bioRxiv Science⌕ Search

Biology subjects

Maalouf, A.

Publications and source records attributed to Maalouf, A..

2 recordsLinked to original sources

Network modularity reveals context and state-dependent reorganization of time-varying functional connectivity in single-cell resolved neural activity recordings

An important goal of neuroscience is to understand how biological neural networks organize activity at multiple scales to enable complex information processing and behavioral output. To address this challenge, large-scale neural activity datasets with increased resolution and wider coverage have become more prevalent across many model systems. However, bridging the gap in scale between changes in pairwise functional connectivity between neurons and changes in brain-wide organization of activity remains a key challenge. In this work, we demonstrate application of modularity-based community detection and network modularity to single-cell resolved recordings, for the first time, as a method to summarize complex changes in time-varying functional connectivity, facilitating comparisons across multiple time windows, recordings, and conditions. We apply these methods to both single-cell resolved multi-cell and whole-brain activity recordings. In the multi-cell recordings, we find that food odor changes functional connectivity between existing network modules in a C. elegans locomotory interneuron network, rather than reorganizing them. In spontaneous whole-brain activity, we identify several key hub neurons and combinations that significantly destabilize module assignments when silenced. Together, these results demonstrate community detection and modularity as a method for detecting context and network state-dependent changes in functional connectivity at the intermediate scale of network modules in single-cell resolved neural activity. Results from these analyses facilitate future investigation of mechanisms that mediate organization of neural activity at intermediate scales.

neuroscience↗

Dual Probe Ligation In Situ Hybridization with Rolling-Circle Amplification for High-Plex Spatial Transcriptomics

New biological insights are increasingly dependent upon a deeper understanding of tissue architectures. Critical to such studies are spatial transcriptomics technologies, especially those amenable to analysis of the most widely available human tissue type, formalin-fixed and paraffin-embedded (FFPE) clinical specimens. Here we build on our previous oligonucleotide probe ligation-based approach to accurately analyze FFPE mRNA, which suffers from variable levels of degradation. Ligation In Situ Hybridization followed by rolling circle amplification (LISH-LocknRoll or LISH-LnR), provides a streamlined method to detect the spatial location of specific mRNA isoforms within FFPE tissue architectures. Iterative fluorescent probe hybridization and imaging enables highly multiplexed spatial transcriptomic studies, as demonstrated herein for fixed specimens from inclusion body myositis patients and pediatric rhabdomyosarcoma patients. We additionally demonstrate a system of molecular rheostats that can be used to fine tune the performance of the LISH-LnR assay. Combined with LISH-seq and LISH-QC, the LISH-LnR methodology provides a powerful approach to spatial transcriptomics.

molecular biology↗