Strongylocentrotus purpuratus

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Strongylocentrotus purpuratus
Strongylocentrotus purpuratus 1.jpg
Scientific classification OOjs UI icon edit-ltr.svg
Domain: Eukaryota
Kingdom: Animalia
Phylum: Echinodermata
Class: Echinoidea
Order: Echinoida
Family: Strongylocentrotidae
Genus: Strongylocentrotus
Species:
S. purpuratus
Binomial name
Strongylocentrotus purpuratus
(Stimpson, 1857)
Strongylocentrotus purpuratus range.png
Oral surface of Strongylocentrotus purpuratus showing teeth of Aristotle's Lantern, spines and tube feet. Strongylocentrotus purpuratus 020313.JPG
Oral surface of Strongylocentrotus purpuratus showing teeth of Aristotle's Lantern, spines and tube feet.
Strongylocentrotus purpuratus Strongylocentrotus purpuratus California.JPG
Strongylocentrotus purpuratus

Strongylocentrotus purpuratus, the purple sea urchin, lives along the eastern edge of the Pacific Ocean extending from Ensenada, Mexico, to British Columbia, Canada. [1] This sea urchin species is deep purple in color, and lives in lower inter-tidal and nearshore sub-tidal communities. Its eggs are orange when secreted in water. [2] January, February, and March function as the typical active reproductive months for the species. Sexual maturity is reached around two years. [3] It normally grows to a diameter of about 10 cm (4 inches) and may live as long as 70 years. [4]

Contents

S. purpuratus is used as a model organism and its genome was the first echinoderm genome to be sequenced. [5]

Role in biomedical research

The initial discovery of three distinct eukaryotic DNA-dependent RNA polymerases was made using S. purpuratus as a model organism. [6] While embryonic development is still a major part of the utilization of the sea urchin, studies on urchin's position as an evolutionary marvel have become increasingly frequent. Orthologs to human diseases have led scientists to investigate potential therapeutic uses for the sequences found in Strongylocentrotus purpuratus. For instance, in 2012, scientists at the University of St Andrews began investigating the "2A" viral region in the S. purpuratus genome [7] [8] which may be useful for Alzheimer's disease and cancer research. The study identified a sequence that can return cells to a 'stem-cell' like state, allowing for better treatment options. [7] The species has also been a candidate in longevity studies, particularly because of its ability to regenerate damaged or aging tissue. Another study comparing 'young' vs. 'old' suggested that even in species with varying lifespans, the 'regenerative potential' was upheld in older specimens as they suffered no significant disadvantages compared to younger ones. [9]

Genome

The genome of the purple sea urchin was completely sequenced and annotated in 2006 by teams of scientists from over 70 institutions including the Kerckhoff Marine Laboratory at the California Institute of Technology as well as the Human Genome Sequencing Center at the Baylor College of Medicine. [10] A new improved version of the purple sea urchin genome, Strongylocentrotus purpuratus v5.0, is now available on Echinobase. S. purpuratus is one of several biomedical research model organisms in cell and developmental biology. [11] The sea urchin is the first animal with a sequenced genome that (1) is a free-living, motile marine invertebrate; (2) has a bilaterally organized embryo but a radial adult body plan; (3) has the endoskeleton and water vascular system found only in echinoderms; and (4) has a nonadaptive immune system that is unique in the enormous complexity of its receptor repertoire. [12]

The sea urchin genome is estimated to encode about 23,500 genes. The S. purpuratus has 353 protein kinases, containing members of 97% of human kinase subfamilies. [13] Many of these genes were previously thought to be vertebrate innovations or were only known from groups outside the deuterostomes. The team sequencing the species concluded that some genes are not vertebrate specific as thought previously, while other genes still were found in the urchin but not the chordate.

