4.7 Article

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

期刊

FRONTIERS OF MEDICINE
卷 10, 期 3, 页码 297-310

出版社

SPRINGER
DOI: 10.1007/s11684-016-0452-0

关键词

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

资金

  1. National Twelfth Five-Year Plan for Science & Technology Support [2013BAI01B09]
  2. National Natural Science Foundation of China [31471115, 31401160, 31201097, 31301199, 31401260]
  3. National Key Scientific Instrument and Equipment Development Projects of China [2011YQ03013404]
  4. National High Technology Research and Development Program of China [2015AA020101, 2015AA020108, 2013AA020107]
  5. State Key Laboratory of Experimental Hematology Pilot Project Grant [ZK13-05]
  6. Guangzhou Health Care and Cooperative Innovation Major Project [201400000003]
  7. Guangdong Major Scientific and Technological Project [2013A022100005]

向作者/读者索取更多资源

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.

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