HIV: The two sides of Tat
Like all viruses, human immunodeficiency virus (HIV) must engage with the cells of its host to be able to replicate. Compared to other retroviruses, this interaction is particularly complex in the case of HIV because its genome encodes many proteins that take advantage of various cell processes and counteract host defenses. One of these proteins is called transactivator of transcription (Tat) and it is essential for the expression of HIV genes in host cells. Now, in eLife, Ivan D’Orso of the University of Texas Southwestern Medical Center (UTSW) and colleagues – including Jonathan Reeder and Youn-Tae Kwak of UTSW as joint first authors – demonstrate that Tat can also regulate the expression of many host genes (Reeder et al., 2015).
In the first stage of gene expression, a gene is “transcribed” to make messenger RNA (mRNA) by an enzyme called RNA polymerase II (Pol II). After Pol II binds to the promoter region of a gene and starts to make an mRNA molecule, the enzyme stops due to the actions of pause-inducing factors. The ability of Pol II to continue to transcribe the gene (in a step called elongation) depends on a cellular protein complex called P-TEFb (short for positive transcription elongation factor b). In the case of HIV, the situation is very similar. Pol II pauses soon after initiating from the promoter of the viral genome producing only short mRNAs. However, Tat can override this transcriptional block by recruiting P-TEFb to Pol II via a RNA stem-loop structure called the transactivation response element, which is found at the beginning of all virus mRNAs (Ott et al., 2011).
While most researchers have focused on understanding how Tat activates the transcription of HIV, some studies have demonstrated that Tat also alters the expression of host genes to promote the production and spread of HIV. For example, Tat manipulates immune T cells in its host to allow the virus to infect and replicate in them (Li et al., 1997, Huang et al., 1998). Moreover, Tat induces the expression of chemokines that attract uninfected T cells and macrophages, facilitating expansion of HIV in the host (Izmailova et al., 2003). On the other side, Tat can also contribute to the depletion of T cells during AIDS progression by up-regulating cellular pro-apoptotic genes (Kim et al., 2010). Finally, Tat is able to repress the transcription of several genes encoding receptors of the innate immune system responses. However, we still do not have a comprehensive view of the host genes that Tat targets, or how Tat alters the transcription of these genes.
Reeder, Kwak, D'Orso and two colleagues – Ryan McNamara (UTSW) and Christian Forst (Icahn School of Medicine at Mount Sinai) – took on this challenge by analyzing T cells that produced the Tat protein with a series of genome-wide approaches. They identified close to 3000 sites in the human genome that are occupied by Tat. The presence of Tat changed the expression of about 2000 host genes, and almost quarter of these were classified as direct targets because Tat bound to their promoters or to other sites in the genes. About half of these direct targets were up-regulated by Tat, while the rest were down-regulated. Further experiments revealed that for a subset of the target genes, Tat is able to regulate either the initiation or elongation by Pol II.
Next, Reeder, Kwak et al. investigated how Tat can modulate different steps in the transcription of host genes. For example, to stimulate or inhibit the start of transcription, Tat regulates the loading Pol II to cellular promoters. Of note, at the majority of up-regulated genes, Tat appears to facilitate Pol II promoter presence from sites within gene bodies by inducing DNA looping. However, to regulate elongation, Tat can either promote or prevent the recruitment of P-TEFb to specific genes. Importantly, Reeder, Kwak et al.’s further findings suggest that, unlike what happens with viral genes, Tat does not seem to rely on RNA structures similar to the HIV transactivation response element to regulate target host genes. Instead, Tat co-opts some of the master transcriptional regulators of its host that also control cellular gene transcription in uninfected cells.
In agreement with an earlier report (Marban et al., 2011), Reeder, Kwak et al. found that binding sites for the master regulator called ETS1 were, among others, most frequent near the genomic regions that Tat occupies. Tat interacts with ETS1 protein and knocking down the ETS1 gene abolished the recruitment of Tat to some target genes, thus preventing it from being able to modulate their transcription. Moreover, ETS1 motifs are found at both up-regulated and down-regulated Tat targets, underscoring that gene-specific circumstances determine the effect of Tat. Curiously, HIV itself contains an ETS1 binding site upstream of its promoter, and this allows ETS1 to stimulate viral gene expression in collaboration with other transcription factors of the cell (Sieweke et al., 1998; Yang et al., 2009).
The report by Reeder, Kwak et al. arguably represents the most thorough characterization of the role of Tat on host gene expression. While making sure that the HIV genome is transcribed, Tat also fine-tunes two critical steps in the expression of specific cellular genes. Is this tweaking of host gene transcription a necessary survival strategy for HIV, or merely a side effect of the presence of potent transcriptional regulator Tat in the cell nucleus? Or has this possible side effect been transformed through evolution into a winning strategy of the virus? Whatever the correct answer might be, Reeder, Kwak et al. confirmed that the expression of many Tat target genes changed as expected during HIV infection. Moreover, many of these genes appear to be involved in signaling pathways and biological processes that could help HIV to spread in the host.
