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MiR-3960 binding sites with mRNA of human genes
The importance of miRNA in cellular regulation is gaining momentum. Therefore, it is of interest to study miRNA in human genes. Hence, the humanmRNA sequences (12,175) were searched for miRNA binding sites and 2,563predicted sites were found. We observed that the miR-3960 has more than 1000mRNA bind...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Biomedical Informatics
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4135290/ https://www.ncbi.nlm.nih.gov/pubmed/25187682 http://dx.doi.org/10.6026/97320630010423 |
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author | Ivashchenko, Anatoly Berillo, Olga Pyrkova, Anna Niyazova, Raigul Atambayeva, Shara |
author_facet | Ivashchenko, Anatoly Berillo, Olga Pyrkova, Anna Niyazova, Raigul Atambayeva, Shara |
author_sort | Ivashchenko, Anatoly |
collection | PubMed |
description | The importance of miRNA in cellular regulation is gaining momentum. Therefore, it is of interest to study miRNA in human genes. Hence, the humanmRNA sequences (12,175) were searched for miRNA binding sites and 2,563predicted sites were found. We observed that the miR-3960 has more than 1000mRNA binding sites with high affinity (with ΔG/ΔG(m) values greater than or equal to 90%) for 375genes. The miR-3960 has 565 binding sites in the 5'UTRs and 515 sites in theCDS of mRNAs. Nucleotide sequences of the binding sites in CDS encode for polyalanine orpolyproline. It is observed that miR-3960 has binding sites in 73 mRNAs of target genesencoded transcription factors. Thus, we document predictedproperties (polysites, sites in CDS) of uncharacterized miR-3960 binding sites. The studying of the miRNA properties is important for creation of diagnostic methods of cancer. |
format | Online Article Text |
id | pubmed-4135290 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Biomedical Informatics |
record_format | MEDLINE/PubMed |
spelling | pubmed-41352902014-09-03 MiR-3960 binding sites with mRNA of human genes Ivashchenko, Anatoly Berillo, Olga Pyrkova, Anna Niyazova, Raigul Atambayeva, Shara Bioinformation Hypothesis The importance of miRNA in cellular regulation is gaining momentum. Therefore, it is of interest to study miRNA in human genes. Hence, the humanmRNA sequences (12,175) were searched for miRNA binding sites and 2,563predicted sites were found. We observed that the miR-3960 has more than 1000mRNA binding sites with high affinity (with ΔG/ΔG(m) values greater than or equal to 90%) for 375genes. The miR-3960 has 565 binding sites in the 5'UTRs and 515 sites in theCDS of mRNAs. Nucleotide sequences of the binding sites in CDS encode for polyalanine orpolyproline. It is observed that miR-3960 has binding sites in 73 mRNAs of target genesencoded transcription factors. Thus, we document predictedproperties (polysites, sites in CDS) of uncharacterized miR-3960 binding sites. The studying of the miRNA properties is important for creation of diagnostic methods of cancer. Biomedical Informatics 2014-07-22 /pmc/articles/PMC4135290/ /pubmed/25187682 http://dx.doi.org/10.6026/97320630010423 Text en © 2014 Biomedical Informatics This is an open-access article, which permits unrestricted use, distribution, and reproduction in any medium, for non-commercial purposes, provided the original author and source are credited. |
spellingShingle | Hypothesis Ivashchenko, Anatoly Berillo, Olga Pyrkova, Anna Niyazova, Raigul Atambayeva, Shara MiR-3960 binding sites with mRNA of human genes |
title | MiR-3960 binding sites with mRNA of human genes |
title_full | MiR-3960 binding sites with mRNA of human genes |
title_fullStr | MiR-3960 binding sites with mRNA of human genes |
title_full_unstemmed | MiR-3960 binding sites with mRNA of human genes |
title_short | MiR-3960 binding sites with mRNA of human genes |
title_sort | mir-3960 binding sites with mrna of human genes |
topic | Hypothesis |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4135290/ https://www.ncbi.nlm.nih.gov/pubmed/25187682 http://dx.doi.org/10.6026/97320630010423 |
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