Please use this identifier to cite or link to this item: https://hdl.handle.net/11147/2280
Title: Checkpoint deficient rad53-11 yeast cannot accumulate dNTPs in response to DNA damage
Authors: Koç, Ahmet
Merrill, Gary F.
Koç, Ahmet
Izmir Institute of Technology. Molecular Biology and Genetics
Keywords: DNA damage
dNTP
EMS
Rad53
Yeast
Issue Date: Feb-2007
Publisher: Elsevier Ltd.
Source: Koç, A., and Merrill, G. F. (2007). Checkpoint deficient rad53-11 yeast cannot accumulate dNTPs in response to DNA damage. Biochemical and Biophysical Research Communications, 353(2), 527-530. doi:10.1016/j.bbrc.2006.12.049
Abstract: Deoxyribonucleotide pools are maintained at levels that support efficient and yet accurate DNA replication and repair. Rad53 is part of a protein kinase regulatory cascade that, conceptually, promotes dNTP accumulation in four ways: (1) it activates the transcription of ribonucleotide reductase subunits by inhibiting the Crt1 repressor; (2) it plays a role in relocalization of ribonucleotide reductase subunits RNR2 and RNR4 from nucleus to cytoplasm; (3) it antagonizes the action of Sml1, a protein that binds and inhibits ribonucleotide reductase; and (4) it blocks cell-cycle progression in response to DNA damage, thus preventing dNTP consumption through replication forks. Although several lines of evidence support the above modes of Rad53 action, an effect of a rad53 mutation on dNTP levels has not been directly demonstrated. In fact, in a previous study, a rad53-11 mutation did not result in lower dNTP levels in asynchronous cells or in synchronized cells that entered the S-phase in the presence of the RNR inhibitor hydroxyurea. These anomalies prompted us to investigate whether the rad53-11 mutation affected dNTP levels in cells exposed to a DNA-damaging dose of ethylmethyl sulfonate (EMS). Although dNTP levels increased by 2- to 3-fold in EMS treated wild-type cells, rad53-11 cells showed no such change. Thus, the results indicate that Rad53 checkpoint function is not required for dNTP pool maintenance in normally growing cells, but is required for dNTP pool expansion in cells exposed to DNA-damaging agents.
URI: http://doi.org/10.1016/j.bbrc.2006.12.049
http://hdl.handle.net/11147/2280
ISSN: 0006-291X
0006-291X
Appears in Collections:Molecular Biology and Genetics / Moleküler Biyoloji ve Genetik
Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection
WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection

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