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.

  • Letter
  • Published:

Origin of avian genome size and structure in non-avian dinosaurs

Abstract

Avian genomes are small and streamlined compared with those of other amniotes by virtue of having fewer repetitive elements and less non-coding DNA1,2. This condition has been suggested to represent a key adaptation for flight in birds, by reducing the metabolic costs associated with having large genome and cell sizes3,4. However, the evolution of genome architecture in birds, or any other lineage, is difficult to study because genomic information is often absent for long-extinct relatives. Here we use a novel bayesian comparative method to show that bone-cell size correlates well with genome size in extant vertebrates, and hence use this relationship to estimate the genome sizes of 31 species of extinct dinosaur, including several species of extinct birds. Our results indicate that the small genomes typically associated with avian flight evolved in the saurischian dinosaur lineage between 230 and 250 million years ago, long before this lineage gave rise to the first birds. By comparison, ornithischian dinosaurs are inferred to have had much larger genomes, which were probably typical for ancestral Dinosauria. Using comparative genomic data, we estimate that genome-wide interspersed mobile elements, a class of repetitive DNA, comprised 5–12% of the total genome size in the saurischian dinosaur lineage, but was 7–19% of total genome size in ornithischian dinosaurs, suggesting that repetitive elements became less active in the saurischian lineage. These genomic characteristics should be added to the list of attributes previously considered avian but now thought to have arisen in non-avian dinosaurs, such as feathers5, pulmonary innovations6, and parental care and nesting7.

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

Access options

Buy this article

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

Figure 1: Primary histological data, distribution of average osteocyte-cell size in extinct dinosaur species, and regression lines derived from data on extant animals used to infer genome size and interspersed repetitive elements.
Figure 2: Haploid genome size (mean of posterior predictive distribution) mapped onto a phylogeny shows a reduction within saurischian dinosaurs, the lineage to which birds belong.
Figure 3: Bar graph of interspersed repetitive elements in a range of extant vertebrate species and extinct dinosaur species inferred from genome size reconstructions and the correlation between repetitive element composition and genome size.

Similar content being viewed by others

References

  1. Hillier, L. W. et al. Sequence and comparative analysis of the chicken genome provide unique perspectives on vertebrate evolution. Nature 432, 695–716 (2004)

    Article  ADS  CAS  Google Scholar 

  2. Ellengren, H. The avian genome uncovered. Trends Ecol. Evol. 20, 180–186 (2005)

    Article  Google Scholar 

  3. Hughes, A. L. Adaptive Evolution of Genes and Genomes. (Oxford Univ. Press, Oxford, 1999)

    Google Scholar 

  4. Hughes, A. L. & Hughes, M. K. Small genomes for better flyers. Nature 377, 391 (1995)

    Article  ADS  CAS  Google Scholar 

  5. Xu, X., Zhou, Z. & Prum, R. O. Branched integumental structures in Sinornithosaurus and the origin of feathers. Nature 410, 200–204 (2001)

    Article  ADS  CAS  Google Scholar 

  6. O'Connor, P. M. & Claessens, P. A. M. Basic avian pulmonary design and flow-through ventilation in non-avian theropod dinosaurs. Nature 436, 253–256 (2005)

    Article  ADS  CAS  Google Scholar 

  7. Horner, J. R. & Makela, R. Nest of juveniles provides evidence of family structure among dinosaurs. Nature 282, 296–298 (1979)

    Article  ADS  Google Scholar 

  8. Gregory, T. R. Animal Genome Size Databasehttp://www.genomesize.com/〉 (2005)

    Google Scholar 

  9. Van den Bussche, R. A. How bats achieve a small C-value: frequency of repetitive DNA in Macrotus. Mamm. Genome 6, 521–525 (1995)

    Article  CAS  Google Scholar 

  10. Waltari, E. & Edwards, S. V. Evolutionary dynamics of intron size, genome size, and physiological correlates in archosaurs. Am. Nat. 160, 539–552 (2002)

    Article  Google Scholar 

  11. Tiersch, T. R. & Wachtel, S. S. On the evolution of genome size of birds. J. Hered. 82, 363–368 (1991)

    Article  CAS  Google Scholar 

  12. Raup, D. M. Extinction: Bad Genes or Bad Luck? 3–21 (W. W. Norton & Company, New York, 1992)

    Google Scholar 

  13. Conway Morris, S. & Harper, E. Genome size in conodonts (Chordata): inferred variations during 270 million years. Science 241, 1230–1232 (1988)

    Article  ADS  Google Scholar 

  14. Masterson, J. Stomatal size in fossil plants: Evidence for polyploidy in majority of angiosperms. Science 264, 421–423 (1994)

    Article  ADS  CAS  Google Scholar 

  15. Thomson, K. S. & Muraszko, K. Estimation of cell size and DNA content in fossil fishes and amphibians. J. Exp. Zool. 205, 315–320 (1978)

