Unifying the known and unknown microbial coding sequence space

  1. Chiara Vanni
  2. Matthew S Schechter
  3. Silvia G Acinas
  4. Albert Barberán
  5. Pier Luigi Buttigieg
  6. Emilio O Casamayor
  7. Tom O Delmont
  8. Carlos M Duarte
  9. A Murat Eren
  10. Robert D Finn
  11. Renzo Kottmann
  12. Alex Mitchell
  13. Pablo Sánchez
  14. Kimmo Siren
  15. Martin Steinegger
  16. Frank Oliver Gloeckner
  17. Antonio Fernàndez-Guerra  Is a corresponding author
  1. Max Planck Institute for Marine Microbiology, Germany
  2. University of Chicago, United States
  3. Institut de Ciències del Mar-CMIMA (CSIC), Spain
  4. University of Arizona, United States
  5. Alfred Wegener Institute, Germany
  6. Spanish Council for Research, Spain
  7. Genoscope, Institut François Jacob, CEA, CNRS, France
  8. King Abdullah University of Science and Technology, Saudi Arabia
  9. European Molecular Biology Laboratory, United Kingdom
  10. University of Copenhagen, Denmark
  11. Seoul National University, Republic of Korea
  12. University of Bremen, Germany

Abstract

Genes of unknown function are among the biggest challenges in molecular biology, especially in microbial systems, where 40%-60% of the predicted genes are unknown. Despite previous attempts, systematic approaches to include the unknown fraction into analytical workflows are still lacking. Here, we present a conceptual framework, its translation into the computational workflow AGNOSTOS and a demonstration on how we can bridge the known-unknown gap in genomes and metagenomes. By analyzing 415,971,742 genes predicted from 1,749 metagenomes and 28,941 bacterial and archaeal genomes, we quantify the extent of the unknown fraction, its diversity, and its relevance across multiple organisms and environments. The unknown sequence space is exceptionally diverse, phylogenetically more conserved than the known fraction and predominantly taxonomically restricted at the species level. From the 71M genes identified to be of unknown function, we compiled a collection of 283,874 lineage-specific genes of unknown function for Cand. Patescibacteria (also known as Candidate Phyla Radiation, CPR), which provides a significant resource to expand our understanding of their unusual biology. Finally, by identifying a target gene of unknown function for antibiotic resistance, we demonstrate how we can enable the generation of hypotheses that can be used to augment experimental data.

Data availability

We used public data as described in the Methods section and Appendix 1-table 5.The code used for the analyses in the manuscript is available at https://github.com/functional-dark-side/functional-dark-side.github.io/tree/master/scripts. A list with the program versions can be found in https://github.com/functional-dark-side/functional-dark-side.github.io/blob/master/programs_and_versions.txt.The code to create the figures is available at https://github.com/functional-dark-side/vanni_et_al-figures, and the data for the figure can be downloaded from https://doi.org/10.6084/m9.figshare.12738476.v2. A reproducible version of the workflow is available at https://github.com/functional-dark-side/agnostos-wf.The data is publicly available at https://doi.org/10.6084/m9.figshare.12459056.

