{"id":2225,"date":"2017-09-11T09:10:19","date_gmt":"2017-09-11T09:10:19","guid":{"rendered":"https:\/\/askanacademic.com\/uncategorized\/what-is-x-inactivation-1026\/"},"modified":"2019-09-24T13:35:39","modified_gmt":"2019-09-24T13:35:39","slug":"what-is-x-inactivation-1026","status":"publish","type":"post","link":"https:\/\/askanacademic.com\/medical-sciences\/what-is-x-inactivation-1026\/","title":{"rendered":"What is X-inactivation and why is it important?"},"content":{"rendered":"
What is X-inactivation and why is it important?<\/p>\n
X-inactivation is a process that occurs in the nuclei of all female mammals, due to them having two X chromosomes. Two X chromosomes is more than is really necessary in the mammal genome, as evidenced by the fact that 50% of the population (the males) is surviving perfectly well with only one. In order to prevent the overproduction of X-chromosome products, which could cause serious problems, each cell in a female mammal needs to silence one of their X chromosomes.<\/p>\n
In marsupials, it is always the paternal copy of the X chromosome that is inactivated, whereas placental mammals (non-marsupials) inactivate one X chromosome in each cell at random at a very early stage of development. The inactivated X becomes coated in an RNA product called Xist, or \u2018X-inactive specific transcript\u2019, triggering its condensation down into a dense \u2018Barr body\u2019. The Barr body is silenced by packaging into repressive heterochromatin, a form of DNA storage which inhibits transcription of genes.<\/p>\n
Which X will be inactivated in each cell is decided in the early embryo. The descendants of these cells always inactivate the same copy of the X chromosome, creating distinct populations of cells. For a visualisation of the size of these populations, examine a tortoiseshell cat; the genes encoding coat colour in cats are on the X chromosome \u2013 the tortoiseshell pattern is produced by separate populations of cells producing black and orange pigments, depending on which X chromosome is active. This means that all female mammals are effectively genetic mosaics, and explains why females are usually less severely affected by genetic disorders carried on the X chromosome; if their other X chromosome doesn\u2019t also carry the mutation, then only half of their cells will be affected by the condition. This also explains why the symptoms of people with multiple X chromosomes are much less severe than would be expected \u2013 all but one of their X chromosomes are usually inactivated.<\/p>\n
An explanation of X chromosome inactivation in female mammals, and its effects.<\/p>\n","protected":false},"author":1,"featured_media":1940,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[30],"tags":[],"yoast_head":"\n