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Front. Genet., 13 March 2014
Sec. Systems Biology Archive
This article is part of the Research Topic The origins of biological noise View all 6 articles

Biological noise to get a sense of direction: an analogy between chemotaxis and stress response

  • Structural Computational Biology, Spanish National Cancer Research Centre (CNIO), Madrid, Spain

Introduction

From the earliest studies on bacteria (Spudich and Koshland, 1976; Elowitz et al., 2002), it was soon understood that biological processes are often dominated by the stochasticity that pervades the physical world. Biological noise, here defined as the substantial cell-to-cell variation that is observed in populations of genetically identical cells, is more and more recognized as an important factor in biology, thanks to the improvement of single cell analysis techniques. The stochasticity of physical phenomena that underlie cellular processes plays an important role in the origin of noise. Noise manifests itself at different levels. At the smallest scales, the random motion of molecules affects basic cellular processes such as transcription, translation, and signal transduction. At a higher level, the topology and connectivity of biological regulatory circuits is often such that stochastic behavior is observed in the levels of specific factors. Specifically, the topology of regulatory networks can feature multiple types of feedback and feed-forward loops, which create multistability in the system and can amplify the fluctuations originating from molecular noise (Burda et al., 2011). Both of these sources of noise can result in the existence of multiple stable states in cells, each defined by specific gene and protein levels. In isogenic cellular population this produces heterogeneity amongst cells and in time as stochasticity forces transitions between the different stable states (Levine et al., 2013; Sanchez and Golding, 2013). Although there is a clear difference between noise, which does not have a unique definition, and heterogeneity at the population level, the two phenomena are closely connected (Huang, 2009).

At first sight, the complexity of biological behavior would seem to require the strictest control of underlying processes, suggesting a constant evolutionary fight against the inherent disadvantages of noise. This is certainly the case, for example in the evolution of accurate proof-reading mechanisms that ensure faithful DNA replication. However, recent results also support the view that controlled levels of stochasticity are important in cells, proposing noise as a selectable trait. Already in 2004 Raser and O'Shea identified mutations both acting in cis and trans that affected the levels of gene expression noise, which is viewed as an evolvable trait (Raser and O'Shea, 2004). Ansel and colleagues later showed that the levels of expression noise in a single gene can be a heritable trait and they identified three Quantitative Trait Loci associated to it (Ansel et al., 2008). The adaptive importance of noise is exemplified in the concept of bet-hedging, according to which cells maximize their chance of survival by exploring different states in a random fashion (Fehrmann et al., 2013; Viney and Reece, 2013; Yvert et al., 2013).

The positive aspects of noise manifest themselves at many levels at which noise acts. At the molecular level, a control strategy based on dynamic equilibrium of stochastic events, similar to a thermostat regulating temperature, offers more robustness and tunability in processes such as mRNA production and translation (Shalem et al., 2008; Salari et al., 2012; Sanchez and Golding, 2013).

At the level of regulatory networks, topologies, and logic relations allowing oscillations and multistability contribute to higher adaptability of the organism to changing environments. It was recently shown that stress in yeast provokes a clear change in network topology, which can promote phenotype differentiation within a population (Mihalik and Csermely, 2011; Lehtinen et al., 2013). We can hypothesize that the observed loosening of the network could serve to diversify phenotypes in the different cells.

Single cell monitoring of phenotypes in tissues suggests a high degree of heterogeneity even in multi-cellular organisms (Paszek et al., 2010). An important factor in cell-cell communication, NFkB (nuclear factor kappa-light-chain-enhancer of activated B cells), undergoes continuous cycles of nuclear localization, such that in a population only a fraction of the cells at any time will have high levels of this transcription factor's activity (Ashall et al., 2009). In the overall context of a tissue, this heterogeneity in activation levels of NFkB contributes to the maintenance of homeostasis and to tissue responsiveness. Thus, even at the tissue level, the presence of fluctuations in time and across cellular populations serves as a detection tool that ensures fast reaction to any changes in the tissue's condition (Paszek et al., 2010; Levine et al., 2013).

Although the connections between noise at these different levels are still to be elucidated, noise pervades biological life forms across evolutionary time and there does not seem to have been a strong negative evolutionary pressure to eliminate it, with a few exceptions (Lehner, 2008).

