x
Filter:
Filters applied
- DNA and Chromosomes
- Burgers, Peter MRemove Burgers, Peter M filter
- Galletto, RobertoRemove Galletto, Roberto filter
Publication Date
Please choose a date range between 2019 and 2020.
DNA and Chromosomes
2 Results
- DNA and ChromosomesOpen Access
Pif1, RPA, and FEN1 modulate the ability of DNA polymerase δ to overcome protein barriers during DNA synthesis
Journal of Biological ChemistryVol. 295Issue 47p15883–15891Published online: September 10, 2020- Melanie A. Sparks
- Peter M. Burgers
- Roberto Galletto
Cited in Scopus: 10Successful DNA replication requires carefully regulated mechanisms to overcome numerous obstacles that naturally occur throughout chromosomal DNA. Scattered across the genome are tightly bound proteins, such as transcription factors and nucleosomes, that are necessary for cell function, but that also have the potential to impede timely DNA replication. Using biochemically reconstituted systems, we show that two transcription factors, yeast Reb1 and Tbf1, and a tightly positioned nucleosome, are strong blocks to the strand displacement DNA synthesis activity of DNA polymerase δ. - DNA and ChromosomesOpen Access
The telomere-binding protein Rif2 and ATP-bound Rad50 have opposing roles in the activation of yeast Tel1ATM kinase
Journal of Biological ChemistryVol. 294Issue 49p18846–18852Published online: October 22, 2019- Sarem Hailemariam
- Paolo De Bona
- Roberto Galletto
- Marcel Hohl
- John H. Petrini
- Peter M. Burgers
Cited in Scopus: 12Saccharomyces cerevisiae Tel1 is the ortholog of human ATM kinase and initiates a cell cycle checkpoint in response to dsDNA breaks (DSBs). Tel1ATM kinase is activated synergistically by naked dsDNA and the Mre11-Rad50-Xrs2NBS1 complex (MRX). A multisubunit protein complex, which is related to human shelterin, protects telomeres from being recognized as DSBs, thereby preventing a Tel1ATM checkpoint response. However, at very short telomeres, Tel1ATM can be recruited and activated by the MRX complex, resulting in telomere elongation.