4
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access

      Predictive evolution of metabolic phenotypes using model‐designed environments

      research-article

      Read this article at

      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          Adaptive evolution under controlled laboratory conditions has been highly effective in selecting organisms with beneficial phenotypes such as stress tolerance. The evolution route is particularly attractive when the organisms are either difficult to engineer or the genetic basis of the phenotype is complex. However, many desired traits, like metabolite secretion, have been inaccessible to adaptive selection due to their trade‐off with cell growth. Here, we utilize genome‐scale metabolic models to design nutrient environments for selecting lineages with enhanced metabolite secretion. To overcome the growth‐secretion trade‐off, we identify environments wherein growth becomes correlated with a secondary trait termed tacking trait. The latter is selected to be coupled with the desired trait in the application environment where the trait manifestation is required. Thus, adaptive evolution in the model‐designed selection environment and subsequent return to the application environment is predicted to enhance the desired trait. We experimentally validate this strategy by evolving Saccharomyces cerevisiae for increased secretion of aroma compounds, and confirm the predicted flux‐rerouting using genomic, transcriptomic, and proteomic analyses. Overall, model‐designed selection environments open new opportunities for predictive evolution.

          Abstract

          EvolveX, a new algorithm enabling model‐guided design of chemical environments for targeted adaptive evolution, is applied to evolve a wine yeast strain for increased aroma secretion.

          Related collections

          Most cited references100

          • Record: found
          • Abstract: found
          • Article: found
          Is Open Access

          Moderated estimation of fold change and dispersion for RNA-seq data with DESeq2

          In comparative high-throughput sequencing assays, a fundamental task is the analysis of count data, such as read counts per gene in RNA-seq, for evidence of systematic changes across experimental conditions. Small replicate numbers, discreteness, large dynamic range and the presence of outliers require a suitable statistical approach. We present DESeq2, a method for differential analysis of count data, using shrinkage estimation for dispersions and fold changes to improve stability and interpretability of estimates. This enables a more quantitative analysis focused on the strength rather than the mere presence of differential expression. The DESeq2 package is available at http://www.bioconductor.org/packages/release/bioc/html/DESeq2.html. Electronic supplementary material The online version of this article (doi:10.1186/s13059-014-0550-8) contains supplementary material, which is available to authorized users.
            Bookmark
            • Record: found
            • Abstract: found
            • Article: not found

            STAR: ultrafast universal RNA-seq aligner.

            Accurate alignment of high-throughput RNA-seq data is a challenging and yet unsolved problem because of the non-contiguous transcript structure, relatively short read lengths and constantly increasing throughput of the sequencing technologies. Currently available RNA-seq aligners suffer from high mapping error rates, low mapping speed, read length limitation and mapping biases. To align our large (>80 billon reads) ENCODE Transcriptome RNA-seq dataset, we developed the Spliced Transcripts Alignment to a Reference (STAR) software based on a previously undescribed RNA-seq alignment algorithm that uses sequential maximum mappable seed search in uncompressed suffix arrays followed by seed clustering and stitching procedure. STAR outperforms other aligners by a factor of >50 in mapping speed, aligning to the human genome 550 million 2 × 76 bp paired-end reads per hour on a modest 12-core server, while at the same time improving alignment sensitivity and precision. In addition to unbiased de novo detection of canonical junctions, STAR can discover non-canonical splices and chimeric (fusion) transcripts, and is also capable of mapping full-length RNA sequences. Using Roche 454 sequencing of reverse transcription polymerase chain reaction amplicons, we experimentally validated 1960 novel intergenic splice junctions with an 80-90% success rate, corroborating the high precision of the STAR mapping strategy. STAR is implemented as a standalone C++ code. STAR is free open source software distributed under GPLv3 license and can be downloaded from http://code.google.com/p/rna-star/.
              Bookmark
              • Record: found
              • Abstract: found
              • Article: found
              Is Open Access

              limma powers differential expression analyses for RNA-sequencing and microarray studies

