Rat BodyMap transcriptomes reveal unique circular RNA features across tissue types and developmental stages
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Author
Zhou, TongXie, Xueying
Li, Musheng
Shi, Junchao
Zhou, Jin J
Knox, Kenneth S
Wang, Ting
Chen, Qi
Gu, Wanjun
Affiliation
Univ Arizona, Dept Epidemiol & BiostatUniv Arizona, Coll Med Phoenix, Dept Internal Med
Issue Date
2018-08-09
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Zhou, T., Xie, X., Li, M., Shi, J., Zhou, J. J., Knox, K. S., ... & Gu, W. (2018). Rat BodyMap transcriptomes reveal unique circular RNA features across tissue types and developmental stages. Rna, 24(11), 1443-1456.Journal
RNARights
© 2018 Zhou et al. This article, published in RNA, is available under a Creative Commons License (Attribution 4.0 International), as described at http://creativecommons.org/licenses/by/4.0/.Collection Information
This item from the UA Faculty Publications collection is made available by the University of Arizona with support from the University of Arizona Libraries. If you have questions, please contact us at repository@u.library.arizona.edu.Abstract
Circular RNAs (circRNAs) are a novel class of regulatory RNAs. Here, we present a comprehensive investigation of circRNA expression profiles across 11 tissues and four developmental stages in rats, along with cross-species analyses in humans and mice. Although the expression of circRNAs is positively correlated with that of cognate mRNAs, highly expressed genes tend to splice a larger fraction of circular transcripts. Moreover, circRNAs exhibit higher tissue specificity than cognate mRNAs. Intriguingly, while we observed a monotonic increase of circRNA abundance with age in the rat brain, we further discovered a dynamic, age-dependent pattern of circRNA expression in the testes that is characterized by a dramatic increase with advancing stages of sexual maturity and a decrease with aging. The age-sensitive testicular circRNAs are highly associated with spermatogenesis, independent of cognate mRNA expression. The tissue/age implications of circRNAs suggest that they present unique physiological functions rather than simply occurring as occasional by-products of gene transcription.Note
Open access articleISSN
1355-8382EISSN
1469-9001PubMed ID
30093490Version
Final published versionae974a485f413a2113503eed53cd6c53
10.1261/rna.067132.118
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Except where otherwise noted, this item's license is described as © 2018 Zhou et al. This article, published in RNA, is available under a Creative Commons License (Attribution 4.0 International), as described at http://creativecommons.org/licenses/by/4.0/.
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