bioRxiv Science⌕ Search

Biology subjects

Friedlander, T.

Publications and source records attributed to Friedlander, T..

7 recordsLinked to original sources

Volatile but persistent co-existence of self-compatibility and self-incompatibility in plants

Plants employ diverse mating strategies, including self- and cross-fertilization or their combination. Despite the ubiquity of mixed mating - the use of both self- and cross-fertilization within the same population - its evolutionary origins and dynamic stability remain elusive. Here, we study self-incompatibility, in which self-fertilization is disabled by molecular recognition and enabled when mutations disrupt this recognition. Using population-level stochastic simulations, we model the effects of two main parameters on the prevailing mating mode: promiscuity of molecular recognition and inbreeding depression, which penalizes self-compatibility. We reveal a phase diagram with three phases: complete self-incompatibility, complete self-compatibility, and a mixture combining both. The mixed phase exhibits newly-described vigorous, non-decaying fluctuations in the proportions of individuals occupying either mating mode. Pollen limitation extends the parameter range over which complete self-incompatibility is favored, contrary to the commonly held view. This study offers new insight into the evolutionary dynamics of plant reproductive systems.

evolutionary biology↗

Reconciling conflicting selection pressures in the plant collaborative non-self recognition self-incompatibility system

Complex biological systems should often reconcile conflicting selection pressures. In systems based on molecular recognition, molecules must specifically identify certain partners while excluding others. Here we study how such selection pressures shape the evolution of the self-incompatibility system in plants. This system inhibits self-fertilization using specific molecular recognition between proteins, expressed in the plant female and male reproductive organs. We study the impact of these opposing selection pressures on the amino acid frequencies in these proteins recognition domain. We construct a theoretical framework enabling promiscuous recognition between proteins, as found empirically, and employ stochastic simulations to study its evolution. We find that selection exerts asymmetric responses of amino acid frequencies, affecting female proteins considerably, but hardly the male. Using large deviations theory, we well-approximate the simulated frequencies and find agreement with genomic data. Our work offers a general theoretical framework to study the impact of multiple selection pressures, applicable to additional biological systems.

genetics↗

Olive Flowering dependence on winter temperatures - linking empirical results to a dynamic model

Increasing winter temperatures jeopardize the yield of fruit trees requiring a prolonged and sufficiently cold winter to flower. Assessing the exact risk to different crop varieties is the first step in mitigating the harmful effect of climate change. Since empirically testing the impacts of many temperature scenarios is very time-consuming, quantitative predictive models could be extremely helpful in reducing the number of experiments needed. Here, we focus on olive (Olea europaea) - a traditional crop in the Mediterranean basin, a region expected to be severely affected by climatic change. Olive flowering and consequently yield depend on the sufficiency of cold periods and the lack of warm ones during the preceding winter. Yet, a satisfactory quantitative model forecasting its expected flowering under natural temperature conditions is still lacking. Previous models simply summed the number of cold hours during winter, as a proxy for flowering, but exhibited only mediocre agreement with empirical flowering values, possibly because they overlooked the order of occurrence of different temperatures. We empirically tested the effect of different temperature regimes on olive flowering intensity and flowering-gene expression. To predict flowering based on winter temperatures, we constructed a dynamic model, describing the response of a putative flowering factor to the temperature signal. The crucial ingredient in the model is an unstable intermediate, produced and degraded at temperature-dependent rates. Our model accounts not only for the number of cold and warm hours but also for their order. We used sets of empirical flowering and temperature data to fit the model parameters, applying numerical constrained optimization techniques, and successfully validated the model outcomes. Our model more accurately predicts flowering under winters with warm periods yielding low-to-moderate flowering and is more robust compared to previous models. This model is the first step toward a practical predictive tool, applicable under various temperature conditions.

plant biology↗

The role of promiscuous molecular recognition in the evolution of RNase-based self-incompatibility

How do biological networks evolve and expand and which parameters determine their size? We study these questions in the context of the plant collaborative-non-self recognition self-incompatibility system. Self-incompatibility evolved to avoid self-fertilization among hermaphroditic plants. It relies on specific molecular recognition between highly diverse proteins of two families: female and male determinants, such that the combination of alleles an individual possesses determines its mating partners. Though highly diverse, previous models struggled to pinpoint the evolutionary trajectories by which new alleles evolved. Here, we construct a novel theoretical frame-work, that crucially affords interaction promiscuity and multiple distinct partners per protein, empirical findings disregarded by previous models. We demonstrate a dynamic long-term balance between allele emergence and extinction, where their equilibrium number depends on population parameters. Our work highlights the importance of molecular recognition promiscuity to network evolvability. Promiscuity was found in additional systems suggesting that our framework could be more broadly applicable.

evolutionary biology↗

Fitness landscape analysis reveals that the wild type allele is sub-optimal and mutationally robust

