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Changes in snoRNA and snRNA Abundance in the Human, Chimpanzee, Macaque, and Mouse Brain

Small nuclear and nucleolar RNAs (snRNAs and snoRNAs) are known to be functionally and evolutionarily conserved elements of transcript processing machinery. Here, we investigated the expression evolution of snRNAs and snoRNAs by measuring their abundance in the frontal cortex of humans, chimpanzees,...

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Autores principales: Zhang, Bin, Han, Dingding, Korostelev, Yuriy, Yan, Zheng, Shao, Ningyi, Khrameeva, Ekaterina, Velichkovsky, Boris M., Chen, Yi-Ping Phoebe, Gelfand, Mikhail S., Khaitovich, Philipp
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4824147/
https://www.ncbi.nlm.nih.gov/pubmed/26926764
http://dx.doi.org/10.1093/gbe/evw038
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author Zhang, Bin
Han, Dingding
Korostelev, Yuriy
Yan, Zheng
Shao, Ningyi
Khrameeva, Ekaterina
Velichkovsky, Boris M.
Chen, Yi-Ping Phoebe
Gelfand, Mikhail S.
Khaitovich, Philipp
author_facet Zhang, Bin
Han, Dingding
Korostelev, Yuriy
Yan, Zheng
Shao, Ningyi
Khrameeva, Ekaterina
Velichkovsky, Boris M.
Chen, Yi-Ping Phoebe
Gelfand, Mikhail S.
Khaitovich, Philipp
author_sort Zhang, Bin
collection PubMed
description Small nuclear and nucleolar RNAs (snRNAs and snoRNAs) are known to be functionally and evolutionarily conserved elements of transcript processing machinery. Here, we investigated the expression evolution of snRNAs and snoRNAs by measuring their abundance in the frontal cortex of humans, chimpanzees, rhesus monkeys, and mice. Although snRNA expression is largely conserved, 44% of the 185 measured snoRNA and 40% of the 134 snoRNA families showed significant expression divergence among species. The snRNA and snoRNA expression divergence included drastic changes unique to humans: A 10-fold elevated expression of U1 snRNA and a 1,000-fold drop in expression of SNORA29. The decreased expression of SNORA29 might be due to two mutations that affect secondary structure stability. Using in situ hybridization, we further localized SNORA29 expression to nucleolar regions of neuronal cells. Our study presents the first observation of snoRNA abundance changes specific to the human lineage and suggests a possible mechanism underlying these changes.
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spelling pubmed-48241472016-04-08 Changes in snoRNA and snRNA Abundance in the Human, Chimpanzee, Macaque, and Mouse Brain Zhang, Bin Han, Dingding Korostelev, Yuriy Yan, Zheng Shao, Ningyi Khrameeva, Ekaterina Velichkovsky, Boris M. Chen, Yi-Ping Phoebe Gelfand, Mikhail S. Khaitovich, Philipp Genome Biol Evol Research Article Small nuclear and nucleolar RNAs (snRNAs and snoRNAs) are known to be functionally and evolutionarily conserved elements of transcript processing machinery. Here, we investigated the expression evolution of snRNAs and snoRNAs by measuring their abundance in the frontal cortex of humans, chimpanzees, rhesus monkeys, and mice. Although snRNA expression is largely conserved, 44% of the 185 measured snoRNA and 40% of the 134 snoRNA families showed significant expression divergence among species. The snRNA and snoRNA expression divergence included drastic changes unique to humans: A 10-fold elevated expression of U1 snRNA and a 1,000-fold drop in expression of SNORA29. The decreased expression of SNORA29 might be due to two mutations that affect secondary structure stability. Using in situ hybridization, we further localized SNORA29 expression to nucleolar regions of neuronal cells. Our study presents the first observation of snoRNA abundance changes specific to the human lineage and suggests a possible mechanism underlying these changes. Oxford University Press 2016-02-28 /pmc/articles/PMC4824147/ /pubmed/26926764 http://dx.doi.org/10.1093/gbe/evw038 Text en © The Author 2016. Published by Oxford University Press on behalf of the Society for Molecular Biology and Evolution. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Research Article
Zhang, Bin
Han, Dingding
Korostelev, Yuriy
Yan, Zheng
Shao, Ningyi
Khrameeva, Ekaterina
Velichkovsky, Boris M.
Chen, Yi-Ping Phoebe
Gelfand, Mikhail S.
Khaitovich, Philipp
Changes in snoRNA and snRNA Abundance in the Human, Chimpanzee, Macaque, and Mouse Brain
title Changes in snoRNA and snRNA Abundance in the Human, Chimpanzee, Macaque, and Mouse Brain
title_full Changes in snoRNA and snRNA Abundance in the Human, Chimpanzee, Macaque, and Mouse Brain
title_fullStr Changes in snoRNA and snRNA Abundance in the Human, Chimpanzee, Macaque, and Mouse Brain
title_full_unstemmed Changes in snoRNA and snRNA Abundance in the Human, Chimpanzee, Macaque, and Mouse Brain
title_short Changes in snoRNA and snRNA Abundance in the Human, Chimpanzee, Macaque, and Mouse Brain
title_sort changes in snorna and snrna abundance in the human, chimpanzee, macaque, and mouse brain
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4824147/
https://www.ncbi.nlm.nih.gov/pubmed/26926764
http://dx.doi.org/10.1093/gbe/evw038
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