¨Ubung Bioinformatik Von RNA- Und Proteinstrukturen

Total Page:16

File Type:pdf, Size:1020Kb

¨Ubung Bioinformatik Von RNA- Und Proteinstrukturen Ubung¨ Bioinformatik von RNA- und Proteinstrukturen Ronny Lorenz [email protected] Bioinformatik University of Leipzig Leipzig, Germany, April 14, 2014 RNA Secondary structure prediction Secondary structures can be uniquely decomposed into loops interior base pairs interior base pair closing base pair CG A A G 5 G U G 5 5 C 3 U C 3 3 CA C U AA closing base pair closing base pair stacking pair hairpin loop multi loop interior base pair closing base pair C G A GA G 5 5 A 3 3 CU C 5 3 AU G interior base pair UAUACGCA closing base pair interior loop bulge exterior loop RNA Secondary structure prediction X E(S) = E(L) L2S i j N 1 • The free energy of a secondary structure is the sum of the free energy of the loops its composed of • Loop energies depend on loop type, loop size and sequence • Energy parameters are measured experimentally or extrapolated by mathematical models RNA Secondary structure prediction Decomposition scheme F i,j = | i j i i+1 j i k k+1 j Ci,j = | | i j i j i d e j i uu+1 j Mi,j = | | i j i j−1j i uu+1j i u u+1 j ^ Mi,j = | i j i j−1j i j Programs / Program suites • Unafold / mfold (M. Zuker) http://mfold.rna.albany.edu/ ...the ’inventor’ of the DP recursion scheme • RNAstructure (D. Mathews) http://rna.urmc.rochester.edu/RNAstructure.html http://rna.urmc.rochester.edu/NNDB/ ...the energy parameter guys • ViennaRNA Package (I. Hofacker) http://www.tbi.univie.ac.at/RNA/ http://www.tbi.univie.ac.at/~ronny/RNA/ ...comprehensive compilation and very fast implementation of RNA structure prediction algorithms RNA/DNA sequence file formats • Simple textfile (ViennaRNA) CAAAGGCGACUCUCCUUAGACUCUAUAAAUAGUAAAUAGCUCCUAGGGACAAGGCUUACG • SEQ file (RNAstructure) ; There can be any number of comments. A title must immediately follow on the next line and be on one line. AAA GCGG UUTGTT UTCUTaaTCTXXXXUCAGG1 • FASTA >some random sequence CAAAGGCGACUCUCCUUAGACUCUAUAAAU AGUAAAUAGCUCCUAGGGACAAGGCUUACG • GenBank http://www.ncbi.nlm.nih.gov/Sitemap/samplerecord.html • EMBL http://www.ebi.ac.uk/ena/ • RNAML XML style storage of RNA sequence- and structure data • Clustal format for sequence alignments (used by many alignment programs) • Stockholm format sequence alignments (http://rfam.sanger.ac.uk/) RNA/DNA structure file formats • dot parenthesis (a.k.a. dot-bracket) notation UGGGAAUAGUCUCUUCCGAGUCUCGCGGGCGACGGGCGAUCUUCGAAAGUGGAAUCCGUA ..(((....((.(((.((((..((((.........))))..)))).))).))..)))... • BPSEQ format 1 G 8 2 G 7 3 C 0 4 A 0 5 U 0 6 U 0 7 C 2 8 C 1 • connectivity table (CT) format 8 1 G 0 2 8 1 2 G 1 3 7 2 3 C 2 4 0 3 4 A 3 5 0 4 5 U 4 6 0 5 6 U 5 7 0 6 7 C 6 8 2 7 8 C 7 0 1 8 • RNAML see also http://www.rnasoft.ca/strand/help.php The ViennaRNA Package www.tbi.univie.ac.at/~ronny/RNA • Source code available • Binary packages available (Fedora, Ubuntu, Debian, Windows) • FAST and accurate!!! http: //www.tbi.univie.ac.at/~ronny/RNA/performance.html • Reads simple sequence files, FASTA, clustal, and Stockholm formats • Produces Postscript plots, dot-bracket structures, other output • ViennaRNA Websuite: rna.tbi.univie.ac.at RNAfold Compute minimum free energy structures (...partition function, base pair probabilities, centroid-, and MEA-structure, etc...) • Sequence file, e.g. FASTA format (sequence.fa) >some random sequence UGGGAAUAGUCUCUUCCGAGUCUCGCGGGCGA CGGGCGAUCUUCGAAAGUGGAAUCCGUA • Run RNAfold $ RNAfold < sequence.fa >some random sequence UGGGAAUAGUCUCUUCCGAGUCUCGCGGGCGACGGGCGAUCUUCGAAAGUGGAAUCCGUA ..