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Mosaic Origin of the Heme Biosynthesis Pathway in Photosynthetic Eukaryotes
Open accessAbstract
Heme biosynthesis represents one of the most essential metabolic pathways in living organisms, providing the precursors for cytochrome prosthetic groups, photosynthetic pigments, and vitamin B(12). Using genomic data, we have compared the heme pathway in the diatom Thalassiosira pseudonana and the red alga Cyanidioschyzon merolae to those of green algae and higher plants, as well as to those of heterotrophic eukaryotes (fungi, apicomplexans, and animals). Phylogenetic analyses showed the mosaic character of this pathway in photosynthetic eukaryotes. Although most of the algal and plant enzymes showed the expected plastid (cyanobacterial) origin, at least one of them (porphobilinogen deaminase) appears to have a mitochondrial (alpha-proteobacterial) origin. Another enzyme, glutamyl-tRNA synthase, obviously originated in the eukaryotic nucleus. Because all the plastid-targeted sequences consistently form a well-supported cluster, this suggests that genes were either transferred from the primary endosymbiont (cyanobacteria) to the primary host nucleus shortly after the primary endosymbiotic event or replaced with genes from other sources at an equally early time, i.e., before the formation of three primary plastid lineages. The one striking exception to this pattern is ferrochelatase, the enzyme catalyzing the first committed step to heme and bilin pigments. In this case, two red algal sequences do not cluster either with the other plastid sequences or with cyanobacterial sequences and appear to have a proteobacterial origin like that of the apicomplexan parasites Plasmodium and Toxoplasma. Although the heterokonts also acquired their plastid via secondary endosymbiosis from a red alga, the diatom has a typical plastid-cyanobacterial ferrochelatase. We have not found any remnants of the plastidlike heme pathway in the nonphotosynthetic heterokonts Phytophthora ramorum and Phytophthora sojae.
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Woese, C. R. (1987) · Microbiological Reviews · doi:10.1128/mr.51.2.221-271.1987 · Cited by 5,042
Martin, W., Rujan, T., Richly, E., Hansen, A., Cornelsen, S., Lins, T., Leister, D., Stoebe, B., Hasegawa, M., & Penny, D. (2002) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.182432999 · Cited by 1,178
The highly reduced genome of an enslaved algal nucleus
Douglas, S., Zauner, S., Fraunholz, M., Beaton, M., Penny, S., Deng, L.-T., Wu, X., Reith, M., Cavalier-Smith, T., & Maier, U.-G. (2001) · Nature · doi:10.1038/35074092 · Cited by 454
Fast, N. M., Kissinger, J. C., Roos, D. S., & Keeling, P. J. (2001) · Molecular Biology and Evolution · doi:10.1093/oxfordjournals.molbev.a003818 · Cited by 418
Cited by
Horizontal gene transfer in eukaryotic evolution
Keeling, P. J., & Palmer, J. D. (2008) · Nature Reviews Genetics · doi:10.1038/nrg2386 · Cited by 1,355
Tetrapyrrole Biosynthesis in Higher Plants
Tanaka, R., & Tanaka, A. (2007) · Annual Review of Plant Biology · doi:10.1146/annurev.arplant.57.032905.105448 · Cited by 818
DNA Transfer from Organelles to the Nucleus: The Idiosyncratic Genetics of Endosymbiosis
Kleine, T., Maier, U. G., & Leister, D. (2009) · Annual Review of Plant Biology · doi:10.1146/annurev.arplant.043008.092119 · Cited by 391
The cell biology of tetrapyrroles: a life and death struggle
Mochizuki, N., Tanaka, R., Grimm, B., Masuda, T., Moulin, M., Smith, A. G., Tanaka, A., & Terry, M. J. (2010) · Trends in Plant Science · doi:10.1016/j.tplants.2010.05.012 · Cited by 320
Tetrapyrrole Metabolism in Arabidopsis thaliana
Tanaka, R., Kobayashi, K., & Masuda, T. (2011) · The Arabidopsis Book · doi:10.1199/tab.0145 · Cited by 281
Metadata
- Authors
- Oborník, M., & Green, B. R.
- Venue
- Molecular Biology and Evolution
- Publisher
- Oxford University Press (OUP)
- Published
- 2005-08-10
- Volume
- 22
- Issue
- 12
- Pages
- 2343-2353
- ISSN
- 0737-4038 (ISSN-L)
- 1537-1719
- OpenAlex
- W1977281120
- Cited by
- 164
- References
- 4
- FWCI
- 2.42
- Type
- journal article
- Language
- en
- Open access
- bronze
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