Our Research
We live in a cyclic environment; days and nights are a common thing to us. We are used to sunrises and sunsets and yet, we normally forget that such constant rhythmicity has sculpted organismal biology since the dawn of times. Biological systems have thus evolved sophisticated molecular devices that allow them to anticipate such daily changes.
Circadian (circa diem) clocks are accurate pacemakers (with ~24 h period length) that allow temporal compartmentalization of a large range of biological process within the cell and also at the organismal level. Interestingly, although the molecular components of circadian clocks differ across phyla, they share the same basic design or blueprints. Therefore, in organisms as diverse as humans, insects and fungi, it is possible to recognize a transcriptional-translational negative feedback loop at the heart of the timing mechanism, with kinases playing a key role in setting up the speed of the clock.
Circadian (circa diem) clocks are accurate pacemakers (with ~24 h period length) that allow temporal compartmentalization of a large range of biological process within the cell and also at the organismal level. Interestingly, although the molecular components of circadian clocks differ across phyla, they share the same basic design or blueprints. Therefore, in organisms as diverse as humans, insects and fungi, it is possible to recognize a transcriptional-translational negative feedback loop at the heart of the timing mechanism, with kinases playing a key role in setting up the speed of the clock.
The Larrondo Lab is interested in different aspects of gene expression. In particular, we study the molecular mechanisms underlying biological oscillators, assessing the impact that circadian clocks have on physiology and in host-pathogen interactions.
Currently, we study various fungal systems to try to understand some of these processes: the filamentous fungus Neurospora crassa, the phytopathogen Botrytis cinerea, the biocontroller Trichoderma atroviride and the yeast Saccharomyces cerevisiae.
Lately, through both optogenetics and synthetic biology approaches, we are additionally exploring the design of new oscillatory circuits capable of starting and sustaining circadian rhythms, while also developing new tools to implement complex circuits to reprogram gene expression.
Lately, through both optogenetics and synthetic biology approaches, we are additionally exploring the design of new oscillatory circuits capable of starting and sustaining circadian rhythms, while also developing new tools to implement complex circuits to reprogram gene expression.
The Neurospora circadian clock: an overview
The Neurospora circadian oscillator is based on a transcriptional/translational negative feedback loop (TTFL) that relies on the negative element FREQUENCY (FRQ). frq expression is under the control of the positive element, the WCC transcriptional complex, which is composed by the GATA type transcription factors (TFs) White Collar 1 (WC-1, which is also a blue light receptor) and White Collar 2 (WC-2). Under constant darkness (DD) WCC binds to the clock-box (c-box), a cis-element within the frq promoter that is both necessary and sufficient for frq rhythmic expression. In the presence of light, the stoichiometry of the WCC changes, which alters its DNA recognition patterns, which results in the WCC binding a different cis-sequence in the frq promoter -the proximal light regulatory element, pLRE-, increasing frq expression and allowing entrainment of the clock to environmental light (summarized in Montenegro-Montero et al., 2015).
The Neurospora circadian oscillator is based on a transcriptional/translational negative feedback loop (TTFL) that relies on the negative element FREQUENCY (FRQ). frq expression is under the control of the positive element, the WCC transcriptional complex, which is composed by the GATA type transcription factors (TFs) White Collar 1 (WC-1, which is also a blue light receptor) and White Collar 2 (WC-2). Under constant darkness (DD) WCC binds to the clock-box (c-box), a cis-element within the frq promoter that is both necessary and sufficient for frq rhythmic expression. In the presence of light, the stoichiometry of the WCC changes, which alters its DNA recognition patterns, which results in the WCC binding a different cis-sequence in the frq promoter -the proximal light regulatory element, pLRE-, increasing frq expression and allowing entrainment of the clock to environmental light (summarized in Montenegro-Montero et al., 2015).
