Ectopic expression of HIV-1 Tat modifies gene expression in cultured B cells: implications for the development of B-cell lymphomas in HIV-1-infected patients
Anna A. Valyaeva,
Maria A. Tikhomirova,
Daria M. Potashnikova,
Alexandra N. Bogomazova,
Galina P. Snigiryova,
Aleksey A. Penin,
Maria D. Logacheva,
Eugene A. Arifulin,
Anna A. Shmakova,
Diego Germini,
Anastasia I. Kachalova,
Aleena A. Saidova,
Anastasia A. Zharikova,
Yana R. Musinova,
Andrey A. Mironov,
Yegor S. Vassetzky,
Eugene V. Sheval
Affiliations
Anna A. Valyaeva
School of Bioengineering and Bioinformatics, Lomonosov Moscow State University, Moscow, Russia
Maria A. Tikhomirova
School of Bioengineering and Bioinformatics, Lomonosov Moscow State University, Moscow, Russia
Daria M. Potashnikova
Department of Cell Biology and Histology, School of Biology, Lomonosov Moscow State University, Moscow, Russia
Alexandra N. Bogomazova
Federal Research and Clinical Center of Physical-Chemical Medicine, Moscow, Russia
Galina P. Snigiryova
Burdenko National Medical Research Center of Neurosurgery, Moscow, Russia
Aleksey A. Penin
Institute for Information Transmission Problems, Moscow, Russia
Maria D. Logacheva
Belozersky Institute of Physico-Chemical Biology, Lomonosov Moscow State University, Moscow, Russia
Eugene A. Arifulin
Belozersky Institute of Physico-Chemical Biology, Lomonosov Moscow State University, Moscow, Russia
Anna A. Shmakova
Koltzov Institute of Developmental Biology, Moscow, Russia
Diego Germini
UMR9018 (CNRS – Institut Gustave Roussy – Université Paris Saclay), Centre National de Recherche Scientifique, Villejuif, France, France
Anastasia I. Kachalova
Department of Cell Biology and Histology, School of Biology, Lomonosov Moscow State University, Moscow, Russia
Aleena A. Saidova
Department of Cell Biology and Histology, School of Biology, Lomonosov Moscow State University, Moscow, Russia
Anastasia A. Zharikova
School of Bioengineering and Bioinformatics, Lomonosov Moscow State University, Moscow, Russia
Yana R. Musinova
Belozersky Institute of Physico-Chemical Biology, Lomonosov Moscow State University, Moscow, Russia
Andrey A. Mironov
School of Bioengineering and Bioinformatics, Lomonosov Moscow State University, Moscow, Russia
Yegor S. Vassetzky
Koltzov Institute of Developmental Biology, Moscow, Russia
Eugene V. Sheval
School of Bioengineering and Bioinformatics, Lomonosov Moscow State University, Moscow, Russia
An increased frequency of B-cell lymphomas is observed in human immunodeficiency virus-1 (HIV-1)-infected patients, although HIV-1 does not infect B cells. Development of B-cell lymphomas may be potentially due to the action of the HIV-1 Tat protein, which is actively released from HIV-1-infected cells, on uninfected B cells. The exact mechanism of Tat-induced B-cell lymphomagenesis has not yet been precisely identified. Here, we ectopically expressed either Tat or its TatC22G mutant devoid of transactivation activity in the RPMI 8866 lymphoblastoid B cell line and performed a genome-wide analysis of host gene expression. Stable expression of both Tat and TatC22G led to substantial modifications of the host transcriptome, including pronounced changes in antiviral response and cell cycle pathways. We did not find any strong action of Tat on cell proliferation, but during prolonged culturing, Tat-expressing cells were displaced by non-expressing cells, indicating that Tat expression slightly inhibited cell growth. We also found an increased frequency of chromosome aberrations in cells expressing Tat. Thus, Tat can modify gene expression in cultured B cells, leading to subtle modifications in cellular growth and chromosome instability, which could promote lymphomagenesis over time.