A possible generalized interpretation of the above observations is that fluctuations, and hence noise at multiple levels, are instrumental in granting a robust control strategy to organisms enabling them to adapt to changing environments. We will try to substantiate this claim through two examples that lead us to make an analogy between bacteria aiming to reach a source of food and a population of yeast aiming to reach a state of optimal growth in a varying environment.

Chemotaxis: Charting the Map with Biased Random Walks

Bacteria can identify sources of food and repellent substances based on the presence of just a few molecules in a background concentration spanning many orders of magnitude (Wadhams and Armitage, 2004). It was discovered that bacteria can either swim in a specific direction or tumble, that is rotate on themselves, and hence randomly change their direction. These two different actions are determined by the sense of rotation of their flagella, which is the output of a complex signaling network. Combining the two types of motion, evolution has selected a strategy that allows bacteria to explore their environment in search for food, performing what is effectively a random walk biased by the concentration field. When the bacterium swims across increasing food concentration, the tumble motion is suppressed, whereas, when there is no clear concentration gradient, tumbling is favored and a new random direction is chosen. A closer look at the mechanism behind this phenomenon reveals that random motion, combined with signal processing and feedback can explain this behavior (Sourjik and Wingreen, 2012).

Thus, stochastic behavior is at the origin of cells' ability to navigate their environment. We can say that the cell is building a model of the “world” outside and with time it keeps re-adjusting it. Each stochastic tumble-swim event brings an occasion to confront the model with the environment, through detection of the actual chemical concentration gradient. Moreover, when an entire population of bacteria is present, stochastic mechanisms ensure that each individual will have a sufficiently different behavior from the others to efficiently explore the entire space (Korobkova et al., 2004; Emonet and Cluzel, 2008). This strategy is likely to be under selection, as the capacity to navigate environments, find food and avoid repellents is a clearly important trait for bacteria and is even conserved in the immune system (Luster, 2001).

Mechanisms of Stress Response and Adaptation in Yeast

Yeast cells perform very broad rearrangements of their transcriptional program upon stress treatment (Gasch et al., 2000; Gasch, 2007; Berry and Gasch, 2008; Chen et al., 2008; Lackner et al., 2012) that allow the cell to produce the correct amount of proteins that it needs to deal with challenges, including de-toxifying agents and chaperones, and regulate its cell cycle. Growth and cell division genes are down-regulated concomitantly with the temporary arrest of the cell cycle, while genes involved in stress protection are up-regulated (Pancaldi et al., 2010). It is generally observed that each cell can either choose to grow faster, reducing its resilience to changes in the conditions, or grow slower, allowing it to better survive external changes (López-Maury et al., 2008).

In recent experiments with budding yeast, stress was seen to increment morphological variability at the population level, possibly through an effect related to HSP90 (Hsieh et al., 2013), an important chaperone buffering the effects of multiple genetic mutations (Rutherford and Lindquist, 1998). Investigations on single cell growth rates in budding yeast propose that keeping a wide distribution of values for this parameter can be exploited as a stress defense mechanism against severe heat stress (Levy et al., 2012). Sequence variants in yeast are known to affect gene expression variability (Fehrmann et al., 2013) but, importantly, in this case, the presence of a distribution of growth rates in the population is found not to depend on the genetic make-up of the single cells, as the character is not heritable. Instead, it is attributed to a large number of epigenetic states which determine the growth rate and hence affect the propensity to resist stress in each cell. This was verified by following the progeny of cells that displayed a particular low or high growth rate and observing the cells revert to the original distribution after a few tens of generations (Levy et al., 2012). Particular types of stress, like nitrogen starvation, even prompt yeast to perform meiosis and produce spores, more resistant cells that can survive in a dormant state until external conditions have improved (Su et al., 1996; Otsubo and Yamamoto, 2012). Meiosis involves homologous recombination, which could be interpreted as a further attempt to maximize the variability within the population. Once again the presence of a wide distribution of values of a specific character, in this case of growth rate, confers an advantage to the whole population, which will thus avoid extinction when its perfectly adapted fast growing cells are killed.