The genome is largely non-redundant, making it very comparable to vertebrates, but without the complexity. For example, 200 to 700 chemosensory genes were found that lacked introns, a feature typical of vertebrates. [13] Thus the sea urchin genome provides a comparison to our own and those of other deuterostomes, the larger group to which both echinoderms and humans belong. [12] Sea urchins are also the closest living relative to chordates. [13] Using the strictest measure, the purple sea urchin and humans share 7,700 genes. [14] Many of these genes are involved in sensing the environment, [15] a fact surprising for an animal lacking a head structure.

The sea urchin also has a chemical 'defensome' that reacts when stress is sensed to eliminate potentially toxic chemicals. [13] S. purpuratus's immune systems contains innate pathogen receptors like Toll-like receptors and genes that encode for LRR . There were genes identified for Biomineralization that were not counterparts of the typical human vertebrate variety SCCPs, and encode for transmembrane proteins like P16. Many orthologs exist for genes associated with human diseases, such as Reelin (from Norman-Roberts lissencephaly syndrome) and many cytoskeletal proteins of the Usher syndrome network like usherin and VLGR1. [13]

Increasing carbon dioxide concentrations affect the epigenome, gene expression, and phenotype of the purple sea urchin. Carbon dioxide concentration also reduces the size of its larvae, which indicates that fitness of the larvae could be negatively impacted. [16] [17]

Ecology

The purple sea urchin, along with sea otters and abalones, is a prominent member of the kelp forest community. [18] The purple sea urchin also plays a key role in the disappearance of kelp forests that is currently occurring due to climate change. [19]

Use as food

Sea urchins like the purple sea urchin have been used for food by the indigenous peoples of California, who ate the yellow egg mass raw. [20] [21]

In California, the peak gonad growth season (and therefore peak of edibility) is September–October. [22] Early in the season, the gonads are still growing and the yield will be smaller. From November onwards the gonads are developed, however harvesting stress can induce spawning, decreasing quality.

Close up of Strongylocentrotus purpuratus clearly showing tube feet. Strongylocentrotus purpuratus.jpg
Close up of Strongylocentrotus purpuratus clearly showing tube feet.

See also

Related Research Articles

<span class="mw-page-title-main">Echinoderm</span> Exclusively marine phylum of animals with generally 5-point radial symmetry

An echinoderm is any member of the phylum Echinodermata. The adults are recognisable by their radial symmetry, and include starfish, brittle stars, sea urchins, sand dollars, and sea cucumbers, as well as the sea lilies or "stone lilies". Adult echinoderms are found on the sea bed at every ocean depth, from the intertidal zone to the abyssal zone. The phylum contains about 7,000 living species, making it the second-largest grouping of deuterostomes, after the chordates. Echinoderms are the largest entirely marine phylum. The first definitive echinoderms appeared near the start of the Cambrian.

<span class="mw-page-title-main">Sea urchin</span> Class of marine invertebrates

Sea urchins are spiny, globular echinoderms in the class Echinoidea. About 950 species of sea urchin are distributed on the seabeds of every ocean and inhabit every depth zone from the intertidal seashore down to 5,000 meters. The spherical, hard shells (tests) of sea urchins are round and covered in spines. Most urchin spines range in length from 3 to 10 cm, with outliers such as the black sea urchin possessing spines as long as 30 cm (12 in). Sea urchins move slowly, crawling with tube feet, and also propel themselves with their spines. Although algae are the primary diet, sea urchins also eat slow-moving (sessile) animals. Predators that eat sea urchins include a wide variety of fish, starfish, crabs, marine mammals, and humans.

<span class="mw-page-title-main">Codon usage bias</span> Genetic bias in coding DNA

Codon usage bias refers to differences in the frequency of occurrence of synonymous codons in coding DNA. A codon is a series of three nucleotides that encodes a specific amino acid residue in a polypeptide chain or for the termination of translation.

<span class="mw-page-title-main">Genome project</span>

Genome projects are scientific endeavours that ultimately aim to determine the complete genome sequence of an organism and to annotate protein-coding genes and other important genome-encoded features. The genome sequence of an organism includes the collective DNA sequences of each chromosome in the organism. For a bacterium containing a single chromosome, a genome project will aim to map the sequence of that chromosome. For the human species, whose genome includes 22 pairs of autosomes and 2 sex chromosomes, a complete genome sequence will involve 46 separate chromosome sequences.