              limma is an R/Bioconductor software package that provides an integrated solution for analysing data from gene expression experiments. It contains rich features for handling complex experimental designs and for information borrowing to overcome the problem of small sample sizes. Over the past decade, limma has been a popular choice for gene discovery through differential expression analyses of microarray and high-throughput PCR data. The package contains particularly strong facilities for reading, normalizing and exploring such data. Recently, the capabilities of limma have been significantly expanded in two important directions. First, the package can now perform both differential expression and differential splicing analyses of RNA sequencing (RNA-seq) data. All the downstream analysis tools previously restricted to microarray data are now available for RNA-seq as well. These capabilities allow users to analyse both RNA-seq and microarray data with very similar pipelines. Second, the package is now able to go past the traditional gene-wise expression analyses in a variety of ways, analysing expression profiles in terms of co-regulated sets of genes or in terms of higher-order expression signatures. This provides enhanced possibilities for biological interpretation of gene expression differences. This article reviews the philosophy and design of the limma package, summarizing both new and historical features, with an emphasis on recent enhancements and features that have not been previously described.
                Bookmark

                Author and article information

                Contributors
                kp533@cam.ac.uk
                Journal
                Mol Syst Biol
                Mol Syst Biol
                10.1002/(ISSN)1744-4292
                MSB
                msb
                Molecular Systems Biology
                John Wiley and Sons Inc. (Hoboken )
                1744-4292
                06 October 2022
                October 2022
                : 18
                : 10 ( doiID: 10.1002/msb.v18.10 )
                : e10980
                Affiliations
                [ 1 ] European Molecular Biology Laboratory Heidelberg Germany
                [ 2 ] VTT Technical Research Centre of Finland Ltd Espoo Finland
                [ 3 ] Department of Bioproducts and Biosystems Aalto University Espoo Finland
                [ 4 ] Department of Chemistry and Molecular Biology University of Gothenburg Gothenburg Sweden
                [ 5 ] Departament Bioquímica i Biotecnologia, Facultat d'Enologia Universitat Rovira i Virgili Tarragona Spain
                [ 6 ] Department of Biotechnology and Food Science NTNU – Norwegian University of Science and Technology Trondheim Norway
                [ 7 ] Instituto de Ciencias de la Vid y delVino (CSIC, Gobierno de la Rioja, Universidad de La Rioja) Finca La Grajera Logroño Spain
                [ 8 ] Medical Research Council (MRC) Toxicology Unit University of Cambridge Cambridge UK
                Author notes
                [*] [* ]Corresponding author. Tel: +44 01223 3 35640; E‐mail: kp533@ 123456cam.ac.uk
                [ † ]

                These authors contributed equally to this work

                Author information
                https://orcid.org/0000-0003-1075-7448
                https://orcid.org/0000-0002-9125-326X
                https://orcid.org/0000-0002-0763-1679
                https://orcid.org/0000-0001-6144-2740
                https://orcid.org/0000-0002-0130-6111
                https://orcid.org/0000-0002-6166-8640
                Article
                MSB202210980
                10.15252/msb.202210980
                9536503
                36201279
                648a1aee-75e6-4826-8055-fdd0bd28af7e
                © 2022 The Authors. Published under the terms of the CC BY 4.0 license.

                This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.

                History
                : 24 August 2022
                : 16 February 2022
                : 26 August 2022
                Page count
                Figures: 5, Tables: 1, Pages: 18, Words: 16945
                Funding
                Funded by: Academy of Finland (AKA) , doi 10.13039/501100002341;
                Award ID: 310514
                Award ID: 314125
                Award ID: 329930
                Funded by: Bundesministerium für Bildung und Forschung (BMBF) , doi 10.13039/501100002347;
                Award ID: 031A605
                Funded by: EC ¦ H2020 ¦ PRIORITY 'Excellent science' ¦ H2020 European Research Council (ERC) , doi 10.13039/100010663;
                Award ID: 866028
                Funded by: MInistry of Science, Innovation, and Universities, Spain
                Award ID: PCI2018‐092962
                Funded by: The Research Council of Norway
                Award ID: 245160
                Categories
                Article
                Articles
                Custom metadata
                2.0
                October 2022
                Converter:WILEY_ML3GV2_TO_JATSPMC version:6.2.0 mode:remove_FC converted:06.10.2022

                Quantitative & Systems biology
                adaptive evolution,genome‐scale metabolic model,predictive evolution,saccharomyces cerevisiae,wine aroma,biotechnology & synthetic biology,metabolism,methods & resources

                Comments

                Comment on this article