High-resolution genome-wide expression analysis of single myofibers using SMART-Seq

被引:29
作者
Blackburn, Darren M. [1 ,2 ]
Lazure, Felicia [1 ,2 ]
Corchado, Aldo H. [1 ]
Perkins, Theodore J. [3 ,4 ]
Najafabadi, Hamed S. [1 ,2 ]
Soleimani, Vahab D. [1 ]
机构
[1] McGill Univ, Dept Human Genet, 3640 Rue Univ, Montreal, PQ H3A 0C7, Canada
[2] Jewish Gen Hosp, Lady Davis Inst Med Res, Mol & Regenerat Med Axis, Montreal, PQ H3T 1E2, Canada
[3] Ottawa Hosp Res Inst, Sprott Ctr Stem Cell Res, Ottawa, ON K1H 8L6, Canada
[4] Univ Ottawa, Dept Biochem Microbiol & Immunol, Ottawa, ON K1H 8M5, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
muscle; RNA; gene expression; molecular cell biology; molecular biology; SMART-Seq; MOUSE SKELETAL-MUSCLE; ENDOTHELIAL-CELLS; STEM-CELLS; PROGENITORS; CHEMOKINE; EXERCISE; BINDING; NECDIN; RNA;
D O I
10.1074/jbc.RA119.011506
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Skeletal muscle is a heterogeneous tissue. Individual myofibers that make up muscle tissue exhibit variation in their metabolic and contractile properties. Although biochemical and histological assays are available to study myofiber heterogeneity, efficient methods to analyze the whole transcriptome of individual myofibers are lacking. Here, we report on a single-myofiber RNA-sequencing (smfRNA-Seq) approach to analyze the whole transcriptome of individual myofibers by combining single-fiber isolation with Switching Mechanism at 5? end of RNA Template (SMART) technology. Using smfRNA-Seq, we first determined the genes that are expressed in the whole muscle, including in nonmyogenic cells. We also analyzed the differences in the transcriptome of myofibers from young and old mice to validate the effectiveness of this new method. Our results suggest that aging leads to significant changes in the expression of metabolic genes, such as Nos1, and structural genes, such as Myl1, in myofibers. We conclude that smfRNA-Seq is a powerful tool to study developmental, disease-related, and age-related changes in the gene expression profile of skeletal muscle.
引用
收藏
页码:20097 / 20108
页数:12
相关论文
共 52 条
[1]
Not just a marker: CD34 on human hematopoietic stem/progenitor cells dominates vascular selectin binding along with CD44 [J].
AbuSamra, Dina B. ;
Aleisa, Fajr A. ;
Al-Amoodi, Asma S. ;
Ahmed, Heba M. Jalal ;
Chin, Chee Jia ;
Abuelela, Ayman F. ;
Bergam, Ptissam ;
Sougrat, Rachid ;
Merzaban, Jasmeen S. .
BLOOD ADVANCES, 2017, 1 (27) :2799-2816
[2]
Regulation of satellite cell function in sarcopenia [J].
Alway, Stephen E. ;
Myers, Matthew J. ;
Mohamed, Junaith S. .
FRONTIERS IN AGING NEUROSCIENCE, 2014, 6
[3]
Adipogenic progenitors keep muscle stem cells young [J].
Ancel, Sara ;
Mashinchian, Omid ;
Feige, Jerome N. .
AGING-US, 2019, 11 (18) :7331-7333
[4]
HTSeq-a Python']Python framework to work with high-throughput sequencing data [J].
Anders, Simon ;
Pyl, Paul Theodor ;
Huber, Wolfgang .
BIOINFORMATICS, 2015, 31 (02) :166-169
[5]
Inflammatory monocytes recruited after skeletal muscle injury switch into antiinflammatory macrophages to support myogenesis [J].
Arnold, Ludovic ;
Henry, Adeline ;
Poron, Francoise ;
Baba-Amer, Yasmine ;
van Rooijen, Nico ;
Plonquet, Anne ;
Gherardi, Romain K. ;
Chazaud, Benedicte .
JOURNAL OF EXPERIMENTAL MEDICINE, 2007, 204 (05) :1057-1069
[6]
Reciprocal signalling by Notch-Collagen V-CALCR retains muscle stem cells in their niche [J].
Baghdadi, Meryem B. ;
Castel, David ;
Machado, Leo ;
Fukada, So-ichiro ;
Birk, David E. ;
Relaix, Frederic ;
Tajbakhsh, Shahragim ;
Mourikis, Philippos .
NATURE, 2018, 557 (7707) :714-+
[7]
The Critical Role of Metabolic Pathways in Aging [J].
Barzilai, Nir ;
Huffman, Derek M. ;
Muzumdar, Radhika H. ;
Bartke, Andrzej .
DIABETES, 2012, 61 (06) :1315-1322
[8]
Ageing muscles lose T Reg-eneration [J].
Bird, Lucy .
NATURE REVIEWS IMMUNOLOGY, 2016, 16 (04) :204-204
[9]
3 MYOSIN ADENOSINE TRIPHOSPHATASE SYSTEMS - NATURE OF THEIR PH LABILITY AND SULFHYDRYL DEPENDENCE [J].
BROOKE, MH ;
KAISER, KK .
JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY, 1970, 18 (09) :670-&
[10]
The aged niche disrupts muscle stem cell quiescence [J].
Chakkalakal, Joe V. ;
Jones, Kieran M. ;
Basson, M. Albert ;
Brack, Andrew S. .
NATURE, 2012, 490 (7420) :355-+