Identify Myeloid Differentiation-Related MiRNAs Response to ATRA Induction by RNA Sequencing and CRISPR/Cas9 Gene Editing.
10.19746/j.cnki.issn.1009-2137.2021.02.006
- Author:
Ling-Yan WANG
1
;
Ren-Zhang LIN
2
;
Pei-Fang JIANG
1
;
Yun ZHANG
1
;
Jia-Zheng LI
1
;
Yu-Wen CHEN
1
;
Jian-Da HU
3
Author Information
1. Department of Hematology, Fujian Medical University Union Hospital, Fujian Institute of Hematology, Fujian Provincial Key Laboratory of Hematologic Disease, Fuzhou 350001, Fujian Province, China.
2. Department of Molecular and Cellular Biology, Beckman Research Institute of City of Hope, Duarte 91010, CA, USA.
3. Department of Hematology, Fujian Medical University Union Hospital, Fujian Institute of Hematology, Fujian Provincial Key Laboratory of Hematologic Disease, Fuzhou 350001, Fujian Province, China,E-mail: drjiandahu@163.com.
- Publication Type:Journal Article
- MeSH:
CRISPR-Cas Systems;
Cell Differentiation;
Gene Editing;
MicroRNAs/genetics*;
Sequence Analysis, RNA;
Tretinoin
- From:
Journal of Experimental Hematology
2021;29(2):339-347
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVE:To identify differentiation related miRNA and evaluate roles of miRNA during ATRA induced myeloid differentiation.
METHODS:The small RNA sequencing was used to analyze differential expressed miRNAs in ATRA induced NB4 cells. Then the several up or down-regulated miRNA were selected as the research candidates. SgRNAs targeting the genome of each miRNA were designed and NB4 cells with inducible expression of Cas9 protein were generated. After transduced sgRNA into NB4/Cas9 cells, the mutation level by PCR and surveyor assay were evaluated. The cell differentiation level was investigated by surface CD11b expression via flow cytometry.
RESULTS:A total of 410 mature miRNAs which expressed in NB4 cells were detected out after treated by ATRA, 74 miRNAs were up-regulated and 55 were down-regulated miRNAs with DNA cleavage generated by CRISPR/Cas9 was assayed directly by PCR or surveyor assay, quantitative PCR showed that the expression of miRNA was downregulated, which evaluated that gene edition successfully inhibitied the expression of mature miRNA. MiR-223 knockout showed the myeloid differentation of NB4 significantly inhibitied, while miRNA-155 knockout showed the myeloid differentation of NB4 cells significantly increased.
CONCLUSION:CRISPR/Cas9 is a powerful tool for gene editing and can lead to miRNA knockout. Knockouts of miR-223 and miR-155 have shown a differentiation-related phenotype, and the potential mechanism is the integrative regulation of target genes.
