Movatterモバイル変換


[0]ホーム

URL:


Skip to main content

Thank you for visiting nature.com. You are using a browser version with limited support for CSS. To obtain the best experience, we recommend you use a more up to date browser (or turn off compatibility mode in Internet Explorer). In the meantime, to ensure continued support, we are displaying the site without styles and JavaScript.

Advertisement

Nature Ecology & Evolution
  • Article
  • Published:

Random sequences are an abundant source of bioactive RNAs or peptides

Nature Ecology & Evolutionvolume 1, Article number: 0127 (2017)Cite this article

Subjects

Abstract

It is generally assumed that new genes arise through duplication and/or recombination of existing genes. The probability that a new functional gene could arise out of random non-coding DNA is so far considered to be negligible, as it seems unlikely that such an RNA or protein sequence could have an initial function that influences the fitness of an organism. Here, we have tested this question systematically, by expressing clones with random sequences inEscherichia coli and subjecting them to competitive growth. Contrary to expectations, we find that random sequences with bioactivity are not rare. In our experiments we find that up to 25% of the evaluated clones enhance the growth rate of their cells and up to 52% inhibit growth. Testing of individual clones in competition assays confirms their activity and provides an indication that their activity could be exerted by either the transcribed RNA or the translated peptide. This suggests that transcribed and translated random parts of the genome could indeed have a high potential to become functional. The results also suggest that random sequences may become an effective new source of molecules for studying cellular functions, as well as for pharmacological activity screening.

This is a preview of subscription content,access via your institution

Access options

Access through your institution

Access Nature and 54 other Nature Portfolio journals

Get Nature+, our best-value online-access subscription

9,800 Yen / 30 days

cancel any time

Subscribe to this journal

Receive 12 digital issues and online access to articles

¥14,900 per year

only ¥1,242 per issue

Buy this article

  • Purchase on SpringerLink
  • Instant access to full article PDF

Prices may be subject to local taxes which are calculated during checkout

Figure 1: Induction of expression through IPTG drives changes in clone frequency over time.
Figure 2: Examples of four clones with significant changes in frequency over time.
Figure 3: Assessment of read depth on detection power.
Figure 4: Expression of peptides.
Figure 5: Growth competition experiment with three selected clones.

Similar content being viewed by others

References

  1. Jacob, F. Evolution and tinkering.Science196, 1161–1166 (1977).

    Article CAS  Google Scholar 

  2. Tautz, D. The discovery ofde novo gene evolution.Perspect. Biol. Med.57, 149–161 (2014).

    Article  Google Scholar 

  3. Chothia, C. Proteins. One thousand families for the molecular biologist.Nature357, 543–544 (1992).

    Article CAS  Google Scholar 

  4. Lupas, A. N., Ponting, C. P. & Russell, R. B. On the evolution of protein folds: are similar motifs in different protein folds the result of convergence, insertion, or relics of an ancient peptide world?J. Struct. Biol.134, 191–203 (2001).

    Article CAS  Google Scholar 

  5. Orengo, C. A. & Thornton, J. M. Protein families and their evolution—a structural perspective.Annu. Rev. Biochem.74, 867–900 (2005).

    Article CAS  Google Scholar 

  6. Carvunis, A. R. et al. Proto-genes andde novo gene birth.Nature487, 370–374 (2012).

    Article CAS  Google Scholar 

  7. Reinhardt, J. A. et al.De novo ORFs inDrosophila are important to organismal fitness and evolved rapidly from previously non-coding sequences.PLoS Genet.9, e1003860 (2013).

    Article  Google Scholar 

  8. Zhao, L., Saelao, P., Jones, C. D. & Begun, D. J. Origin and spread ofde novo genes inDrosophila melanogaster populations.Science343, 769–772 (2014).

    Article CAS  Google Scholar 

  9. Neme, R. & Tautz, D. Fast turnover of genome transcription across evolutionary time exposes entire non-coding DNA tode novo gene emergence.eLife5, e09977 (2016).

    Article  Google Scholar 

  10. Tautz, D. & Domazet-Loso, T. The evolutionary origin of orphan genes.Nat. Rev. Genet.12, 692–702 (2011).

    Article CAS  Google Scholar 

  11. Xie, C. et al. Hominoid-specificde novo protein-coding genes originating from long non-coding RNAs.PLoS Genet.8, e1002942 (2012).

    Article CAS  Google Scholar 

  12. Ruiz-Orera, J., Messeguer, X., Subirana, J. A. & Alba, M. M. Long non-coding RNAs as a source of new peptides.Elife3, e03523 (2014).

    Article  Google Scholar 

  13. Barrick, J. E. & Lenski, R. E. Genome dynamics during experimental evolution.Nat. Rev. Genet.14, 827–839 (2013).

    Article CAS  Google Scholar 

  14. Stepanov, V. G. & Fox, G. E. Stress-drivenin vivo selection of a functional mini-gene from a randomized DNA library expressing combinatorial peptides inEscherichia coli.Mol. Biol. Evol.24, 1480–1491 (2007).

    Article CAS  Google Scholar 

  15. Love, M. I., Huber, W. & Anders, S. Moderated estimation of fold change and dispersion for RNA-seq data with DESeq2.Genome Biol.15, 550 (2014).

