Cargando…
A fluorescence-based assay suitable for quantitative analysis of deadenylase enzyme activity
In eukaryotic cells, the shortening and removal of the poly(A) tail of cytoplasmic mRNA by deadenylase enzymes is a critical step in post-transcriptional gene regulation. The ribonuclease activity of deadenylase enzymes is attributed to either a DEDD (Asp-Glu-Asp-Asp) or an endonuclease–exonuclease–...
Autores principales: | Maryati, Maryati, Kaur, Ishwinder, Jadhav, Gopal P., Olotu-Umoren, Loyin, Oveh, Blessing, Hashmi, Lubna, Fischer, Peter M., Winkler, G. Sebastiaan |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2014
|
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3950723/ https://www.ncbi.nlm.nih.gov/pubmed/24170810 http://dx.doi.org/10.1093/nar/gkt972 |
Ejemplares similares
-
Discovery, synthesis and biochemical profiling of purine-2,6-dione derivatives as inhibitors of the human poly(A)-selective ribonuclease Caf1
por: Jadhav, Gopal P., et al.
Publicado: (2015) -
The enzyme activities of Caf1 and Ccr4 are both required for deadenylation by the human Ccr4–Not nuclease module
por: Maryati, Maryati, et al.
Publicado: (2015) -
A Deadenylase Assay by Size-Exclusion Chromatography
por: He, Guang-Jun, et al.
Publicado: (2012) -
Error evaluation in the laboratory testing process and laboratory information systems
por: Arifin, Azila, et al.
Publicado: (2022) -
1‐Hydroxy‐xanthine derivatives inhibit the human Caf1 nuclease and Caf1‐containing nuclease complexes via Mg(2+)‐dependent binding
por: Airhihen, Blessing, et al.
Publicado: (2019)