Somatic cell

A somatic cell (from Ancient Greek σῶμα sôma, meaning "body"), or vegetal cell, is any biological cell forming the body of an organism; that is, in a multicellular organism, any cell other than a gamete, germ cell, gametocyte or undifferentiated stem cell.[1]

The cell which takes part in composition of the body of an organism and divides through the process of binary fission and miotic division is called somatic cell.

In contrast, gametes are cells that fuse during sexual reproduction, germ cells are cells that give rise to gametes, and stem cells are cells that can divide through mitosis and differentiate into diverse specialized cell types. For example, in mammals, somatic cells make up all the internal organs, skin, bones, blood and connective tissue, while mammalian germ cells give rise to spermatozoa and ova which fuse during fertilization to produce a cell called a zygote, which divides and differentiates into the cells of an embryo. There are approximately 220 types of somatic cell in the human body.[1]

Theoretically, these cells are not germ cells (the source of gametes); they transmit their mutations, to their cellular descendants (if they have any), but not to the organism's descendants. However, in sponges, non-differentiated somatic cells form the germ line and, in Cnidaria, differentiated somatic cells are the source of the germline. Mitotic cell division is only seen in diploid somatic cells. Only some cells like germ cells take part in reproduction.[2]

Evolution

As multicellularity evolved many times, sterile somatic cells did too. The evolution of an immortal germline producing specialized somatic cells involved the emergence of mortality, and can be viewed in its simplest version in volvocine algae.[3] Those species with a separation between sterile somatic cells and a germline are called Weismannists. However, Weismannist development is relatively rare (e.g., vertebrates, arthropods, Volvox), as a great number of species have the capacity for somatic embryogenesis (e.g., land plants, most algae, many invertebrates).[4][5]

Genetics and chromosome content

Like all cells, somatic cells contain DNA arranged in chromosomes. If a somatic cell contains chromosomes arranged in pairs, it is called diploid and the organism is called a diploid organism. (The gametes of diploid organisms contain only single unpaired chromosomes and are called haploid.) Each pair of chromosomes comprises one chromosome inherited from the father and one inherited from the mother. For example, in humans, somatic cells contain 46 chromosomes organized into 23 pairs. By contrast, gametes of diploid organisms contain only half as many chromosomes. In humans, this is 23 unpaired chromosomes. When two gametes (i.e. a spermatozoon and an ovum) meet during conception, they fuse together, creating a zygote. Due to the fusion of the two gametes, a human zygote contains 46 chromosomes (i.e. 23 pairs).

However, a large number of species have the chromosomes in their somatic cells arranged in fours ("tetraploid") or even sixes ("hexaploid"). Thus, they can have diploid or even triploid germline cells. An example of this is the modern cultivated species of wheat, Triticum aestivum L., a hexaploid species whose somatic cells contain six copies of every chromatid.

The frequency of spontaneous mutations is significantly lower in advanced male germ cells than in somatic cell types from the same individual.[6] Female germ cells also show a mutation frequency that is lower than that in corresponding somatic cells and similar to that in male germ cells.[7] These findings appear to reflect employment of more effective mechanisms to limit the initial occurrence of spontaneous mutations in germ cells than in somatic cells. Such mechanisms likely include elevated levels of DNA repair enzymes that ameliorate most potentially mutagenic DNA damages.[7]

Cloning

In recent years, the technique of cloning whole organisms has been developed in mammals, allowing almost identical genetic clones of an animal to be produced. One method of doing this is called "somatic cell nuclear transfer" and involves removing the nucleus from a somatic cell, usually a skin cell. This nucleus contains all of the genetic information needed to produce the organism it was removed from. This nucleus is then injected into an ovum of the same species which has had its own genetic material removed. The ovum now no longer needs to be fertilized, because it contains the correct amount of genetic material (a diploid number of chromosomes). In theory, the ovum can be implanted into the uterus of a same-species animal and allowed to develop. The resulting animal will be a nearly genetically identical clone to the animal from which the nucleus was taken. The only difference is caused by any mitochondrial DNA that is retained in the ovum, which is different from the cell that donated the nucleus. In practice, this technique has so far been problematic, although there have been a few high-profile successes, such as Dolly the Sheep and, more recently, Snuppy, the first cloned dog. Somatic cells have also been collected in the practice of cryoconservation of animal genetic resources as a means of conserving animal genetic material, including to clone livestock.

Genetic modifications

Development of biotechnology has allowed for the genetic manipulation of somatic cells, whether for the modelling of chronic disease or for the prevention of malaise conditions.[8][9]

Genetic engineering of somatic cells has resulted in some controversies, although the International Summit on Human Gene Editing has released a statement in support of genetic modification of somatic cells, as the modifications thereof are not passed on to offspring.[10]

See also

References
  1. Campbell, Neil A.; Reece, Jane B.; Urry, Lisa A.; Cain, Michael L.; Wasserman, Steven A.; Minorsky, Peter V.; Jackson, Robert B. (2009). Biology (9th ed.). p. 229. ISBN 978-0-8053-6844-4.
  2. Chernis, P J (1985). "Petrographic analyses of URL-2 and URL-6 special thermal conductivity samples". Cite journal requires |journal= (help)
  3. Hallmann A (2011). "Evolution of reproductive development in the volvocine algae". Sex. Plant Reprod. 24 (2): 97–112. doi:10.1007/s00497-010-0158-4. PMC 3098969. PMID 21174128.
  4. Ridley M (2004) Evolution, 3rd edition. Blackwell Publishing, p. 29-297.
  5. Niklas, K. J. (2014) The evolutionary-developmental origins of multicellularity.
  6. Walter CA, Intano GW, McCarrey JR, McMahan CA, Walter RB (1998). "Mutation frequency declines during spermatogenesis in young mice but increases in old mice". Proc. Natl. Acad. Sci. U.S.A. 95 (17): 10015–9. Bibcode:1998PNAS...9510015W. doi:10.1073/pnas.95.17.10015. PMC 21453. PMID 9707592.
  7. Murphey P, McLean DJ, McMahan CA, Walter CA, McCarrey JR (2013). "Enhanced genetic integrity in mouse germ cells". Biol. Reprod. 88 (1): 6. doi:10.1095/biolreprod.112.103481. PMC 4434944. PMID 23153565.
  8. "Somatic genome editing with CRISPR/Cas9 generates and corrects a metabolic disease". Retrieved 5 July 2018.
  9. "NIH Commits $190M to Somatic Gene-Editing Tools/Tech Research". Retrieved 5 July 2018.
  10. "Why Treat Gene Editing Differently In Two Types Of Human Cells?". Retrieved 5 July 2018.
This article is issued from Wikipedia. The text is licensed under Creative Commons - Attribution - Sharealike. Additional terms may apply for the media files.