Background

Overview

Recent observations lead to the idea that genes, not in the same operon but spatially close, are highly co-transcribed, even in the absence of regulatory factors at their promoter regions.

The iGEM Paris-Saclay project aims at studying the effects of DNA topology on gene expression in E. coli by answering this question:

Does bringing two differentialy regulated promoters close to each others influences the expression level of genes located downstream?

We have designed a new tool based on the CRISPR/Cas9 system to bring two specific DNA regions closer. This system is composed of two different dCas9s fused with each part of the FRB / FKBP12 dimerization system. Each dCas9 will target a specific DNA sequence, one on the chromosome and one on a plasmid, whereas the dimerization system will promote the joining of the two dCas9s when rapalog is added.

In order to assess whether or not this system works, we have also designed a new tool to visualize the interaction between both dCas9s. This tool is composed of a split GFP attached to two dCas9s. These two small GFP tags will interact with the complementary GFP detector only if the two dCas9s are close enough to interact.

Theoretical basis

The transcription and its regulation

Transcription is the first step of the Central dogma of molecular biology. It is the process in which an RNA molecule is created based on the sequence of a DNA template. In this case the template is a gene, a region of DNA whose RNAs can be translated into proteins, which perform different functions within the cell. Because the environment of bacteria is constantly changing, cells have to adapt. A part of adaptation consists in using different proteins present at different times in the cell. These changes can be the result of transcriptional regulations.

Sequences called promoters are small DNA sequences upstream of genes. RNA polymerase is the protein that performs transcription by binding to promoters before starting transcription. RNA polymerase is composed of several parts, each of them called a “subunit”. In bacteria, it is one of these subunits that binds first to the promoter. It is called “σ-factor” [Fig. 1].

But other factors can be necessary to begin transcription or to prevent it, especially when the promoter is not strong enough to keep the σ-factor attached to it. All of the proteins that can bind to DNA are called DNA binding proteins. The binding of a multisubunit RNA polymerase or general transcription factors to a specialized transcription promoter DNA sequence is an essential step in initiating DNA transcription in all organisms (Friedman 2013).

Numerous molecules and factors are involved in the mechanism of transcription and can be involved in its regulation. Transcription factors are proteins that enhance or prevent transcription; other factors such as small molecules, DNA sequence properties, and chromosome structure also play a role even though these mechanisms are diverse and often poorly understood (Browning 2002) [Fig. 2].

DNA binding proteins

These DNA binding proteins are able to bind to DNA with different strengths also called affinities. Some proteins bind DNA with the same affinity regardless of the DNA sequence, others can only be recruited by specific sequences. Four mechanisms by which a DNA binding protein finds its target sequence are known: sliding, when the protein slides along DNA [Fig. 4a]; hopping, when the protein unbinds a DNA segment and binds to another one [Fig. 4b]; intersegment transfer, when the protein binds two different segments of DNA before releasing one; and looping, which consists on the binding of two DNA segments leading to a loop (Bustamante 1999, Bondos 2015) [Fig. 4c,d]. Among these, only the one-dimensional sliding is independent of spatial organization in the chromosome, that’s why the structural organization of genomes is very important for transcriptional regulation.

Competition for binding within a cell

These four mechanisms allow for dynamic binding of proteins to their target sequences, despite the fact that these proteins are not present in large concentrations. For example, the number of genes in Escherichia coli is about 5 000 and the number of active RNA polymerases is about 200 per cell, of which 140 only transcribe 2% of the genes leaving 60 polymerases for the other 4995 genes.

Thus, there is tight competition between genes to get transcribed: competition between the same σ-factor for several promoters, competition between σ-factors for the rest of the RNA polymerase or competition between a σ-factor and other DNA binding proteins. These competitions are fundamental in the mechanism of transcriptional regulation. They are often allowed or prevented by remodeling of the chromosome topology (Haugen 2008) [Fig. 4].

This is why the link between genome topology and gene regulation is a major research topic in the subject of transcription. Although the mechanisms of global gene regulation by changes in DNA organization are well established, the fine tuning of transcription is particularly hard to study and not very well understood. Considering this gap in knowledge, new studies have to be conducted without a priori in order to determine if fine tuning of the DNA topology takes place during transcriptional regulation and if so, how does such regulation work.