Stress Response Variability as Mapping in Time

Thus, stress response in cells is similar to chemotaxis, in the sense that predicting in which direction to go to get to the food corresponds to a yeast population deciding on whether growth conditions are going to get better or worse. In this case we can imagine the gradient of attractant or repellent to correspond to the increasing concentration of a chemical stress agent, for example hydrogen peroxide in a yeast culture. Until the cells are kept in good growth conditions, they simply optimize their growth rate, focussing their gene expression program and protein composition onto this task. In our analogy, this corresponds to a chemotacting cell, swimming almost straight toward a source of attractant. On the other hand, upon stress, the clear goal of optimal growth is substituted by the need to ensure survival. In the case of persistent insults, a variety of genes can be regulated to promote a more resilient state through differentiation of the single cell responses while changes in the interaction network topology further enhance it. In our analogy, this is the equivalent of the increased random tumbling motion in bacteria (Figure 1).

FIGURE 1
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Figure 1. A schematic diagram of the proposed analogy. (A) A bacterium moving toward a source of food through a random walk biased by the chemical concentration gradient. (B) A bacterium tumbling most of the time and performing a non-biased random walk in the absence of a chemical gradient. (C) A phenotypically homogeneous yeast population growing in a rich medium in the absence of a perturbation. (D) A phenotypically heterogeneous yeast population growing under a chemical perturbation, where presumably the heterogeneity is a strategy to ensure survival of at least a few cells during the perturbation. (E) A fitness landscape with clear minima (valleys) and where the homogeneous population is coordinately descending toward the global minimum. (F) A flatter fitness landscape where, in absence of a clear gradient, the population explores various regions through heterogeneity in the single-cell phenotype.

Just like bacteria in the absence of a clear gradient will freely spread in space maximizing their chance that at least one of them finds a gradient to follow, yeast populations in adverse environmental conditions will maximize cell-cell variability to more efficiently explore the fitness landscape.

These phenomena could be a consequence of the relaxation of control mechanisms that usually act to minimize the effects of noise, or there might be an evolved strategy to promote variability beyond that naturally present. In the first case, the resources the cell needs to keep the fluctuations at bay are not available in hostile environments or, in the second case, resources cost in guaranteeing variability at the population level has been evolutionarily selected as it is ultimately beneficial.

Conclusion

In a sense, the diversification of gene expression, genetic and non-genetic features in single cells during stress corresponds to an exploration of the environment, which allows cells to achieve states that are better adapted to the external conditions. The few cells that will randomly achieve a phenotype that is appropriate for the environment will survive, at the expense of the ones whose phenotype is not favorable. Thus, it seems that the inevitable stochasticity of biological processes, accompanied by larger scale variability, could confer robustness to the entire colony in the face of external challenges. The whole population is navigating in a changing fitness landscape, similarly to a cell navigating a chemotactic gradient.

Two very different phenomena, chemotaxis and stress response, share the common feature of enabling the cells to orient themselves, in respectively spatially and temporally varying environments. Both mechanisms rely on the presence of two stochastic processes, the tumbling motion in chemotaxis and the single cell variability of gene expression in stress response. We thus support a very general interpretation of the pervasive noisy nature of biological processes, not only as a consequence of the underlying stochastic physical processes, but also as an important tool for cells that need to adapt to changing conditions.

Acknowledgments

The author acknowledges a long-term FEBS fellowship and thanks Alfonso Valencia for hosting her in his laboratory. The author is also grateful to David Juan, Daniel Rico, and Alfonso Valencia for interesting discussions on this topic and an anonymous referee for useful comments on a previous version of the manuscript.

References

Ansel, J., Bottin, H., Rodriguez-Beltran, C., Damon, C., Nagarajan, M., Fehrmann, S., et al. (2008). Cell-to-cell stochastic variation in gene expression is a complex genetic trait. PLoS Genet. 4:e1000049. doi: 10.1371/journal.pgen.1000049

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Ashall, L., Horton, C. A., Nelson, D. E., Paszek, P., Harper, C. V., Sillitoe, K., et al. (2009). Pulsatile stimulation determines timing and specificity of NF-kappaB-dependent transcription. Science 324, 242–246. doi: 10.1126/science.1164860

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Berry, D. B., and Gasch, A. P. (2008). Stress-activated genomic expression changes serve a preparative role for impending stress in yeast. Mol. Biol. Cell 19, 4580–4587. doi: 10.1091/mbc.E07

