Literature DB >> 28941008

Non-canonical Bases in the Genome: The Regulatory Information Layer in DNA.

Thomas Carell1, Matthias Q Kurz1, Markus Müller1, Martin Rossa1, Fabio Spada1.   

Abstract

Multicellular organisms developed the concept of specialized cells that perform specific functions. Examples are neurons and fibroblast to name just two out of more than 200. These cellular differences are established based on the same sequence information stored in the cell nucleus of all cells of an organism. The sequence information needs consequently different interpretations by the different cell types. During cellular development this interpretation of the genetic code has to be tightly regulated in space and time. Interpretation of the sequence information involves the controlled activation and silencing of specific genes so that certain proteins are made in one cell type but not in others. This involves an additional regulatory information layer beyond the pure base sequence. One aspect of this regulatory information layer relies on functional groups that are attached to the C(5) position of the canonical base dC. Currently four regulatory, non-canonical bases with a methyl (CH3 )-, a hydroxymethyl (CH2 OH)-, a formyl (CHO)- and a carboxyl (COOH)- group are known. While 5-methyl-cytidine is long recognised to be a regulatory base in the genome, the other three bases and the enzymes responsible for generating them, were just recently discovered.
© 2018 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

Entities:  

Keywords:  demethylation; epigenetics; nucleosides; oxidized dC-derivatives; regulatory layer

Mesh:

Substances:

Year:  2018        PMID: 28941008     DOI: 10.1002/anie.201708228

Source DB:  PubMed          Journal:  Angew Chem Int Ed Engl        ISSN: 1433-7851            Impact factor:   15.336


  17 in total

1.  Interplay of Guanine Oxidation and G-Quadruplex Folding in Gene Promoters.

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Authors:  Aaron M Fleming; Anton Alenko; Jay P Kitt; Anita M Orendt; Peter F Flynn; Joel M Harris; Cynthia J Burrows
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4.  Optochemical Control of TET Dioxygenases Enables Kinetic Insights into the Domain-Dependent Interplay of TET1 and MBD1 while Oxidizing and Reading 5-Methylcytosine.

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5.  Kinetics and thermodynamics of BI-BII interconversion altered by T:G mismatches in DNA.

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Journal:  Curr Opin Biotechnol       Date:  2018-10-13       Impact factor: 9.740

7.  5-Hydroxymethyl-, 5-Formyl- and 5-Carboxydeoxycytidines as Oxidative Lesions and Epigenetic Marks.

Authors:  Florian Schelter; Angie Kirchner; Franziska R Traube; Markus Müller; Wolfgang Steglich; Thomas Carell
Journal:  Chemistry       Date:  2021-05-01       Impact factor: 5.236

Review 8.  Repurposing enzymatic transferase reactions for targeted labeling and analysis of DNA and RNA.

Authors:  Miglė Tomkuvienė; Milda Mickutė; Giedrius Vilkaitis; Saulius Klimašauskas
Journal:  Curr Opin Biotechnol       Date:  2018-10-06       Impact factor: 9.740

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Journal:  Nat Commun       Date:  2021-07-02       Impact factor: 14.919

Review 10.  Modified nucleic acids: replication, evolution, and next-generation therapeutics.

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Journal:  BMC Biol       Date:  2020-09-02       Impact factor: 7.431

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