Fitness landscape mapping and the prediction of evolutionary trajectories on these landscapes are major tasks in evolutionary biology research. Evolutionary dynamics is tightly linked to the landscape topography, but this relation is not straightforward. Here, we analyze a fitness landscape of a yeast tRNA gene, previously measured under four different conditions. We find that the wild type allele is sub-optimal, and 8%-10% of its variants are fitter. We rule out the possibilities that the wild type is fittest on average on multiple conditions or located on a local fitness maximum. Instead, we find that the wild type is mutationally robust ( flat), while more fit variants are typically mutationally fragile. Similar observations of mutational robustness or flatness have been so far made in very few cases, predominantly in viral genomes.

evolutionary biology↗

Cell-free DNA as a biomarker for prostate cancer: elevated concentration and decreased fragment size

PurposeProstate cancer is the most commonly diagnosed neoplasm in American men. Although existing biomarkers may detect localized prostate cancer, additional strategies are necessary for improving detection and identifying aggressive disease that may require further intervention. One promising, minimally invasive biomarker is cell-free DNA (cfDNA), which consist of short DNA fragments released into circulation by dying or lysed cells that may reflect underlying cancer. Here we investigated whether differences in cfDNA concentration and cfDNA fragment size could improve the sensitivity for detecting more advanced and aggressive prostate cancer. Materials and MethodsThis study included 268 individuals: 34 healthy controls, 112 men with localized prostate cancer who underwent radical prostatectomy (RP), and 122 men with metastatic castration-resistant prostate cancer (mCRPC). Plasma cfDNA concentration and fragment size were quantified with the Qubit 3.0 and the 2100 Bioanalyzer. The potential relationship between cfDNA concentration or fragment size and localized or mCRPC prostate cancer was evaluated with descriptive statistics, logistic regression, and area under the curve analysis with cross-validation. ResultsPlasma cfDNA concentrations were elevated in mCRPC patients in comparison to localized disease (OR5 ng/mL = 1.34, P = 0.027) or to being a control (OR5 ng/mL = 1.69, P = 0.034). Decreased average fragment size was associated with an increased risk of localized disease compared to controls (OR5bp = 0.77, P = 0.0008). ConclusionThis study suggests that cfDNA concentration and average cfDNA fragment size may provide a quick, cost-effective approach to help determine which patients will benefit most from further screening and/or disease monitoring to help improve prostate cancer outcomes.

cancer biology↗

Transcriptional crosstalk varies between regulatory strategies

Genes differ in the frequency at which they are expressed and in the form of regulation used to control their activity. In particular, positive or negative regulation can lead to activation of a gene in response to an external signal. Previous works proposed that the form of regulation of a gene correlates with its frequency of usage: positive regulation when the gene is frequently expressed and negative regulation when infrequently expressed. Such network design means that, in the absence of their regulators, the genes are found in their least required activity state, hence regulatory intervention is often necessary. Due to the multitude of genes and regulators, spurious binding and unbinding events, called \"crosstalk\", could occur. To determine how the form of regulation affects the global crosstalk in the network, we used a mathematical model that includes multiple regulators and multiple target genes. We found that crosstalk depends non-monotonically on the availability of regulators. Our analysis showed that excess use of regulation entailed by the formerly suggested network design caused high crosstalk levels in a large part of the parameter space. We therefore considered the opposite idle design, where the default unregulated state of genes is their frequently required activity state. We found, that idle design minimized the use of regulation and thus minimized crosstalk. In addition, we estimated global crosstalk of S. cerevisiae using transcription factors binding data. We demonstrated that even partial network data could suffice to estimate its global crosstalk, suggesting its applicability to additional organisms. We found that S. cerevisiae estimated crosstalk is lower than that of a random network, suggesting that natural selection reduces crosstalk. In summary, our study highlights a new type of protein production cost which is typically overlooked: that of regulatory interference caused by the presence of excess regulators in the cell. It demonstrates the importance of whole-network descriptions, which could show effects missed by single-gene models.\n\nAuthor SummaryGenes differ in the frequency at which they are expressed and in the form of regulation used to control their activity. The basic level of regulation is mediated by different types of DNA-binding proteins, where each type regulates particular gene(s). We distinguish between two basic forms of regulation: positive - if a gene is activated by the binding of its regulatory protein, and negative - if it is active unless bound by its regulatory protein. Due to the multitude of genes and regulators, spurious binding and unbinding events, called \"crosstalk\", could occur. How does the form of regulation, positive or negative, affect the extent of regulatory crosstalk? To address this question, we used a mathematical model integrating many genes and many regulators. As intuition suggests, we found that in most of the parameter space, crosstalk increased with the availability of regulators. We propose, that crosstalk is usually reduced when networks are designed such that minimal regulation is needed, which we call the idle design. In other words: a frequently needed gene will use negative regulation and conversely, a scarcely needed gene will employ positive regulation. In both cases, the requirement for the regulators is minimized. In addition, we demonstrate how crosstalk can be calculated from available datasets and discuss the technical challenges in such calculation, specifically data incompleteness.

systems biology↗