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Gene Families With Stochastic Exclusive Gene Choice Underlie Cell Adhesion in Mammalian Cells
JournalArticle (Originalarbeit in einer wissenschaftlichen Zeitschrift)
 
ID 4619690
Author(s) Iakovlev, Mikhail; Faravelli, Simone; Becskei, Attila
Author(s) at UniBasel Becskei, Attila
Faravelli, Simone
Iakovlev, Mikhail
Year 2021
Title Gene Families With Stochastic Exclusive Gene Choice Underlie Cell Adhesion in Mammalian Cells
Journal Frontiers in Cell and Developmental Biology
Volume 9
Pages / Article-Number 642212
Keywords Poisson-binomial distribution; allelic exclusion; basigin; carbonic anhydrase; cell identity; mouse; olfactory receptor; single-cell RNA-seq
Abstract Exclusive stochastic gene choice combines precision with diversity. This regulation enables most T-cells to express exactly one T-cell receptor isoform chosen from a large repertoire, and to react precisely against diverse antigens. Some cells express two receptor isoforms, revealing the stochastic nature of this process. A similar regulation of odorant receptors and protocadherins enable cells to recognize odors and confer individuality to cells in neuronal interaction networks, respectively. We explored whether genes in other families are expressed exclusively by analyzing single-cell RNA-seq data with a simple metric. This metric can detect exclusivity independently of the mean value and the monoallelic nature of gene expression. Chromosomal segments and gene families are more likely to express genes concurrently than exclusively, possibly due to the evolutionary and biophysical aspects of shared regulation. Nonetheless, gene families with exclusive gene choice were detected in multiple cell types, most of them are membrane proteins involved in ion transport and cell adhesion, suggesting the coordination of these two functions. Thus, stochastic exclusive expression extends beyond the prototypical families, permitting precision in gene choice to be combined with the diversity of intercellular interactions.
Publisher Frontiers Media
ISSN/ISBN 2296-634X
edoc-URL https://edoc.unibas.ch/83092/
Full Text on edoc Available
Digital Object Identifier DOI 10.3389/fcell.2021.642212
PubMed ID http://www.ncbi.nlm.nih.gov/pubmed/33996799
Document type (ISI) Journal Article
 
   

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