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Chemical Synthesis of U1 snRNA Derivatives
[Image: see text] U1 snRNA is an interesting biological tool for splicing correction and regulation of gene expression. However, U1 snRNA has never been chemically synthesized. In this study, the first chemical synthesis of U1snRNA and its analogues was carried out. Moreover, it was found that the b...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2013
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3901379/ https://www.ncbi.nlm.nih.gov/pubmed/23952175 http://dx.doi.org/10.1021/ol401917r |
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author | Ohkubo, Akihiro Kondo, Yasushi Suzuki, Makoto Kobayashi, Haruki Kanamori, Takashi Masaki, Yoshiaki Seio, Kohji Nagai, Kiyoshi Sekine, Mitsuo |
author_facet | Ohkubo, Akihiro Kondo, Yasushi Suzuki, Makoto Kobayashi, Haruki Kanamori, Takashi Masaki, Yoshiaki Seio, Kohji Nagai, Kiyoshi Sekine, Mitsuo |
author_sort | Ohkubo, Akihiro |
collection | PubMed |
description | [Image: see text] U1 snRNA is an interesting biological tool for splicing correction and regulation of gene expression. However, U1 snRNA has never been chemically synthesized. In this study, the first chemical synthesis of U1snRNA and its analogues was carried out. Moreover, it was found that the binding affinity of the modified U1 snRNA with an ethylene glycol linkage to snurportin 1 (nuclear import adaptor) was as high as that of the unmodified RNA. |
format | Online Article Text |
id | pubmed-3901379 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-39013792014-01-24 Chemical Synthesis of U1 snRNA Derivatives Ohkubo, Akihiro Kondo, Yasushi Suzuki, Makoto Kobayashi, Haruki Kanamori, Takashi Masaki, Yoshiaki Seio, Kohji Nagai, Kiyoshi Sekine, Mitsuo Org Lett [Image: see text] U1 snRNA is an interesting biological tool for splicing correction and regulation of gene expression. However, U1 snRNA has never been chemically synthesized. In this study, the first chemical synthesis of U1snRNA and its analogues was carried out. Moreover, it was found that the binding affinity of the modified U1 snRNA with an ethylene glycol linkage to snurportin 1 (nuclear import adaptor) was as high as that of the unmodified RNA. American Chemical Society 2013-08-16 2013-09-06 /pmc/articles/PMC3901379/ /pubmed/23952175 http://dx.doi.org/10.1021/ol401917r Text en Copyright © 2013 American Chemical Society Terms of Use CC-BY-NC-ND (http://pubs.acs.org/page/policy/authorchoice_ccbyncnd_termsofuse.html) |
spellingShingle | Ohkubo, Akihiro Kondo, Yasushi Suzuki, Makoto Kobayashi, Haruki Kanamori, Takashi Masaki, Yoshiaki Seio, Kohji Nagai, Kiyoshi Sekine, Mitsuo Chemical Synthesis of U1 snRNA Derivatives |
title | Chemical Synthesis of U1 snRNA Derivatives |
title_full | Chemical Synthesis of U1 snRNA Derivatives |
title_fullStr | Chemical Synthesis of U1 snRNA Derivatives |
title_full_unstemmed | Chemical Synthesis of U1 snRNA Derivatives |
title_short | Chemical Synthesis of U1 snRNA Derivatives |
title_sort | chemical synthesis of u1 snrna derivatives |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3901379/ https://www.ncbi.nlm.nih.gov/pubmed/23952175 http://dx.doi.org/10.1021/ol401917r |
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