HMGB Proteins as DNA Chaperones That Modulate Chromatin Activity


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HMGB proteins are involved in structural rearrangements caused by regulatory chromatin remodeling factors. Particular interest is attracted to a DNA chaperone mechanism, suggesting that the HMGB proteins introduce bends into the double helix, thus rendering DNA accessible to effector proteins and facilitating their activity. The review discusses the role that the HMBG proteins play in key intranuclear processes, including assembly of the preinitiation complex during transcription of ribosomal genes; transcription by RNA polymerases I, II, and III; recruitment of the SWI/SNF complex during transcription of nonribosomal genes; DNA repair; etc. The functions of the HMGB proteins are considered in detail with the examples of yeast HMO1 and NHP6. The two proteins possess unique features in adition to properties characteristic of the HMGB proteins. Thus, NHP6 stimulates a large-scale ATP-independent unwrapping of nucleosomal DNA by the FACT complex, while in its absence FACT stabilizes the nucleosome. HMO1 acts as an alternative linker histone. Both HMO1 and NHP6 are of applied interest primarly because they are homologs of human HMGB1, an important therapeutic target of anticancer and anti-inflammatory treatments.

作者简介

A. Kozlova

Biological Faculty, Moscow State University

Email: vasily.studitsky@fccc.edu
俄罗斯联邦, Moscow, 119234

M. Valieva

Biological Faculty, Moscow State University

Email: vasily.studitsky@fccc.edu
俄罗斯联邦, Moscow, 119234

N. Maluchenko

Biological Faculty, Moscow State University

编辑信件的主要联系方式.
Email: mal_nat@mail.ru
俄罗斯联邦, Moscow, 119234

V. Studitsky

Biological Faculty, Moscow State University; Cancer Epigenetics Program, Fox Chase Cancer Center

编辑信件的主要联系方式.
Email: vasily.studitsky@fccc.edu
俄罗斯联邦, Moscow, 119234; Philadelphia, PA 19111

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