Enhanced prime editing systems by manipulating cellular determinants of editing outcomes

PJ Chen, JA Hussmann, J Yan, F Knip**… - Cell, 2021 - cell.com
While prime editing enables precise sequence changes in DNA, cellular determinants of
prime editing remain poorly understood. Using pooled CRISPRi screens, we discovered that …

Mismatch repair

R Fishel, JB Lee - … , and Repair: Molecular Mechanisms and Pathology, 2016 - Springer
The concept of mismatch repair (MMR) was formulated independently in 1964 to explain the
removal of brominated nucleotides from DNA as well as gene conversion during genetic …

Lynch syndrome, molecular mechanisms and variant classification

AB Abildgaard, SV Nielsen, I Bernstein, A Stein… - British journal of …, 2023 - nature.com
Patients with the heritable cancer disease, Lynch syndrome, carry germline variants in the
MLH1, MSH2, MSH6 and PMS2 genes, encoding the central components of the DNA …

ELM—the eukaryotic linear motif resource in 2020

M Kumar, M Gouw, S Michael… - Nucleic acids …, 2020 - academic.oup.com
Studies on the DNA-binding properties of transcription factors are important in searching for
the downstream genes regulated by these factors. In the present study, we report on the …

Exonuclease 1-dependent and independent mismatch repair

EM Goellner, CD Putnam, RD Kolodner - DNA repair, 2015 - Elsevier
DNA mismatch repair (MMR) acts to repair mispaired bases resulting from misincorporation
errors during DNA replication and also recognizes mispaired bases in recombination (HR) …

New insights into the mechanism of DNA mismatch repair

GX Reyes, TT Schmidt, RD Kolodner, H Hombauer - Chromosoma, 2015 - Springer
The genome of all organisms is constantly being challenged by endogenous and
exogenous sources of DNA damage. Errors like base: base mismatches or small insertions …

[HTML][HTML] Strand discrimination in DNA mismatch repair

CD Putnam - DNA repair, 2021 - Elsevier
DNA mismatch repair (MMR) corrects non-Watson-Crick basepairs generated by replication
errors, recombination intermediates, and some forms of chemical damage to DNA. In MutS …

Mlh1-Mlh3, a meiotic crossover and DNA mismatch repair factor, is a Msh2-Msh3-stimulated endonuclease

MV Rogacheva, CM Manhart, C Chen, A Guarne… - Journal of Biological …, 2014 - ASBMB
Crossing over between homologous chromosomes is initiated in meiotic prophase in most
sexually reproducing organisms by the appearance of programmed double strand breaks …

Roles for mismatch repair family proteins in promoting meiotic crossing over

CM Manhart, E Alani - DNA repair, 2016 - Elsevier
The mismatch repair (MMR) family complexes Msh4-Msh5 and Mlh1-Mlh3 act with Exo1 and
Sgs1-Top3-Rmi1 in a meiotic double strand break repair pathway that results in the …

The Saccharomyces cerevisiae Mlh1-Mlh3 heterodimer is an endonuclease that preferentially binds to Holliday junctions

L Ranjha, R Anand, P Cejka - Journal of Biological Chemistry, 2014 - ASBMB
MutLγ, a heterodimer of the MutL homologues Mlh1 and Mlh3, plays a critical role during
meiotic homologous recombination. The meiotic function of Mlh3 is fully dependent on the …