AI Article Synopsis

  • Recent advancements in transcriptional profiling are identifying new cell types and markers quickly, with single cell RNA sequencing being a popular method for analyzing diverse cell types.
  • The newly developed Probe-Seq technique enhances this by isolating specific cell populations based on RNA characteristics using fluorescent labeling and sorting.
  • This method works with preserved samples and allows for the simultaneous profiling of multiple cell types, making it versatile for various organisms.

Article Abstract

Recent transcriptional profiling technologies are uncovering previously-undefined cell populations and molecular markers at an unprecedented pace. While single cell RNA (scRNA) sequencing is an attractive approach for unbiased transcriptional profiling of all cell types, a complementary method to isolate and sequence specific cell populations from heterogeneous tissue remains challenging. Here, we developed Probe-Seq, which allows deep transcriptional profiling of specific cell types isolated using RNA as the defining feature. Dissociated cells are labeled using fluorescent in situ hybridization (FISH) for RNA, and then isolated by fluorescent activated cell sorting (FACS). We used Probe-Seq to purify and profile specific cell types from mouse, human, and chick retinas, as well as from midguts. Probe-Seq is compatible with frozen nuclei, making cell types within archival tissue immediately accessible. As it can be multiplexed, combinations of markers can be used to create specificity. Multiplexing also allows for the isolation of multiple cell types from one cell preparation. Probe-Seq should enable RNA profiling of specific cell types from any organism.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6901332PMC
http://dx.doi.org/10.7554/eLife.51452DOI Listing

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