Molecular Biology and Evolution, Vol 14, 56-68, Copyright © 1997 by Society for Molecular Biology and Evolution
SM Chaw, A Zharkikh, HM Sung, TC Lau and WH Li
To study the evolutionary relationships among the four living gymnosperm
orders and the interfamilial relationships in each order, a set of 65
nuclear 18S rRNA sequences from ferns, gymnosperms, and angiosperms was
analyzed using the neighbor-joining and maximum- parsimony methods. With
Selaginella as the outgroup, the analysis strongly indicates that the seed
plants form a monophyletic group with the ferns as a sister group. Within
the seed plants the angiosperms are clearly a monophyletic group. Although
the bootstrap support for the monophyly of the gymnosperm clade is
moderate, the monophyly is further supported by its lack of
angiosperm-specific indels. Within the gymnosperms there appear to be three
monophyletic clades: Cycadales- Ginkgoales, Gnetales, and Coniferales. The
cycad-ginkgo clade is the earliest gymnosperm lineage. Given the strong
support for the sister group relationship between Gnetales and Coniferales,
it is unlikely that Gnetales is a sister group of the angiosperms, contrary
to the view of many plant taxonomists. Within Coniferales, Pinaceae is
monophyletic and basal to the remaining conifer families, among which there
are three monophyletic clades: Phyllocladaceae-Podocarpaceae,
Araucariaceae, and Sciadopityaceae-Taxaceae-Cephalotaxaceae-Taxodiacea
e-Cupressaceae. Within the latter clade, Sciadopityaceae may be an outgroup
to the other four families. Among the angiosperms, no significant cluster
at the level of subclass was found, but there was evidence that
Nymphaeaceae branched off first. Within the remaining angiosperms, the
monocots included in this study are nested and form a monophyletic group.
This study attests to the utility of nuclear 18S rRNA sequences in
addressing relationships among living gymnosperms. Considerable variation
in substitution rates was observed among the ferns and seed plants.
ORIGINAL ARTICLE
Molecular phylogeny of extant gymnosperms and seed plant evolution: analysis of nuclear 18S rRNA sequences
Institute of Botany, Academia Sinica, Taipei, Taiwan, Republic of China. bochaw@ccvax.sinica.edu.tw
![]()
CiteULike
Connotea
Del.icio.us What's this?
This article has been cited by other articles:
![]() |
M. Nepi, P. von Aderkas, R. Wagner, S. Mugnaini, A. Coulter, and E. Pacini Nectar and pollination drops: how different are they? Ann. Bot., August 1, 2009; 104(2): 205 - 219. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. Mathews Phylogenetic relationships among seed plants: Persistent questions and the limits of molecular data Am. J. Botany, January 1, 2009; 96(1): 228 - 236. [Abstract] [Full Text] [PDF] |
||||
![]() |
S.-M. Chaw, A. Chun-Chieh Shih, D. Wang, Y.-W. Wu, S.-M. Liu, and T.-Y. Chou The Mitochondrial Genome of the Gymnosperm Cycas taitungensis Contains a Novel Family of Short Interspersed Elements, Bpu Sequences, and Abundant RNA Editing Sites Mol. Biol. Evol., March 1, 2008; 25(3): 603 - 615. [Abstract] [Full Text] [PDF] |
||||
![]() |
G. Theissen and R. Melzer Molecular Mechanisms Underlying Origin and Diversification of the Angiosperm Flower Ann. Bot., September 1, 2007; 100(3): 603 - 619. [Abstract] [Full Text] [PDF] |
||||
![]() |
C.-S. Wu, Y.-N. Wang, S.-M. Liu, and S.-M. Chaw Chloroplast Genome (cpDNA) of Cycas taitungensis and 56 cp Protein-Coding Genes of Gnetum parvifolium: Insights into cpDNA Evolution and Phylogeny of Extant Seed Plants Mol. Biol. Evol., June 1, 2007; 24(6): 1366 - 1379. [Abstract] [Full Text] [PDF] |
||||
![]() |