The following data sets were generated
The following previously published data sets were used
    1. Anna Kopf
    2. Mesude Bicak
    3. Renzo Kottmann
    4. Julia Schnetzer
    5. Ivaylo Kostadinov
    6. Katja Lehmann
    7. Antonio Fernandez-Guerra
    8. Christian Jeanthon
    9. Eyal Rahav
    10. Matthias Ullrich
    11. Antje Wichels
    12. Gunnar Gerdts
    13. Paraskevi Polymenakou
    14. Giorgos Kotoulas
    15. Rania Siam
    16. Rehab Z Abdallah
    17. Eva C Sonnenschein
    18. Thierry Cariou
    19. Fergal O'Gara
    20. Stephen Jackson
    21. Sandi Orlic
    22. Michael Steinke
    23. Julia Busch
    24. Bernardo Duarte
    25. Isabel Caçador
    26. João Canning-Clode
    27. Oleksandra Bobrova
    28. Viggo Marteinsson
    29. Eyjolfur Reynisson
    30. Clara Magalhães Loureiro
    31. Gian Marco Luna
    32. Grazia Marina Quero
    33. Carolin R Löscher
    34. Anke Kremp
    35. Marie E DeLorenzo
    36. Lise Øvreås
    37. Jennifer Tolman
    38. Julie LaRoche
    39. Antonella Penna
    40. Marc Frischer
    41. Timothy Davis
    42. Barker Katherine
    43. Christopher P Meyer
    44. Sandra Ramos
    45. Catarina Magalhães
    46. Florence Jude-Lemeilleur
    47. Ma Leopoldina Aguirre-Macedo
    48. Shiao Wang
    49. Nicole Poulton
    50. Scott Jones
    51. Rachel Collin
    52. Jed A Fuhrman
    53. Pascal Conan
    54. Cecilia Alonso
    55. Noga Stambler
    56. Kelly Goodwin
    57. Michael M Yakimov
    58. Federico Baltar
    59. Levente Bodrossy
    60. Jodie Van De Kamp
    61. Dion MF Frampton
    62. Martin Ostrowski
    63. Paul Van Ruth
    64. Paul Malthouse
    65. Simon Claus
    66. Klaas Deneudt
    67. Jonas Mortelmans
    68. Sophie Pitois
    69. David Wallom
    70. Ian Salter
    71. Rodrigo Costa
    72. Declan C Schroeder
    73. Mahrous M Kandil
    74. Valentina Amaral
    75. Florencia Biancalana
    76. Rafael Santana
    77. Maria Luiza Pedrotti
    78. Takashi Yoshida
    79. Hiroyuki Ogata
    80. Tim Ingleton
    81. Kate Munnik
    82. Naiara Rodriguez-Ezpeleta
    83. Veronique Berteaux-Lecellier
    84. Patricia Wecker
    85. Ibon Cancio
    86. Daniel Vaulot
    87. Christina Bienhold
    88. Hassan Ghazal
    89. Bouchra Chaouni
    90. Soumya Essayeh
    91. Sara Ettamimi
    92. El Houcine Zaid
    93. Noureddine Boukhatem
    94. Abderrahim Bouali
    95. Rajaa Chahboune
    96. Said Barrijal
    97. Mohammed Timinouni
    98. Fatima El Otmani
    99. Mohamed Bennani
    100. Marianna Mea
    101. Nadezhda Todorova
    102. Ventzislav Karamfilov
    103. Petra ten Hoopen
    104. Guy Cochrane
    105. Stephane L'Haridon
    106. Kemal Can Bizsel
    107. Alessandro Vezzi
    108. Federico M Lauro
    109. Patrick Martin
    110. Rachelle M Jensen
    111. Jamie Hinks
    112. Susan Gebbels
    113. Riccardo Rosselli
    114. Fabio De Pascale
    115. Riccardo Schiavon
    116. Antonina dos Santos
    117. Emilie Villar
    118. Stéphane Pesant
    119. Bruno Cataletto
    120. Francesca Malfatti
    121. Ranjith Edirisinghe
    122. Jorge A Herrera Silveira
    123. Michele Barbier
    124. Valentina Turk
    125. Tinkara Tinta
    126. Wayne J Fuller
    127. Ilkay Salihoglu
    128. Nedime Serakinci
    129. Mahmut Cerkez Ergoren
    130. Eileen Bresnan
    131. Juan Iriberri
    132. Paul Anders Fronth Nyhus
    133. Edvardsen Bente
    134. Hans Erik Karlsen
    135. Peter N Golyshin
    136. Josep M Gasol
    137. Snejana Moncheva
    138. Nina Dzhembekova
    139. Zackary Johnson
    140. Christopher David Sinigalliano
    141. Maribeth Louise Gidley
    142. Adriana Zingone
    143. Roberto Danovaro
    144. George Tsiamis
    145. Melody S Clark
    146. Ana Cristina Costa
    147. Monia El Bour
    148. Ana M Martins
    149. R Eric Collins
    150. Anne-Lise Ducluzeau
    151. Jonathan Martinez
    152. Mark J Costello
    153. Linda A Amaral-Zettler
    154. Jack A Gilbert
    155. Neil Davies
    156. Dawn Field & Frank Oliver Glöckner
    (2015) Ocean Sampling Day
    OSD.