(((....((.(((.((((..((((.........))))..)))).))).))..)))... (-13.40) • Postscript structure plot U A U G A G A U U C U C G G G G G C C U U C G A G C U G U C G C A C C G G A A G C U U G U G A A U A A G C G C U G A G C RNAplot Draw and annotate RNA secondary structure plots • Sequence/Structure pair input, e.g. output of RNAfold >some random sequence UGGGAAUAGUCUCUUCCGAGUCUCGCGGGCGACGGGCGAUCUUCGAAAGUGGAAUCCGUA ..(((....((.(((.((((..((((.........))))..)))).))).))..)))... (-13.40) • Run RNAplot with different layout algorithm $ RNAfold < sequence.fa | RNAplot -t 0 C A G C G G G G G G C C G G C A U U C C U U G G C U A G A A U C U C G G C G G A G C A U U C G C U AG G C C G C U G G U G A U C G G C A A U A A A G G G G A U C C U U U C G G U G G C G U C C G A G U C G C C A C UG G G U U C A C C U G G G A A G A C C U A C U U A G C G G A U U U U G A A C U A G G A U A G C A U G C U U G C G U A G A A U U C A C G G A U A U G G • Run RNAplot with --pre="" option to create annotation macros $ RNAfold < sequence.fa | RNAplot --pre="" open resulting postscript plot in a text editor and investigate macros RNAeval Evaluate the free energy of a sequence/structure pair • Simple check if RNAfold and RNAeval score equally $ RNAfold < sequence.fa >some random sequence UGGGAAUAGUCUCUUCCGAGUCUCGCGGGCGACGGGCGAUCUUCGAAAGUGGAAUCCGUA ..(((....((.(((.((((..((((.........))))..)))).))).))..)))... (-13.40) $ RNAfold < sequence.fa | RNAeval UGGGAAUAGUCUCUUCCGAGUCUCGCGGGCGACGGGCGAUCUUCGAAAGUGGAAUCCGUA ..(((....((.(((.((((..((((.........))))..)))).))).))..)))... (-13.40) • Evaluate at 20°C and dangle model 1 $ RNAfold < sequence.fa | RNAeval -d 1 -T 20. UGGGAAUAGUCUCUUCCGAGUCUCGCGGGCGACGGGCGAUCUUCGAAAGUGGAAUCCGUA ..(((....((.(((.((((..((((.........))))..)))).))).))..)))... (-20.28) RNAeval Evaluate the free energy of a sequence/structure pair • Verbose output $ RNAfold < sequence.fa | RNAeval -v External loop : -140 Interior loop ( 3, 57) GC; ( 4, 56) GC: -330 Interior loop ( 4, 56) GC; ( 5, 55) AU: -240 Interior loop ( 5, 55) AU; ( 10, 52) UG: 380 Interior loop ( 10, 52) UG; ( 11, 51) CG: -150 Interior loop ( 11, 51) CG; ( 13, 49) CG: -10 Interior loop ( 13, 49) CG; ( 14, 48) UA: -210 Interior loop ( 14, 48) UA; ( 15, 47) UA: -90 Interior loop ( 15, 47) UA; ( 17, 45) CG: 120 Interior loop ( 17, 45) CG; ( 18, 44) GC: -240 Interior loop ( 18, 44) GC; ( 19, 43) AU: -240 Interior loop ( 19, 43) AU; ( 20, 42) GU: -60 Interior loop ( 20, 42) GU; ( 23, 39) UA: 290 Interior loop ( 23, 39) UA; ( 24, 38) CG: -240 Interior loop ( 24, 38) CG; ( 25, 37) GC: -240 Interior loop ( 25, 37) GC; ( 26, 36) CG: -340 Hairpin loop ( 26, 36) CG : 400 UGGGAAUAGUCUCUUCCGAGUCUCGCGGGCGACGGGCGAUCUUCGAAAGUGGAAUCCGUA ..(((....((.(((.((((..((((.........))))..)))).))).))..)))... (-13.40).
