RNAe: an effective method for targeted protein translation enhancement by artificial non-coding RNA with SINEB2 repeat. Issue 9 (26th February 2015)
- Record Type:
- Journal Article
- Title:
- RNAe: an effective method for targeted protein translation enhancement by artificial non-coding RNA with SINEB2 repeat. Issue 9 (26th February 2015)
- Main Title:
- RNAe: an effective method for targeted protein translation enhancement by artificial non-coding RNA with SINEB2 repeat
- Authors:
- Yao, Yi
Jin, Shouhong
Long, Haizhou
Yu, Yingting
Zhang, Zhenming
Cheng, Ge
Xu, Chengwei
Ding, Yan
Guan, Qian
Li, Ning
Fu, Suneng
Chen, Xiang-Jun
Yan, Yong-Bin
Zhang, Hanshuo
Tong, Pei
Tan, Yue
Yu, Yang
Fu, Shushu
Li, Juan
He, Guang-Jun
Wu, Qiong - Abstract:
- Abstract: In this study, a universal protein expression enhancement RNA tool, termed RNAe, was developed by modifying a recently discovered natural long non-coding RNA. At the moment, RNAe is the only technology for gene expression enhancement, as opposed to silencing, at the post-transcriptional level. With this technology, an expression enhancement of 50–1000% is achievable, with more than 200% enhancement achieved in most cases. This work identified the sufficient and necessary element for RNAe function, which was found to be merely 300 nucleotides long and was named minRNAe. It contains a 72-nt 5' pairing sequence which determines the specificity, a 167-nt short non-pairing interspersed nuclear element (SINE) B2 sequence which enhances ribosome recruitment to the target mRNA, and a poly(A) tail, provided together on a plasmid bearing the appropriate sequences. Cellular delivery of RNAe was achieved using routine transfection. The RNAe platform was validated in several widely-used mammalian cell lines. It was proven to be efficient and flexible in specifically enhancing the expression of various endogenous and exogenous proteins of diverse functions in a dose-dependent manner. Compared to the expression-inhibitory tool RNAi, the RNAe tool has a comparable effect size, with an enhancing as opposed to inhibitory effect. One may predict that this brand new technology for enhancing the production of proteins will find wide applications in both research and biopharmaceuticalAbstract: In this study, a universal protein expression enhancement RNA tool, termed RNAe, was developed by modifying a recently discovered natural long non-coding RNA. At the moment, RNAe is the only technology for gene expression enhancement, as opposed to silencing, at the post-transcriptional level. With this technology, an expression enhancement of 50–1000% is achievable, with more than 200% enhancement achieved in most cases. This work identified the sufficient and necessary element for RNAe function, which was found to be merely 300 nucleotides long and was named minRNAe. It contains a 72-nt 5' pairing sequence which determines the specificity, a 167-nt short non-pairing interspersed nuclear element (SINE) B2 sequence which enhances ribosome recruitment to the target mRNA, and a poly(A) tail, provided together on a plasmid bearing the appropriate sequences. Cellular delivery of RNAe was achieved using routine transfection. The RNAe platform was validated in several widely-used mammalian cell lines. It was proven to be efficient and flexible in specifically enhancing the expression of various endogenous and exogenous proteins of diverse functions in a dose-dependent manner. Compared to the expression-inhibitory tool RNAi, the RNAe tool has a comparable effect size, with an enhancing as opposed to inhibitory effect. One may predict that this brand new technology for enhancing the production of proteins will find wide applications in both research and biopharmaceutical production. … (more)
- Is Part Of:
- Nucleic acids research. Volume 43:Issue 9(2015)
- Journal:
- Nucleic acids research
- Issue:
- Volume 43:Issue 9(2015)
- Issue Display:
- Volume 43, Issue 9 (2015)
- Year:
- 2015
- Volume:
- 43
- Issue:
- 9
- Issue Sort Value:
- 2015-0043-0009-0000
- Page Start:
- e58
- Page End:
- e58
- Publication Date:
- 2015-02-26
- Subjects:
- Nucleic acids -- Periodicals
Molecular biology -- Periodicals
572.805 - Journal URLs:
- http://nar.oxfordjournals.org/ ↗
http://www.ncbi.nlm.nih.gov/pmc/journals/4 ↗
http://ukcatalogue.oup.com/ ↗
http://firstsearch.oclc.org ↗ - DOI:
- 10.1093/nar/gkv125 ↗
- Languages:
- English
- ISSNs:
- 0305-1048
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6183.850000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 22039.xml