High-resolution temporal profiling of E. coli transcriptional response.
Arianna MianoKevin RychelAndrew LeziaAnand SastryBernhard PalssonJeff HastyPublished in: Nature communications (2023)
Understanding how cells dynamically adapt to their environment is a primary focus of biology research. Temporal information about cellular behavior is often limited by both small numbers of data time-points and the methods used to analyze this data. Here, we apply unsupervised machine learning to a data set containing the activity of 1805 native promoters in E. coli measured every 10 minutes in a high-throughput microfluidic device via fluorescence time-lapse microscopy. Specifically, this data set reveals E. coli transcriptome dynamics when exposed to different heavy metal ions. We use a bioinformatics pipeline based on Independent Component Analysis (ICA) to generate insights and hypotheses from this data. We discovered three primary, time-dependent stages of promoter activation to heavy metal stress (fast, intermediate, and steady). Furthermore, we uncovered a global strategy E. coli uses to reallocate resources from stress-related promoters to growth-related promoters following exposure to heavy metal stress.
Keyphrases
- heavy metals
- high throughput
- machine learning
- electronic health record
- big data
- escherichia coli
- high resolution
- single cell
- gene expression
- transcription factor
- risk assessment
- healthcare
- dna methylation
- health risk assessment
- artificial intelligence
- cell death
- heat stress
- genome wide
- circulating tumor cells
- signaling pathway
- cell cycle arrest
- pi k akt
- heat shock protein
- heat shock
- liquid chromatography