Jump to content

Nullisomic

From Wikipedia, the free encyclopedia

This is an old revision of this page, as edited by TheImaCow (talk | contribs) at 10:24, 11 May 2020 (Removed {{Citations broken}} tag (TW)). The present address (URL) is a permanent link to this revision, which may differ significantly from the current revision.

Nullisomic is a genetic condition involving the lack of both the normal chromosomal pairs for a species (2n-2).[1] Humans with this condition will not survive.[2]

Causes

Nullisomy is caused by non-disjunction, during meiosis that causes two of the gametes to have no chromosomal material, leaving the other two gametes to have double the amount of chromosomal material (disomic). Due to the lack of genetic information, the nullisomic gametes are rendered unviable for fertilization.[3]

References

  1. ^ HAKANSSON, ARTUR (2010). "Meiosis In a Nullisomic and in an Ayndetic Godetia Whitneyi". Hereditas. 29 (1): 179–190. doi:10.1111/j.1601-5223.1943.tb02722.x.
  2. ^ http://www.molecular-plant-biotechnology.info/mutations/nullisomic.htm Archived December 19, 2007, at the Wayback Machine
  3. ^ Cunningham F, Leveno K.J., Bloom S.L., Spong C.Y., Dashe J.S., Hoffman B.L., Casey B.M., Sheffield J.S. (2013). Genetics. In Cunningham F, Leveno K.J., Bloom S.L., Spong C.Y., Dashe J.S., Hoffman B.L., Casey B.M., Sheffield J.S. (Eds), Williams Obstetrics, Twenty-Fourth Edition. Retrieved September 28, 2015 from http://accessmedicine.mhmedical.com/content.aspx?bookid=1057 Archived 2017-09-26 at the Wayback Machine