Biology subjects

Pinsky, M.

Publications and source records attributed to Pinsky, M..

6 recordsLinked to original sources

bioRxiv2025

Causal modelling reveals lower coral genetic diversity in more heterogenous reef environments

Conserving genetic diversity is crucial for maintaining species evolutionary potential and resilience to environmental change. Yet, directly measuring genetic diversity across large spatial scales remains resource-intensive and impractical for conservation planning. Identifying reliable, accessible, and cost-effective spatial predictors of genetic diversity would significantly enhance our ability to incorporate genetic diversity into conservation efforts. Caribbean coral reefs represent a compelling system for investigating such predictors, as these ecosystems face unprecedented threats from disease outbreaks and climate change. Here, we investigate the utility of several environmental proxies as surrogates for genetic diversity, which may be useful for conservation planning in resource- or data-poor regions. To achieve this goal, we used reduced-representation genomic sequencing to estimate intraspecific genetic diversity, and in doing so, identified two genetically distinct and sympatric cryptic coral species in the Agaricia tenuifolia species complex. We employed a causal inference approach to assess the relationships between genetic alpha diversity and habitat area and connectivity, habitat heterogeneity, and temperature. Statistical investigations revealed that increased habitat heterogeneity, derived from remotely sensed habitat maps, was associated with lower genetic diversity within coral populations, suggesting that habitat characteristics promoting species diversity may not maintain high genetic diversity within a single species. Habitat area and connectivity, and temperature have predominantly negative effects on genetic diversity with coral habitat area and connectivity showing markedly contrasting responses in two cryptic taxa. Thus, our findings reveal that context matters greatly, as results differ between cryptic species, across variables, and among spatial scales.

evolutionary biology↗

bioRxiv2024

Marine spatial planning to enhance coral adaptive potential

Ocean warming interacts with local stressors to negatively affect coral reefs. The adaptive capacity of reefs to survive these stressors is driven by ecological and evolutionary processes occurring at multiple spatial scales. Marine protected area (MPA) networks are one solution that can address both local and regional threats, yet the impacts of MPA network design on adaptive processes remains unclear. In this paper, we used an eco-evolutionary model to simulate hypothetical MPA configurations in the Caribbean, Southwest Pacific and Coral Triangle under projected warming. We found that protecting thermal refugia (i.e., cooler reefs) largely benefited corals inside the refugia while other reefs declined. In contrast, protecting a diverse habitat portfolio led to increased coral cover both inside and outside of the MPA network. We then quantified the thermal habitat and connectivity representations of reefs both inside and outside existing MPA networks across each region. Most strikingly, reefs in current MPA networks in the Southwest Pacific and Coral Triangle are approximately 2 {degrees}C cooler than reefs outside the MPA networks, while the Caribbeans MPA network is approximately 1 {degrees}C warmer than reefs outside the network, based on mean temperatures from 2008-2018. These results suggest that the Caribbean MPA network is poised to protect sources of warm-adapted larvae but not destinations, and the opposite is true of the Southwest Pacific and Coral Triangle. Our results suggest that 1) by protecting sites with particular temperature and connectivity characteristics, marine spatial planning may alter eco-evolutionary processes to enhance or inhibit the adaptive capacity of a reef network and 2) the distribution, extent, and effectiveness of local interventions have the potential to affect regional distributions of coral cover beyond what would be expected from local benefits alone, due to the potentially wide-reaching effects of larval dispersal and gene flow.

