Principles for Predicting RNA Secondary Structure Design Difficulty. Issue 5 (27th February 2016)
- Record Type:
- Journal Article
- Title:
- Principles for Predicting RNA Secondary Structure Design Difficulty. Issue 5 (27th February 2016)
- Main Title:
- Principles for Predicting RNA Secondary Structure Design Difficulty
- Authors:
- Anderson-Lee, Jeff
Fisker, Eli
Kosaraju, Vineet
Wu, Michelle
Kong, Justin
Lee, Jeehyung
Lee, Minjae
Zada, Mathew
Treuille, Adrien
Das, Rhiju - Abstract:
- Abstract: Designing RNAs that form specific secondary structures is enabling better understanding and control of living systems through RNA-guided silencing, genome editing and protein organization. Little is known, however, about which RNA secondary structures might be tractable for downstream sequence design, increasing the time and expense of design efforts due to inefficient secondary structure choices. Here, we present insights into specific structural features that increase the difficulty of finding sequences that fold into a target RNA secondary structure, summarizing the design efforts of tens of thousands of human participants and three automated algorithms (RNAInverse, INFO-RNA and RNA-SSD) in the Eterna massive open laboratory. Subsequent tests through three independent RNA design algorithms (NUPACK, DSS-Opt and MODENA) confirmed the hypothesized importance of several features in determining design difficulty, including sequence length, mean stem length, symmetry and specific difficult-to-design motifs such as zigzags. Based on these results, we have compiled an Eterna100 benchmark of 100 secondary structure design challenges that span a large range in design difficulty to help test future efforts. Our in silico results suggest new routes for improving computational RNA design methods and for extending these insights to assess "designability" of single RNA structures, as well as of switches for in vitro and in vivo applications. Graphical abstract: Highlights: WeAbstract: Designing RNAs that form specific secondary structures is enabling better understanding and control of living systems through RNA-guided silencing, genome editing and protein organization. Little is known, however, about which RNA secondary structures might be tractable for downstream sequence design, increasing the time and expense of design efforts due to inefficient secondary structure choices. Here, we present insights into specific structural features that increase the difficulty of finding sequences that fold into a target RNA secondary structure, summarizing the design efforts of tens of thousands of human participants and three automated algorithms (RNAInverse, INFO-RNA and RNA-SSD) in the Eterna massive open laboratory. Subsequent tests through three independent RNA design algorithms (NUPACK, DSS-Opt and MODENA) confirmed the hypothesized importance of several features in determining design difficulty, including sequence length, mean stem length, symmetry and specific difficult-to-design motifs such as zigzags. Based on these results, we have compiled an Eterna100 benchmark of 100 secondary structure design challenges that span a large range in design difficulty to help test future efforts. Our in silico results suggest new routes for improving computational RNA design methods and for extending these insights to assess "designability" of single RNA structures, as well as of switches for in vitro and in vivo applications. Graphical abstract: Highlights: We outline several secondary structure elements and structural idiosyncrasies that lead to difficult RNA design problems, and we test a principle of least elements. We describe the contributions of symmetry to design difficulty and its interplay with the presence and repetition of difficult secondary structure elements. We introduce the Eterna100 benchmark for evaluating RNA design methods and evaluate six existing algorithms using this benchmark. This is the first paper based on dominant writing contributions—and co-lead authorship—by non-expert citizen scientists recruited through a video game. … (more)
- Is Part Of:
- Journal of molecular biology. Volume 428:Issue 5 Part A(2016:Mar. 01)
- Journal:
- Journal of molecular biology
- Issue:
- Volume 428:Issue 5 Part A(2016:Mar. 01)
- Issue Display:
- Volume 428, Issue 5, Part 1 (2016)
- Year:
- 2016
- Volume:
- 428
- Issue:
- 5
- Part:
- 1
- Issue Sort Value:
- 2016-0428-0005-0001
- Page Start:
- 748
- Page End:
- 757
- Publication Date:
- 2016-02-27
- Subjects:
- RNA design -- RNA secondary structure -- inverse folding -- benchmark -- citizen science
Molecular biology -- Periodicals
Biology -- Periodicals
Biochemistry -- Periodicals
Bacteriology -- Periodicals
Molecular Biology -- Periodicals
Biochemistry -- Periodicals
Biologie moléculaire -- Périodiques
Biologie -- Périodiques
Biochimie -- Périodiques
Moleculaire biologie
Biochemistry
Biology
Molecular biology
Periodicals
572.805 - Journal URLs:
- http://www.sciencedirect.com/science/journal/00222836 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.jmb.2015.11.013 ↗
- Languages:
- English
- ISSNs:
- 0022-2836
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 5020.700000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 8098.xml