Literature DB >> 17662851

Measuring editing activity and identifying cytidine-to-uridine mRNA editing factors in cells and biochemical isolates.

Harold C Smith1.   

Abstract

Cytidine deaminases with the capacity to act on nucleic acids play a critical role in regulating the proteome through diversification of expressed sequence beyond that encoded in the genome. A family of these enzymes, known as the APOBEC family of cytidine deaminases, has been identified in mammalian cells. APOBEC-1 edits messenger RNA, whereas other family members affect mRNA coding capacity by editing single-stranded DNA in expressed regions of the genomes. Biochemical isolation and analysis of APOBEC proteins and their interacting factors have led to an understanding of the diverse cellular processes including lipoprotein metabolism, antibody production, viral infectivity, and cancer. Practical approaches will be described for the measurement of editing activity and the analysis of proteins involved in C-to-U and dC-to-dU editing.

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Year:  2007        PMID: 17662851     DOI: 10.1016/S0076-6879(07)24018-2

Source DB:  PubMed          Journal:  Methods Enzymol        ISSN: 0076-6879            Impact factor:   1.600


  14 in total

Review 1.  When you can't trust the DNA: RNA editing changes transcript sequences.

Authors:  Volker Knoop
Journal:  Cell Mol Life Sci       Date:  2010-10-12       Impact factor: 9.261

Review 2.  Functions and regulation of the APOBEC family of proteins.

Authors:  Harold C Smith; Ryan P Bennett; Ayse Kizilyer; William M McDougall; Kimberly M Prohaska
Journal:  Semin Cell Dev Biol       Date:  2011-10-06       Impact factor: 7.727

3.  Deaminase activity on single-stranded DNA (ssDNA) occurs in vitro when APOBEC3G cytidine deaminase forms homotetramers and higher-order complexes.

Authors:  William M McDougall; Chinelo Okany; Harold C Smith
Journal:  J Biol Chem       Date:  2011-07-07       Impact factor: 5.157

4.  Metabolic regulation of APOBEC-1 complementation factor trafficking in mouse models of obesity and its positive correlation with the expression of ApoB protein in hepatocytes.

Authors:  Chad A Galloway; John Ashton; Janet D Sparks; Robert A Mooney; Harold C Smith
Journal:  Biochim Biophys Acta       Date:  2010-06-09

5.  APOBEC-1 complementation factor (ACF) forms RNA-dependent multimers.

Authors:  C A Galloway; A Kumar; J Krucinska; H C Smith
Journal:  Biochem Biophys Res Commun       Date:  2010-06-10       Impact factor: 3.575

6.  Structural and functional assessment of APOBEC3G macromolecular complexes.

Authors:  Bogdan Polevoda; William M McDougall; Ryan P Bennett; Jason D Salter; Harold C Smith
Journal:  Methods       Date:  2016-03-14       Impact factor: 3.608

7.  RNA binding to APOBEC3G induces the disassembly of functional deaminase complexes by displacing single-stranded DNA substrates.

Authors:  Bogdan Polevoda; William M McDougall; Bradley N Tun; Michael Cheung; Jason D Salter; Alan E Friedman; Harold C Smith
Journal:  Nucleic Acids Res       Date:  2015-09-30       Impact factor: 16.971

8.  DNA mutagenic activity and capacity for HIV-1 restriction of the cytidine deaminase APOBEC3G depend on whether DNA or RNA binds to tyrosine 315.

Authors:  Bogdan Polevoda; Rebecca Joseph; Alan E Friedman; Ryan P Bennett; Rebecca Greiner; Thareendra De Zoysa; Ryan A Stewart; Harold C Smith
Journal:  J Biol Chem       Date:  2017-04-05       Impact factor: 5.157

9.  APOBEC3G subunits self-associate via the C-terminal deaminase domain.

Authors:  Ryan P Bennett; Jason D Salter; Xiang Liu; Joseph E Wedekind; Harold C Smith
Journal:  J Biol Chem       Date:  2008-10-08       Impact factor: 5.157

10.  DRONE: Direct Tracking of DNA Cytidine Deamination and Other DNA Modifying Activities.

Authors:  Tomoaki Sasaki; Shalley N Kudalkar; Nicole Bertoletti; Karen S Anderson
Journal:  Anal Chem       Date:  2018-09-28       Impact factor: 6.986

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