The Effect of Inactivating Heterozygous Mutation in NBS1 Gene on DNA Damage and Repair Markers and Apoptosis Markers in Mice

We studied the state of the DNA repair system and apoptosis in young mice carrying heterozygous inactivating mutation in the NBS1 gene (c.1971insT, p.Arg658Stop). In the peripheral blood cells of 4-month-old NBS1insT males, the %DNA in the comet tail was higher by 10% than in wild-type mice (wt) (p<0.05). In hepatocytes of NBS1insT mice, the proportion of γH2AX+ nuclear regions marking DNA double-strand breaks was lower by 2 times than in wt mice (p<0.05), which can be an indicator of less efficient DNA repair. In the kidney tissue of NBS1insT mice, a tendency towards the proapoptotic ratio of Bax and Bcl-2 protein markers was revealed against the background of their reduced expression. Thus, the disturbances detected NBS1insT mice in young age suggest that this model is promising for further studies of carcinogenesis..

Medienart:

E-Artikel

Erscheinungsjahr:

2023

Erschienen:

2023

Enthalten in:

Zur Gesamtaufnahme - volume:175

Enthalten in:

Bulletin of experimental biology and medicine - 175(2023), 2 vom: Juni, Seite 234-238

Sprache:

Englisch

Beteiligte Personen:

Yurova, M. N. [VerfasserIn]
Golubev, A. G. [VerfasserIn]
Aleksakhina, S. N. [VerfasserIn]
Fedoros, E. I. [VerfasserIn]
Tumanyan, I. A. [VerfasserIn]
Otradnova, E. A. [VerfasserIn]
Soloviev, I. V. [VerfasserIn]
Sergiev, P. V. [VerfasserIn]
Imyanitov, E. N. [VerfasserIn]

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© Springer Science+Business Media, LLC, part of Springer Nature 2023. Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law.

doi:

10.1007/s10517-023-05841-y

funding:

Förderinstitution / Projekttitel:

PPN (Katalog-ID):

SPR052549763