Academic Journal

Resveratrol induces H3 and H4K16 deacetylation and H2A.X phosphorylation in Toxoplasma gondii

التفاصيل البيبلوغرافية
العنوان: Resveratrol induces H3 and H4K16 deacetylation and H2A.X phosphorylation in Toxoplasma gondii
المؤلفون: Contreras, Susana M., Ganuza, Agustina, Corvi, María M., Angel, Sergio O.
المساهمون: Foundation for the National Institutes of Health, Agencia Nacional de Promoción Científica y Tecnológica, Consejo Nacional de Investigaciones Científicas y Técnicas
المصدر: BMC Research Notes ; volume 14, issue 1 ; ISSN 1756-0500
بيانات النشر: Springer Science and Business Media LLC
سنة النشر: 2021
الوصف: Objective Resveratrol (RSV) is a multitarget drug that has demonstrated activity against Toxoplasma gondii in macrophage and human foreskin fibroblast (HFF) cell line infection models. However, the mechanism of action of RSV has not yet been determined. Thus, with the aim of identifying a possible mechanism of the anti- T. gondii activity of this compound, we analyzed the effects of RSV on histones H3 and H4 lysine 16 acetylation (H4K16). We also analyzed RSV-induced DNA damage to intracellular tachyzoites by using the DNA damage marker phosphorylated histone H2A.X (γH2AX). Results RSV inhibited intracellular T. gondii tachyzoite growth at concentrations below the toxic threshold for host cells. The IC 50 value after 24 h of treatment was 53 μM. RSV induced a reduction in H4K16 acetylation (H4K16ac), a marker associated with transcription, DNA replication and homologous recombination repair. A similar deacetylation effect was observed on histone H3. RSV also increased T. gondii H2A.X phosphorylation at the SQE motif (termed γH2A.X), which is a DNA damage-associated posttranslational modification. Our findings suggest a possible link between RSV and DNA damage or repair processes that is possibly associated with DNA replication stress.
نوع الوثيقة: article in journal/newspaper
اللغة: English
DOI: 10.1186/s13104-020-05416-4
DOI: 10.1186/s13104-020-05416-4.pdf
DOI: 10.1186/s13104-020-05416-4/fulltext.html
الاتاحة: http://dx.doi.org/10.1186/s13104-020-05416-4
http://link.springer.com/content/pdf/10.1186/s13104-020-05416-4.pdf
http://link.springer.com/article/10.1186/s13104-020-05416-4/fulltext.html
Rights: http://creativecommons.org/licenses/by/4.0/ ; http://creativecommons.org/licenses/by/4.0/
رقم الانضمام: edsbas.FCAD4287
قاعدة البيانات: BASE
الوصف
DOI:10.1186/s13104-020-05416-4