Literature DB >> 27272188

Global transcriptome analysis for identification of interactions between coding and noncoding RNAs during human erythroid differentiation.

Nan Ding1,2, Jiafei Xi3,4, Yanming Li1, Xiaoyan Xie3,4, Jian Shi1,2, Zhaojun Zhang1, Yanhua Li3,4, Fang Fang3,4, Sihan Wang3,4, Wen Yue3,4, Xuetao Pei5,6, Xiangdong Fang7.   

Abstract

Studies on coding genes, miRNAs, and lncRNAs during erythroid development have been performed in recent years. However, analysis focusing on the integration of the three RNA types has yet to be done. In the present study, we compared the dynamics of coding genes, miRNA, and lncRNA expression profiles. To explore dynamic changes in erythropoiesis and potential mechanisms that control these changes in the transcriptome level, we took advantage of high throughput sequencing technologies to obtain transcriptome data from cord blood hematopoietic stem cells and the following four erythroid differentiation stages, as well as from mature red blood cells. Results indicated that lncRNAs were promising cell marker candidates for erythroid differentiation. Clustering analysis classified the differentially expressed genes into four subtypes that corresponded to dynamic changes during stemness maintenance, mid-differentiation, and maturation. Integrated analysis revealed that noncoding RNAs potentially participated in controlling blood cell maturation, and especially associated with heme metabolism and responses to oxygen species and DNA damage. These regulatory interactions were displayed in a comprehensive network, thereby inferring correlations between RNAs and their associated functions. These data provided a substantial resource for the study of normal erythropoiesis, which will permit further investigation and understanding of erythroid development and acquired erythroid disorders.

Entities:  

Keywords:  RNA-seq; erythroid differentiation; hematopoietic stem cell; lncRNA; miRNA

Mesh:

Substances:

Year:  2016        PMID: 27272188     DOI: 10.1007/s11684-016-0452-0

Source DB:  PubMed          Journal:  Front Med        ISSN: 2095-0217            Impact factor:   4.592


  57 in total

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