Recommended publications
  • Degeneracy and Genetic Assimilation in RNA Evolution Reza Rezazadegan1* and Christian Reidys1,2
    Rezazadegan and Reidys BMC Bioinformatics (2018) 19:543 https://doi.org/10.1186/s12859-018-2497-3 RESEARCH ARTICLE Open Access Degeneracy and genetic assimilation in RNA evolution Reza Rezazadegan1* and Christian Reidys1,2 Abstract Background: The neutral theory of Motoo Kimura stipulates that evolution is mostly driven by neutral mutations. However adaptive pressure eventually leads to changes in phenotype that involve non-neutral mutations. The relation between neutrality and adaptation has been studied in the context of RNA before and here we further study transitional mutations in the context of degenerate (plastic) RNA sequences and genetic assimilation. We propose quasineutral mutations, i.e. mutations which preserve an element of the phenotype set, as minimal mutations and study their properties. We also propose a general probabilistic interpretation of genetic assimilation and specialize it to the Boltzmann ensemble of RNA sequences. Results: We show that degenerate sequences i.e. sequences with more than one structure at the MFE level have the highest evolvability among all sequences and are central to evolutionary innovation. Degenerate sequences also tend to cluster together in the sequence space. The selective pressure in an evolutionary simulation causes the population to move towards regions with more degenerate sequences, i.e. regions at the intersection of different neutral networks, and this causes the number of such sequences to increase well beyond the average percentage of degenerate sequences in the sequence space. We also observe that evolution by quasineutral mutations tends to conserve the number of base pairs in structures and thereby maintains structural integrity even in the presence of pressure to the contrary.
    [Show full text]
  • Folding RNA/DNA Hybrid Duplexes
    Vol. 00 no. 00 BIOINFORMATICS Pages 1–2 Folding RNA/DNA hybrid duplexes Ronny Lorenz 1,∗, Ivo L Hofacker 1,2 and Stephan H Bernhart 2,∗ 1Institute for Theoretical Chemistry, University Vienna, Wahringer¨ Straße 17, 1090 Vienna, Austria 2Research group BCB, Faculty of Computer Science, University Vienna 3Department of Bioinformatics, University of Leipzig, Haertelstraße 16-18, 04109 Leipzig, Germany Received on XXXXX; revised on XXXXX; accepted on XXXXX Associate Editor: XXXXXXX ABSTRACT (for a review see e.g. [11]) or even their dimers, there is, to our Motivation: While there are numerous programs that can predict knowledge, no program that also includes the possibility to predict RNA or DNA secondary structures, a program that predicts RNA/DNA the full secondary structure of RNA/DNA hetero-dimers. This may hetero-dimers is still missing. The lack of easy to use tools for be due to the lack of compiled energy parameters, as there are only predicting their structure may be in part responsible for the small stacking energies available today. We introduce here a possibility number of reports of biologically relevant RNA/DNA hetero-dimers. to predict the secondary structure of such hetero-dimers within the Results: We present here an extension to the widely used widely used ViennaRNA Package. ViennaRNA Package [6] for the prediction of the structure of RNA/DNA hetero-dimers. Availability: http://www.tbi.univie.ac.at/˜ronny/RNA/vrna2.html 2 APPROACH Contact: [email protected] 2.1 Adaptation of the ViennaRNA Package For the prediction of RNA/DNA hetero-dimers, three distinct energy 1 INTRODUCTION parameter sets (RNA, DNA and mixed) are necessary.
