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Conservation defines functional motifs in the squint/nodal-related 1 RNA dorsal localization element

RNA localization is emerging as a general principle of sub-cellular protein localization and cellular organization. However, the sequence and structural requirements in many RNA localization elements remain poorly understood. Whereas transcription factor-binding sites in DNA can be recognized as sho...

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Autores principales: Gilligan, Patrick C., Kumari, Pooja, Lim, Shimin, Cheong, Albert, Chang, Alex, Sampath, Karuna
Formato: Texto
Lenguaje:English
Publicado: Oxford University Press 2011
Materias:
RNA
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3082914/
https://www.ncbi.nlm.nih.gov/pubmed/21149265
http://dx.doi.org/10.1093/nar/gkq1185
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author Gilligan, Patrick C.
Kumari, Pooja
Lim, Shimin
Cheong, Albert
Chang, Alex
Sampath, Karuna
author_facet Gilligan, Patrick C.
Kumari, Pooja
Lim, Shimin
Cheong, Albert
Chang, Alex
Sampath, Karuna
author_sort Gilligan, Patrick C.
collection PubMed
description RNA localization is emerging as a general principle of sub-cellular protein localization and cellular organization. However, the sequence and structural requirements in many RNA localization elements remain poorly understood. Whereas transcription factor-binding sites in DNA can be recognized as short degenerate motifs, and consensus binding sites readily inferred, protein-binding sites in RNA often contain structural features, and can be difficult to infer. We previously showed that zebrafish squint/nodal-related 1 (sqt/ndr1) RNA localizes to the future dorsal side of the embryo. Interestingly, mammalian nodal RNA can also localize to dorsal when injected into zebrafish embryos, suggesting that the sequence motif(s) may be conserved, even though the fish and mammal UTRs cannot be aligned. To define potential sequence and structural features, we obtained ndr1 3′-UTR sequences from approximately 50 fishes that are closely, or distantly, related to zebrafish, for high-resolution phylogenetic footprinting. We identify conserved sequence and structural motifs within the zebrafish/carp family and catfish. We find that two novel motifs, a single-stranded AGCAC motif and a small stem-loop, are required for efficient sqt RNA localization. These findings show that comparative sequencing in the zebrafish/carp family is an efficient approach for identifying weak consensus binding sites for RNA regulatory proteins.
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spelling pubmed-30829142011-04-27 Conservation defines functional motifs in the squint/nodal-related 1 RNA dorsal localization element Gilligan, Patrick C. Kumari, Pooja Lim, Shimin Cheong, Albert Chang, Alex Sampath, Karuna Nucleic Acids Res RNA RNA localization is emerging as a general principle of sub-cellular protein localization and cellular organization. However, the sequence and structural requirements in many RNA localization elements remain poorly understood. Whereas transcription factor-binding sites in DNA can be recognized as short degenerate motifs, and consensus binding sites readily inferred, protein-binding sites in RNA often contain structural features, and can be difficult to infer. We previously showed that zebrafish squint/nodal-related 1 (sqt/ndr1) RNA localizes to the future dorsal side of the embryo. Interestingly, mammalian nodal RNA can also localize to dorsal when injected into zebrafish embryos, suggesting that the sequence motif(s) may be conserved, even though the fish and mammal UTRs cannot be aligned. To define potential sequence and structural features, we obtained ndr1 3′-UTR sequences from approximately 50 fishes that are closely, or distantly, related to zebrafish, for high-resolution phylogenetic footprinting. We identify conserved sequence and structural motifs within the zebrafish/carp family and catfish. We find that two novel motifs, a single-stranded AGCAC motif and a small stem-loop, are required for efficient sqt RNA localization. These findings show that comparative sequencing in the zebrafish/carp family is an efficient approach for identifying weak consensus binding sites for RNA regulatory proteins. Oxford University Press 2011-04 2010-12-10 /pmc/articles/PMC3082914/ /pubmed/21149265 http://dx.doi.org/10.1093/nar/gkq1185 Text en © The Author(s) 2010. Published by Oxford University Press. http://creativecommons.org/licenses/by-nc/2.5 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.5), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle RNA
Gilligan, Patrick C.
Kumari, Pooja
Lim, Shimin
Cheong, Albert
Chang, Alex
Sampath, Karuna
Conservation defines functional motifs in the squint/nodal-related 1 RNA dorsal localization element
title Conservation defines functional motifs in the squint/nodal-related 1 RNA dorsal localization element
title_full Conservation defines functional motifs in the squint/nodal-related 1 RNA dorsal localization element
title_fullStr Conservation defines functional motifs in the squint/nodal-related 1 RNA dorsal localization element
title_full_unstemmed Conservation defines functional motifs in the squint/nodal-related 1 RNA dorsal localization element
title_short Conservation defines functional motifs in the squint/nodal-related 1 RNA dorsal localization element
title_sort conservation defines functional motifs in the squint/nodal-related 1 rna dorsal localization element
topic RNA
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3082914/
https://www.ncbi.nlm.nih.gov/pubmed/21149265
http://dx.doi.org/10.1093/nar/gkq1185
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