Rad27 and Exo1 function in different excision pathways for mismatch repair in Saccharomyces cerevisiae
Defects in DNA mismatch repair (MMR) have been linked to inherited and sporadic cancers. Here the authors demonstrate that the DNA repair protein Rad27 (human FEN1) functions in one of three redundant mispair excision pathways, where its flap endonuclease activity catalyzes mispair excision.
Guardado en:
Autores principales: | Felipe A. Calil, Bin-Zhong Li, Kendall A. Torres, Katarina Nguyen, Nikki Bowen, Christopher D. Putnam, Richard D. Kolodner |
---|---|
Formato: | article |
Lenguaje: | EN |
Publicado: |
Nature Portfolio
2021
|
Materias: | |
Acceso en línea: | https://doaj.org/article/edd8c42e20fe4ec2a4fcf1e024649b17 |
Etiquetas: |
Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
|
Ejemplares similares
-
Cryo-EM structure of TFIIH/Rad4–Rad23–Rad33 in damaged DNA opening in nucleotide excision repair
por: Trevor van Eeuwen, et al.
Publicado: (2021) -
A genetic network that suppresses genome rearrangements in Saccharomyces cerevisiae and contains defects in cancers
por: Christopher D. Putnam, et al.
Publicado: (2016) -
Correction: Publisher Correction: Base excision repair AP endonucleases and mismatch repair act together to induce checkpoint-mediated autophagy
por: Tanima SenGupta, et al.
Publicado: (2018) -
Nucleotide Excision Repair Protein Rad23 Regulates Cell Virulence Independent of Rad4 in <named-content content-type="genus-species">Candida albicans</named-content>
por: Jia Feng, et al.
Publicado: (2020) -
Catalase enzyme in mitochondria of Saccharomyces cerevisiae
por: Petrova,Ventsislava Yankova, et al.
Publicado: (2002)