TY - JOUR
T1 - A whole-tissue RNA-seq toolkit for organism-wide studies of gene expression with PME-seq
AU - Pandey, Surya
AU - Takahama, Michihiro
AU - Gruenbaum, Adam
AU - Zewde, Makda
AU - Cheronis, Katerina
AU - Chevrier, Nicolas
N1 - Funding Information:
We thank M. Kadoki, T. Matsui and S. Tay for helpful discussions. This work was supported by an Overseas Research Fellowship from the Astellas Foundation for Research on Metabolic Disorders (M.T.), an NIH Director’s New Innovator Award DP2 (AI145100), an Institutional Research Grant (IRG-16-222-56) from the American Cancer Society, the University of Chicago Medicine Comprehensive Cancer Center Support Grant (P30 CA14599), the Elliot and Ruth Sigal MRA Young Investigator Award (571146) and funds from the Pritzker School of Molecular Engineering (N.C.).
Publisher Copyright:
© 2020, The Author(s), under exclusive licence to Springer Nature Limited.
PY - 2020/4/1
Y1 - 2020/4/1
N2 - The immune system operates at the scale of the whole organism in mammals. We currently lack experimental approaches to systematically track and study organism-wide molecular processes in mice. Here we describe an integrated toolkit for measuring gene expression in whole tissues, 3-prime mRNA extension sequencing, that is applicable to most mouse organs and any mouse model of interest. Further, the methods of RNA-seq described in this protocol are broadly applicable to other sample types beyond whole organs, such as tissue samples or isolated cell populations. We report procedures to collect, store and lyse a dozen organ types using conditions compatible with the extraction of high-quality RNA. In addition, we detail protocols to perform high-throughput and low-cost RNA extraction and sequencing, as well as downstream data analysis. The protocol takes 5 d to process 384 mouse organs from collecting tissues to obtaining raw sequencing data, with additional time required for data analysis and mining. The protocol is accessible to individuals with basic skills in (i) mouse perfusion and dissection for sample collection and (ii) computation using Unix and R for data analysis. Overall, the methods presented here fill a gap in our toolbox for studying organism-wide processes in immunology and physiology.
AB - The immune system operates at the scale of the whole organism in mammals. We currently lack experimental approaches to systematically track and study organism-wide molecular processes in mice. Here we describe an integrated toolkit for measuring gene expression in whole tissues, 3-prime mRNA extension sequencing, that is applicable to most mouse organs and any mouse model of interest. Further, the methods of RNA-seq described in this protocol are broadly applicable to other sample types beyond whole organs, such as tissue samples or isolated cell populations. We report procedures to collect, store and lyse a dozen organ types using conditions compatible with the extraction of high-quality RNA. In addition, we detail protocols to perform high-throughput and low-cost RNA extraction and sequencing, as well as downstream data analysis. The protocol takes 5 d to process 384 mouse organs from collecting tissues to obtaining raw sequencing data, with additional time required for data analysis and mining. The protocol is accessible to individuals with basic skills in (i) mouse perfusion and dissection for sample collection and (ii) computation using Unix and R for data analysis. Overall, the methods presented here fill a gap in our toolbox for studying organism-wide processes in immunology and physiology.
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U2 - 10.1038/s41596-019-0291-y
DO - 10.1038/s41596-019-0291-y
M3 - Article
C2 - 32076350
AN - SCOPUS:85079796582
SN - 1754-2189
VL - 15
SP - 1459
EP - 1483
JO - Nature Protocols
JF - Nature Protocols
IS - 4
ER -