Literature DB >> 21652314

Monocot relationships: an overview.

Mark W Chase1.   

Abstract

In 10 years, the monocots have gone from being one of the least studied and most phylogenetically misunderstood groups of the angiosperms to one of the best characterized. Based on analyses of seven genes representing all three genomes, the following clades have high bootstrap support: Acorales (with the single genus Acorus) is sister to the rest of the monocots, followed successively by Alismatales (including Araceae and Tofieldiaceae), Petrosaviales, Dioscoreales/Pandanales, Liliales, Asparagales, and finally a polytomy of Arecales, Commelinales/Zingiberales, Dasypogonaceae, and Poales. Many of these results also have support from at least some morphological data, but some are unique to the trees created from DNA sequence data. Monocots have been shown in molecular clock studies to be at least 140 million years old, and all major clades and most families date to well before the end of the Cretaceous. More data are required to clarify the positions of the remaining unclearly placed orders, Asparagles, Liliales, and Arecales, as well as Dasypogonaceae. More sequences from the nuclear and mitochondrial genomes are also needed to complement those from the plastid genome, which is the most sampled and thus far most pattern-rich.

Entities:  

Year:  2004        PMID: 21652314     DOI: 10.3732/ajb.91.10.1645

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


  28 in total

1.  Pollination and late-acting self-incompatibility in Cyrtanthus breviflorus (Amaryllidaceae): implications for seed production.

Authors:  Glenda Vaughton; Mike Ramsey; Steven D Johnson
Journal:  Ann Bot       Date:  2010-07-19       Impact factor: 4.357

2.  Comparative sequencing of plant genomes: choices to make.

Authors:  Scott Jackson; Steve Rounsley; Michael Purugganan
Journal:  Plant Cell       Date:  2006-05       Impact factor: 11.277

3.  Breakdown and delayed cospeciation in the arbuscular mycorrhizal mutualism.

Authors:  Vincent Merckx; Martin I Bidartondo
Journal:  Proc Biol Sci       Date:  2008-05-07       Impact factor: 5.349

4.  Release of developmental constraints on tetrad shape is confirmed in inaperturate pollen of Potamogeton.

Authors:  Elaine Lopes Pereira Nunes; Cleusa Bona; Maria Cecília de Chiara Moço; Alessandra Ike Coan
Journal:  Ann Bot       Date:  2009-06-30       Impact factor: 4.357

5.  The frequency of polyploid speciation in vascular plants.

Authors:  Troy E Wood; Naoki Takebayashi; Michael S Barker; Itay Mayrose; Philip B Greenspoon; Loren H Rieseberg
Journal:  Proc Natl Acad Sci U S A       Date:  2009-08-10       Impact factor: 11.205

6.  Tropical forests are both evolutionary cradles and museums of leaf beetle diversity.

Authors:  Duane D McKenna; Brian D Farrell
Journal:  Proc Natl Acad Sci U S A       Date:  2006-07-03       Impact factor: 11.205

Review 7.  A re-examination of the root cortex in wetland flowering plants with respect to aerenchyma.

Authors:  James L Seago; Leland C Marsh; Kevin J Stevens; Ales Soukup; Olga Votrubová; Daryl E Enstone
Journal:  Ann Bot       Date:  2005-08-04       Impact factor: 4.357

8.  Expression of a polyubiquitin promoter isolated from Gladiolus.

Authors:  Young Hee Joung; Kathryn Kamo
Journal:  Plant Cell Rep       Date:  2006-06-08       Impact factor: 4.570

9.  An analysis of flavonoid compounds in leaves of Japonolirion (Petrosaviaceae).

Authors:  Tsukasa Iwashina; Junichi Kitajima; Takako Kato; Hiroshi Tobe
Journal:  J Plant Res       Date:  2005-02-10       Impact factor: 2.629

10.  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

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