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Burda, Z., Krzywicki, A., Martin, O. C., and Zagorski, M. (2011). Motifs emerge from function in model gene regulatory networks. Proc. Natl. Acad. Sci. U.S.A. 108, 17263–17268. doi: 10.1073/pnas.1109435108

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Chen, D., Wilkinson, C. R., Watt, S., Penkett, C. J., Toone, W. M., Jones, N., et al. (2008). Multiple pathways differentially regulate global oxidative stress responses in fission yeast. Mol. Biol. Cell 19, 308–317. doi: 10.1091/mbc.E07-08-0735

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Elowitz, M. B., Levine, A. J., Siggia, E. D., and Swain, P. S. (2002). Stochastic gene expression in a single cell. Science 297, 1183–1186. doi: 10.1126/science.1070919

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Emonet, T., and Cluzel, P. (2008). Relationship between cellular response and behavioral variability in bacterial chemotaxis. Proc. Natl. Acad. Sci. U.S.A. 105, 3304–3309. doi: 10.1073/pnas.0705463105

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Fehrmann, S., Bottin-Duplus, H., Leonidou, A., Mollereau, E., Barthelaix, A., Wei, W., et al. (2013). Natural sequence variants of yeast environmental sensors confer cell-to-cell expression variability. Mol. Syst. Biol. 9, 695. doi: 10.1038/msb.2013.53

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Gasch, A. P. (2007). Comparative genomics of the environmental stress response in ascomycete fungi. Yeast (Chichester, England) 24, 961–976. doi: 10.1002/yea.1512

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Gasch, A. P., Spellman, P. T., Kao, C. M., Carmel-Harel, O., Eisen, M. B., Storz, G., et al. (2000). Genomic expression programs in the response of yeast cells to environmental changes. Mol. Biol. Cell 12, 4241–4257. doi: 10.1091/mbc.11.12.4241

CrossRef Full Text

Hsieh, Y.-Y., Hung, P.-H., and Leu, J.-Y. (2013). Hsp90 regulates nongenetic variation in response to environmental stress. Mol. Cell 50, 82–92. doi: 10.1016/j.molcel.2013.01.026

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Huang, S. (2009). Non-genetic heterogeneity of cells in development: more than just noise. Development 136, 3853–3862. doi: 10.1242/dev.035139

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Korobkova, E., Emonet, T., Vilar, J. M. G., Shimizu, T. S., and Cluzel, P. (2004). From molecular noise to behavioural variability in a single bacterium. Nature 428, 574–578. doi: 10.1038/nature02404

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Lackner, D. H., Schmidt, M. W., Wu, S., Wolf, D. A., and Bähler, J. (2012). Regulation of transcriptome, translation, and proteome in response to environmental stress in fission yeast. Genome Biol. 13, R25. doi: 10.1186/gb-2012-13-4-r25

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Lehner, B. (2008). Selection to minimise noise in living systems and its implications for the evolution of gene expression. Mol. Syst. Biol. 4, 170. doi: 10.1038/msb.2008.11

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Lehtinen, S., Marsellach, F. X., Codlin, S., Schmidt, A., Clément-Ziza, M., Beyer, A., et al. (2013). Stress induces remodelling of yeast interaction and co-expression networks. Mol. Biosyst. 9, 1697–1707. doi: 10.1039/c3mb25548d

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Levine, J. H., Lin, Y., and Elowitz, M. B. (2013). Functional roles of pulsing in genetic circuits. Science 342, 1193–1200. doi: 10.1126/science.1239999

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Levy, S. F., Ziv, N., and Siegal, M. L. (2012). Bet hedging in yeast by heterogeneous, age-correlated expression of a stress protectant. PLoS Biol. 10:e1001325. doi: 10.1371/journal.pbio.1001325

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

López-Maury, L., Marguerat, S., and Bähler, J. (2008). Tuning gene expression to changing environments: from rapid responses to evolutionary adaptation. Nat. Rev. Genet. 8, 583–593. doi: 10.1038/nrg2398

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Luster, A. D. (2001). Chemotaxis: Role in Immune Response. Chichester: John Wiley & Sons, Ltd. doi: 10.1038/npg.els.0000507