    [Show full text]
  • Supplemental Material Predicting Transfer RNA Gene Activity From
    Supplemental Material Predicting transfer RNA gene activity from sequence and genome context 1 1,2 1 1 Bryan P. Thornlow ,​ Joel Armstrong ,​ Andrew D. Holmes ,​ Jonathan M. Howard ,​ Russell B. 1,2 ​ 1,2 ​ ​ ​ Corbett-Detig ,​ Todd M. Lowe ​ ​ 1 2 D​ epartment of Biomolecular Engineering, University of California, Santa Cruz, CA 95064; G​ enomics ​ Institute, University of California, Santa Cruz, CA 95064 Supplemental Material Supplemental Text Supplemental Methods Supplemental Figure S1 Supplemental Figure S2 Supplemental Figure S3 Supplemental Figure S4 Supplemental Figure S5 Supplemental Figure S6 Supplemental Figure S7 Supplemental Figure S8 Supplemental Figure S9 Supplemental Figure S10 Supplemental Figure S11 Supplemental References SUPPLEMENTAL TEXT: Possible tRNA gene classification and assembly errors. Ideally, we would observe that all species ​ contained at least one tRNA gene per expected anticodon (excluding anticodons for which no active tRNA gene is observed in human or mouse). We found three exceptions to this rule. C. hircus (goat) is the only ​ ​ species without a predicted active tRNA-Ser-TGA gene. C. hircus is also one of only three species that has ​ ​ any tRNA-Ser-GGA genes, and it has 27 such genes, one of which was predicted active. These 27 tRNA-Ser-GGA genes do exhibit some sequence similarity, as 21 of these share a 10-base 3’ flanking motif (AGAAGGAAAT). They may therefore reflect a very recent proliferation event. However, it is more likely that they represent assembly errors, because we have previously shown that the immediate 3’ flanking regions of tRNA genes experience high mutation rates (Thornlow et al. 2018), these 27 tRNA genes are found on 15 ​ ​ different chromosomes, and Ser-GGA is not a standard eukaryotic tRNA (Grosjean et al.
    [Show full text]
  • Ribotoolkit: an Integrated Platform for Analysis and Annotation of Ribosome Profiling Data to Decode Mrna Translation at Codon R
    W218–W229 Nucleic Acids Research, 2020, Vol. 48, Web Server issue Published online 19 May 2020 doi: 10.1093/nar/gkaa395 RiboToolkit: an integrated platform for analysis and annotation of ribosome profiling data to decode mRNA translation at codon resolution Qi Liu1,2,*, Tanya Shvarts3, Piotr Sliz2,3 and Richard I. Gregory 1,2,4,5,6,* 1Stem Cell Program, Division of Hematology/Oncology, Boston Children’s Hospital, Boston, MA 02115, USA, 2Department of Biological Chemistry and Molecular Pharmacology, Harvard Medical School, Boston, MA 02115, USA, 3Computational Health Informatics Program, Boston Children’s Hospital, Boston, MA 02115, USA, 4Department of Pediatrics, Harvard Medical School, Boston, MA 02115, USA, 5Harvard Initiative for RNA Medicine, Boston, MA 02115, USA and 6Harvard Stem Cell Institute, Cambridge, MA 02138, USA Received March 06, 2020; Revised April 23, 2020; Editorial Decision May 02, 2020; Accepted May 15, 2020 ABSTRACT INTRODUCTION Ribosome profiling (Ribo-seq) is a powerful technol- Ribosome profiling (Ribo-seq), also known as ribosome ogy for globally monitoring RNA translation; ranging footprinting, has revolutionized the ‘translatomics’ field from codon occupancy profiling, identification of ac- by mapping the position of ribosome-protected fragments tively translated open reading frames (ORFs), to the (RPFs), which typically range in length from 26 to 34 nu- quantification of translational efficiency under vari- cleotides (nt), over the entire transcriptome (1,2). The sci- entific community has employed Ribo-seq to answer awide ous physiological or experimental conditions. How- range of questions, ranging from the identification of trans- ever, analyzing and decoding translation information lated open reading frames (ORFs) to the quantification from Ribo-seq data is not trivial.
