Literature DB >> 26363379

Evolutionary conservation and function of the human embryonic stem cell specific miR-302/367 cluster.

Liang Chen1, Liisa Heikkinen2, K Emily Knott2, Yanchun Liang3, Garry Wong4.   

Abstract

miRNA clusters define a group of related miRNAs closely localized in the genome with an evolution that remains poorly understood. The miR-302/367 cluster represents a single polycistronic transcript that produces five precursor miRNAs. The cluster is highly expressed and essential for maintenance of human embryonic stem cells. We found the cluster to be highly conserved and present in most mammals. In primates, seed sequence and miRNA structure are conserved, but inter-precursor sequences are evolving. Insertions of new miRNAs, deletions of individual miRNAs, and a cluster duplication observed in different species suggest an actively evolving cluster. Core transcriptional machinery consisting of NANOG and OCT-4 transcription factors that define stem cells are present upstream of the miR-302/367 cluster. Interestingly, we found the miR-302/367 cluster flanking region to be enriched as a target site of other miRNAs suggesting a mechanism for feedback control. Analysis of miR-302 and miR-367 targets demonstrated concordance of gene set enrichment groups at high gene ontology levels. This cluster also expresses isomiRs providing another means of establishing sequence diversity. Finally, using three different kidney tumor datasets, we observed consistent expression of miR-302 family members in normal tissue while adjacent tumor tissue showed a significant lack of expression. Clustering expression levels of miR-302 validated target genes showed a significant correlation between miR-302/367 cluster miRNAs and a subset of validated gene targets in healthy and adjacent tumor tissues. Taken together, our data show a highly conserved and still evolving miRNA cluster that may have additional unrecognized functions.
Copyright © 2015. Published by Elsevier Inc.

Entities:  

Keywords:  Cancer; Functional genomics; Stem cells; Target analysis; miRNA

Mesh:

Substances:

Year:  2015        PMID: 26363379     DOI: 10.1016/j.cbd.2015.08.002

Source DB:  PubMed          Journal:  Comp Biochem Physiol Part D Genomics Proteomics        ISSN: 1744-117X            Impact factor:   2.674


  6 in total

1.  miR-302/367/LATS2/YAP pathway is essential for prostate tumor-propagating cells and promotes the development of castration resistance.

Authors:  Y Guo; J Cui; Z Ji; C Cheng; K Zhang; C Zhang; M Chu; Q Zhao; Z Yu; Y Zhang; Y-X Fang; W-Q Gao; H H Zhu
Journal:  Oncogene       Date:  2017-07-24       Impact factor: 9.867

2.  Trimester-specific plasma exosome microRNA expression profiles in preeclampsia.

Authors:  Eric Devor; Donna Santillan; Sabrina Scroggins; Akshaya Warrier; Mark Santillan
Journal:  J Matern Fetal Neonatal Med       Date:  2019-01-30

3.  miR-371a-3p, miR-373-3p and miR-367-3p as Serum Biomarkers in Metastatic Testicular Germ Cell Cancers Before, During and After Chemotherapy.

Authors:  Ximena Rosas Plaza; Ton van Agthoven; Coby Meijer; Marcel A T M van Vugt; Steven de Jong; Jourik A Gietema; Leendert H J Looijenga
Journal:  Cells       Date:  2019-10-08       Impact factor: 6.600

4.  ADAR1 Suppresses Interferon Signaling in Gastric Cancer Cells by MicroRNA-302a-Mediated IRF9/STAT1 Regulation.

Authors:  Lushang Jiang; Min Ji Park; Charles J Cho; Kihak Lee; Min Kyo Jung; Chan Gi Pack; Seung-Jae Myung; Suhwan Chang
Journal:  Int J Mol Sci       Date:  2020-08-27       Impact factor: 5.923

5.  The Evolution of Imprinted microRNAs and Their RNA Targets.

Authors:  David Haig; Avantika Mainieri
Journal:  Genes (Basel)       Date:  2020-09-03       Impact factor: 4.096

Review 6.  Insight into the Key Points of Preeclampsia Pathophysiology: Uterine Artery Remodeling and the Role of MicroRNAs.

Authors:  Katarzyna Pankiewicz; Anna Fijałkowska; Tadeusz Issat; Tomasz M Maciejewski
Journal:  Int J Mol Sci       Date:  2021-03-19       Impact factor: 5.923

  6 in total

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