Alterations in chromatin accessibility during osteoblast and adipocyte differentiation in human mesenchymal stem cells

被引:6
作者
Liu, Jianyun [1 ]
Gan, Lijun [1 ]
Ma, Baichen [1 ]
He, Shan [1 ]
Wu, Ping [1 ]
Li, Huiming [1 ]
Xiong, Jianjun [1 ]
机构
[1] Jiujiang Univ, Jiangxi Prov Key Lab Syst Biomed, Jiujiang 332000, Peoples R China
基金
中国国家自然科学基金;
关键词
MSC; ATAC-seq; RNA-seq; Adipogenic; Osteogenic; TRANSCRIPTION FACTOR; ADIPOGENESIS; LANDSCAPE; MARROW;
D O I
10.1186/s12920-022-01168-1
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Although differential expression of genes is apparent during the adipogenic/osteogenic differentiation of marrow mesenchymal stem cells (MSCs), it is not known whether this is associated with changes in chromosomal structure. In this study, we used ATAC-sequencing technology to observe variations in chromatin assembly during the early stages of MSC differentiation. This showed significant changes in the number and distribution of chromosome accessibility at different time points of adipogenic/osteogenic differentiation. Sequencing of differential peaks indicated alterations in transcription factor motifs involved in MSC differentiation. Gene Ontology (GO) and pathway analysis indicated that changes in biological function resulted from the alterations in chromatin accessibility. We then integrated ATAC-seq and RNA-seq and found that only a small proportion of the overlapping genes were screened out from ATAC-seq and RNA-seq overlapping. Through GO and pathway analysis of these overlapped genes, we not only observed some known biological functions related to adipogenic/osteogenic differentiation but also noticed some unusual biological clustering during MSC differentiation. In summary, our work not only presents the landscape of chromatin accessibility of MSC during differentiation but also helps to further our understanding of the underlying mechanisms of gene expression in these processes.
引用
收藏
页数:13
相关论文
共 34 条
[1]   Integration of ATAC-seq and RNA-seq identifies human alpha cell and beta cell signature genes [J].
Ackermann, Amanda M. ;
Wang, Zhiping ;
Schug, Jonathan ;
Naji, Ali ;
Kaestner, Klaus H. .
MOLECULAR METABOLISM, 2016, 5 (03) :233-244
[2]   One billion years of bZIP transcription factor evolution: Conservation and change in dimerization and DNA-binding site specificity [J].
Amoutzias, G. D. ;
Veron, A. S. ;
Weiner, J., III ;
Robinson-Rechavi, M. ;
Bornberg-Bauer, E. ;
Oliver, S. G. ;
Robertson, D. L. .
MOLECULAR BIOLOGY AND EVOLUTION, 2007, 24 (03) :827-835
[3]   A role for bone morphogenetic protein-4 in adipocyte development [J].
Bowers, Robert R. ;
Lane, M. Daniel .
CELL CYCLE, 2007, 6 (04) :385-389
[4]  
Bruder SP, 1997, J CELL BIOCHEM, V64, P278, DOI 10.1002/(SICI)1097-4644(199702)64:2<278::AID-JCB11>3.0.CO
[5]  
2-F
[6]  
Buenrostro Jason D, 2015, Curr Protoc Mol Biol, V109, DOI 10.1002/0471142727.mb2129s109
[7]  
Buenrostro JD, 2013, NAT METHODS, V10, P1213, DOI [10.1038/nmeth.2688, 10.1038/NMETH.2688]
[8]   Transcriptomic Analyses of Adipocyte Differentiation From Human Mesenchymal Stromal-Cells (MSC) [J].
Casado-Diaz, Antonio ;
Anter, Jaouad ;
Mueller, Soeren ;
Winter, Peter ;
Manuel Quesada-Gomez, Jose ;
Dorado, Gabriel .
JOURNAL OF CELLULAR PHYSIOLOGY, 2017, 232 (04) :771-784
[9]   Lineage-specific and single-cell chromatin accessibility charts human hematopoiesis and leukemia evolution [J].
Corces, M. Ryan ;
Buenrostro, Jason D. ;
Wu, Beijing ;
Greenside, Peyton G. ;
Chan, Steven M. ;
Koenig, Julie L. ;
Snyder, Michael P. ;
Pritchard, Jonathan K. ;
Kundaje, Anshul ;
Gkeenleaf, William J. ;
Majeti, Ravindra ;
Chang, Howard Y. .
NATURE GENETICS, 2016, 48 (10) :1193-1203
[10]   Reduction of Cellular Lipid Content by a Knockdown of Drosophila PDP1 gamma and Mammalian Hepatic Leukemia Factor [J].
Dzitoyeva, Svetlana ;
Manev, Hari .
JOURNAL OF LIPIDS, 2013, 2013