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A Potential Regulatory Role for Intronic microRNA-338-3p for Its Host Gene Encoding Apoptosis-Associated Tyrosine Kinase

MicroRNAs (miRNAs) are important gene regulators that are abundantly expressed in both the developing and adult mammalian brain. These non-coding gene transcripts are involved in post-transcriptional regulatory processes by binding to specific target mRNAs. Approximately one third of known miRNA gen...

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Autores principales: Kos, Aron, Olde Loohuis, Nikkie F. M., Wieczorek, Martha L., Glennon, Jeffrey C., Martens, Gerard J. M., Kolk, Sharon M., Aschrafi, Armaz
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3281898/
https://www.ncbi.nlm.nih.gov/pubmed/22363537
http://dx.doi.org/10.1371/journal.pone.0031022
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author Kos, Aron
Olde Loohuis, Nikkie F. M.
Wieczorek, Martha L.
Glennon, Jeffrey C.
Martens, Gerard J. M.
Kolk, Sharon M.
Aschrafi, Armaz
author_facet Kos, Aron
Olde Loohuis, Nikkie F. M.
Wieczorek, Martha L.
Glennon, Jeffrey C.
Martens, Gerard J. M.
Kolk, Sharon M.
Aschrafi, Armaz
author_sort Kos, Aron
collection PubMed
description MicroRNAs (miRNAs) are important gene regulators that are abundantly expressed in both the developing and adult mammalian brain. These non-coding gene transcripts are involved in post-transcriptional regulatory processes by binding to specific target mRNAs. Approximately one third of known miRNA genes are located within intronic regions of protein coding and non-coding regions, and previous studies have suggested a role for intronic miRNAs as negative feedback regulators of their host genes. In the present study, we monitored the dynamic gene expression changes of the intronic miR-338-3p and miR-338-5p and their host gene Apoptosis-associated Tyrosine Kinase (AATK) during the maturation of rat hippocampal neurons. This revealed an uncorrelated expression pattern of mature miR-338 strands with their host gene. Sequence analysis of the 3′ untranslated region (UTR) of rat AATK mRNA revealed the presence of two putative binding sites for miR-338-3p. Thus, miR-338-3p may have the capacity to modulate AATK mRNA levels in neurons. Transfection of miR-338-3p mimics into rat B35 neuroblastoma cells resulted in a significant decrease of AATK mRNA levels, while the transfection of synthetic miR-338-5p mimics did not alter AATK levels. Our results point to a possible molecular mechanism by which miR-338-3p participates in the regulation of its host gene by modulating the levels of AATK mRNA, a kinase which plays a role during differentiation, apoptosis and possibly in neuronal degeneration.
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spelling pubmed-32818982012-02-23 A Potential Regulatory Role for Intronic microRNA-338-3p for Its Host Gene Encoding Apoptosis-Associated Tyrosine Kinase Kos, Aron Olde Loohuis, Nikkie F. M. Wieczorek, Martha L. Glennon, Jeffrey C. Martens, Gerard J. M. Kolk, Sharon M. Aschrafi, Armaz PLoS One Research Article MicroRNAs (miRNAs) are important gene regulators that are abundantly expressed in both the developing and adult mammalian brain. These non-coding gene transcripts are involved in post-transcriptional regulatory processes by binding to specific target mRNAs. Approximately one third of known miRNA genes are located within intronic regions of protein coding and non-coding regions, and previous studies have suggested a role for intronic miRNAs as negative feedback regulators of their host genes. In the present study, we monitored the dynamic gene expression changes of the intronic miR-338-3p and miR-338-5p and their host gene Apoptosis-associated Tyrosine Kinase (AATK) during the maturation of rat hippocampal neurons. This revealed an uncorrelated expression pattern of mature miR-338 strands with their host gene. Sequence analysis of the 3′ untranslated region (UTR) of rat AATK mRNA revealed the presence of two putative binding sites for miR-338-3p. Thus, miR-338-3p may have the capacity to modulate AATK mRNA levels in neurons. Transfection of miR-338-3p mimics into rat B35 neuroblastoma cells resulted in a significant decrease of AATK mRNA levels, while the transfection of synthetic miR-338-5p mimics did not alter AATK levels. Our results point to a possible molecular mechanism by which miR-338-3p participates in the regulation of its host gene by modulating the levels of AATK mRNA, a kinase which plays a role during differentiation, apoptosis and possibly in neuronal degeneration. Public Library of Science 2012-02-17 /pmc/articles/PMC3281898/ /pubmed/22363537 http://dx.doi.org/10.1371/journal.pone.0031022 Text en Kos et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Kos, Aron
Olde Loohuis, Nikkie F. M.
Wieczorek, Martha L.
Glennon, Jeffrey C.
Martens, Gerard J. M.
Kolk, Sharon M.
Aschrafi, Armaz
A Potential Regulatory Role for Intronic microRNA-338-3p for Its Host Gene Encoding Apoptosis-Associated Tyrosine Kinase
title A Potential Regulatory Role for Intronic microRNA-338-3p for Its Host Gene Encoding Apoptosis-Associated Tyrosine Kinase
title_full A Potential Regulatory Role for Intronic microRNA-338-3p for Its Host Gene Encoding Apoptosis-Associated Tyrosine Kinase
title_fullStr A Potential Regulatory Role for Intronic microRNA-338-3p for Its Host Gene Encoding Apoptosis-Associated Tyrosine Kinase
title_full_unstemmed A Potential Regulatory Role for Intronic microRNA-338-3p for Its Host Gene Encoding Apoptosis-Associated Tyrosine Kinase
title_short A Potential Regulatory Role for Intronic microRNA-338-3p for Its Host Gene Encoding Apoptosis-Associated Tyrosine Kinase
title_sort potential regulatory role for intronic microrna-338-3p for its host gene encoding apoptosis-associated tyrosine kinase
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3281898/
https://www.ncbi.nlm.nih.gov/pubmed/22363537
http://dx.doi.org/10.1371/journal.pone.0031022
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