Y. Wang, X. Tang, Z. Cheng, L. Mueller, J. Giovannoni, and S. D. Tanksley Euchromatin and Pericentromeric Heterochromatin: Comparative Composition in the Tomato Genome Genetics, April 1, 2006; 172(4): 2529 - 2540. [Abstract] [Full Text] [PDF] |
||||
![]() |
C.-C. Chang, H.-C. Lin, I-P. Lin, T.-Y. Chow, H.-H. Chen, W.-H. Chen, C.-H. Cheng, C.-Y. Lin, S.-M. Liu, C.-C. Chang, et al. The Chloroplast Genome of Phalaenopsis aphrodite (Orchidaceae): Comparative Analysis of Evolutionary Rate with that of Grasses and Its Phylogenetic Implications Mol. Biol. Evol., February 1, 2006; 23(2): 279 - 291. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. Syring, A. Willyard, R. Cronn, and A. Liston Evolutionary relationships among Pinus (Pinaceae) subsections inferred from multiple low-copy nuclear loci Am. J. Botany, December 1, 2005; 92(12): 2086 - 2100. [Abstract] [Full Text] [PDF] |
||||
![]() |
Patterns of segregation and convergence in the evolution of fern and seed plant leaf morphologies Paleobiology, January 1, 2005; 31(1): 117 - 140. |
||||
![]() |
W. E. Friedman, R. C. Moore, and M. D. Purugganan The evolution of plant development Am. J. Botany, October 1, 2004; 91(10): 1726 - 1741. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. G. Burleigh and S. Mathews Phylogenetic signal in nucleotide data from seed plants: implications for resolving the seed plant tree of life Am. J. Botany, September 1, 2004; 91(10): 1599 - 1613. [Abstract] [Full Text] [PDF] |
||||
![]() |
Z.-Q. WANG A New Permian Gnetalean Cone as Fossil Evidence for Supporting Current Molecular Phylogeny Ann. Bot., August 1, 2004; 94(2): 281 - 288. [Abstract] [Full Text] [PDF] |
||||
![]() |
D. M. Martin, J. Faldt, and J. Bohlmann Functional Characterization of Nine Norway Spruce TPS Genes and Evolution of Gymnosperm Terpene Synthases of the TPS-d Subfamily Plant Physiology, August 1, 2004; 135(4): 1908 - 1927. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. Jager, A. Hassanin, M. Manuel, H. L. Guyader, and J. Deutsch MADS-Box Genes in Ginkgo biloba and the Evolution of the AGAMOUS Family Mol. Biol. Evol., May 1, 2003; 20(5): 842 - 854. [Abstract] [Full Text] [PDF] |
||||
![]() |
Ecological conservatism in the "living fossil" Ginkgo Paleobiology, March 1, 2003; 29(1): 84 - 104. |
||||
![]() |
K. Vissenberg, V. Van Sandt, S. C. Fry, and J-P. Verbelen Xyloglucan endotransglucosylase action is high in the root elongation zone and in the trichoblasts of all vascular plants from Selaginella to Zea mays J. Exp. Bot., January 2, 2003; 54(381): 335 - 344. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. Farjon and S. Ortiz Garcia Cone and ovule development in Cunninghamia and Taiwania (Cupressaceae sensu lato) and its significance for conifer evolution Am. J. Botany, January 1, 2003; 90(1): 8 - 16. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. Magallon and M. J. Sanderson Relationships among seed plants inferred from highly conserved genes: sorting conflicting phylogenetic signals among ancient lineages Am. J. Botany, December 1, 2002; 89(12): 1991 - 2006. [Abstract] [Full Text] [PDF] |
||||
![]() |
D. E. Soltis, P. S. Soltis, and M. J. Zanis Phylogeny of seed plants based on evidence from eight genes Am. J. Botany, October 1, 2002; 89(10): 1670 - 1681. [Abstract] [Full Text] [PDF] |
||||
![]() |
L. C. Grubisha, J. M. Trappe, R. Molina, and J. W. Spatafora Biology of the ectomycorrhizal genus Rhizopogon. VI. Re-examination of infrageneric relationships inferred from phylogenetic analyses of ITS sequences Mycologia, July 1, 2002; 94(4): 607 - 619. [Abstract] [Full Text] [PDF] |
||||
![]() |
C. C. Labandeira, B. A. LePage, and A. H. Johnson A Dendroctonus bark engraving (Coleoptera: Scolytidae) from a middle Eocene Larix (Coniferales: Pinaceae): early or delayed colonization? Am. J. Botany, November 1, 2001; 88(11): 2026 - 2039. [Abstract] [Full Text] [PDF] |
