Literature DB >> 21653455

Amborella not a "basal angiosperm"? Not so fast.

Douglas E Soltis1, Pamela S Soltis.   

Abstract

The sequence of the plastid genome of Amborella trichopoda, the putative sister to all other extant angiosperms, was recently reported (Molecular Biology and Evolution 20: 1499-1505). Goremykin et al. used sequence data for 61 plastid genes from Amborella and 12 other embryophytes in phylogenetic analyses and concluded that Amborella is not the sister to the remaining flowering plants; the monocots instead occupy this position. The authors attributed their results, which differ substantially from all recent phylogenetic analyses of angiosperms, to the increased character sampling (30 017 nucleotides in their aligned matrix) in their analysis relative to published studies that included fewer genes but more taxa. We hypothesized that the difference in topology is not due to limited character sampling in previous studies but to limited taxon sampling in the analysis by Goremykin et al. To test this, we conducted a series of phylogenetic analyses using a three-gene, 12 (or more)-taxon data set to evaluate the topological effects of (i) including three vs. 61 genes for (nearly) the same set of taxa, (ii) analyzing different codon positions, (iii) substituting representatives of other basal lineages for Amborella, (iv) replacing the grasses used to represent the monocots with other monocots, selected either for their phylogenetic position or randomly, and (v) adding other basal taxa-Nymphaea, Austrobaileya, magnoliids, and monocots-to the 12-taxon data set. Our results demonstrate that the "monocots basal" topology obtained by Goremykin et al. is not due to increased character sampling of the plastid genome; their topology was obtained using only two plastid genes or two plastid genes and one nuclear gene. This topology was also retained when either Nymphaea or Austrobaileya was substituted for Amborella, demonstrating that any of the three basal lineages will attach to Calycanthus for lack of any other close branch. Furthermore, the "monocots basal" topology is not robust to changes in sampling of monocots. Simply adding Oncidium, for example, places Amborella sister to the other angiosperms. Thus, limited taxon sampling, focusing on organisms with complete genome sequences, can lead to artifactual results.

Entities:  

Year:  2004        PMID: 21653455     DOI: 10.3732/ajb.91.6.997

Source DB:  PubMed          Journal:  Am J Bot        ISSN: 0002-9122            Impact factor:   3.844


  22 in total

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Review 2.  Molecular mechanisms underlying origin and diversification of the angiosperm flower.

Authors:  Guenter Theissen; Rainer Melzer
Journal:  Ann Bot       Date:  2007-07-31       Impact factor: 4.357

3.  Phylogenetic analysis of 83 plastid genes further resolves the early diversification of eudicots.

Authors:  Michael J Moore; Pamela S Soltis; Charles D Bell; J Gordon Burleigh; Douglas E Soltis
Journal:  Proc Natl Acad Sci U S A       Date:  2010-02-22       Impact factor: 11.205

4.  Analysis of 81 genes from 64 plastid genomes resolves relationships in angiosperms and identifies genome-scale evolutionary patterns.

Authors:  Robert K Jansen; Zhengqiu Cai; Linda A Raubeson; Henry Daniell; Claude W Depamphilis; James Leebens-Mack; Kai F Müller; Mary Guisinger-Bellian; Rosemarie C Haberle; Anne K Hansen; Timothy W Chumley; Seung-Bum Lee; Rhiannon Peery; Joel R McNeal; Jennifer V Kuehl; Jeffrey L Boore
Journal:  Proc Natl Acad Sci U S A       Date:  2007-11-28       Impact factor: 11.205

5.  The Complete Plastid Genome Sequence of Madagascar Periwinkle Catharanthus roseus (L.) G. Don: Plastid Genome Evolution, Molecular Marker Identification, and Phylogenetic Implications in Asterids.

Authors:  Chuan Ku; Wan-Chia Chung; Ling-Ling Chen; Chih-Horng Kuo
Journal:  PLoS One       Date:  2013-06-18       Impact factor: 3.240

6.  Increased gene sampling strengthens support for higher-level groups within leaf-mining moths and relatives (Lepidoptera: Gracillariidae).

Authors:  Akito Y Kawahara; Issei Ohshima; Atsushi Kawakita; Jerome C Regier; Charles Mitter; Michael P Cummings; Donald R Davis; David L Wagner; Jurate De Prins; Carlos Lopez-Vaamonde
Journal:  BMC Evol Biol       Date:  2011-06-24       Impact factor: 3.260

7.  Phylogenetic analyses of Vitis (Vitaceae) based on complete chloroplast genome sequences: effects of taxon sampling and phylogenetic methods on resolving relationships among rosids.

Authors:  Robert K Jansen; Charalambos Kaittanis; Christopher Saski; Seung-Bum Lee; Jeffrey Tomkins; Andrew J Alverson; Henry Daniell
Journal:  BMC Evol Biol       Date:  2006-04-09       Impact factor: 3.260

8.  Inferring phylogenies with incomplete data sets: a 5-gene, 567-taxon analysis of angiosperms.

Authors:  J Gordon Burleigh; Khidir W Hilu; Douglas E Soltis
Journal:  BMC Evol Biol       Date:  2009-03-17       Impact factor: 3.260

9.  Implications of the plastid genome sequence of typha (typhaceae, poales) for understanding genome evolution in poaceae.

Authors:  Mary M Guisinger; Timothy W Chumley; Jennifer V Kuehl; Jeffrey L Boore; Robert K Jansen
Journal:  J Mol Evol       Date:  2010-01-21       Impact factor: 2.395

10.  An extreme case of plant-insect codiversification: figs and fig-pollinating wasps.

Authors:  Astrid Cruaud; Nina Rønsted; Bhanumas Chantarasuwan; Lien Siang Chou; Wendy L Clement; Arnaud Couloux; Benjamin Cousins; Gwenaëlle Genson; Rhett D Harrison; Paul E Hanson; Martine Hossaert-McKey; Roula Jabbour-Zahab; Emmanuelle Jousselin; Carole Kerdelhué; Finn Kjellberg; Carlos Lopez-Vaamonde; John Peebles; Yan-Qiong Peng; Rodrigo Augusto Santinelo Pereira; Tselil Schramm; Rosichon Ubaidillah; Simon van Noort; George D Weiblen; Da-Rong Yang; Anak Yodpinyanee; Ran Libeskind-Hadas; James M Cook; Jean-Yves Rasplus; Vincent Savolainen
Journal:  Syst Biol       Date:  2012-07-30       Impact factor: 15.683

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