    Article  Google Scholar 

  16. Keefe, A. D. & Szostak, J. W. Functional proteins from a random-sequence library.Nature410, 715–718 (2001).

    Article CAS  Google Scholar 

  17. Uversky, V. N. & Dunker, A. K. Understanding protein non-folding.BBA-Proteins Proteom.1804, 1231–1264 (2010).

    Article CAS  Google Scholar 

  18. Tompa, P., Schad, E., Tantos, A. & Kalmar, L. Intrinsically disordered proteins: emerging interaction specialists.Curr. Opin. Struct. Biol.35, 49–59 (2015).

    Article CAS  Google Scholar 

  19. Cumberworth, A., Lamour, G., Babu, M. M. & Gsponer, J. Promiscuity as a functional trait: intrinsically disordered regions as central players of interactomes.Biochem. J.454, 361–369 (2013).

    Article CAS  Google Scholar 

  20. Tompa, P., Davey, N. E., Gibson, T. J. & Babu, M. M. A million peptide motifs for the molecular biologist.Mol. Cell55, 161–169 (2014).

    Article CAS  Google Scholar 

  21. Sims, D. et al. High-throughput RNA interference screening using pooled shRNA libraries and next generation sequencing.Genome Biol.12, R104 (2011).

    Article CAS  Google Scholar 

  22. Edgar, R. C. Search and clustering orders of magnitude faster than BLAST.Bioinformatics26, 2460–2461 (2010).

    Article CAS  Google Scholar 

  23. Rice, P., Longden, I. & Bleasby, A. EMBOSS: the European molecular biology open software suite.Trends Genet.16, 276–277 (2000).

    Article CAS  Google Scholar 

  24. Sedlazeck, F. J., Rescheneder, P. & von Haeseler, A. NextGenMap: fast and accurate read mapping in highly polymorphic genomes.Bioinformatics29, 2790–2791 (2013).

    Article CAS  Google Scholar 

  25. Li, H. et al. The sequence alignment/map format and SAMtools.Bioinformatics25, 2078–2079 (2009).

    Article  Google Scholar 

  26. Buchfink, B., Xie, C. & Huson, D. H. Fast and sensitive protein alignment using DIAMOND.Nat. Methods12, 59–60 (2015).

    Article CAS  Google Scholar 

  27. Xiao, N., Cao, D. S., Zhu, M. F. & Xu, Q. S . protr/ProtrWeb: R package and web server for generating various numerical representation schemes of protein sequences.Bioinformatics31, 1857–1859 (2015).

    Article CAS  Google Scholar 

Download references

Acknowledgements

We thank S. Künzel for sequencing and E. Özkurt for contributions during her rotation project. The project was financed through an ERC advanced grant to D.T. (NewGenes—322564).

Author information

Author notes
  1. Rafik Neme & Cristina Amador

    Present address: †Present addresses: Department of Biochemistry and Molecular Biophysics, Columbia University Medical Center, 1212 Amsterdam Avenue, New York, NY 10027, USA (R.N.); Technical University of Denmark, Department of Biotechnology and Biomedicine, 2800 Kgs Lyngby, Denmark (C.A.),

Authors and Affiliations

  1. Max-Planck Institute for Evolutionary Biology, August-Thienemannstrasse 2, Plön, 24306, Germany.

    Rafik Neme, Cristina Amador, Burcin Yildirim, Ellen McConnell & Diethard Tautz

Authors
  1. Rafik Neme

    You can also search for this author inPubMed Google Scholar

  2. Cristina Amador

    You can also search for this author inPubMed Google Scholar

  3. Burcin Yildirim

    You can also search for this author inPubMed Google Scholar

  4. Ellen McConnell

    You can also search for this author inPubMed Google Scholar

  5. Diethard Tautz

    You can also search for this author inPubMed Google Scholar

Contributions

R.N. and D.T. designed the experiment, C.A. constructed the library, C.A., B.Y. and E.M. conducted the experiments, R.N. did the bioinformatic analysis, and R.N. and D.T. wrote the paper.

Corresponding author

Correspondence toDiethard Tautz.

Ethics declarations

Competing interests

The work described in this publication is subject to patent application by the Max-Planck Society.

Supplementary information

Supplementary Figures

Supplementary Figures 1–3 (PDF 661 kb)

Supplementary Table 1

Supplementary Table 1 (XLSX 116 kb)

Rights and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Neme, R., Amador, C., Yildirim, B.et al. Random sequences are an abundant source of bioactive RNAs or peptides.Nat Ecol Evol1, 0127 (2017). https://doi.org/10.1038/s41559-017-0127

Download citation

Access through your institution
Buy or subscribe

Associated content

No beneficial fitness effects of random peptides

  • Michael Knopp
  • Dan I. Andersson
Nature Ecology & EvolutionCorrespondence

Reply to ‘No beneficial fitness effects of random peptides’

  • Diethard Tautz
  • Rafik Neme
Nature Ecology & EvolutionCorrespondence

Advertisement

Search

Advanced search

Quick links

Nature Briefing

Sign up for theNature Briefing newsletter — what matters in science, free to your inbox daily.

Get the most important science stories of the day, free in your inbox.Sign up for Nature Briefing

[8]ページ先頭

©2009-2025 Movatter.jp