Published online on September 8, 2003, 10.1073/pnas.1833775100
PNAS | September 16, 2003 | vol. 100 | no. 19 | 10824-10829
Previous Article |
Table of Contents
| Next Article
EVOLUTION
Horizontal gene transfer from flowering plants to Gnetum
Hyosig Won
, and
Susanne S. Renner
Department of Biology, University of Missouri, 8001 Natural Bridge Road, St. Louis, MO 63121; and
Missouri Botanical Garden, P.O. Box 299, St. Louis, MO 63166
Edited by Barbara A. Schaal, Washington University, St. Louis, MO, and approved July 18, 2003
(received for review June 12, 2003)
Although horizontal gene transfer is well documented in microbial genomes, no case has been reported in higher plants. We discovered horizontal transfer of the mitochondrial nad1 intron 2 and adjacent exons b and c from an asterid to Gnetum (Gnetales, gymnosperms). Gnetum has two copies of intron 2, a group II intron, that differ in their exons, nucleotide composition, domain lengths, and structural characteristics. One of the copies, limited to an Asian clade of Gnetum, is almost identical to the homologous locus in angiosperms, and partial sequences of its exons b and c show characteristic substitutions unique to angiosperms. Analyses of 70 seed plant nad1 exons b and c and intron 2 sequences, including representatives of all angiosperm clades, support that this copy originated from a euasterid and was horizontally transferred to Gnetum. Molecular clock dating, using calibrations provided by gnetalean macrofossils, suggests an age of 5 to 2 million years for the Asian clade that received the horizontal transfer.
This paper was submitted directly (Track II) to the PNAS office.
Abbreviations: mt, mitochondrial; my, million years.
Data deposition: The DNA sequences reported in this paper have been deposited in the GenBank database (accession nos. AY230269AY230316, AY231296AY231300, AY243113, AY243121, AY243125, AY243129AY243131, AY256880AY256885, and AY283607AY283610). For a full listing of accession numbers, see Table 2, which is published as supporting information on the PNAS web site, www.pnas.org.
To whom correspondence should be addressed. E-mail: renner{at}umsl.edu.

CiteULike
Complore
Connotea
Del.icio.us
Digg What's this?
This article has been cited by other articles in HighWire Press-hosted journals:

|
 |

|
 |
 
C. J. Willson, P. S. Manos, and R. B. Jackson
Hydraulic traits are influenced by phylogenetic history in the drought-resistant, invasive genus Juniperus (Cupressaceae)
Am. J. Botany,
March 1, 2008;
95(3):
299 - 314.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
C.-Y. Qiao, J.-H. Ran, Y. Li, and X.-Q. Wang
Phylogeny and Biogeography of Cedrus (Pinaceae) Inferred from Sequences of Seven Paternal Chloroplast and Maternal Mitochondrial DNA Regions
Ann. Bot.,
September 1, 2007;
100(3):
573 - 580.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
A. O. Richardson and J. D. Palmer
Horizontal gene transfer in plants
J. Exp. Bot.,
January 1, 2007;
58(1):
1 - 9.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
R. M. Bateman, J. Hilton, and P. J. Rudall
Morphological and molecular phylogenetic context of the angiosperms: contrasting the 'top-down' and 'bottom-up' approaches used to infer the likely characteristics of the first flowers
J. Exp. Bot.,
October 1, 2006;
57(13):
3471 - 3503.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
Y. Inagaki, E. Susko, and A. J. Roger
Recombination between elongation factor 1{alpha} genes from distantly related archaeal lineages
PNAS,
March 21, 2006;
103(12):
4528 - 4533.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
S. Kim, P. S. Soltis, K. Wall, and D. E. Soltis
Phylogeny and Domain Evolution in the APETALA2-like Gene Family
Mol. Biol. Evol.,
January 1, 2006;
23(1):
107 - 120.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
M. Habetha and T. C. G. Bosch
Symbiotic Hydra express a plant-like peroxidase gene during oogenesis
J. Exp. Biol.,
June 1, 2005;
208(11):
2157 - 2165.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
S.-H. Oh and D. Potter
Molecular phylogenetic systematics and biogeography of tribe Neillieae (Rosaceae) using DNA sequences of cpDNA, rDNA, and LEAFY
Am. J. Botany,
January 1, 2005;
92(1):
179 - 192.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
U. Bergthorsson, A. O. Richardson, G. J. Young, L. R. Goertzen, and J. D. Palmer
From the Cover: Massive horizontal transfer of mitochondrial genes from diverse land plant donors to the basal angiosperm Amborella
PNAS,
December 21, 2004;
101(51):
17747 - 17752.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
C. C. Davis and K. J. Wurdack
Host-to-Parasite Gene Transfer in Flowering Plants: Phylogenetic Evidence from Malpighiales
Science,
July 30, 2004;
305(5684):
676 - 678.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
T. J. Barkman, S.-H. Lim, K. M. Salleh, and J. Nais
From the Cover: Mitochondrial DNA sequences reveal the photosynthetic relatives of Rafflesia, the world's largest flower
PNAS,
January 20, 2004;
101(3):
787 - 792.
[Abstract]
[Full Text]
[PDF]
|
 |
|