miR-218 Inhibits Erythroid Differentiation and Alters Iron Metabolism by Targeting ALAS2 in K562 Cells

microRNAs (miRNAs) are involved in a variety of biological processes. The regulatory function and potential role of miRNAs targeting the mRNA of the 5′-aminolevulinate synthase 2 (ALAS2) in erythropoiesis were investigated in order to identify miRNAs which play a role in erythroid iron metabolism an...

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Main Authors: Yanming Li, Shuge Liu, Hongying Sun, Yadong Yang, Heyuan Qi, Nan Ding, Jiawen Zheng, Xunong Dong, Hongzhu Qu, Zhaojun Zhang, Xiangdong Fang
Format: Article
Language:English
Published: MDPI AG 2015-11-01
Series:International Journal of Molecular Sciences
Subjects:
Online Access:http://www.mdpi.com/1422-0067/16/12/26088
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spelling doaj-f332c3f05cd74632a63c9c46d380a7ea2020-11-25T01:00:59ZengMDPI AGInternational Journal of Molecular Sciences1422-00672015-11-011612281562816810.3390/ijms161226088ijms161226088miR-218 Inhibits Erythroid Differentiation and Alters Iron Metabolism by Targeting ALAS2 in K562 CellsYanming Li0Shuge Liu1Hongying Sun2Yadong Yang3Heyuan Qi4Nan Ding5Jiawen Zheng6Xunong Dong7Hongzhu Qu8Zhaojun Zhang9Xiangdong Fang10CAS Key Laboratory of Genome Sciences and Information, Beijing Institute of Genomics, Chinese Academy of Sciences, Beijing 100101, ChinaCAS Key Laboratory of Genome Sciences and Information, Beijing Institute of Genomics, Chinese Academy of Sciences, Beijing 100101, ChinaCAS Key Laboratory of Genome Sciences and Information, Beijing Institute of Genomics, Chinese Academy of Sciences, Beijing 100101, ChinaCAS Key Laboratory of Genome Sciences and Information, Beijing Institute of Genomics, Chinese Academy of Sciences, Beijing 100101, ChinaCAS Key Laboratory of Genome Sciences and Information, Beijing Institute of Genomics, Chinese Academy of Sciences, Beijing 100101, ChinaCAS Key Laboratory of Genome Sciences and Information, Beijing Institute of Genomics, Chinese Academy of Sciences, Beijing 100101, ChinaCAS Key Laboratory of Genome Sciences and Information, Beijing Institute of Genomics, Chinese Academy of Sciences, Beijing 100101, ChinaCAS Key Laboratory of Genome Sciences and Information, Beijing Institute of Genomics, Chinese Academy of Sciences, Beijing 100101, ChinaCAS Key Laboratory of Genome Sciences and Information, Beijing Institute of Genomics, Chinese Academy of Sciences, Beijing 100101, ChinaCAS Key Laboratory of Genome Sciences and Information, Beijing Institute of Genomics, Chinese Academy of Sciences, Beijing 100101, ChinaCAS Key Laboratory of Genome Sciences and Information, Beijing Institute of Genomics, Chinese Academy of Sciences, Beijing 100101, ChinamicroRNAs (miRNAs) are involved in a variety of biological processes. The regulatory function and potential role of miRNAs targeting the mRNA of the 5′-aminolevulinate synthase 2 (ALAS2) in erythropoiesis were investigated in order to identify miRNAs which play a role in erythroid iron metabolism and differentiation. Firstly, the role of ALAS2 in erythroid differentiation and iron metabolism in human erythroid leukemia cells (K562) was confirmed by ALAS2 knockdown. Through a series of screening strategies and experimental validations, it was identified that hsa-miR-218 (miR-218) targets and represses the expression of ALAS2 by binding to the 3′-untranslated region (UTR). Overexpression of miR-218 repressed erythroid differentiation and altered iron metabolism in K562 cells similar to that seen in the ALAS2 knockdown in K562 cells. In addition to iron metabolism and erythroid differentiation, miR-218 was found to be responsible for a reduction in K562 cell growth. Taken together, our results show that miR-218 inhibits erythroid differentiation and alters iron metabolism by targeting ALAS2 in K562 cells.http://www.mdpi.com/1422-0067/16/12/26088miR-218ALAS2erythroid differentiationiron metabolism
collection DOAJ
language English
format Article
sources DOAJ
author Yanming Li
Shuge Liu
Hongying Sun
Yadong Yang
Heyuan Qi
Nan Ding
Jiawen Zheng
Xunong Dong
Hongzhu Qu
Zhaojun Zhang
Xiangdong Fang
spellingShingle Yanming Li
Shuge Liu
Hongying Sun
Yadong Yang
Heyuan Qi
Nan Ding
Jiawen Zheng
Xunong Dong
Hongzhu Qu
Zhaojun Zhang
Xiangdong Fang
miR-218 Inhibits Erythroid Differentiation and Alters Iron Metabolism by Targeting ALAS2 in K562 Cells
International Journal of Molecular Sciences
miR-218
ALAS2
erythroid differentiation
iron metabolism
author_facet Yanming Li
Shuge Liu
Hongying Sun
Yadong Yang
Heyuan Qi
Nan Ding
Jiawen Zheng
Xunong Dong
Hongzhu Qu
Zhaojun Zhang
Xiangdong Fang
author_sort Yanming Li
title miR-218 Inhibits Erythroid Differentiation and Alters Iron Metabolism by Targeting ALAS2 in K562 Cells
title_short miR-218 Inhibits Erythroid Differentiation and Alters Iron Metabolism by Targeting ALAS2 in K562 Cells
title_full miR-218 Inhibits Erythroid Differentiation and Alters Iron Metabolism by Targeting ALAS2 in K562 Cells
title_fullStr miR-218 Inhibits Erythroid Differentiation and Alters Iron Metabolism by Targeting ALAS2 in K562 Cells
title_full_unstemmed miR-218 Inhibits Erythroid Differentiation and Alters Iron Metabolism by Targeting ALAS2 in K562 Cells
title_sort mir-218 inhibits erythroid differentiation and alters iron metabolism by targeting alas2 in k562 cells
publisher MDPI AG
series International Journal of Molecular Sciences
issn 1422-0067
publishDate 2015-11-01
description microRNAs (miRNAs) are involved in a variety of biological processes. The regulatory function and potential role of miRNAs targeting the mRNA of the 5′-aminolevulinate synthase 2 (ALAS2) in erythropoiesis were investigated in order to identify miRNAs which play a role in erythroid iron metabolism and differentiation. Firstly, the role of ALAS2 in erythroid differentiation and iron metabolism in human erythroid leukemia cells (K562) was confirmed by ALAS2 knockdown. Through a series of screening strategies and experimental validations, it was identified that hsa-miR-218 (miR-218) targets and represses the expression of ALAS2 by binding to the 3′-untranslated region (UTR). Overexpression of miR-218 repressed erythroid differentiation and altered iron metabolism in K562 cells similar to that seen in the ALAS2 knockdown in K562 cells. In addition to iron metabolism and erythroid differentiation, miR-218 was found to be responsible for a reduction in K562 cell growth. Taken together, our results show that miR-218 inhibits erythroid differentiation and alters iron metabolism by targeting ALAS2 in K562 cells.
topic miR-218
ALAS2
erythroid differentiation
iron metabolism
url http://www.mdpi.com/1422-0067/16/12/26088
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