The recombination-activating genes (RAGs) encode parts of a protein complex that plays important roles in the rearrangement and recombination of the genes encoding immunoglobulin and T cell receptor molecules. There are two recombination-activating genes RAG1 and RAG2, whose cellular expression is restricted to lymphocytes during their developmental stages. The enzymes encoded by these genes, RAG-1 and RAG-2, are essential to the generation of mature B cells and T cells, two types of lymphocyte that are crucial components of the adaptive immune system.

Eric Harris Davidson was an American developmental biologist at the California Institute of Technology. Davidson was best known for his pioneering work on the role of gene regulation in evolution, on embryonic specification and for spearheading the effort to sequence the genome of the purple sea urchin, Strongylocentrotus purpuratus. He devoted a large part of his professional career to developing an understanding of embryogenesis at the genetic level. He wrote many academic works describing his work, including a textbook on early animal development.

In genetics, an isochore is a large region of genomic DNA with a high degree of uniformity in GC content; that is, guanine (G) and cytosine (C) bases. The distribution of bases within a genome is non-random: different regions of the genome have different amounts of G-C base pairs, such that regions can be classified and identified by the proportion of G-C base pairs they contain.

Gretchen Hofmann is professor of ecological physiology of marine organisms at the University of California, Santa Barbara. She holds a B.S. from the University of Wyoming, and an M.S. and Ph.D. from the University of Colorado at Boulder in Environmental, Population and Organismal Biology.

<span class="mw-page-title-main">MCOLN3</span> Protein-coding gene in the species Homo sapiens

Mucolipin-3 also known as TRPML3 is a protein that in humans is encoded by the MCOLN3 gene. It is a member of the small family of the TRPML channels, a subgroup of the large protein family of TRP ion channels.

<span class="mw-page-title-main">Deuterostome</span> Superphylum of bilateral animals

Deuterostomia or deuterostomes are bilaterian animals typically characterized by their anus forming before their mouth during embryonic development. The three major clades of extant deuterostomes include chordates, echinoderms and hemichordates.

Skeletogenesis is a key morphogenetic event in the embryonic development of vertebrates and is of equal, although transient, importance in the development of the sea urchin, a marine invertebrate. The larval sea urchin does not resemble its adult form, because the sea urchin is an indirect developer, meaning its larva form must undergo metamorphosis to form the juvenile adult. Here, the focus is on skeletogenesis in the sea urchin species Strongylocentrotus purpuratus, as this species has been most thoroughly studied and characterized.

<span class="mw-page-title-main">Stereom</span>

Stereom is a calcium carbonate material that makes up the internal skeletons found in all echinoderms, both living and fossilized forms. It is a sponge-like porous structure which, in a sea urchin may be 50% by volume living cells, and the rest being a matrix of calcite crystals. The size of openings in stereom varies in different species and in different places within the same organism. When an echinoderm becomes a fossil, microscopic examination is used to reveal the structure and such examination is often an important tool to classify the fossil as an echinoderm or related creature.

<span class="mw-page-title-main">Compositional domain</span>

A compositional domain in genetics is a region of DNA with a distinct guanine (G) and cytosine (C) G-C and C-G content. The homogeneity of compositional domains is compared to that of the chromosome on which they reside. As such, compositional domains can be homogeneous or nonhomogeneous domains. Compositionally homogeneous domains that are sufficiently long are termed isochores or isochoric domains.

<span class="mw-page-title-main">Mosaic protein</span> Protein made up of multiple protein domains

A mosaic protein is a protein that is made up of different protein domains, giving the protein multiple functions. These proteins have quaternary structures, as they are made up of multiple tertiary structured protein domains. Protein domains can combine to form different types of proteins, creating a diversity of proteins. These domains are spread throughout the genome because they are mobile, which is why some domains can be found in a variety of proteins, even though they are seemingly unrelated. This also allows the domains to fold independently, and so they don't become deformed and unfolded in a new environment.