CrossRef Full Text

Mihalik, Á., and Csermely, P. (2011). Heat shock partially dissociates the overlapping modules of the yeast protein-protein interaction network: a systems level model of adaptation. PLoS Comput. Biol. 7:e1002187. doi: 10.1371/journal.pcbi.1002187

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Otsubo, Y., and Yamamoto, M. (2012). Signaling pathways for fission yeast sexual differentiation at a glance. J. Cell Sci. 125(Pt 12), 2789–2793. doi: 10.1242/jcs.094771

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Pancaldi, V., Schubert, F., and Bähler, J. (2010). Meta-analysis of genome regulation and expression variability across hundreds of environmental and genetic perturbations in fission yeast. Mol. Biosyst. 6, 543–552. doi: 10.1039/b913876p

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Paszek, P., Ryan, S., Ashall, L., Sillitoe, K., Harper, C. V., Spiller, D. G., et al. (2010). Population robustness arising from cellular heterogeneity. Proc. Natl. Acad. Sci. U.S.A. 107, 11644–11649. doi: 10.1073/pnas.0913798107

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Raser, J. M., and O'Shea, E. K. (2004). Control of stochasticity in eukaryotic gene expression. Science 304, 1811–1814. doi: 10.1126/science.1098641

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Rutherford, S. L., and Lindquist, S. (1998). Hsp90 as a capacitor for morphological evolution. Nature 396, 336–342. doi: 10.1038/24550

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Salari, R., Wojtowicz, D., Zheng, J., Levens, D., Pilpel, Y., and Przytycka, T. M. (2012). Teasing apart translational and transcriptional components of stochastic variations in eukaryotic gene expression. PLoS Comput. Biol. 8:e1002644. doi: 10.1371/journal.pcbi.1002644

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Sanchez, A., and Golding, I. (2013). Genetic determinants and cellular constraints in noisy gene expression. Science 342, 1188–1193. doi: 10.1126/science.1242975

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Shalem, O., Dahan, O., Levo, M., Martinez, M. R., Furman, I., Segal, E., et al. (2008). Transient transcriptional responses to stress are generated by opposing effects of mRNA production and degradation. Mol. Syst. Biol. 4, 223. doi: 10.1038/msb.2008.59

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Sourjik, V., and Wingreen, N. S. (2012). Responding to chemical gradients: bacterial chemotaxis. Curr. Opin. Cell Biol. 24, 262–268. doi: 10.1016/j.ceb.2011.11.008

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Spudich, J. L., and Koshland, D. E. (1976). Non-genetic individuality: chance in the single cell. Nature 262, 467–471. doi: 10.1038/262467a0

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Su, S. S., Tanaka, Y., Samejima, I., Tanaka, K., and Yanagida, M. (1996). A nitrogen starvation-induced dormant G0 state in fission yeast: the establishment from uncommitted G1 state and its delay for return to proliferation. J. Cell Sci. 109(Pt 6), 1347–1357.

Pubmed Abstract | Pubmed Full Text

Viney, M., and Reece, S. E. (2013). Adaptive noise. Proc. Biol. Sci. 280:20131104. doi: 10.1098/rspb.2013.1104

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Wadhams, G. H., and Armitage, J. P. (2004). Making sense of it all: bacterial chemotaxis. Nat. Rev. Mol. Cell Biol. 5, 1024–1037. doi: 10.1038/nrm1524

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Yvert, G., Ohnuki, S., Nogami, S., Imanaga, Y., Fehrmann, S., Schacherer, J., et al. (2013). Single-cell phenomics reveals intra-species variation of phenotypic noise in yeast. BMC Syst. Biol. 7:54. doi: 10.1186/1752-0509-7-54

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Keywords: biological noise, heterogeneity, chemotaxis, stress response, adaptation

Citation: Pancaldi V (2014) Biological noise to get a sense of direction: an analogy between chemotaxis and stress response. Front. Genet. 5:52. doi: 10.3389/fgene.2014.00052

Received: 01 February 2014; Accepted: 21 February 2014;
Published online: 13 March 2014.

Edited by:

Daniel Hebenstreit, University of Warwick, UK

Reviewed by:

Pawel Paszek, University of Manchester, UK

Copyright © 2014 Pancaldi. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: vpancaldi@cnio.es

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