ecology↗

bioRxiv2022

Regulation of heme utilization and homeostasis in Candida albicans

Heme (iron-protoporphyrin IX) is an essential but potentially toxic cellular cofactor. While most organisms are heme prototrophs, many microorganisms can utilize environmental heme as iron source. The pathogenic yeast Candida albicans can utilize host heme in the iron-poor host environment, using an extracellular cascade of soluble anchored hemophores, and plasma membrane ferric reductase-like proteins. To gain additional insight into the C. albicans heme uptake pathway, we performed an unbiased genetic selection for mutants resistant to the toxic heme analog Ga3+-protoporphyrin IX at neutral pH, and a secondary screen for inability to utilize heme as iron source. Among the mutants isolated were the genes of the pH-responsive RIM pathway, and a zinc finger transcription factor, HUF1. In the presence of hemin in the medium, HUF1 is induced, the Huf1 protein is stabilized and Huf1-GFP localizes to the nucleus. In the huf1 mutant, cytoplasmic heme levels are elevated, while influx of extracellular heme is lower. Gene expression analysis indicated that in the presence of extracellular hemin, Huf1 activates the heme oxygenase HMX1, which breaks down excess cytoplasmic heme, while at the same time it also activates all the known heme uptake genes. These results indicate that Huf1 is a heme-responsive transcription factor that plays a role both in cytoplasmic heme homeostasis and in utilization of extracellular heme. The induction of heme uptake genes by Huf1 under iron satiety indicates that preferential utilization of host heme can be a dietary strategy in a heme prototroph.

microbiology↗

bioRxiv2022

Ferric reductase-related proteins mediate fungal heme acquisition

Heme can serve as iron source in many environments, including the iron-poor animal host environment. The fungal pathobiont Candida albicans expresses a family of extracellular CFEM hemophores that capture heme from host proteins and transfer it across the cell wall to the cell membrane, to be endocytosed and utilized as heme or iron source. Here we identified Frp1 and Frp2, two ferric reductase (FRE)-related proteins that lack an extracellular N-terminal substrate-binding domain, as being required for hemoglobin heme utilization and for sensitivity to toxic heme analogs. Frp1/2 redistribute from the ER to the plasma membrane in the presence of hemoglobin, consistent with a direct role in heme trafficking. Expression of Frp1 with the CFEM hemophore Pga7 can promote heme utilization in Saccharomyces cerevisiae as well, confirming the functional interaction between these proteins. Sequence and structure comparison reveals that the CFEM hemophores are related to the FRE substrate-binding domain that is missing in Frp1/2. We conclude that Frp1/2 and the CFEM hemophores form a functional complex that evolved from ferric reductases to enable extracellular heme uptake.

microbiology↗

bioRxiv2020

Using genetically encoded heme sensors to probe the mechanisms of heme uptake and homeostasis in Candida albicans

Candida albicans is a major fungal pathogen that can utilize hemin and hemoglobin as iron sources in the iron-scarce host environment. While C. albicans is a heme prototroph, we show here that it can also efficiently utilize external heme as a cellular heme source. Using genetically encoded ratiometric fluorescent heme sensors, we show that heme extracted from hemoglobin and free hemin enter the cells with different kinetics. Heme supplied as hemoglobin is taken up via the CFEM (Common in Fungal Extracellular Membrane) hemophore cascade, and reaches the cytoplasm over several hours, whereas entry of free hemin via CFEM-dependent and independent pathways is much faster, less than an hour. To prevent an influx of extracellular heme from reaching toxic levels in the cytoplasm, the cells deploy Hmx1, a heme oxygenase. Hmx1 was previously suggested to be involved in utilization of hemoglobin and hemin as iron sources, but we find that it is primarily required to prevent heme toxicity. Taken together, the combination of novel heme sensors with genetic analysis revealed new details of the fungal mechanisms of heme import and homeostasis, necessary to balance the uses of heme as essential cofactor and potential iron source against its toxicity.

microbiology↗

bioRxiv2018

Genomic signatures of evolutionary rescue in bats surviving white-nose syndrome

Rapid evolution of advantageous traits following abrupt environmental change can help populations grow and avoid extinction through evolutionary rescue. Here, we provide the first genetic evidence for rapid evolution in bat populations affected by white-nose syndrome (WNS). By comparing genetic samples from before and after little brown bat populations were decimated by WNS, we identified signatures of soft selection on standing genetic variation. This selection occurred at multiple loci in genes linked to hibernation behavior rather than immune function, suggesting that differences in hibernation strategy have allowed these bats to survive infection with WNS. Through these findings, we suggest that evolutionary rescue can be a conservationrelevant process even in slowly reproducing taxa threatened with extinction.

evolutionary biology↗