Tautomeric and anionic Watson-Crick-like mismatches have important roles in replication and translation errors through mechanisms that are not fully understood. Here, using NMR relaxation dispersion, we resolve a sequence-dependent kinetic network connecting G•T/U wobbles with three distinct Watson-Crick mismatches: two rapidly exchanging tautomeric species (G•T/UG•T/U; population less than 0.4%) and one anionic species (G•T/U; population around 0.001% at neutral pH). The sequence-dependent tautomerization or ionization step was inserted into a minimal kinetic mechanism for correct incorporation during replication after the initial binding of the nucleotide, leading to accurate predictions of the probability of dG•dT misincorporation across different polymerases and pH conditions and for a chemically modified nucleotide, and providing mechanisms for sequence-dependent misincorporation. Our results indicate that the energetic penalty for tautomerization and/or ionization accounts for an approximately 10 to 10-fold discrimination against misincorporation, which proceeds primarily via tautomeric dG•dT and dG•dT, with contributions from anionic dG•dT dominant at pH 8.4 and above or for some mutagenic nucleotides.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5808992PMC
http://dx.doi.org/10.1038/nature25487DOI Listing

Publication Analysis

Top Keywords

dg•dt misincorporation
8
tautomerization ionization
8
dg•dt
5
dynamic basis
4
basis dg•dt
4
misincorporation
4
misincorporation tautomerization
4
ionization tautomeric
4
tautomeric anionic
4
anionic watson-crick-like
4

Similar Publications

PNKP safeguards stalled replication forks from nuclease-dependent degradation during replication stress.

Cell Rep

December 2024

Department of Oncology, Faculty of Medicine & Dentistry, University of Alberta, 11560 University Avenue, Edmonton, AB T6G 1Z2, Canada; Biophysics Department, Faculty of Science, Cairo University, Giza 12613, Egypt. Electronic address:

Uncontrolled degradation and collapse of stalled replication forks (RFs) are primary sources of genomic instability, yet the molecular mechanisms for protecting forks from degradation/collapse remain to be fully elaborated. Here, we show that polynucleotide kinase-phosphatase (PNKP) localizes at stalled forks and protects stalled forks from excessive degradation. The loss of PNKP results in nucleolytic degradation of nascent DNA at stalled RFs.

View Article and Find Full Text PDF
Article Synopsis
  • Plants use toxic metabolites to outcompete others for resources, targeting key processes like protein synthesis.
  • Nonproteogenic amino acids (NPAAs), such as azetidine-2-carboxylic acid (Aze), can disrupt root growth in plants like Arabidopsis by getting incorrectly incorporated into proteins.
  • The incorporation of Aze leads to misfolded proteins and triggers a stress response, revealing important pathways for enhancing crop resilience.
View Article and Find Full Text PDF

T7 RNA Polymerase (RNAP) is a widely used enzyme with recent applications in the production of RNA vaccines. For over 50 years denaturing sequencing gels have been used as key analysis tools for probing the nucleotide addition mechanisms of T7 RNAP and other polymerases. However, sequencing gels are low-throughput limiting their utility for comprehensive enzyme analysis.

View Article and Find Full Text PDF

The mechanism of transcription proceeds through the formation of R-loop structures containing a DNA-RNA heteroduplex and a single-stranded DNA segment that should be placed inside the elongation complex; therefore, these nucleic acid segments are limited in length. The attachment of each nucleotide to the 3' end of an RNA strand requires a repeating cycle of incoming nucleoside triphosphate binding, catalysis, and enzyme translocation. Within these steps of transcription elongation, RNA polymerase sequentially goes through several states and is post-translocated, catalytic, and pre-translocated.

View Article and Find Full Text PDF

Messenger RNA (mRNA) translation is a tightly controlled process frequently deregulated in cancer. Key to this deregulation are transfer RNAs (tRNAs), whose expression, processing and post-transcriptional modifications are often altered in cancer to support cellular transformation. In conditions of limiting levels of amino acids, this deregulated control of protein synthesis leads to aberrant protein production in the form of ribosomal frameshifting or misincorporation of non-cognate amino acids.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!