Brinkley Meyers ◽  
Daniel P. Flaherty ◽  
...  

Staphylococcus aureus RnpA is thought to be a unique dual functional antimicrobial target that is required for two essential cellular processes, precursor tRNA processing and messenger RNA degradation. Herein, we used a previously described whole cell-based mupirocin synergy assay to screen members of a 53,000 compound small molecule diversity library and simultaneously enrich for agents with cellular RnpA inhibitory activity. A medicinal chemistry-based campaign was launched to generate a preliminary structure activity relationship and guide early optimization of two novel chemical classes of RnpA inhibitors identified, phenylcarbamoyl cyclic thiophene and piperidinecarboxamide. Representatives of each chemical class displayed potent anti-staphylococcal activity, limited the protein’s in vitro ptRNA processing and mRNA degradation activities, and exhibited favorable therapeutic indexes. The most potent piperidinecarboxamide RnpA inhibitor, JC2, displayed inhibition of cellular RnpA mRNA turnover, RnpA-depletion strain hypersusceptibility, and exhibited antimicrobial efficacy in a wax worm model of S. aureus infection. Taken together, these results establish that the whole cell screening assay used is amenable to identifying small molecule RnpA inhibitors within large chemical libraries and that the chemical classes identified here may represent progenitors of new classes of antimicrobials that target RnpA.


2018 ◽  
Vol 23 (6) ◽  
pp. 493-506 ◽  
Author(s):  
John Lalith Charles Richard ◽  
Pieter Johan Adam Eichhorn

Prior to the sequencing of the human genome, it was presumed that most of the DNA coded for proteins. However, with the advent of next-generation sequencing, it has now been recognized that most complex eukaryotic genomes are in fact transcribed into noncoding RNAs (ncRNAs), including a family of transcripts referred to as long noncoding RNAs (lncRNAs). LncRNAs have been implicated in many biological processes ranging from housekeeping functions such as transcription to more specialized functions such as dosage compensation or genomic imprinting, among others. Interestingly, lncRNAs are not limited to a defined set of functions but can regulate varied activities such as messenger RNA degradation, translation, and protein kinetics or function as RNA decoys or scaffolds. Although still in its infancy, research into the biology of lncRNAs has demonstrated the importance of lncRNAs in development and disease. However, the specific mechanisms through which these lncRNAs act remain poorly defined. Focused research into a small number of these lncRNAs has provided important clues into the heterogeneous nature of this family of ncRNAs. Due to the complex diversity of lncRNA function, in this review, we provide an update on the platforms available for investigators to aid in the identification of lncRNA function.


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