||||
![]() |
Y.-L. Qiu, J. Lee, B. A. Whitlock, F. Bernasconi-Quadroni, and O. Dombrovska Was the ANITA Rooting of the Angiosperm Phylogeny Affected by Long-Branch Attraction? Mol. Biol. Evol., September 1, 2001; 18(9): 1745 - 1753. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. Kumar and B. E. Ellis The Phenylalanine Ammonia-Lyase Gene Family in Raspberry. Structure, Expression, and Evolution Plant Physiology, September 1, 2001; 127(1): 230 - 239. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. J. Sanderson and J. A. Doyle Sources of error and confidence intervals in estimating the age of angiosperms from rbcL and 18S rDNA data Am. J. Botany, August 1, 2001; 88(8): 1499 - 1516. [Full Text] |
||||
![]() |
S. W. Graham and R. G. Olmstead Utility of 17 chloroplast genes for inferring the phylogeny of the basal angiosperms Am. J. Botany, November 1, 2000; 87(11): 1712 - 1730. [Abstract] [Full Text] |
||||
![]() |
A. Becker, K.-U. Winter, B. Meyer, H. Saedler, and G. Thei{beta}en MADS-Box Gene Diversity in Seed Plants 300 Million Years Ago Mol. Biol. Evol., October 1, 2000; 17(10): 1425 - 1434. [Abstract] [Full Text] [PDF] |
||||
![]() |
P. A. Gadek, D. L. Alpers, M. M. Heslewood, and C. J. Quinn Relationships within Cupressaceae sensu lato: a combined morphological and molecular approach Am. J. Botany, July 1, 2000; 87(7): 1044 - 1057. [Abstract] [Full Text] |
||||
![]() |
X.-Q. Wang, D. C. Tank, and T. Sang Phylogeny and Divergence Times in Pinaceae: Evidence from Three Genomes Mol. Biol. Evol., May 1, 2000; 17(5): 773 - 781. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. J. Sanderson, M. F. Wojciechowski, J.-M. Hu, T. S. Khan, and S. G. Brady Error, Bias, and Long-Branch Attraction in Data for Two Chloroplast Photosystem Genes in Seed Plants Mol. Biol. Evol., May 1, 2000; 17(5): 782 - 797. [Abstract] [Full Text] [PDF] |
||||
![]() |
S.-M. Chaw, C. L. Parkinson, Y. Cheng, T. M. Vincent, and J. D. Palmer Seed plant phylogeny inferred from all three plant genomes: Monophyly of extant gymnosperms and origin of Gnetales from conifers PNAS, April 11, 2000; 97(8): 4086 - 4091. [Abstract] [Full Text] [PDF] |
||||
![]() |
L. M. Bowe, G. Coat, and C. W. dePamphilis Phylogeny of seed plants based on all three genomic compartments: Extant gymnosperms are monophyletic and Gnetales' closest relatives are conifers PNAS, April 11, 2000; 97(8): 4092 - 4097. [Abstract] [Full Text] [PDF] |
||||
![]() |
R. Alba, P. M. Kelmenson, M.-M. Cordonnier-Pratt, and L. H. Pratt The Phytochrome Gene Family in Tomato and the Rapid Differential Evolution of this Family in Angiosperms Mol. Biol. Evol., March 1, 2000; 17(3): 362 - 373. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. W. Frohlich MADS about Gnetales PNAS, August 3, 1999; 96(16): 8811 - 8813. [Full Text] [PDF] |
||||
![]() |
K.-U. Winter, A. Becker, T. Munster, J. T. Kim, H. Saedler, and G. Theissen MADS-box genes reveal that gnetophytes are more closely related to conifers than to flowering plants PNAS, June 22, 1999; 96(13): 7342 - 7347. [Abstract] [Full Text] [PDF] |
||||
![]() |
D. S. Gernandt and A. Liston Internal transcribed spacer region evolution in Larix and Pseudotsuga (Pinaceae) Am. J. Botany, May 1, 1999; 86(5): 711 - 723. [Abstract] [Full Text] [PDF] |
||||
![]() |
R. J. Duff and D. L. Nickrent Phylogenetic relationships of land plants using mitochondrial small-subunit rDNA sequences Am. J. Botany, March 1, 1999; 86(3): 372 - 386. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. Bohlmann, G. Meyer-Gauen, and R. Croteau Plant terpenoid synthases: Molecular biology and phylogenetic analysis PNAS, April 14, 1998; 95(8): 4126 - 4133. [Abstract] [Full Text] [PDF] |
||||








