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

被引:582
作者
Moore, Michael J. [1 ]
Soltis, Pamela S. [2 ]
Bell, Charles D. [3 ]
Burleigh, J. Gordon [4 ]
Soltis, Douglas E. [4 ]
机构
[1] Oberlin Coll, Dept Biol, Oberlin, OH 44074 USA
[2] Univ Florida, Florida Museum Nat Hist, Gainesville, FL 32611 USA
[3] Univ New Orleans, Dept Biol Sci, New Orleans, LA 70148 USA
[4] Univ Florida, Dept Biol, Gainesville, FL 32611 USA
基金
美国国家科学基金会;
关键词
Angiosperm Tree of Life; Pentapetalae; plastid genome; BASAL ANGIOSPERM; DNA-SEQUENCES; DATA SETS; 18S RDNA; RBCL; CONFIDENCE; AMBORELLA; EVOLUTION; ATPB; RADIATION;
D O I
10.1073/pnas.0907801107
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Although Pentapetalae (comprising all core eudicots except Gunnerales) include approximate to 70% of all angiosperms, the origin of and relationships among the major lineages of this clade have remained largely unresolved. Phylogenetic analyses of 83 protein-coding and rRNA genes from the plastid genome for 86 species of seed plants, including new sequences from 25 eudicots, indicate that soon after its origin, Pentapetalae diverged into three clades: (i) a "superrosid" clade consisting of Rosidae, Vitaceae, and Saxifragales; (ii) a "superasterid" clade consisting of Berberidopsidales, Santalales, Caryophyllales, and Asteridae; and (iii) Dilleniaceae. Maximum-likelihood analyses support the position of Dilleniaceae as sister to superrosids, but topology tests did not reject alternative positions of Dilleniaceae as sister to Asteridae or all remaining Pentapetalae. Molecular dating analyses suggest that the major lineages within both superrosids and superasterids arose in as little as 5 million years. This phylogenetic hypothesis provides a crucial historical framework for future studies aimed at elucidating the underlying causes of the morphological and species diversity in Pentapetalae.
引用
收藏
页码:4623 / 4628
页数:6
相关论文
共 56 条
[1]   Dating phylogenetically basal eudicots using rbcL sequences and multiple fossil reference points [J].
Anderson, CL ;
Bremer, K ;
Friis, EM .
AMERICAN JOURNAL OF BOTANY, 2005, 92 (10) :1737-1748
[2]  
[Anonymous], 2011, PAUP*: phylogenetic analysis using parsimony
[3]   The age of the angiosperms: A molecular timescale without a clock [J].
Bell, CD ;
Soltis, DE ;
Soltis, PS .
EVOLUTION, 2005, 59 (06) :1245-1258
[4]   Dating the dipsacales: Comparing models, genes, and evolutionary implications [J].
Bell, CD ;
Donoghue, MJ .
AMERICAN JOURNAL OF BOTANY, 2005, 92 (02) :284-296
[5]   Inferring phylogenies with incomplete data sets: a 5-gene, 567-taxon analysis of angiosperms [J].
Burleigh, J. Gordon ;
Hilu, Khidir W. ;
Soltis, Douglas E. .
BMC EVOLUTIONARY BIOLOGY, 2009, 9
[6]  
Cantino PD, 2007, TAXON, V56, P822, DOI 10.2307/25065865
[7]   PHYLOGENETICS OF SEED PLANTS - AN ANALYSIS OF NUCLEOTIDE-SEQUENCES FROM THE PLASTID GENE RBCL [J].
CHASE, MW ;
SOLTIS, DE ;
OLMSTEAD, RG ;
MORGAN, D ;
LES, DH ;
MISHLER, BD ;
DUVALL, MR ;
PRICE, RA ;
HILLS, HG ;
QIU, YL ;
KRON, KA ;
RETTIG, JH ;
CONTI, E ;
PALMER, JD ;
MANHART, JR ;
SYTSMA, KJ ;
MICHAELS, HJ ;
KRESS, WJ ;
KAROL, KG ;
CLARK, WD ;
HEDREN, M ;
GAUT, BS ;
JANSEN, RK ;
KIM, KJ ;
WIMPEE, CF ;
SMITH, JF ;
FURNIER, GR ;
STRAUSS, SH ;
XIANG, QY ;
PLUNKETT, GM ;
SOLTIS, PS ;
SWENSEN, SM ;
WILLIAMS, SE ;
GADEK, PA ;
QUINN, CJ ;
EGUIARTE, LE ;
GOLENBERG, E ;
LEARN, GH ;
GRAHAM, SW ;
BARRETT, SCH ;
DAYANANDAN, S ;
ALBERT, VA .
ANNALS OF THE MISSOURI BOTANICAL GARDEN, 1993, 80 (03) :528-580
[8]  
Cronquist A, 1981, INTEGRATED SYSTEM CL
[9]   Darwin's abominable mystery: Insights from a supertree of the angiosperms [J].
Davies, TJ ;
Barraclough, TG ;
Chase, MW ;
Soltis, PS ;
Soltis, DE ;
Savolainen, V .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (07) :1904-1909
[10]  
DRINNAN AN, 1994, PL SYST EVOL S, V8, P93