Note to users. If you're seeing this message, it means that your browser cannot find this page's style/presentation instructions -- or possibly that you are using a browser that does not support current Web standards. Find out more about why this message is appearing, and what you can do to make your experience of our site the best it can be.
Click Me!

Site Tools

  • AAAS
  • Subscribe
  • Feedback

Site Search

Search Advanced

Published Online July 15, 2004
Science DOI: 10.1126/science.1100671

Reports

Submitted on May 25, 2004
Accepted on July 6, 2004

Host-to-Parasite Gene Transfer in Flowering Plants: Phylogenetic Evidence from Malpighiales

Charles C. Davis 1* and Kenneth J. Wurdack 2

1 Ecology and Evolutionary Biology, University of Michigan Herbarium, 3600 Varsity Drive, Ann Arbor, MI 48108-2287, USA.
2 Department of Botany and Laboratories of Analytical Biology, Smithsonian Institution, 4210 Silver Hill Road, Suitland, MD 20746, USA.

* To whom correspondence should be addressed.
Charles C. Davis , E-mail: chdavis{at}umich.edu

Horizontal gene transfer (HGT) between sexually unrelated species has recently been documented for higher plants, but mechanistic explanations for HGTs have remained speculative. We show that a parasitic relationship may facilitate HGT between flowering plants. The endophytic parasites Rafflesiaceae are placed in the diverse order Malpighiales. Our multigene phylogenetic analyses of Malpighiales show that mitochrodrial (matR) and nuclear loci (18S rDNA and PHYC) place Rafflesiaceae in Malpighiales, perhaps near Ochnaceae/Clusiaceae. Mitochondrial nad1B-C, however, groups them within Vitaceae, sister to their obligate host, Tetrastigma. These discordant phylogenetic hypotheses strongly suggest that part of the mitochondrial genome in Rafflesiaceae was acquired via HGT from their hosts.


THIS ARTICLE HAS BEEN CITED BY OTHER ARTICLES:
Plastid Genome Sequence of the Cryptophyte Alga Rhodomonas salina CCMP1319: Lateral Transfer of Putative DNA Replication Machinery and a Test of Chromist Plastid Phylogeny.
H. Khan, N. Parks, C. Kozera, B. A. Curtis, B. J. Parsons, S. Bowman, and J. M. Archibald (2007)
Mol. Biol. Evol. 24, 1832-1842
   Abstract »    Full Text »    PDF »
Mitochondrial Genome Haplotype Hypervariation Within the Isopod Parasitic Nematode Thaumamermis cosgrovei.
S. Tang and B. C. Hyman (2007)
Genetics 176, 1139-1150
   Abstract »    Full Text »    PDF »
Floral Gigantism in Rafflesiaceae.
C. C. Davis, M. Latvis, D. L. Nickrent, K. J. Wurdack, and D. A. Baum (2007)
Science 315, 1812
   Abstract »    Full Text »    PDF »
Horizontal gene transfer in plants.
A. O. Richardson and J. D. Palmer (2007)
J. Exp. Bot. 58, 1-9
   Abstract »    Full Text »    PDF »
Patterns of anomalous floral development in the Asian Passiflora (subgenus Decaloba: supersection Disemma).
S. E. Krosnick, E. M. Harris, and J. V. Freudenstein (2006)
Am. J. Botany 93, 620-636
   Abstract »    Full Text »    PDF »
Comprehensive Multigene Phylogenies of Excavate Protists Reveal the Evolutionary Positions of "Primitive" Eukaryotes.
A. G. B. Simpson, Y. Inagaki, and A. J. Roger (2006)
Mol. Biol. Evol. 23, 615-625
   Abstract »    Full Text »    PDF »
Molecular phylogenetic analysis of uniovulate Euphorbiaceae (Euphorbiaceae sensu stricto) using plastid RBCL and TRNL-F DNA sequences.
K. J. Wurdack, P. Hoffmann, and M. W. Chase (2005)
Am. J. Botany 92, 1397-1420
   Abstract »    Full Text »    PDF »
From the Cover: Massive horizontal transfer of mitochondrial genes from diverse land plant donors to the basal angiosperm Amborella.
U. Bergthorsson, A. O. Richardson, G. J. Young, L. R. Goertzen, and J. D. Palmer (2004)
PNAS 101, 17747-17752
   Abstract »    Full Text »    PDF »
A question concerning the identity of Streptomyces sp. MSU-2110.
G. A. Strobel, D. Ezra, U. Castillo, and W. M. Hess (2004)
Microbiology 150, 3094-3096
   Full Text »    PDF »



ADVERTISEMENT
Click Me!

ADVERTISEMENT
Click Me!

To Advertise     Find Products