Detecting gene expression in Caenorhabditis elegans

被引:0
作者
Calarco, John A. [1 ]
Taylor, Seth R. [2 ]
Miller III, David M. [3 ,4 ]
机构
[1] Univ Toronto, Dept Cell & Syst Biol, Toronto, ON, Canada
[2] Brigham Young Univ, Dept Cell Biol & Physiol, Provo, UT 84602 USA
[3] Vanderbilt Univ, Dept Cell & Dev Biol, Nashville, TN 37240 USA
[4] Vanderbilt Univ, Neurosci Program, Nashville, TN 37240 USA
基金
加拿大自然科学与工程研究理事会; 加拿大健康研究院;
关键词
gene expression; RNA sequencing; FISH; live-cell reporters; single-cell RNA sequencing; WormBook; GENOME-WIDE EXPRESSION; IN-SITU HYBRIDIZATION; CELL RNA-SEQ; C-ELEGANS; MESSENGER-RNA; ALTERNATIVE POLYADENYLATION; PROTEOME ANALYSIS; BINDING PROTEINS; SENSORY NEURONS; OPEN CHROMATIN;
D O I
10.1093/genetics/iyae167
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Reliable methods for detecting and analyzing gene expression are necessary tools for understanding development and investigating biological responses to genetic and environmental perturbation. With its fully sequenced genome, invariant cell lineage, transparent body, wiring diagram, detailed anatomy, and wide array of genetic tools, Caenorhabditis elegans is an exceptionally useful model organism for linking gene expression to cellular phenotypes. The development of new techniques in recent years has greatly expanded our ability to detect gene expression at high resolution. Here, we provide an overview of gene expression methods for C. elegans, including techniques for detecting transcripts and proteins in situ, bulk RNA sequencing of whole worms and specific tissues and cells, single-cell RNA sequencing, and high-throughput proteomics. We discuss important considerations for choosing among these techniques and provide an overview of publicly available online resources for gene expression data.
引用
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页数:45
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