{"id":30428,"date":"2014-04-22T09:46:44","date_gmt":"2014-04-22T13:46:44","guid":{"rendered":"http:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/revealed-scientists-edit-dna-to-correct-adult-genes-and-cure-diseases\/"},"modified":"2014-04-22T09:46:44","modified_gmt":"2014-04-22T13:46:44","slug":"revealed-scientists-edit-dna-to-correct-adult-genes-and-cure-diseases","status":"publish","type":"post","link":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/transhuman-news-blog\/genome\/revealed-scientists-edit-dna-to-correct-adult-genes-and-cure-diseases\/","title":{"rendered":"Revealed: Scientists edit DNA to correct adult genes and cure diseases"},"content":{"rendered":"<p><p>A genetic disease has been cured in living, adult animals for the  first time using a revolutionary genome-editing technique that  can make the smallest changes to the vast database of the DNA  molecule with pinpoint accuracy.  <\/p>\n<p>    Scientists have used the genome-editing technology to cure    adult laboratory mice of an inherited liver disease by    correcting a single \"letter\" of the genetic alphabet which had    been mutated in a vital gene involved in liver metabolism.  <\/p>\n<p>    A similar mutation in the same gene causes the equivalent    inherited liver disease in humans - and the successful repair    of the genetic defect in laboratory mice raises hopes that the    first clinical trials on patients could begin within a few    years, scientists said.  <\/p>\n<p>    The success is the latest achievement in the field of genome    editing. This has been transformed by the discovery of Crispr,    a technology that allows scientists to make almost any DNA    changes at precisely defined points on the chromosomes of    animals or plants. Crispr  pronounced \"crisper\"  was    initially discovered in 1987 as an immune defence used by    bacteria against invading viruses. Its powerful genome-editing    potential in higher animals, including humans, was only fully    realised in 2012 and 2013 when scientists showed that it can be    combined with a DNA-sniping enzyme called Cas9 and used to edit    the human genome.Scientists have used the genome-editing    technology to cure adult laboratory mice of an inherited liver    disease by correcting a single \"letter\" of the genetic alphabet    which had been mutated in a vital gene involved in liver    metabolism.  <\/p>\n<p>    A similar mutation in the same gene causes the equivalent    inherited liver disease in humans - and the successful repair    of the genetic defect in laboratory mice raises hopes that the    first clinical trials on patients could begin within a few    years, scientists said.  <\/p>\n<p>    The success is the latest achievement in the field of genome    editing. This has been transformed by the discovery of Crispr,    a technology that allows scientists to make almost any DNA    changes at precisely defined points on the chromosomes of    animals or plants. Crispr  pronounced \"crisper\"  was    initially discovered in 1987 as an immune defence used by    bacteria against invading viruses. Its powerful genome-editing    potential in higher animals, including humans, was only fully    realised in 2012 and 2013 when scientists showed that it can be    combined with a DNA-sniping enzyme called Cas9 and used to edit    the human genome.  <\/p>\n<p>    Since then there has been an explosion of interest in the    technology because it is such a simple method of changing the    individual letters of the human genome  the 3 billion \"base    pairs\" of the DNA molecule  with an accuracy equivalent to    correcting a single misspelt word in a 23-volume encyclopaedia.  <\/p>\n<p>    In the latest study, scientists at the Massachusetts Institute    of Technology (MIT) used Crispr to locate and correct the    single mutated DNA base pair in a liver gene known as LAH,    which can lead to a fatal build-up of the amino acid tyrosine    in humans and has to be treated with drugs and a special diet.  <\/p>\n<p>    The researchers effectively cured mice suffering from the    disease by altering the genetic make-up of about a third of    their liver cells using the Crispr technique, which was    delivered by high-pressure intravenous injections.  <\/p>\n<p>    \"We basically showed you could use the Crispr system in an    animal to cure a genetic disease, and the one we picked was a    disease in the liver which is very similar to one found in    humans,\" said Professor Daniel Anderson of MIT, who led the    study.  <\/p>\n<p><!-- Auto Generated --><\/p>\n<p>Read more:<br \/>\n<a target=\"_blank\" href=\"http:\/\/timesofindia.feedsportal.com\/c\/33039\/f\/533922\/s\/399e8f8c\/l\/0Ltimesofindia0Bindiatimes0N0Chome0Cscience0CRevealed0EScientists0Eedit0EDNA0Eto0Ecorrect0Eadult0Egenes0Eand0Ecure0Ediseases0Carticleshow0C340A763590Bcms\/story01.htm\/RS=^ADAPznwlvx4l0Kyq3bODj3iV38TnuQ-\" title=\"Revealed: Scientists edit DNA to correct adult genes and cure diseases\">Revealed: Scientists edit DNA to correct adult genes and cure diseases<\/a><\/p>\n","protected":false},"excerpt":{"rendered":"<p> A genetic disease has been cured in living, adult animals for the first time using a revolutionary genome-editing technique that can make the smallest changes to the vast database of the DNA molecule with pinpoint accuracy. Scientists have used the genome-editing technology to cure adult laboratory mice of an inherited liver disease by correcting a single \"letter\" of the genetic alphabet which had been mutated in a vital gene involved in liver metabolism <a href=\"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/transhuman-news-blog\/genome\/revealed-scientists-edit-dna-to-correct-adult-genes-and-cure-diseases\/\">Continue reading <span class=\"meta-nav\">&rarr;<\/span><\/a><\/p>\n","protected":false},"author":1,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[25],"tags":[],"class_list":["post-30428","post","type-post","status-publish","format-standard","hentry","category-genome"],"_links":{"self":[{"href":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/wp-json\/wp\/v2\/posts\/30428"}],"collection":[{"href":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/wp-json\/wp\/v2\/comments?post=30428"}],"version-history":[{"count":0,"href":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/wp-json\/wp\/v2\/posts\/30428\/revisions"}],"wp:attachment":[{"href":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/wp-json\/wp\/v2\/media?parent=30428"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/wp-json\/wp\/v2\/categories?post=30428"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/wp-json\/wp\/v2\/tags?post=30428"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}