This study raises further questions. Does Tat modulate the expression of hundreds of previously identified host proteins that interact with HIV gene products or are critical to replication of the virus? Is Tat also capable of regulating the termination of transcription at host genes? How exactly do the interactions between Tat, master transcriptional regulators like ETS1, and host proteins lead to changes in gene expression? Further, has HIV devised one strategy to promote very high levels of transcription of its own genome, while exploiting cellular transcriptional regulators to provoke only modest (but beneficial) changes in the expression of host genes? Answers to these and other questions shall advance our understanding of how and why HIV Tat reprograms its host.
References
-
Tat protein induces human immunodeficiency virus type 1 (hIV-1) coreceptors and promotes infection with both macrophage-tropic and t-lymphotropic HIV-1 strainsJournal of Virology 72:8952–8960.
-
Tat protein induces self-perpetuating permissivity for productive HIV-1 infectionProceedings of the National Academy of Sciences USA 94:8116–8120.https://doi.org/10.1073/pnas.94.15.8116
-
The control of HIV transcription: keeping RNA polymerase II on trackCell Host & Microbe 10:426–435.https://doi.org/10.1016/j.chom.2011.11.002
-
Isolation of a cellular factor that can reactivate latent HIV-1 without t cell activationProceedings of the National Academy of Sciences USA 106:6321–6326.https://doi.org/10.1073/pnas.0809536106
Article and author information
Author details
Publication history
- Version of Record published: January 19, 2016 (version 1)
Copyright
© 2016, Barboric et al.
This article is distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use and redistribution provided that the original author and source are credited.
Metrics
-
- 1,822
- Page views
-
- 232
- Downloads
-
- 5
- Citations
Article citation count generated by polling the highest count across the following sources: Crossref, PubMed Central, Scopus.
Download links
Downloads (link to download the article as PDF)
Open citations (links to open the citations from this article in various online reference manager services)
Cite this article (links to download the citations from this article in formats compatible with various reference manager tools)
Further reading
-
- Chromosomes and Gene Expression
Chromatin accessibility is modulated in a variety of ways to create open and closed chromatin states, both of which are critical for eukaryotic gene regulation. At the single molecule level, how accessibility is regulated of the chromatin fiber composed of canonical or variant nucleosomes is a fundamental question in the field. Here, we developed a single-molecule tracking method where we could analyze thousands of canonical H3 and centromeric variant nucleosomes imaged by high-speed atomic force microscopy. This approach allowed us to investigate how changes in nucleosome dynamics in vitro inform us about transcriptional potential in vivo. By high-speed atomic force microscopy, we tracked chromatin dynamics in real time and determined the mean square displacement and diffusion constant for the variant centromeric CENP-A nucleosome. Furthermore, we found that an essential kinetochore protein CENP-C reduces the diffusion constant and mobility of centromeric nucleosomes along the chromatin fiber. We subsequently interrogated how CENP-C modulates CENP-A chromatin dynamics in vivo. Overexpressing CENP-C resulted in reduced centromeric transcription and impaired loading of new CENP-A molecules. From these data, we speculate that factors altering nucleosome mobility in vitro, also correspondingly alter transcription in vivo. Subsequently, we propose a model in which variant nucleosomes encode their own diffusion kinetics and mobility, and where binding partners can suppress or enhance nucleosome mobility.
-
- Cell Biology
- Chromosomes and Gene Expression
The cohesin complex plays essential roles in chromosome segregation, 3D genome organisation, and DNA damage repair through its ability to modify DNA topology. In higher eukaryotes, meiotic chromosome function, and therefore fertility, requires cohesin complexes containing meiosis-specific kleisin subunits: REC8 and RAD21L in mammals and REC-8 and COH-3/4 in Caenorhabditis elegans. How these complexes perform the multiple functions of cohesin during meiosis and whether this involves different modes of DNA binding or dynamic association with chromosomes is poorly understood. Combining time-resolved methods of protein removal with live imaging and exploiting the temporospatial organisation of the C. elegans germline, we show that REC-8 complexes provide sister chromatid cohesion (SCC) and DNA repair, while COH-3/4 complexes control higher-order chromosome structure. High-abundance COH-3/4 complexes associate dynamically with individual chromatids in a manner dependent on cohesin loading (SCC-2) and removal (WAPL-1) factors. In contrast, low-abundance REC-8 complexes associate stably with chromosomes, tethering sister chromatids from S-phase until the meiotic divisions. Our results reveal that kleisin identity determines the function of meiotic cohesin by controlling the mode and regulation of cohesin–DNA association, and are consistent with a model in which SCC and DNA looping are performed by variant cohesin complexes that coexist on chromosomes.