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Sando, S. R.

Publications and source records attributed to Sando, S. R..

2 recordsLinked to original sources

Transcriptional landscape of a hypoxia response identifies cell-specific pathways for adaptation

Hypoxia (low oxygen) activates diverse cellular responses driven primarily by a single transcription factor, the hypoxia-inducible factor HIF-1. Here we identify at single-cell resolution HIF-1-dependent transcriptional responses in neuronal, intestinal, and muscle tissues of the nematode Caenorhabditis elegans. We report that while all three tissues share HIF-1-dependent modulation of pathways for central-carbon metabolism, individual tissues and specific cell subtypes exhibit broader transcriptional responses that differ extensively among cellular contexts. Using supervised machine learning to provide a deeper multivariate analysis, we observed that genotype-defined HIF-1 activation states were distinguishable within each tissue and that the highest-ranked predictive genes varied substantially among tissues. The differential-expression and machine-learning analyses together revealed a hierarchical contextualization of HIF-1-dependent transcriptomes: in response to HIF-1 activation, different tissues express distinct transcriptional programs, and cell subtypes within each tissue express further distinct programs. We validated representative tissue- and cell-type-specific responses in vivo and demonstrated that a gene that is HIF-1-responsive in a specific muscle cell subtype functions in that cell type to regulate HIF-1-driven hypersensitivity to the cholinergic agonist levamisole. Overall, our findings provide a systems-level view of HIF-1 activity and show that a broadly expressed transcription factor can generate both a shared core response and diverse context-dependent transcriptional programs.

genetics↗

An Hourglass Circuit Motif Transforms a Motor Program via Subcellularly Localized Calcium Signaling in Muscle

Neural control of muscle function is fundamental to animal behavior. Many muscles can generate multiple distinct behaviors. Nonetheless, individual muscle cells are generally regarded as the smallest units of motor control. We report that muscle cells can alter behavior by contracting subcellularly. We previously discovered that noxious tastes reverse the net flow of particles through the C. elegans pharynx, a neuromuscular pump, resulting in spitting. We now show that spitting results from the subcellular contraction of the anterior region of the pm3 muscle cell. Subcellularly localized calcium increases accompany this contraction. Spitting is controlled by an "hourglass" circuit motif: parallel neural pathways converge onto a single motor neuron that differentially controls multiple muscles and the critical subcellular muscle compartment. We conclude that subcellular muscle units enable modulatory motor control and propose that subcellular muscle contraction is a fundamental mechanism by which neurons can reshape behavior.

neuroscience↗