Skip Navigation


MBE Advance Access originally published online on September 21, 2006
Molecular Biology and Evolution 2007 24(1):54-62; doi:10.1093/molbev/msl129
This Article
Right arrow Full Text Freely available
Right arrow FREE Full Text (PDF) Freely available
Right arrow Supplemantary Material
Right arrow All Versions of this Article:
24/1/54    most recent
msl129v1
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrowRequest Permissions
Google Scholar
Right arrow Articles by Rogers, M. B.
Right arrow Articles by Keeling, P. J.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Rogers, M. B.
Right arrow Articles by Keeling, P. J.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

© The Author 2006. Published by Oxford University Press on behalf of the Society for Molecular Biology and Evolution. All rights reserved. For permissions, please e-mail: journals.permissions@oxfordjournals.org

Research Articles

The Complete Chloroplast Genome of the Chlorarachniophyte Bigelowiella natans: Evidence for Independent Origins of Chlorarachniophyte and Euglenid Secondary Endosymbionts

Matthew B. Rogers*, Paul R. Gilson{dagger}, Vanessa Su{ddagger}, Geoffrey I. McFadden{ddagger} and Patrick J. Keeling*

* Botany Department, University of British Columbia, British Columbia, Canada
{dagger} The Walter and Eliza Hall Institute of Medical Research, Parkville, Victoria, Australia
{ddagger} School of Botany, University of Melbourne, Victoria, Australia

E-mail: pkeeling{at}interchange.ubc.ca.

Accepted for publication September 18, 2006.

Chlorarachniophytes are amoeboflagellate cercozoans that acquired a plastid by secondary endosymbiosis. Chlorarachniophytes are the last major group of algae for which there is no completely sequenced plastid genome. Here we describe the 69.2-kbp chloroplast genome of the model chlorarachniophyte Bigelowiella natans. The genome is highly reduced in size compared with plastids of other photosynthetic algae and is closer in size to genomes of several nonphotosynthetic plastids. Unlike nonphotosynthetic plastids, however, the B. natans chloroplast genome has not sustained a massive loss of genes, and it retains nearly all of the functional photosynthesis-related genes represented in the genomes of other green algae. Instead, the genome is highly compacted and gene dense. The genes are organized with a strong strand bias, and several unusual rearrangements and inversions also characterize the genome; notably, an inversion in the small-subunit rRNA gene, a translocation of 3 genes in the major ribosomal protein operon, and the fragmentation of the cluster encoding the large photosystem proteins PsaA and PsaB. The chloroplast endosymbiont is known to be a green alga, but its evolutionary origin and relationship to other primary and secondary green plastids has been much debated. A recent hypothesis proposes that the endosymbionts of chlorarachniophytes and euglenids share a common origin (the Cabozoa hypothesis). We inferred phylogenies using individual and concatenated gene sequences for all genes in the genome. Concatenated gene phylogenies show a relationship between the B. natans plastid and the ulvophyte–trebouxiophyte–chlorophyte clade of green algae to the exclusion of Euglena. The B. natans plastid is thus not closely related to that of Euglena, which suggests that plastids originated independently in these 2 groups and the Cabozoa hypothesis is false.

Key Words: plastid • genome • chlorarachniophyte • phylogeny • endosymbiosis


Charles Delwiche, Associate Editor


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
Mol Biol EvolHome page
C. Grauvogel, H. Brinkmann, and J. Petersen
Evolution of the Glucose-6-Phosphate Isomerase: The Plasticity of Primary Metabolism in Photosynthetic Eukaryotes
Mol. Biol. Evol., August 1, 2007; 24(8): 1611 - 1621.
[Abstract] [Full Text] [PDF]


Home page
Mol Biol EvolHome page
J. D. Hackett, H. S. Yoon, S. Li, A. Reyes-Prieto, S. E. Rummele, and D. Bhattacharya
Phylogenomic Analysis Supports the Monophyly of Cryptophytes and Haptophytes and the Association of Rhizaria with Chromalveolates
Mol. Biol. Evol., August 1, 2007; 24(8): 1702 - 1713.
[Abstract] [Full Text] [PDF]


Home page
Mol Biol EvolHome page
H. Khan, N. Parks, C. Kozera, B. A. Curtis, B. J. Parsons, S. Bowman, and J. M. Archibald
Plastid Genome Sequence of the Cryptophyte Alga Rhodomonas salina CCMP1319: Lateral Transfer of Putative DNA Replication Machinery and a Test of Chromist Plastid Phylogeny
Mol. Biol. Evol., August 1, 2007; 24(8): 1832 - 1842.
[Abstract] [Full Text] [PDF]


Home page
Plant Physiol.Home page
A. G. Koziol, T. Borza, K.-I. Ishida, P. Keeling, R. W. Lee, and D. G. Durnford
Tracing the Evolution of the Light-Harvesting Antennae in Chlorophyll a/b-Containing Organisms
Plant Physiology, April 1, 2007; 143(4): 1802 - 1816.
[Abstract] [Full Text] [PDF]



Disclaimer:
Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.