Donna R. Maglott is a staff scientist at the National Center for Biotechnology Information known for her research on large-scale genomics projects, including the mouse genome and development of databases required for genomics research.

Fred Huffman Wilt is an American biologist who was elected a Fellow of the American Association for the Advancement of Science. His research currently includes the endoskeletal spicule of sea urchin embryos, and its biomineralization relative to its cellular and molecular foundation.

Echinobase is a Model Organism Database (MOD). It supports the international research community by providing a centralized, integrated web based resource to access the diverse and rich, functional genomics data of echinoderm evolution, development and gene regulatory networks.

Patricia Jean Johnson is a Professor of Microbiology at University of California, Los Angeles (UCLA). She works on the parasite Trichomonas vaginalis, which is responsible for the most prevalent sexually transmitted infections in the United States, Trichomoniasis. She was elected a member of the National Academy of Sciences (NAS) in 2019.

Cytochrome P450, family 27, also known as CYP27, is a Deuterostome cytochrome P450 monooxygenase family found in human genome. This family belongs to Mitochondrial clan CYPs, which is located in the inner membrane of mitochondria(IMM). There are three members in the human genome, CYP27A1, CYP27B1 and CYP27C1, and an ortholog CYP27F1 in sea urchins, Strongylocentrotus purpuratus.