    [Show full text]
  • Comparative Ribosome Profiling Uncovers a Dominant Role for Translational Control in Toxoplasma Gondii
    Comparative ribosome profiling uncovers a dominant role for translational control in Toxoplasma gondii The MIT Faculty has made this article openly available. Please share how this access benefits you. Your story matters. Citation Hassan, Musa A. et al. "Comparative ribosome profiling uncovers a dominant role for translational control in Toxoplasma gondii." BMC Genomics 18 (December 2017): 961 © 2017 The Author(s) As Published http://dx.doi.org/10.1186/s12864-017-4362-6 Publisher BioMed Central Version Final published version Citable link http://hdl.handle.net/1721.1/114431 Terms of Use Creative Commons Attribution Detailed Terms http://creativecommons.org/licenses/by/4.0/ Hassan et al. BMC Genomics (2017) 18:961 DOI 10.1186/s12864-017-4362-6 RESEARCH ARTICLE Open Access Comparative ribosome profiling uncovers a dominant role for translational control in Toxoplasma gondii Musa A. Hassan1,2*, Juan J. Vasquez3,8, Chew Guo-Liang4, Markus Meissner5,6 and T. Nicolai Siegel3,6,7 Abstract Background: The lytic cycle of the protozoan parasite Toxoplasma gondii, which involves a brief sojourn in the extracellular space, is characterized by defined transcriptional profiles. For an obligate intracellular parasite that is shielded from the cytosolic host immune factors by a parasitophorous vacuole, the brief entry into the extracellular space is likely to exert enormous stress. Due to its role in cellular stress response, we hypothesize that translational control plays an important role in regulating gene expression in Toxoplasma during the lytic cycle. Unlike transcriptional profiles, insights into genome-wide translational profiles of Toxoplasma gondii are lacking. Methods: We have performed genome-wide ribosome profiling, coupled with high throughput RNA sequencing, in intracellular and extracellular Toxoplasma gondii parasites to investigate translational control during the lytic cycle.
    [Show full text]
  • Assessing the Quality of Cotranscriptional Folding Simulations
    bioRxiv preprint doi: https://doi.org/10.1101/2020.01.06.895607; this version posted January 6, 2020. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY 4.0 International license. Assessing the Quality of Cotranscriptional Folding Simulations Felix Kühnl, Peter F. Stadler, and Sven Findeiß Abstract Structural changes in RNAs are an important contributor to controlling gene expression not only at the post-transcriptional stage but also during transcription. A subclass of riboswitches and RNA thermometers located in the 5’ region of the primary transcript regulates the downstream functional unit – usually an ORF – through premature termination of transcription. Such elements not only occur naturally but they are also attractive devices in synthetic biology. The possibility to design such riboswitches or RNA thermometers is thus of considerable practical interest. Since these functional RNA elements act already during transcription, it is important to model and understand the dynamics of folding and, in particular, the formation of intermediate structures concurrently with transcription. Cotranscriptional folding simulations are therefore an important step to verify the functionality of design constructs before conducting expensive and labour-intensive wet lab experiments. For RNAs, full-fledged molecular dynamics simulations are far beyond practical reach both because of the size of the molecules and the time scales of interest. Even at the simplified level of secondary structures further approximations are necessary. The BarMap approach is based on representing the secondary structure landscape F.
