Microbes residing in cryoconite holes (debris, water, and nutrient-rich ecosystems) on the glacier surface actively participate in carbon and nutrient cycling. Not much is known about how these communities and their functions change during the summer melt-season when intense ablation and runoff alter the influx and outflux of nutrients and microbes. Here, we use high-throughput-amplicon sequencing, predictive metabolic tools and Phenotype MicroArray techniques to track changes in bacterial communities and functions in cryoconite holes in a coastal Antarctic site and the surrounding fjord, during the summer season. The bacterial diversity in cryoconite hole meltwater was predominantly composed of heterotrophs (Proteobacteria) throughout the season. The associated functional potentials were related to heterotrophic-assimilatory and -dissimilatory pathways. Autotrophic Cyanobacterial lineages dominated the debris community at the beginning and end of summer, while heterotrophic Bacteroidota- and Proteobacteria-related phyla increased during the peak melt period. Predictive functional analyses based on taxonomy show a shift from predominantly phototrophy-related functions to heterotrophic assimilatory pathways as the melt-season progressed. This shift from autotrophic to heterotrophic communities within cryoconite holes can affect carbon drawdown and nutrient liberation from the glacier surface during the summer. In addition, the flushing out and export of cryoconite hole communities to the fjord could influence the biogeochemical dynamics of the fjord ecosystem.
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The functional and optimal expression of genes is crucial
for survival of all living organisms. Numerous experiments
and efforts have been performed to reveal the mechanisms
required for the functional and optimal expression of human
genes. The yeast Saccharomyces cerevisiae has evolved
independently of humans for billions of years. Nevertheless,
S. cerevisiae has many conserved genes and expression mechanisms
that are similar to those in humans. Yeast is the most
commonly used model organism for studying the function
and expression mechanisms of human genes because it has
a relatively simple genome structure, which is easy to manipulate.
Many previous studies have focused on understanding
the functions and mechanisms of human proteins using
orthologous genes and biological systems of yeast. In this
review, we mainly introduce two recent studies that replaced
human genes and nucleosomes with those of yeast. Here, we
suggest that, although yeast is a relatively small eukaryotic
cell, its humanization is useful for the direct study of human
proteins. In addition, yeast can be used as a model organism
in a broader range of studies, including drug screening.
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