References

  1. Ricketts EF, Calvin J. Between Pacific Tides. 3rd Rev. edn. 1962 by J.W. Hedgpeth. XII 516. Stanford University Press, Stanford, CA. 1939
  2. "Sea Urchin Research | ASU - Ask A Biologist". askabiologist.asu.edu. 2010-04-16. Retrieved 2016-12-05.
  3. "Strongylocentrotus purpuratus". Animal Diversity Web. Retrieved 2016-12-05.
  4. T.A. Ebert, J. R. Southon, 2003. Fish. Bull. 101, 915
  5. Arshinoff, Bradley I; Cary, Gregory A; Karimi, Kamran; Foley, Saoirse; Agalakov, Sergei; Delgado, Francisco; Lotay, Vaneet S; Ku, Carolyn J; Pells, Troy J; Beatman, Thomas R; Kim, Eugene; Cameron, R Andrew; Vize, Peter D; Telmer, Cheryl A; Croce, Jenifer C; Ettensohn, Charles A; Hinman, Veronica F (7 January 2022). "Echinobase: leveraging an extant model organism database to build a knowledgebase supporting research on the genomics and biology of echinoderms". Nucleic Acids Research. 50 (D1): D970–D979. doi: 10.1093/nar/gkab1005 . PMC   8728261 . PMID   34791383.
  6. Roeder, R. G.; Rutter, W. J. (1969). "Multiple Forms of DNA-dependent in Eukaryotic Organisms" (PDF). Nature. 224 (5216): 234–237. doi:10.1038/224234a0. PMID   5344598. S2CID   4283528.
  7. 1 2 "Sea urchins could contain the genetic key to curing some diseases" . Retrieved 2016-12-05.
  8. Ryan, Dr Martin. "M. Ryan". www.st-andrews.ac.uk. Archived from the original on 2016-12-30. Retrieved 2016-12-12.
  9. Bodnar, Andrea G.; Coffman, James A. (2016-08-01). "Maintenance of somatic tissue regeneration with age in short- and long-lived species of sea urchins". Aging Cell. 15 (4): 778–787. doi:10.1111/acel.12487. ISSN   1474-9726. PMC   4933669 . PMID   27095483.
  10. "California Purple Sea-Urchin Genome Sequenced by International Team | Caltech". The California Institute of Technology. Retrieved 2016-12-05.
  11. "SU White Paper" (PDF). Archived from the original (PDF) on 2016-03-03. Retrieved 2009-10-31.
  12. 1 2 Sodergren, E.; Sodergren, G. M.; Weinstock, E. H.; Davidson, R. A.; Cameron, R. A.; Gibbs, R. C.; Angerer, L. M.; Angerer, M. I.; Arnone, D. R.; Burgess, R. D.; Burke, J. A.; Coffman, M.; Dean, M. R.; Elphick, C. A.; Ettensohn, K. R.; Foltz, A.; Hamdoun, R. O.; Hynes, W. H.; Klein, W.; Marzluff, D. R.; McClay, R. L.; Morris, A.; Mushegian, J. P.; Rast, L. C.; Smith, M. C.; Thorndyke, V. D.; Vacquier, G. M.; Wessel, G.; Wray, L.; et al. (2006). "The Genome of the Sea Urchin Strongylocentrotus purpuratus". Science. 314 (5801): 941–952. Bibcode:2006Sci...314..941S. doi:10.1126/science.1133609. PMC   3159423 . PMID   17095691.
  13. 1 2 3 4 5 Sodergren, E; Weinstock, GM; Davidson, EH; et al. (2006-11-10). "The Genome of the Sea Urchin Strongylocentrotus purpuratus". Science. 314 (5801): 941–952. Bibcode:2006Sci...314..941S. doi:10.1126/science.1133609. ISSN   0036-8075. PMC   3159423 . PMID   17095691.
  14. Materna, S.C., K. Berney, and R.A. Cameron. 2006a. The S. purpuratus genome: A comparative perspective" Dev. Biol. 300: 485-495.
  15. Burke, R.D.; Angerer, L.M.; Elphick, M.R.; Humphrey, G.W.; Yaguchi, S.; Kiyama, T.; Liang, S.; Mu, X.; Agca, C.; Klein, W.H.; Brandhorst, B.P.; Rowe, M.; Wilson, K.; Churcher, A.M.; Taylor, J.S.; Chen, N.; Murray, G.; Wang, D.; Mellott, D.; Olinski, R.; Hallböök, F.; Thorndyke, M.C. (2006). "A genomic view of the sea urchin nervous system". Dev. Biol. 300 (1): 434–460. doi:10.1016/j.ydbio.2006.08.007. PMC   1950334 . PMID   16965768.
  16. Doney, Scott C.; Busch, D. Shallin; Cooley, Sarah R.; Kroeker, Kristy J. (2020-10-17). "The Impacts of Ocean Acidification on Marine Ecosystems and Reliant Human Communities". Annual Review of Environment and Resources. 45 (1): 83–112. doi: 10.1146/annurev-environ-012320-083019 . ISSN   1543-5938.
  17. Kelly, Morgan W.; Padilla-Gamiño, Jacqueline L.; Hofmann, Gretchen E. (August 2013). "Natural variation and the capacity to adapt to ocean acidification in the keystone sea urchin Strongylocentrotus purpuratus". Global Change Biology. 19 (8): 2536–2546. Bibcode:2013GCBio..19.2536K. doi:10.1111/gcb.12251. PMID   23661315. S2CID   27096322.
  18. Pearse, J. S. (2006). "The ecological role of purple sea urchins". Science. 314 (5801): 940–941. Bibcode:2006Sci...314..940P. doi: 10.1126/science.1131888 . PMID   17095690.
  19. Provost, Euan J.; Kelaher, Brendan P. (2017). "Climate‐driven disparities among ecological interactions threaten kelp forest persistence". Global Change Biology . 23 (1): 353–361. Bibcode:2017GCBio..23..353P. doi:10.1111/gcb.13414. PMID   27392308. S2CID   205143756.
  20. D. Sweetnam et al., Calif. Coop. Oceanic Fish. Invest. Rep. 46: 10 (2005).
  21. Heizer, Robert Fleming; Elsasser, Albert B. (1980-01-01). The Natural World of the California Indians . University of California Press. ISBN   9780520038967.
  22. "Purple Sea Urchin | California Sea Grant". caseagrant.ucsd.edu. Retrieved 2020-12-14.