Статья

Functional diversity of non-histone chromosomal protein hmgb1

E. Chikhirzhina, T. Starkova, A. Beljajev, A. Polyanichko, A. Tomilin,
2021

The functioning of DNA in the cell nucleus is ensured by a multitude of proteins, whose interactions with DNA as well as with other proteins lead to the formation of a complicated, organized, and quite dynamic system known as chromatin. This review is devoted to the description of properties and structure of the progenitors of the most abundant non-histone protein of the HMGB family—the HmgB1 protein. The proteins of the HMGB family are also known as “architectural factors” of chromatin, which play an important role in gene expression, transcription, DNA replication, and repair. However, as soon as HmgB1 goes outside the nucleus, it acquires completely different functions, post-translational modifications, and change of its redox state. Despite a lot of evidence of the functional activity of HmgB1, there are still many issues to be solved related to the mechanisms of the influence of HmgB1 on the development and treatment of different diseases—from oncological and cardiovascular diseases to pathologies during pregnancy and childbirth. Here, we describe molecular structure of the HmgB1 protein and discuss general mechanisms of its interactions with other proteins and DNA in cell. © 2020 by the authors. Licensee MDPI, Basel, Switzerland.

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Версии

  • 1. Version of Record от 2021-04-27

Метаданные

Об авторах
  • E. Chikhirzhina
    Institute of Cytology of the Russian Academy of Sciences, Laboratory of Molecular Biology of Stem Cells, Tikhoretsky Av. 4, St. Petersburg, 194064, Russian Federation
  • T. Starkova
  • A. Beljajev
  • A. Polyanichko
  • A. Tomilin
Название журнала
  • International Journal of Molecular Sciences
Том
  • 21
Выпуск
  • 21
Страницы
  • 1-29
Ключевые слова
  • chromosome protein; high mobility group B1 protein; nonhistone protein; adenosine diphosphate ribosylation; cell nucleus; chromatin; DNA repair; DNA replication; gene expression; genetic transcription; human; nonhuman; oxidation reduction state; protein acetylation; protein DNA binding; protein function; protein glycosylation; protein methylation; protein phosphorylation; protein processing; protein protein interaction; protein structure; Review
Издатель
  • MDPI AG
Тип документа
  • Review
Тип лицензии Creative Commons
  • CC
Правовой статус документа
  • Свободная лицензия
Источник
  • scopus