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When FRQ is produced, it associates with FRH, a RNA-helicase, and this complex blocks the activity of the WCC, thus creating a negative feedback loop (that’s why FRQ is called the negative element of the clock). Shortly after its synthesis, FRQ is progressively phosphorylated up until the point in which its ability to repress the WCC is lost and FRQ eventually becomes degraded via the proteosome. Each cycle of this TTFL takes about 22.5 hours, which can be observed as daily oscillations of frq and FRQ levels and as rhythmic gene expression of 10-40% of its transcriptome, impacting, for instance, metabolism and leading to overt rhythms in conidiation. These rhythms can easily be tracked through a phenotypic assay based on “race tubes”, which allows visualization of daily rhythms in conidia production (visible as “bands” of spores, see figure on the right).
Additional information on the Neurospora circadian clock, a field that encompasses the work of several labs for over 25 years, can be found in Montenegro-Montero et al. (2015) and references therein. |
From Montenegro-Montero A & Larrondo LF (2013). The Neurospora Circadian System: From Genes to Proteins and Back in Less Than 24 hours, in Neurospora: Genomics and Molecular Biology.
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Current Projects
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I. Neurospora clock mechanisms
An important advancement in the past years has been the use of luciferase-based real-time reporters to monitor circadian gene expression in Neurospora (Gooch et al., 2008). This, together with the ease of modifying loci at will through allele replacement strategies (Larrondo et al., 2009), has allowed to further track FRQ dynamics with high spatial and temporal resolution (Larrondo et al., 2012). With such tools, we have been able to redefine some long-standing paradigms regarding period determination and FRQ stability, showing that FRQ posttranslational modifications (the quality of FRQ) rather than its quantity and degradation is crucial for determining period length (Larrondo et al., 2015; Montenegro-Montero et al., 2015). |
From Larondo et al., (2015). Circadian rhythms. Decoupling circadian clock protein turnover from circadian period determination.
Science. 347(6221):1257277 |
In addition, our results have highlighted the role of the co-repressor RCO-1 as a modulator of amplitude, period and metabolic compensation (Olivares-Yañez et al., 2016).
We are also interested in other aspects of circadian regulation in Neurospora, such as the cross-talk between metabolism and clock regulation and its effect on cellulose degradation (Díaz-Choque R, Ph.D. thesis, 2016). We have also studied the role of second messengers and the effect of several drugs on clock dynamics (Alessandri P, B.Sc. thesis 2015), together with actively examining the role of diverse transcription factors in regulating not only core-clock function, but also circadian output pathways, that is, the different circuits and mechanisms through which the clock controls rhythms in a variety of processes in Neurospora. Whether the Neurospora clock regulates rhythmic gene expression mainly at the level of transcription or at the post-transcriptional level, is still a matter of debate (Montenegro-Montero & Larrondo 2016; Montenegro-Montero et al. 2015)
Our general interest in gene regulation in Neurospora have additionally led us to be a part of a major effort aimed at understanding overall transcription factor specificity in eukaryotes (Weirauch et al., 2014).
We are also interested in other aspects of circadian regulation in Neurospora, such as the cross-talk between metabolism and clock regulation and its effect on cellulose degradation (Díaz-Choque R, Ph.D. thesis, 2016). We have also studied the role of second messengers and the effect of several drugs on clock dynamics (Alessandri P, B.Sc. thesis 2015), together with actively examining the role of diverse transcription factors in regulating not only core-clock function, but also circadian output pathways, that is, the different circuits and mechanisms through which the clock controls rhythms in a variety of processes in Neurospora. Whether the Neurospora clock regulates rhythmic gene expression mainly at the level of transcription or at the post-transcriptional level, is still a matter of debate (Montenegro-Montero & Larrondo 2016; Montenegro-Montero et al. 2015)
Our general interest in gene regulation in Neurospora have additionally led us to be a part of a major effort aimed at understanding overall transcription factor specificity in eukaryotes (Weirauch et al., 2014).
