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Modulation of base excision repair of 8-oxoguanine by the nucleotide sequence

Nucleic acids research. Bd. 41. H. 18. Oxford: Oxford Univ. Press 2013 S. 8559 - 8571

Erscheinungsjahr: 2013

ISBN/ISSN: 0305-1048

Publikationstyp: Zeitschriftenaufsatz

Sprache: Englisch

Doi/URN: 10.1093/nar/gkt620

Volltext über DOI/URN

Geprüft:Bibliothek

Inhaltszusammenfassung


8-Oxoguanine (8-oxoG) is a major product of oxidative DNA damage, which induces replication errors and interferes with transcription. By varying the position of single 8-oxoG in a functional gene and manipulating the nucleotide sequence surrounding the lesion, we found that the degree of transcriptional inhibition is independent of the distance from the transcription start or the localization within the transcribed or the non-transcribed DNA strand. However, it is strongly dependent on the se...8-Oxoguanine (8-oxoG) is a major product of oxidative DNA damage, which induces replication errors and interferes with transcription. By varying the position of single 8-oxoG in a functional gene and manipulating the nucleotide sequence surrounding the lesion, we found that the degree of transcriptional inhibition is independent of the distance from the transcription start or the localization within the transcribed or the non-transcribed DNA strand. However, it is strongly dependent on the sequence context and also proportional to cellular expression of 8-oxoguanine DNA glycosylase (OGG1)-demonstrating that transcriptional arrest does not take place at unrepaired 8-oxoG and proving a causal connection between 8-oxoG excision and the inhibition of transcription. We identified the 5'-CAGGGC[8-oxoG]GACTG-3' motif as having only minimal transcription-inhibitory potential in cells, based on which we predicted that 8-oxoG excision is particularly inefficient in this sequence context. This anticipation was fully confirmed by direct biochemical assays. Furthermore, in DNA containing a bistranded Cp[8-oxoG]/Cp[8-oxoG] clustered lesion, the excision rates differed between the two strands at least by a factor of 9, clearly demonstrating that the excision preference is defined by the DNA strand asymmetry rather than the overall geometry of the double helix or local duplex stability.» weiterlesen» einklappen

Autoren


Allgayer, Julia (Autor)
Kitsera, Nataliya (Autor)
Lippen, Carina von der (Autor)
Epe, Bernd (Autor)
Khobta, Andriy (Autor)

Klassifikation


DFG Fachgebiet:
2.11 - Grundlagen der Biologie und Medizin

DDC Sachgruppe:
Naturwissenschaften