» Articles » PMID: 19448611

DUTP Incorporation into Genomic DNA is Linked to Transcription in Yeast

Overview
Journal Nature
Specialty Science
Date 2009 May 19
PMID 19448611
Citations 39
Authors
Affiliations
Soon will be listed here.
Abstract

Highly activated transcription is associated with eukaryotic genome instability, resulting in increased rates of mitotic recombination and mutagenesis. The association between high transcription and genome stability is probably due to a variety of factors including an enhanced accumulation of DNA damage, transcription-associated supercoiling, collision between replication forks and the transcription machinery, and the persistence of RNA-DNA hybrids. In the case of transcription-associated mutagenesis, we previously showed that there is a direct proportionality between the level of transcription and the mutation rate in the yeast Saccharomyces cerevisiae, and that the molecular nature of the mutations is affected by highly activated transcription. Here we show that the accumulation of apurinic/apyrimidinic sites is greatly enhanced in highly transcribed yeast DNA. We further demonstrate that most apurinic/apyrimidinic sites in highly transcribed DNA are derived from the removal of uracil, the presence of which is linked to direct incorporation of dUTP in place of dTTP. These results show an unexpected relationship between transcription and the fidelity of DNA synthesis, and raise intriguing cell biological issues with regard to nucleotide pool compartmentalization.

Citing Articles

ERCC2 mutations alter the genomic distribution pattern of somatic mutations and are independently prognostic in bladder cancer.

Barbour J, Ou T, Yang H, Fang H, Yue N, Zhu X Cell Genom. 2024; 4(8):100627.

PMID: 39096913 PMC: 11406173. DOI: 10.1016/j.xgen.2024.100627.


Dynamic alternative DNA structures in biology and disease.

Wang G, Vasquez K Nat Rev Genet. 2022; 24(4):211-234.

PMID: 36316397 PMC: 11634456. DOI: 10.1038/s41576-022-00539-9.


Complex genomic patterns of abasic sites in mammalian DNA revealed by a high-resolution SSiNGLe-AP method.

Cai Y, Cao H, Wang F, Zhang Y, Kapranov P Nat Commun. 2022; 13(1):5868.

PMID: 36198706 PMC: 9534904. DOI: 10.1038/s41467-022-33594-1.


Efficient DNA fluorescence labeling via base excision trapping.

Jun Y, Harcourt E, Xiao L, Wilson D, Kool E Nat Commun. 2022; 13(1):5043.

PMID: 36028479 PMC: 9418136. DOI: 10.1038/s41467-022-32494-8.


Giardia intestinalis thymidine kinase is a high-affinity enzyme crucial for DNA synthesis and an exploitable target for drug discovery.

Krakovka S, Ranjbarian F, Lujan L, Saura A, Larsen N, Jimenez-Gonzalez A J Biol Chem. 2022; 298(6):102028.

PMID: 35568200 PMC: 9190010. DOI: 10.1016/j.jbc.2022.102028.


References
1.
Kim N, Abdulovic A, Gealy R, Lippert M, Jinks-Robertson S . Transcription-associated mutagenesis in yeast is directly proportional to the level of gene expression and influenced by the direction of DNA replication. DNA Repair (Amst). 2007; 6(9):1285-96. PMC: 2034516. DOI: 10.1016/j.dnarep.2007.02.023. View

2.
Senturker S, van der Kemp P, You H, Doetsch P, Dizdaroglu M, Boiteux S . Substrate specificities of the ntg1 and ntg2 proteins of Saccharomyces cerevisiae for oxidized DNA bases are not identical. Nucleic Acids Res. 1998; 26(23):5270-6. PMC: 148016. DOI: 10.1093/nar/26.23.5270. View

3.
Swanson R, Morey N, Doetsch P . Overlapping specificities of base excision repair, nucleotide excision repair, recombination, and translesion synthesis pathways for DNA base damage in Saccharomyces cerevisiae. Mol Cell Biol. 1999; 19(4):2929-35. PMC: 84087. DOI: 10.1128/MCB.19.4.2929. View

4.
Harfe B . Removal of frameshift intermediates by mismatch repair proteins in Saccharomyces cerevisiae. Mol Cell Biol. 1999; 19(7):4766-73. PMC: 84275. DOI: 10.1128/MCB.19.7.4766. View

5.
Popoff S, Spira A, Johnson A, Demple B . Yeast structural gene (APN1) for the major apurinic endonuclease: homology to Escherichia coli endonuclease IV. Proc Natl Acad Sci U S A. 1990; 87(11):4193-7. PMC: 54074. DOI: 10.1073/pnas.87.11.4193. View