    [Show full text]
  • Control of RNA Function by Conformational Design
    DISSERTATION / DOCTORAL THESIS Titel der Dissertation /Title of the Doctoral Thesis Control of RNA function by conformational design verfasst von / submitted by Mag. rer. nat. Stefan Badelt angestrebter akademischer Grad / in partial fulfilment of the requirements for the degree of Doctor of Philosophy (PhD) Wien, 2016 / Vienna, 2016 Studienkennzahl lt. Studienblatt / A 794 685 490 degree programme code as it appears on the student record sheet: Dissertationsgebiet lt. Studienblatt / Molekulare Biologie field of study as it appears on the student record sheet: Betreut von / Supervisor: Univ.-Prof. Dipl.-Phys. Dr. Ivo Hofacker Design landscapes >Output Input AGGAACAGUCGCACU ACCCACCUCGACAUC AGCAACA GUAAAUCAAAUUGGA AGGAUCU ACUGAAGCCCUUGGU AGGAUCA CUGGAGUCACCAGGG objective function AGGAACA GGUUUACGUACUACU design Energy landscapes 0.7 0.7 >Input -8.0 Output 3.9 3.7 1.1 2.8 1.2 1.3 2.3 0.8 AGGAACAGUCGCACU 3.5 2.6 2.6 2.8 3.9 2.3 -10.0 3.0 4.2 1.2 0.7 2.3 1.2 4.4 1.3 0.599999 1.3 2.4 1.0 0.8 100 1.5 2.0 1.2 0.8 97 98 99 2.8 1.4 1.0 94 95 93 96 92 2.3 0.7 2.6 0.8 91 1.5 1.3 2.0 2.6 1.6 89 90 1.9 0.8 2.0 86 88 87 2.9 2.3 1.9 1.3 1.3 ACCCACCUCGACAUC 0.6 83 85 84 82 2.6 1.0 0.8 0.8 77 81 79 78 80 0.7 76 1.9 74 75 73 1.5 72 0.7 -12.0 0.8 0.8 70 71 1.1 0.799999 1.2 0.8 69 68 0.8 0.8 0.8 63 65 64 66 67 0.9 1.2 1.2 59 60 58 61 62 1.2 1.4 1.7 1.2 55 54 57 56 3.1 3.0 4.2 52 53 51 49 50 0.7 1.0 45 44 46 47 48 42 43 41 3.5 1.0 38 39 40 1.3 0.6 2.6 1.3 0.8 0.8 0.8 GUAAAUCAAAUUGGA 37 35 36 34 32 33 31 30 28 29 27 1.2 0.8 24 25 26 23 -14.0 22 20 21 2.4 17
    [Show full text]
  • Machine Learning a Model for RNA Structure Prediction
    Machine learning a model for RNA structure prediction Nicola Calonaci1, Alisha Jones2,3, Francesca Cuturello1, Michael Sattler2,3, and Giovanni Bussi1 1International School for Advanced Studies, via Bonomea 265, 34136 Trieste, Italy 2Institute of Structural Biology, Helmoltz Zentrum M¨unchen, Neuherberg 85764, Germany 3Center for Integrated Protein Science M¨unchen and Bavarian NMR Center at Department of Chemistry, Technical University of Munich, Garching 85757, Germany Abstract RNA function crucially depends on its structure. Thermodynamic models currently used for secondary structure prediction rely on com- puting the partition function of folding ensembles, and can thus esti- mate minimum free-energy structures and ensemble populations. These models sometimes fail in identifying native structures unless comple- mented by auxiliary experimental data. Here, we build a set of mod- els that combine thermodynamic parameters, chemical probing data (DMS, SHAPE), and co-evolutionary data (Direct Coupling Analysis, DCA) through a network that outputs perturbations to the ensemble free energy. Perturbations are trained to increase the ensemble popu- lations of a representative set of known native RNA structures. In the chemical probing nodes of the network, a convolutional window com- bines neighboring reactivities, enlightening their structural information arXiv:2004.00351v2 [q-bio.BM] 5 Oct 2020 content and the contribution of local conformational ensembles. Regu- larization is used to limit overfitting and improve transferability. The most transferable model is selected through a cross-validation strategy that estimates the performance of models on systems on which they are not trained. With the selected model we obtain increased ensem- ble populations for native structures and more accurate predictions in an independent validation set.