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II. Fungal Clocks, Light and Virulence
The circadian clock of the model plant Arabidopsis thaliana modulates defense mechanisms, which impact plant-pathogen interaction dynamics. The effect of the time of day on the virulence of plant pathogenic fungi on the other hand, has not been explored in detail and moreover, molecular description of clocks in fungi other than Neurospora had not been reported. We therefore first focused on characterizing the circadian system of the plant pathogen Botrytis cinerea, one of the most scientifically/economically important fungal pathogens. We have shown the existence of a functional clock in B. cinerea, which shares similar components and circuitry with the Neurospora circadian system (Hevia et al., 2015). Notably, we have additionally described how circadian regulation affects the pathogenic potential in this fungus (Hevia et al., 2015; Hevia et al., 2016), such that the time of the day at which the first interaction between Botrytis and a plant (A. thaliana) occurs, defines the outcome of the interaction: bigger lesions are observed when the fungus interacts at dusk, compared to dawn. |
From Hevia et al. (2015). Circadian clocks and the regulation of virulence in fungi: Getting up to speed. Semin Cell Dev Biol. 57:147-55.
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Unexpectedly, our Botrytis data show novel, extra-circadian functions for the conserved clock protein FRQ, something that we are actively pursuing (Muller-Esparza H, B. Sc. thesis 2015; Hevia et al., 2016). Moreover, as light is a key environmental cue that allows clock entrainment, we have become interested in different aspects of fungal photobiology and reported for instance, that light perception can modulate B. cinerea virulence (Canessa et al., 2013).
We are also interested in how environmental conditions shape the interaction between B. cinerea and the biocontroller T. atroviride, research that we are developing as part of an international collaboration.
We are also interested in how environmental conditions shape the interaction between B. cinerea and the biocontroller T. atroviride, research that we are developing as part of an international collaboration.
III. Plant Cell Wall Deconstruction
We have participated in various fungal genome projects and we have been actively involved in the genome annotation of several fungi capable of lignin and cellulose degradation (Fernandez-Fueyo et al., 2012; Floudas et al., 2012; Hori et al., 2014)
In addition to these computational efforts, we have studied specific transcription factors (TFs) and environmental conditions modulating some of these processes, for instance, a URSB1/SRE-1 type TF and iron availability (Canessa et al., 2012; Canessa and Larrondo, 2013).
We have additionally described that in N. crassa, the bZIP TF HAC-1 is involved in the unfolded protein response, and that this protein, and the ability to properly activate UPR, is key in allowing growth on media containing cellulose as the sole carbon source, unveiling new aspects of the degradation of this relevant plant cell-wall component (Montenegro-Montero et al., 2015).
As mentioned earlier, we are also actively assessing the effect that clock-regulation has on the ability of Neurospora to degrade cellulose (Díaz-Choque R, Ph.D. Thesis 2016).
We have participated in various fungal genome projects and we have been actively involved in the genome annotation of several fungi capable of lignin and cellulose degradation (Fernandez-Fueyo et al., 2012; Floudas et al., 2012; Hori et al., 2014)
In addition to these computational efforts, we have studied specific transcription factors (TFs) and environmental conditions modulating some of these processes, for instance, a URSB1/SRE-1 type TF and iron availability (Canessa et al., 2012; Canessa and Larrondo, 2013).
We have additionally described that in N. crassa, the bZIP TF HAC-1 is involved in the unfolded protein response, and that this protein, and the ability to properly activate UPR, is key in allowing growth on media containing cellulose as the sole carbon source, unveiling new aspects of the degradation of this relevant plant cell-wall component (Montenegro-Montero et al., 2015).
As mentioned earlier, we are also actively assessing the effect that clock-regulation has on the ability of Neurospora to degrade cellulose (Díaz-Choque R, Ph.D. Thesis 2016).
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IV. Optogenetics and Synthetic Biology
Together with synbio approaches aimed at modifying the Neurospora circadian system, we are also interested in designing and implementing additional circuits in both Neurospora and in S. cerevisiae. We have been involved in several projects, including the development of optogenetic tools in yeast (Salinas et al., 2018; Salinas et al., 2017) , aimed at the dissection of basic cellular processes as well as at improving biotechnologically relevant properties (Rojas V, Bs.c Thesis 2016). Some of our research, such as the “Live Canvas” project, lays at the interphase between fundamental science and art. Stay tuned to learn more about this and other ongoing projects. |
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