Interaction of two tumor suppressors: Phosphatase CTDSPL and Rb protein


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Earlier we established that CTDSPL gene encoding small carboxy-terminal domain serine phosphatase can be considered a classical tumor suppressor gene. Besides, transfection of tumor cell line MCF-7 with CTDSPL led to the content decrease of inactive phosphorylated form of another tumor suppressor, retinoblastoma protein (Rb), and subsequently to cell cycle arrest at the G1/S boundary. This result implied that small phosphatase CTDSPL is able to specifically dephosphorylate and activate Rb protein. In order to add some fuel to this hypothesis, in the present work we studied the interaction of two tumor suppressors CTDSPL and Rb in vitro. GST pool-down assay revealed that CTDSPL is able to precipitate Rb protein from MCF-7 cell extracts, while surface plasmon resonance technique showed that interaction of the two proteins is direct. Results of this study reassert that phosphatase CTDSPL and Rb could be involved in the common mechanism of cell cycle regulation.

作者简介

A. Beniaminov

Engelhardt Institute of Molecular Biology

编辑信件的主要联系方式.
Email: abeniaminov@mail.ru
俄罗斯联邦, Moscow, 119991

G. Krasnov

Engelhardt Institute of Molecular Biology

Email: abeniaminov@mail.ru
俄罗斯联邦, Moscow, 119991

A. Dmitriev

Engelhardt Institute of Molecular Biology

Email: abeniaminov@mail.ru
俄罗斯联邦, Moscow, 119991

G. Puzanov

Engelhardt Institute of Molecular Biology

Email: abeniaminov@mail.ru
俄罗斯联邦, Moscow, 119991

B. Snopok

Lashkaryov Institute of Semiconductor Physics

Email: abeniaminov@mail.ru
乌克兰, Kiev, 03028

V. Senchenko

Engelhardt Institute of Molecular Biology

Email: abeniaminov@mail.ru
俄罗斯联邦, Moscow, 119991

V. Kashuba

Department of Molecular Oncogenetics, Institute of Molecular Biology and Genetics

Email: abeniaminov@mail.ru
乌克兰, Kiev, 03680

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