4.8 Article

On the Origin of Isoprenoid Biosynthesis

期刊

MOLECULAR BIOLOGY AND EVOLUTION
卷 35, 期 9, 页码 2185-2197

出版社

OXFORD UNIV PRESS
DOI: 10.1093/molbev/msy120

关键词

isoprenoid; mevalonate pathway; candidate phyla radiation; GHMP superfamily

资金

  1. Agouron Institute Postdoctoral Fellowship
  2. Department of Defense, Army Research Office [W911NF-16-1-0372]
  3. Human Frontier Science Program grant [RGP0041]
  4. National Institute of Health [R01AR069137]
  5. NATIONAL INSTITUTE OF ARTHRITIS AND MUSCULOSKELETAL AND SKIN DISEASES [R01AR069137] Funding Source: NIH RePORTER

向作者/读者索取更多资源

Isoprenoids and their derivatives represent the largest group of organic compounds in nature and are distributed universally in the three domains of life. Isoprenoids are biosynthesized from isoprenyl diphosphate units, generated by two distinctive biosynthetic pathways: mevalonate pathway and methylerthritol 4-phosphate pathway. Archaea and eukaryotes exclusively have the former pathway, while most bacteria have the latter. Some bacteria, however, are known to possess the mevalonate pathway genes. Understanding the evolutionary history of these two isoprenoid biosynthesis pathways in each domain of life is critical since isoprenoids are so interweaved in the architecture of life that they would have had indispensable roles in the early evolution of life. Our study provides a detailed phylogenetic analysis of enzymes involved in the mevalonate pathway and sheds new light on its evolutionary history. The results suggest that a potential mevalonate pathway is present in the recently discovered superphylum Candidate Phyla Radiation (CPR), and further suggest a strong evolutionary relationship exists between archaea and CPR. Interestingly, CPR harbors the characteristics of both the bacterial-type and archaeal-type mevalonate pathways and may retain signatures regarding the ancestral isoprenoid biosynthesis pathway in the last universal common ancestor. Our study supports the ancient origin of the mevalonate pathway in the three domains of life as previously inferred, but concludes that the evolution of the mevalonate pathway was more complex.

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