    Article  CAS  Google Scholar 

  16. Gregory, T. R. The bigger the C-value, the larger the cell: Genome size and red blood cell size in vertebrates. Blood Cells Mol. Dis. 27, 830–843 (2001)

    Article  CAS  Google Scholar 

  17. Pagel, M. D. Inferring evolutionary processes from phylogenies. Zool. Scr. 26, 331–348 (1997)

    Article  Google Scholar 

  18. Pagel, M. D. Inferring the historical patterns of biological evolution. Nature 401, 877–884 (1999)

    Article  ADS  CAS  Google Scholar 

  19. Gregory, T. R. & Hebert, P. D. N. The modulation of DNA content: proximate causes and ultimate consequences. Genome Res. 9, 317–324 (1999)

    CAS  PubMed  Google Scholar 

  20. Langer, M. C. in The Dinosauria (eds Weishampel, D. B., Dodson, P. & Osmólska, H.) 25–46 (Univ. California Press, Berkeley, 2004)

    Book  Google Scholar 

  21. Kazazian, H. H. Mobile elements: Drivers of genome evolution. Science 303, 1626–1632 (2004)

    Article  ADS  CAS  Google Scholar 

  22. Shedlock, A. M. et al. Phylogenomics of non-avian reptiles and the structure of the ancestral amniote genome. Proc. Natl Acad. Sci. USA 104, 2767–2772 (2007)

    Article  ADS  CAS  Google Scholar 

  23. Shedlock, A. M. Phylogenomic investigation of CR1 LINE diversity in reptiles. Syst. Biol. 55, 902–911 (2006)

    Article  Google Scholar 

  24. Petrov, D. A. Evolution of genome size: new approaches to an old problem. Trends Genet. 17, 23–28 (2001)

    Article  CAS  Google Scholar 

  25. Kozlowski, J., Konarzewski, M. & Gawelczyk, A. T. Cell size as a link between noncoding DNA and metabolic rate scaling. Proc. Natl Acad. Sci. USA 100, 14080–14085 (2003)

    Article  ADS  CAS  Google Scholar 

  26. Cavalier-Smith, T. in The Evolution of Genome Size (ed. Cavalier-Smith, T.) 104–184 (John Wiley & Sons, Chichester, 1985)

    Google Scholar 

  27. Szarski, H. Cell size and the concept of wasteful and frugal evolutionary strategies. J. Theor. Biol. 105, 201–209 (1983)

    Article  CAS  Google Scholar 

  28. Erickson, G. M., Curry-Rogers, K. & Yerby, S. A. Dinosaurian growth patterns and rapid avian growth rates. Nature 412, 429–433 (2001)

    Article  ADS  CAS  Google Scholar 

  29. Padian, K., Horner, J. R. & de Ricqlès, A. J. Growth in small dinosaurs and pterosaurs: the evolution of archosaurian growth strategies. J. Vert. Paleontol. 24, 555–571 (2004)

    Article  Google Scholar 

  30. Gilks, W. R., Richardson, S. & Spiegelhalter, D. J. in Markov Chain Monte Carlo in Practice (eds Gilks, W. R., Richardson, S. & Spiegelhalter, D. J.) 1–19 (Chapman and Hall, London, 1996)

    MATH  Google Scholar 

Download references

Acknowledgements

We thank the Museum of Comparative Zoology at Harvard University and the Gabriel Laboratory for Cellular and Molecular Paleontology at the Museum of the Rockies for access to histology sections. We also thank D. Smith at the Imaging Center in the Department of Cellular and Molecular Biology, Harvard University for facilitating microscopy, A. Crompton and J. Horner for offering materials, laboratory space, and discussions on palaeohistology, and D. Jablonski and T. Garland for discussions. We are grateful for comments from B. Jennings, N. Hobbs and M. Laurin, which have improved this manuscript. This research was supported by an NIH Postdoctoral Fellowship granted to C.L.O., an NSF grant to S.V.E. and a NERC grant to M.P.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Chris L. Organ.

Ethics declarations

Competing interests

Reprints and permissions information is available at www.nature.com/reprints. The authors declare no competing financial interests.

Supplementary information

Supplementary Information

This file contains Supplementary Notes, Supplementary Data, Supplementary Figure 1, Supplementary Tables 1-8 and additional references. (PDF 398 kb)

Rights and permissions

Reprints and permissions

About this article

Cite this article

Organ, C., Shedlock, A., Meade, A. et al. Origin of avian genome size and structure in non-avian dinosaurs. Nature 446, 180–184 (2007). https://doi.org/10.1038/nature05621

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1038/nature05621

This article is cited by

Comments

By submitting a comment you agree to abide by our Terms and Community Guidelines. If you find something abusive or that does not comply with our terms or guidelines please flag it as inappropriate.

Search

Quick links

Nature Briefing

Sign up for the Nature 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