Transcription initiation

Regulation can occur at every step on the pathway to gene expression, but transcription initiation is probably the most frequently regulated step (Haugen 2008). It is the result of:

1. The recognition of a promoter by a σ-factor;
2. The recruitment of the other parts of the RNA polymerase;
3. The formation of an open complex, thus the unwinding of DNA from either side of the promoter;
4. The beginning of RNA synthesis and finally;
5. The release of the σ-factor (Browning 2002).

The first step, in which the σ-factor binds to the promoter, can limit the transcription rate. Moreover one σ-factor can lead to the beginning of transcription of a gene, be released and lead to the beginning of the transcription of an other one. As a result, we think that spatially close promoters can act on each others, for example by doubling the number of sequences which can recruit a σ-factor in a certain area. A strong promoter could recruit a σ-factor and after its release, this σ-factor would have a better probability of being recruited to a weaker promoter. Conversely, a strong promoter could have a better chance of recruiting a σ-factor leading to “starving” of the weaker promoters within the same area.

DNA topology in bacteria

As mentioned above, DNA topology plays a fundamental role in gene regulation and in protein interactions after their synthesis. A growing number of studies have shown a periodically structure of bacterial chromosome in solenoid or in plectoneme at some sub levels of organization [Fig.6]. Such structures could be selected to keep gene pairs close to each other. Indeed, some authors (Wright and al. 2007) have shown that gene pairs are often distant from each others by 117 kb, resulting in possible helix-like structures with this periodicity.

From Wright et al. 2007

Because of this periodicity, regulation could be effective in particular area of the chromosome, leading to a fine, but integral, tuning of the genes involved in the same pathway. That is why concepts such as regulons (genes that are usually geographically scattered but under the control of the same regulatory factor), who were initially described with a 2D vision of the bacterial chromosomes, could be specified with the incorporation of new researches.

From Dorman 2013

In bacteria, translation occurs at the same time as transcription. Products of gene-coding-protein are synthesized near their gene and the pairing of genes can results in an increasing probability for the two proteins to interact with each others (Fig.7) (Dorman 2013). In the same way a single sigma factor, specific of a group of genes, could be recruited from a promoter to another easily because of the DNA topology. Thus, gene pair associations could provide the cell with an other level of regulation of transcription.

Question

To understand transcriptional regulation, we have to study chromosome topology in 4-dimensions (3D + time) and its effect on the recruitment of DNA binding proteins. In this project, we try to answer to a fundamental question: are proximal promoters influencing each other’s transcriptional rates? [Fig. 8].

References

Browning, D.F., and Busby, S.J.W. (2004). The regulation of bacterial transcription initiation. Nature Reviews Microbiology 2, 57–65.

Cases, I., and de Lorenzo, V. (2005). Promoters in the environment: transcriptional regulation in its natural context. Nature Reviews Microbiology 3, 105–118.

Dorman, C.J. (2013). Genome architecture and global gene regulation in bacteria: making progress towards a unified model? Nature Reviews Microbiology 11, 349–355.

Esvelt, K.M., Mali, P., Braff, J.L., Moosburner, M., Yaung, S.J., and Church, G.M. (2013). Orthogonal Cas9 proteins for RNA-guided gene regulation and editing. Nature Methods 10, 1116–1121.

Ishihama, A. (2000). Functional modulation of Escherichia coli RNA polymerase. Annu. Rev. Microbiol. 54, 499–518. Lagomarsino, M.C., Espéli, O., and Junier, I. (2015). From structure to function of bacterial chromosomes: Evolutionary perspectives and ideas for new experiments. FEBS Letters 589, 2996–3004.

Li, X. (2002). Tissue-Specific Regulation of Retinal and Pituitary Precursor Cell Proliferation. Science.

Rud, I. (2006). A synthetic promoter library for constitutive gene expression in Lactobacillus plantarum. Microbiology 152, 1011–1019.

Sanli, I., and Feil, R. (2016). PRC-mediated interaction networks of repressed genes: emerging insights and possible roles. Epigenomics 8, 733–735.

Sobetzko, P., Travers, A., and Muskhelishvili, G. (2012). Gene order and chromosome dynamics coordinate spatiotemporal gene expression during the bacterial growth cycle. Proceedings of the National Academy of Sciences 109, E42–E50.

Travers, A., and Muskhelishvili, G. (2005). DNA supercoiling — a global transcriptional regulator for enterobacterial growth? Nature Reviews Microbiology 3, 157–169.

Wright, M.A., Kharchenko, P., Church, G.M., and Segrè, D. (2007). Chromosomal periodicity of evolutionarily conserved gene pairs. Proceedings of the National Academy of Sciences 104, 10559–10564.