Article and author information

Author details

  1. Chiara Vanni

    Microbial Genomics and Bioinformatics Research G, Max Planck Institute for Marine Microbiology, Bremen, Germany
    Competing interests
    The authors declare that no competing interests exist.
  2. Matthew S Schechter

    Department of Medicine, University of Chicago, Chicago, United States
    Competing interests
    The authors declare that no competing interests exist.
    ORCID icon "This ORCID iD identifies the author of this article:" 0000-0002-8435-3203
  3. Silvia G Acinas

    Department of Marine Biology and Oceanography, Institut de Ciències del Mar-CMIMA (CSIC), Barcelona, Spain
    Competing interests
    The authors declare that no competing interests exist.
  4. Albert Barberán

    Department of Environmental Science, University of Arizona, Tucson, United States
    Competing interests
    The authors declare that no competing interests exist.
  5. Pier Luigi Buttigieg

    Helmholtz Centre for Polar and Marine Research, Alfred Wegener Institute, Bremerhaven, Germany
    Competing interests
    The authors declare that no competing interests exist.
  6. Emilio O Casamayor

    Center for Advanced Studies of Blanes CEAB-CSIC, Spanish Council for Research, Blanes, Spain
    Competing interests
    The authors declare that no competing interests exist.
    ORCID icon "This ORCID iD identifies the author of this article:" 0000-0001-7074-3318
  7. Tom O Delmont

    Génomique Métabolique, Genoscope, Institut François Jacob, CEA, CNRS, Paris, France
    Competing interests
    The authors declare that no competing interests exist.
    ORCID icon "This ORCID iD identifies the author of this article:" 0000-0001-7053-7848
  8. Carlos M Duarte

    Computational Bioscience Research Center, King Abdullah University of Science and Technology, Thuwal, Saudi Arabia
    Competing interests
    The authors declare that no competing interests exist.
  9. A Murat Eren

    Department of Medicine, University of Chicago, Chicago, United States
    Competing interests
    The authors declare that no competing interests exist.
    ORCID icon "This ORCID iD identifies the author of this article:" 0000-0001-9013-4827
  10. Robert D Finn

    European Bioinformatics Institute (EMBL-EBI), European Molecular Biology Laboratory, Hinxton, United Kingdom
    Competing interests
    The authors declare that no competing interests exist.
  11. Renzo Kottmann

    Microbial Genomics and Bioinformatics Research G, Max Planck Institute for Marine Microbiology, Bremen, Germany
    Competing interests
    The authors declare that no competing interests exist.
  12. Alex Mitchell

    European Bioinformatics Institute (EMBL-EBI), European Molecular Biology Laboratory, Hinxton, United Kingdom
    Competing interests
    The authors declare that no competing interests exist.
  13. Pablo Sánchez

    Department of Marine Biology and Oceanography, Institut de Ciències del Mar-CMIMA (CSIC), Barcelona, Spain
    Competing interests
    The authors declare that no competing interests exist.
    ORCID icon "This ORCID iD identifies the author of this article:" 0000-0003-2787-822X
  14. Kimmo Siren

    Section for Evolutionary Genomics, The GLOBE Institute, University of Copenhagen, Copenhagen, Denmark
    Competing interests
    The authors declare that no competing interests exist.
  15. Martin Steinegger

    School of Biological Sciences, Seoul National University, Seoul, Republic of Korea
    Competing interests
    The authors declare that no competing interests exist.
  16. Frank Oliver Gloeckner

    MARUM, Helmholtz Center for Polar and Marine Research, University of Bremen, Bremen, Germany
    Competing interests
    The authors declare that no competing interests exist.
  17. Antonio Fernàndez-Guerra

    Lundbeck Foundation GeoGenetics Centre, GLOBE Institute, University of Copenhagen, Copenhagen, Denmark
    For correspondence
    antonio.fernandez-guerra@sund.ku.dk
    Competing interests
    The authors declare that no competing interests exist.
    ORCID icon "This ORCID iD identifies the author of this article:" 0000-0002-8679-490X

Funding

Max Planck Society

  • Chiara Vanni

European Union's Horizon 2020 (INMARE)

  • Antonio Fernàndez-Guerra

Biotechnology and Biological Sciences Research Council

  • Alex Mitchell

European Molecular Biology Laboratory

  • Robert D Finn

Spanish Agency of Science MICIU/AEI (INTERACTOMA RTI2018-101205-B-I00)

  • Emilio O Casamayor

Spanish Ministry of Economy and Competitiveness (MAGGY (CTM2017-87736-R))

  • Silvia G Acinas
  • Pablo Sánchez

The funders had no role in study design, data collection and interpretation, or the decision to submit the work for publication.

Reviewing Editor

  1. C Titus Brown, University of California, Davis, United States

Version history

  1. Preprint posted: July 1, 2020 (view preprint)
  2. Received: February 18, 2021
  3. Accepted: March 30, 2022
  4. Accepted Manuscript published: March 31, 2022 (version 1)
  5. Version of Record published: May 25, 2022 (version 2)

Copyright

© 2022, Vanni et al.

