Literature DB >> 23608647

Phylogeny and origins of holoparasitism in Orobanchaceae.

Joel R McNeal1, Jonathan R Bennett, Andrea D Wolfe, Sarah Mathews.   

Abstract

PREMISE: Orobanchaceae are a family of angiosperms that range from fully autotrophic and free-living to completely heterotrophic and dependent on their hosts (holoparasites). Most of the ca. 2060 species are hemiparasites that photosynthesize throughout all or part of their life cycles. Certain family members are ecologically important due to direct impacts on community biomass and diversity, plant-herbivore interactions, and nutrient cycling. Other members are among the most economically damaging weeds in the world. Multiple trophic transitions within this family make it ideal for studying molecular evolutionary and physiological changes that accompany the evolution of parasitism. •
METHODS: To establish a phylogenetic framework for such work, we substantially increased taxonomic sampling at loci for which a significant amount of data already existed (nuclear ITS and PHYA, plastid matK and rps2) and added data from the low-copy nuclear locus, PHYB. • KEY
RESULTS: The data provide strong support for relationships among six major clades and for the position of Brandisia hancei Hook. f. The positions of Boschniakia himalaica Hook. f. & Thomson, Centranthera cochinchinensis (Lour.) Merr., Mannagettaea hummelii Harry Sm., and Pterygiella nigrescens Oliv. are confirmed or suggested for the first time. •
CONCLUSIONS: There is a single origin of parasitism, and from within the hemiparasites, holoparasitism has originated three times. Moving from the base to the tips of the Orobanchaceae tree, the successive major splits within the parasitic clade are: Cymbarieae + the rest; Orobancheae + the rest; Brandisia + the rest; Rhinantheae + the rest; and Pedicularideae + Buchnereae.

Entities:  

Keywords:  Orobanchaceae; hemiparasite; parasitism; phylogeny; phytochrome

Mesh:

Substances:

Year:  2013        PMID: 23608647     DOI: 10.3732/ajb.1200448

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


  30 in total

1.  Arabinogalactan protein-rich cell walls, paramural deposits and ergastic globules define the hyaline bodies of rhinanthoid Orobanchaceae haustoria.

Authors:  Anna Pielach; Olivier Leroux; David S Domozych; J Paul Knox; Zoë A Popper
Journal:  Ann Bot       Date:  2014-07-14       Impact factor: 4.357

2.  Hydathode trichomes actively secreting water from leaves play a key role in the physiology and evolution of root-parasitic rhinanthoid Orobanchaceae.

Authors:  Petra Světlíková; Tomáš Hájek; Jakub Těšitel
Journal:  Ann Bot       Date:  2015-05-18       Impact factor: 4.357

3.  Targeted mutagenesis of two homologous ATP-binding cassette subfamily G (ABCG) genes in tomato confers resistance to parasitic weed Phelipanche aegyptiaca.

Authors:  Vinay Kumar Bari; Jackline Abu Nassar; Ayala Meir; Radi Aly
Journal:  J Plant Res       Date:  2021-03-11       Impact factor: 2.629

4.  Mechanistic model of evolutionary rate variation en route to a nonphotosynthetic lifestyle in plants.

Authors:  Susann Wicke; Kai F Müller; Claude W dePamphilis; Dietmar Quandt; Sidonie Bellot; Gerald M Schneeweiss
Journal:  Proc Natl Acad Sci U S A       Date:  2016-07-22       Impact factor: 11.205

5.  Cryptic host-specific diversity among western hemisphere broomrapes (Orobanche s.l., Orobanchaceae).

Authors:  Adam C Schneider; Alison E L Colwell; Gerald M Schneeweiss; Bruce G Baldwin
Journal:  Ann Bot       Date:  2016-08-18       Impact factor: 4.357

6.  Lineage and role in integrative taxonomy of a heterotrophic orchid complex.

Authors:  Craig F Barrett; Mathilda V Santee; Nicole M Fama; John V Freudenstein; Sandra J Simon; Brandon T Sinn
Journal:  Mol Ecol       Date:  2022-07-22       Impact factor: 6.622

7.  Marker Development for Phylogenomics: The Case of Orobanchaceae, a Plant Family with Contrasting Nutritional Modes.

Authors:  Xi Li; Baohai Hao; Da Pan; Gerald M Schneeweiss
Journal:  Front Plant Sci       Date:  2017-11-21       Impact factor: 5.753

8.  Mechanisms of functional and physical genome reduction in photosynthetic and nonphotosynthetic parasitic plants of the broomrape family.

Authors:  Susann Wicke; Kai F Müller; Claude W de Pamphilis; Dietmar Quandt; Norman J Wickett; Yan Zhang; Susanne S Renner; Gerald M Schneeweiss
Journal:  Plant Cell       Date:  2013-10-18       Impact factor: 11.277

9.  Genomic reconfiguration in parasitic plants involves considerable gene losses alongside global genome size inflation and gene births.

Authors:  Peter Lyko; Susann Wicke
Journal:  Plant Physiol       Date:  2021-07-06       Impact factor: 8.340

10.  Comparative transcriptome analyses reveal core parasitism genes and suggest gene duplication and repurposing as sources of structural novelty.

Authors:  Zhenzhen Yang; Eric K Wafula; Loren A Honaas; Huiting Zhang; Malay Das; Monica Fernandez-Aparicio; Kan Huang; Pradeepa C G Bandaranayake; Biao Wu; Joshua P Der; Christopher R Clarke; Paula E Ralph; Lena Landherr; Naomi S Altman; Michael P Timko; John I Yoder; James H Westwood; Claude W dePamphilis
Journal:  Mol Biol Evol       Date:  2014-12-21       Impact factor: 16.240

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