    [Show full text]
  • Alternative DNA Secondary Structure Formation Affects RNA Polymerase II Promoter-Proximal Pausing in Human Karol Szlachta1†, Ryan G
    Szlachta et al. Genome Biology (2018) 19:89 https://doi.org/10.1186/s13059-018-1463-8 RESEARCH Open Access Alternative DNA secondary structure formation affects RNA polymerase II promoter-proximal pausing in human Karol Szlachta1†, Ryan G. Thys1†, Naomi D. Atkin1†, Levi C. T. Pierce2, Stefan Bekiranov1* and Yuh-Hwa Wang1* Abstract Background: Alternative DNA secondary structures can arise from single-stranded DNA when duplex DNA is unwound during DNA processes such as transcription, resulting in the regulationorperturbationofthese processes. We identify sites of high propensity to form stable DNA secondary structure across the human genome using Mfold and ViennaRNA programs with parameters for analyzing DNA. Results: The promoter-proximal regions of genes with paused transcription are significantly and energetically more favorable to form DNA secondary structure than non-paused genes or genes without RNA polymerase II (Pol II) binding. Using Pol II ChIP-seq, GRO-seq, NET-seq, and mNET-seq data, we arrive at a robust set of criteria for Pol II pausing, independent of annotation, and find that a highly stable secondary structure is likely to form about 10–50 nucleotides upstream of a Pol II pausing site. Structure probing data confirm the existence of DNA secondary structures enriched at the promoter-proximal regions of paused genes in human cells. Using an in vitro transcription assay, we demonstrate that Pol II pausing at HSPA1B, a human heat shock gene, is affected by manipulating DNA secondary structure upstream of the pausing site. Conclusions: Our results indicate alternative DNA secondary structure formation as a mechanism for how GC-rich sequences regulate RNA Pol II promoter-proximal pausing genome-wide.
    [Show full text]
  • RNA Secondary Structure Prediction Using Deep Learning with Thermodynamic Integration ✉ Kengo Sato 1 , Manato Akiyama1 & Yasubumi Sakakibara1
    ARTICLE https://doi.org/10.1038/s41467-021-21194-4 OPEN RNA secondary structure prediction using deep learning with thermodynamic integration ✉ Kengo Sato 1 , Manato Akiyama1 & Yasubumi Sakakibara1 Accurate predictions of RNA secondary structures can help uncover the roles of functional non-coding RNAs. Although machine learning-based models have achieved high performance in terms of prediction accuracy, overfitting is a common risk for such highly parameterized fi 1234567890():,; models. Here we show that over tting can be minimized when RNA folding scores learnt using a deep neural network are integrated together with Turner’s nearest-neighbor free energy parameters. Training the model with thermodynamic regularization ensures that folding scores and the calculated free energy are as close as possible. In computational experiments designed for newly discovered non-coding RNAs, our algorithm (MXfold2) achieves the most robust and accurate predictions of RNA secondary structures without sacrificing computational efficiency compared to several other algorithms. The results sug- gest that integrating thermodynamic information could help improve the robustness of deep learning-based predictions of RNA secondary structure. 1 Department of Biosciences and Informatics, Keio University, 3–14–1 Hiyoshi, Kohoku-ku, Yokohama, Japan. ✉email: [email protected] NATURE COMMUNICATIONS | (2021) 12:941 | https://doi.org/10.1038/s41467-021-21194-4 | www.nature.com/naturecommunications 1 ARTICLE NATURE COMMUNICATIONS | https://doi.org/10.1038/s41467-021-21194-4 ecent studies have revealed that functional non-coding ContextFold14, and other methods, and has enabled us to more RNAs (ncRNAs) play essential roles, including transcrip- accurately predict RNA secondary structures. However, rich para- R fi fi tional regulation and guiding modi cation, participating in meterization can easily cause over tting to the training data, thus various biological processes ranging from development to cell preventing robust predictions for a wide range of RNA sequences15.
