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Deep sequencing and proteomic analysis of the microRNA-induced silencing complex in human red blood cells.
Abstract
During maturation, erythropoietic cells extrude their nuclei but retain their ability to respond to oxidant stress by tightly regulating protein translation. Several studies have reported microRNA-mediated regulation of translation during terminal stages of erythropoiesis, even after enucleation. In the present study, we performed a detailed examination of the endogenous microRNA machinery in human red blood cells using a combination of deep sequencing analysis of microRNAs and proteomic analysis of the microRNA-induced silencing complex. Among the 197 different microRNAs detected, miR-451a was the most abundant, representing more than 60% of all read sequences. In addition, miR-451a and its known target, 14-3-3ζ mRNA, were bound to the microRNA-induced silencing complex, implying their direct interaction in red blood cells. The proteomic characterization of endogenous Argonaute 2-associated microRNA-induced silencing complex revealed 26 cofactor candidates. Among these cofactors, we identified several RNA-binding proteins, as well as motor proteins and vesicular trafficking proteins. Our results demonstrate that red blood cells contain complex microRNA machinery, which might enable immature red blood cells to control protein translation independent of de novo nuclei information.
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“the number of genes expressed in mature RBCs (∼8,092 genes) are far less than those of other nuclear blood cells such as peripheral blood mononuclear cells (∼15,743 genes) and erythroid progenitor cells (∼15,113 genes)”
From Red Blood Cells as Potential Repositories of MicroRNAs in the Circulatory System (2020) · cites this paper as Azzouzi et al., 2015
In the citing paper
“However, current investigations have confirmed several different types of long RNAs in RBCs and have shown that the number of genes expressed in mature RBCs (∼8,092 genes) are far less than those of other nuclear blood cells such as peripheral blood mononuclear cells (∼15,743 genes) and erythroid progenitor cells (∼15,113 genes)”
From Red Blood Cells as Potential Repositories of MicroRNAs in the Circulatory System (2020) · cites this paper as Azzouzi et al., 2015
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Cited by
Sorted by citations
Red Blood Cells as Potential Repositories of MicroRNAs in the Circulatory System
Sun, L., Yu, Y., Niu, B., & Wang, D. (2020) · Frontiers in Genetics · doi:10.3389/fgene.2020.00442 · Cited by 83
Metadata
- Authors
- Azzouzi, I., Moest, H., Wollscheid, B., Schmugge, M., Eekels, J. J. M., & Speer, O.
- Venue
- Experimental Hematology
- Publisher
- Elsevier BV
- Published
- 2015-05
- Volume
- 43
- Issue
- 5
- Pages
- 382-392
- ISSN
- 0301-472X
- Cited by
- 39
- References
- 2
- Language
- en
- Licence
- Funders
- Roche (5002248765)
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