Micromi RNA-34a targets protein phosphatase PP1γ to regulate DNA damage toleranceReportar como inadecuado


Micromi RNA-34a targets protein phosphatase PP1γ to regulate DNA damage tolerance


Micromi RNA-34a targets protein phosphatase PP1γ to regulate DNA damage tolerance - Descarga este documento en PDF. Documentación en PDF para descargar gratis. Disponible también para leer online.

Publication Date: 2015-06-25

Journal Title: Cell Cycle

Publisher: Taylor & Francis

Volume: 14

Issue: 24

Pages: 3830-3841

Language: English

Type: Article

Metadata: Show full item record

Citation: Takeda, Y., & Venkitaraman, A. R. (2015). Micro(mi) RNA-34a targets protein phosphatase (PP)1γ to regulate DNA damage tolerance. Cell Cycle, 14 (24), 3830-3841.

Description: This is the author accepted manuscript. The final version is available from Taylor & Francis via http://dx.doi.org/10.1080/15384101.2015.1064202

Abstract: The DNA damage response (DDR) triggers widespread changes in gene expression, mediated partly by alterations in micro(mi) RNA levels, whose nature and significance remain uncertain. Here, we report that miR-34a, which is upregulated during the DDR, modulates the expression of protein phosphatase 1γ (PP1γ) to regulate cellular tolerance to DNA damage. Multiple bio-informatic algorithms predict that miR-34a targets the PP1CCC gene encoding PP1γ protein. Ionising radiation (IR) decreases cellular expression of PP1γ in a dose-dependent manner. An miR-34a-mimic reduces cellular PP1γ protein. Conversely, an miR-34a inhibitor antagonizes IR-induced decreases in PP1γ protein expression. A wild-type (but not mutant) miR-34a seed match sequence from the 3′ untranslated region (UTR) of PP1CCC when transplanted to a luciferase reporter gene makes it responsive to an miR-34a-mimic. Thus, miR-34a upregulation during the DDR targets the 3′ UTR of PP1CCC to decrease PP1γ protein expression. PP1γ is known to antagonize DDR signalling via the ataxia-telangiectasia-mutated (ATM) kinase. Interestingly, we find that cells exposed to DNA damage become more sensitive – in an miR-34a-dependent manner – to a second challenge with damage. Increased sensitivity to the second challenge is marked by enhanced phosphorylation of ATM and p53, increased γH2AX formation, and increased cell death. Increased sensitivity can be partly recapitulated by a miR-34a-mimic, or antagonized by an miR-34a-inhibitor. Thus, our findings suggest a model in which damage-induced miR-34a induction reduces PP1γ expression and enhances ATM signaling to decrease tolerance to repeated genotoxic challenges. This mechanism has implications for tumour suppression and the response of cancers to therapeutic radiation.

Sponsorship: Work in ARV's laboratory is funded by the Medical Research Council.

Identifiers:

This record's URL: http://dx.doi.org/10.1080/15384101.2015.1064202https://www.repository.cam.ac.uk/handle/1810/253057

Rights: Creative Commons Attribution 4.0 International License

Licence URL: http://creativecommons.org/licenses/by/4.0/





Autor: Takeda, YukoVenkitaraman, Ashok R.

Fuente: https://www.repository.cam.ac.uk/handle/1810/253057



DESCARGAR PDF




Documentos relacionados