    [Show full text]
  • A Short Tutorial on RNA Bioinformatics 1 RNA Web Services
    A short Tutorial on RNA Bioinformatics The ViennaRNA Package and related Programs 1 RNA Web Services This tutorial aims to give a basic introduction to using the command line pro- grams in the ViennaRNA Package in a UNIX-like (LINUX) environment. Of course, some of you may ask “Why are there no friendly graphical user inter- faces?”. Well, there are some, especially in the form of web services. If a few simple structure predictions is all you want to do, there are several useful sites for doing RNA structure analysis available on the web. Indeed many of the tasks described below can be performed using various web servers. Useful Web Services • Michael Zuker’s mfold server computes (sub)optimal structures and hy- bridization for DNA and RNA sequences with many options. http://mfold.rna.albany.edu/?q=mfold • BiBiServ, several small services e.g. pseudo-knot prediction pknotsRG, bi- stable structures paRNAss, alignment RNAforester, visualization RNAmovies, suboptimal structures RNAshapes http://bibiserv.techfak.uni-bielefeld.de/ • The ViennaRNA Server offers web access to many tools of the ViennaRNA Package, e.g. RNAfold, RNAalifold, RNAinverse and RNAz http://rna.tbi.univie.ac.at/ • several specialized servers such as pfold consensus structure prediction http://www.daimi.au.dk/~compbio/rnafold/ s-fold stochastic suboptimals and siRNA design http://sfold.wadsworth.org/ StrAl progressiv ncRNA alignment tool http://www.biophys.uni-duesseldorf.de/stral/ Web servers are also a good starting point for novice users since they provide a more intuitive interface. Moreover, the ViennaRNA Server will return the equivalent command line invocation for each request, making the transition from web services to locally installed software easier.
    [Show full text]
  • In Silico Study on RNA Structures of Intronic Mutations of Beta-Globin Gene [Version 1; Peer Review: 1 Approved with Reservations, 1 Not Approved]
    F1000Research 2020, 9:49 Last updated: 03 SEP 2020 RESEARCH ARTICLE In silico study on RNA structures of intronic mutations of beta-globin gene [version 1; peer review: 1 approved with reservations, 1 not approved] Nur Imaniati Sumantri1, Kenny Lischer2,3, Dian Rachma Wijayanti4, Tomy Abuzairi 1,3 1Biomedical Engineering, Department of Electrical Engineering, Faculty of Engineering, Universitas Indonesia, Depok, 16424, Indonesia 2Bioprocess Technology, Department of Chemical Engineering, Faculty of Engineering, Universitas Indonesia, Depok, 16424, Indonesia 3Research Center for Biomedical Engineering, Faculty of Engineering, Universitas Indonesia, Depok, 16424, Indonesia 4Department of Biotechnology, Faculty of Science and Technology, Binawan University, Jakarta, 13630, Indonesia v1 First published: 27 Jan 2020, 9:49 Open Peer Review https://doi.org/10.12688/f1000research.21953.1 Second version: 20 Jul 2020, 9:49 https://doi.org/10.12688/f1000research.21953.2 Reviewer Status Latest published: 01 Sep 2020, 9:49 https://doi.org/10.12688/f1000research.21953.3 Invited Reviewers Abstract 1 2 Background: Mutation of the beta-globin gene (HBB) interferes with primary mRNA transcription, leading to beta-thalassemia disease. The version 3 IVS1nt1 and IVS1nt5 mutations were reported as two of the most (revision) prevalent intronic mutations associated with beta-thalassemia major. 01 Sep 2020 These mutations may affect the mRNA structure of the human beta- globin (HBB) gene. However, the mechanism by which variation in HBB version 2 alters the mRNA structure remains unclear. The objective of this study (revision) report report was to unveil the secondary and tertiary conformation difference of 20 Jul 2020 the mutants compared to the wildtype using in silico analysis.
    [Show full text]