This article is distributed under the terms of the Creative Commons Attribution License permitting unrestricted use and redistribution provided that the original author and source are credited.

Metrics

  • 5,642
    views
  • 887
    downloads
  • 26
    citations

Views, downloads and citations are aggregated across all versions of this paper published by eLife.

Download links

A two-part list of links to download the article, or parts of the article, in various formats.

Downloads (link to download the article as PDF)

Open citations (links to open the citations from this article in various online reference manager services)

Cite this article (links to download the citations from this article in formats compatible with various reference manager tools)

  1. Chiara Vanni
  2. Matthew S Schechter
  3. Silvia G Acinas
  4. Albert Barberán
  5. Pier Luigi Buttigieg
  6. Emilio O Casamayor
  7. Tom O Delmont
  8. Carlos M Duarte
  9. A Murat Eren
  10. Robert D Finn
  11. Renzo Kottmann
  12. Alex Mitchell
  13. Pablo Sánchez
  14. Kimmo Siren
  15. Martin Steinegger
  16. Frank Oliver Gloeckner
  17. Antonio Fernàndez-Guerra
(2022)
Unifying the known and unknown microbial coding sequence space
eLife 11:e67667.
https://doi.org/10.7554/eLife.67667

Share this article

https://doi.org/10.7554/eLife.67667

Further reading

    1. Computational and Systems Biology
    Qianmu Yuan, Chong Tian, Yuedong Yang
    Tools and Resources

    Revealing protein binding sites with other molecules, such as nucleic acids, peptides, or small ligands, sheds light on disease mechanism elucidation and novel drug design. With the explosive growth of proteins in sequence databases, how to accurately and efficiently identify these binding sites from sequences becomes essential. However, current methods mostly rely on expensive multiple sequence alignments or experimental protein structures, limiting their genome-scale applications. Besides, these methods haven’t fully explored the geometry of the protein structures. Here, we propose GPSite, a multi-task network for simultaneously predicting binding residues of DNA, RNA, peptide, protein, ATP, HEM, and metal ions on proteins. GPSite was trained on informative sequence embeddings and predicted structures from protein language models, while comprehensively extracting residual and relational geometric contexts in an end-to-end manner. Experiments demonstrate that GPSite substantially surpasses state-of-the-art sequence-based and structure-based approaches on various benchmark datasets, even when the structures are not well-predicted. The low computational cost of GPSite enables rapid genome-scale binding residue annotations for over 568,000 sequences, providing opportunities to unveil unexplored associations of binding sites with molecular functions, biological processes, and genetic variants. The GPSite webserver and annotation database can be freely accessed at https://bio-web1.nscc-gz.cn/app/GPSite.

    1. Cell Biology
    2. Computational and Systems Biology
    Thomas Grandits, Christoph M Augustin ... Alexander Jung
    Research Article

    Computer models of the human ventricular cardiomyocyte action potential (AP) have reached a level of detail and maturity that has led to an increasing number of applications in the pharmaceutical sector. However, interfacing the models with experimental data can become a significant computational burden. To mitigate the computational burden, the present study introduces a neural network (NN) that emulates the AP for given maximum conductances of selected ion channels, pumps, and exchangers. Its applicability in pharmacological studies was tested on synthetic and experimental data. The NN emulator potentially enables massive speed-ups compared to regular simulations and the forward problem (find drugged AP for pharmacological parameters defined as scaling factors of control maximum conductances) on synthetic data could be solved with average root-mean-square errors (RMSE) of 0.47 mV in normal APs and of 14.5 mV in abnormal APs exhibiting early afterdepolarizations (72.5% of the emulated APs were alining with the abnormality, and the substantial majority of the remaining APs demonstrated pronounced proximity). This demonstrates not only very fast and mostly very accurate AP emulations but also the capability of accounting for discontinuities, a major advantage over existing emulation strategies. Furthermore, the inverse problem (find pharmacological parameters for control and drugged APs through optimization) on synthetic data could be solved with high accuracy shown by a maximum RMSE of 0.22 in the estimated pharmacological parameters. However, notable mismatches were observed between pharmacological parameters estimated from experimental data and distributions obtained from the Comprehensive in vitro Proarrhythmia Assay initiative. This reveals larger inaccuracies which can be attributed particularly to the fact that small tissue preparations were studied while the emulator was trained on single cardiomyocyte data. Overall, our study highlights the potential of NN emulators as powerful tool for an increased efficiency in future quantitative systems pharmacology studies.