@ARTICLE{TreeBASE2Ref20071,
author = {Valerie Lynn Soza and Vietnam Le Huynh and Veronica S. Di Stilio},
title = {Pattern and process in the evolution of the sole dioecious member of Brassicaceae },
year = {2014},
keywords = {allopolyploidy, programmed cell death, dioecy, floral ontogeny, genome size, organ arrest, phylogenetic network, PISTILLATA, sex differentiation, unisexual flowers},
doi = {10.1186/2041-9139-5-42},
url = {http://},
pmid = {},
journal = {EvoDevo},
volume = {5},
number = {},
pages = {42},
abstract = {Background
Lepidium sisymbrioides, a polyploid New Zealand endemic, is the sole dioecious species in Brassicaceae and therefore the closest dioecious relative of the model plant Arabidopsis thaliana. The attractiveness of developing this system for future studies on the genetics of sex determination prompted us to investigate historical and developmental factors surrounding the evolution of its unisexual flowers. Our goal was to determine the evolutionary pattern of polyploidization of L. sisymbrioides and the timing and process of flower reproductive organ abortion. To that end, we used a combination of phylogenetics to place this species within the complex history of polyploidization events in Lepidium and histology to compare its floral ontogeny to that of its closest hermaphroditic relatives and to A. thaliana.
Results
Using a nuclear locus (PISTILLATA), we reconstructed the gene tree among Lepidium taxa and applied a phylogenetic network analysis to identify ancestral genomes that contributed to the evolution of L. sisymbrioides. Combining this phylogenetic framework with cytological and genome size data, we estimated L. sisymbrioides as an allo-octoploid resulting from three hybridization events. Our investigations of flower development showed that unisexual flowers appear to abort reproductive organs by programmed cell death in female flowers and by developmental arrest in male flowers. This selective abortion occurs at the same floral developmental stage in both males and females, corresponding to Arabidopsis stage nine.
Conclusions
Dioecy in Brassicaceae evolved once in L. sisymbrioides following several allopolyploidization events, by a process of selective abortion of reproductive organs at intermediate stages of flower development. Different developmental processes, but similar timing of abortions, affect male versus female flower development. An increased understanding of how and when reproductive organs abort in this species, combined with our estimates of ancestral genome contributions, ploidy and genome size, lay the foundation for future efforts to examine the genetic mechanisms involved in the evolution of unisexual flowers in the closest dioecious relative of the best studied model plant.
}
}
Taxa for tree 55685 of Study 11886

Citation title:
"Pattern and process in the evolution of the sole dioecious member of Brassicaceae ".

Study name:
"Pattern and process in the evolution of the sole dioecious member of Brassicaceae ".

This study is part of submission 11886
(Status: Published).
Taxa
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| ID |
Taxon Label |
NCBI taxid |
uBIO namebankID |
| 852831 |
Altirhinus kurzanovi |
|
6104964
|
| 852846 |
Bactrosaurus johnsoni |
|
6096099
|
| 852844 |
Barilium dawsoni |
|
|
| 852817 |
Callovosaurus leedsi |
|
5665345
|
| 852863 |
Camptosaurus aphanoecetes |
|
|
| 852838 |
Camptosaurus depressus |
|
7062176
|
| 852860 |
Camptosaurus dispar |
|
|
| 852867 |
Camptosaurus valdensis |
|
6178935
|
| 852835 |
Cedrorestes crichtoni |
|
|
| 852871 |
Claosaurus agilis |
|
6638463
|
| 852828 |
Corythosaurus casuarius |
|
5709773
|
| 852842 |
Cumnoria prestwichii |
|
|
| 852859 |
Dakotadon lakotaensis |
|
|
| 852830 |
Dollodon bampingi |
|
|
| 852843 |
Draconyx loureiroi |
|
5665344
|
| 852824 |
Dryosaurus altus |
|
6327240
|
| 852847 |
Dysalotosaurus lettowvorbecki |
|
7101432
|
| 852827 |
Edmontosaurus annectens |
|
5804540
|
| 852851 |
Elrhazosaurus nigeriensis |
|
|
| 852869 |
Eolambia caroljonesa |
|
5642159
|
| 852845 |
Equijubus normani |
|
5530008
|
| 852826 |
Fukuisaurus tetoriensis |
|
5533758
|
| 852833 |
Gilmoreosaurus mongoliensis |
|
|
| 852816 |
Hadrosaurus foulkii |
|
|
| 852857 |
Hypselospinus fittoni |
|
|
| 852855 |
Hypsilophodon foxii |
|
6355423
|
| 852834 |
Iguanodon bernissartensis |
|
5651240
|
| 852841 |
Jeyawati rugoculus |
|
|
| 852858 |
Jintasaurus meniscus |
|
|
| 852853 |
Jinzhousaurus yangi |
|
5635609
|
| 852840 |
Kangnasaurus coetzeei |
|
6415800
|
| 852849 |
Kukufeldia tilgatensis |
|
|
| 852829 |
Lanzhousaurus magnidens |
|
|
| 852861 |
Lesothosaurus diagnosticus |
|
6463968
|
| 852812 |
Levnesovia transoxiana |
|
|
| 852822 |
Lophorhothon atopus |
|
|
| 852814 |
Lurdusaurus arenatus |
|
6041066
|
| 852839 |
Mantellisaurus atherfieldensis |
|
|
| 852832 |
Muttaburrasaurus langdoni |
|
6909768
|
| 852825 |
NHMUK R1831 |
|
|
| 852868 |
NHMUK R8676 |
|
|
| 852856 |
Nanyangosaurus zhugeii |
|
5700698
|
| 852852 |
Ouranosaurus nigeriensis |
|
6113300
|
| 852854 |
Owenodon hoggii |
|
|
| 852837 |
Penelopognathus weishampeli |
|
|
| 852850 |
Planicoxa venenica |
|
5669547
|
| 852823 |
Probactrosaurus gobiensis |
|
5575255
|
| 852815 |
Probactrosaurus mazongshanensis |
|
5575257
|
| 852813 |
Protohadros byrdi |
|
6055337
|
| 852821 |
Rhabdodon Sp. |
|
4328356
|
| 852819 |
Shuangmiaosaurus gilmorei |
|
5530061
|
| 852866 |
Tanius sinensis |
|
6362683
|
| 852864 |
Telmatosaurus transsylvanicus |
|
6325737
|
| 852848 |
Tenontosaurus dossi |
|
6134668
|
| 852870 |
Tenontosaurus tilletti |
|
6240838
|
| 852873 |
Tethyshadros insularis |
|
|
| 852862 |
Theiophytalia kerri |
|
|
| 852820 |
Utah taxon 1 |
|
|
| 852872 |
Utah taxon 2 |
|
|
| 852818 |
Valdosaurus canaliculatus |
|
6178934
|
| 852865 |
Zalmoxes robustus |
|
5529683
|
| 852836 |
Zalmoxes shqiperorum |
|
5529676
|