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Transport and Localization Elements in Myelin Basic Protein mRNA
Myelin basic protein (MBP) mRNA is localized to myelin produced by oligodendrocytes of the central nervous system. MBP mRNA microinjected into oligodendrocytes in primary culture is assembled into granules in the perikaryon, transported along the processes, and localized to the myelin compartment. I...
Autores principales: | , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
The Rockefeller University Press
1997
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2136761/ https://www.ncbi.nlm.nih.gov/pubmed/9281585 |
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author | Ainger, Kevin Avossa, Daniela Diana, Amy S. Barry, Christopher Barbarese, Elisa Carson, John H. |
author_facet | Ainger, Kevin Avossa, Daniela Diana, Amy S. Barry, Christopher Barbarese, Elisa Carson, John H. |
author_sort | Ainger, Kevin |
collection | PubMed |
description | Myelin basic protein (MBP) mRNA is localized to myelin produced by oligodendrocytes of the central nervous system. MBP mRNA microinjected into oligodendrocytes in primary culture is assembled into granules in the perikaryon, transported along the processes, and localized to the myelin compartment. In this work, microinjection of various deleted and chimeric RNAs was used to delineate regions in MBP mRNA that are required for transport and localization in oligodendrocytes. The results indicate that transport requires a 21-nucleotide sequence, termed the RNA transport signal (RTS), in the 3′ UTR of MBP mRNA. Homologous sequences are present in several other localized mRNAs, suggesting that the RTS represents a general transport signal in a variety of different cell types. Insertion of the RTS from MBP mRNA into nontransported mRNAs, causes the RNA to be transported to the oligodendrocyte processes. Localization of mRNA to the myelin compartment requires an additional element, termed the RNA localization region (RLR), contained between nucleotide 1,130 and 1,473 in the 3′ UTR of MBP mRNA. Computer analysis predicts that this region contains a stable secondary structure. If the coding region of the mRNA is deleted, the RLR is no longer required for localization, and the region between nucleotide 667 and 953, containing the RTS, is sufficient for both RNA transport and localization. Thus, localization of coding RNA is RLR dependent, and localization of noncoding RNA is RLR independent, suggesting that they are localized by different pathways. |
format | Text |
id | pubmed-2136761 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1997 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-21367612008-05-01 Transport and Localization Elements in Myelin Basic Protein mRNA Ainger, Kevin Avossa, Daniela Diana, Amy S. Barry, Christopher Barbarese, Elisa Carson, John H. J Cell Biol Article Myelin basic protein (MBP) mRNA is localized to myelin produced by oligodendrocytes of the central nervous system. MBP mRNA microinjected into oligodendrocytes in primary culture is assembled into granules in the perikaryon, transported along the processes, and localized to the myelin compartment. In this work, microinjection of various deleted and chimeric RNAs was used to delineate regions in MBP mRNA that are required for transport and localization in oligodendrocytes. The results indicate that transport requires a 21-nucleotide sequence, termed the RNA transport signal (RTS), in the 3′ UTR of MBP mRNA. Homologous sequences are present in several other localized mRNAs, suggesting that the RTS represents a general transport signal in a variety of different cell types. Insertion of the RTS from MBP mRNA into nontransported mRNAs, causes the RNA to be transported to the oligodendrocyte processes. Localization of mRNA to the myelin compartment requires an additional element, termed the RNA localization region (RLR), contained between nucleotide 1,130 and 1,473 in the 3′ UTR of MBP mRNA. Computer analysis predicts that this region contains a stable secondary structure. If the coding region of the mRNA is deleted, the RLR is no longer required for localization, and the region between nucleotide 667 and 953, containing the RTS, is sufficient for both RNA transport and localization. Thus, localization of coding RNA is RLR dependent, and localization of noncoding RNA is RLR independent, suggesting that they are localized by different pathways. The Rockefeller University Press 1997-09-08 /pmc/articles/PMC2136761/ /pubmed/9281585 Text en This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/). |
spellingShingle | Article Ainger, Kevin Avossa, Daniela Diana, Amy S. Barry, Christopher Barbarese, Elisa Carson, John H. Transport and Localization Elements in Myelin Basic Protein mRNA |
title | Transport and Localization Elements in Myelin Basic Protein mRNA |
title_full | Transport and Localization Elements in Myelin Basic Protein mRNA |
title_fullStr | Transport and Localization Elements in Myelin Basic Protein mRNA |
title_full_unstemmed | Transport and Localization Elements in Myelin Basic Protein mRNA |
title_short | Transport and Localization Elements in Myelin Basic Protein mRNA |
title_sort | transport and localization elements in myelin basic protein mrna |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2136761/ https://www.ncbi.nlm.nih.gov/pubmed/9281585 |
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