Literature DB >> 14770006

Assessing messenger RNA decapping in cellular extracts.

Naomi Bergman1, Joseph Milone, Elizabeth J Bates, Mateusz Opyrchal, Vivian Bellofatto, Jeffrey Wilusz.   

Abstract

Removal of the 5' cap from a messenger RNA (mRNA) is an integral part of all mRNA decay pathways and can be a highly regulated event. Assays designed to assess decapping in vitro need to effectively resolve four products of mRNA decay: 7meGpppG produced by 3'-5' shortening of the transcript by the exosome, 7meGMP produced by the scavenger decapping enzyme DcpS acting on the product of exosomal decay, 7meGDP produced by the Dcp1/2 decapping enzyme, and free phosphate, which can be generated by phosphatases in the extract acting upon either of the two products of decapping noted above. We have outlined both thin-layer chromatography and acrylamide-gel based approaches that can be used to assess decapping activities.

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Year:  2004        PMID: 14770006     DOI: 10.1385/1-59259-750-5:181

Source DB:  PubMed          Journal:  Methods Mol Biol        ISSN: 1064-3745


  1 in total

1.  Identification of the HIT-45 protein from Trypanosoma brucei as an FHIT protein/dinucleoside triphosphatase: substrate specificity studies on the recombinant and endogenous proteins.

Authors:  Hiren Banerjee; Jennifer B Palenchar; Maciej Lukaszewicz; Elzbieta Bojarska; Janusz Stepinski; Jacek Jemielity; Andrzej Guranowski; Stephanie Ng; David A Wah; Edward Darzynkiewicz; Vivian Bellofatto
Journal:  RNA       Date:  2009-06-18       Impact factor: 4.942

  1 in total

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