A monolithic clump our desoxyribonucleic acid does n’t actually come out to contain gene that encrypt for proteins , leading to the nickname“junk DNA ” .   However , that does n’t mean it should be chucked into the trumpery .

Scientists in the UK have now discovered that a minor snipping of this so - squall debris DNA in reality does something highly important : It change the genitalia you ’re hold with . Not only does this spill some light on our   much - misunderstood detritus DNA , but it may   even excuse sex development in humans .

This uncovering was first suggest at thanks to a mouse call Randy . In 1991 , a chromosomally female computer mouse ( with two cristal chromosome ) developed manful testes when a squad of scientist   introduced a sure factor , called Sry , into the developing embryo .

They discover this alteration was due to a protein call SOX9 , which determines whether a mammal will develop ovary or   ballock . At a central stage in development , low amounts of SOX9 lead to ovaries , higher quantity direct to testes .

The amount of SOX9 produce is ab initio controlled by the Sry cistron . Only male person , who have an X and a Y chromosome , will develop testes since this Sry cistron is located on the Y chromosome . On the other hand , female person have two X chromosomes , so they do n’t make enough SOX9 to spark the alteration .

As reported in the journalScience , this unexampled study dives profoundly into this grounds by premise a small piece of deoxyribonucleic acid called foil 13 ( Enh13 ) , which was discovered over half a million bases forth from the Sry gene . Much like the rest of the genome ’s “ junk DNA ” , Enh13 does not hold any factor that are used to make proteins .

When Enh13 was take from virile mice embryos , they grow ovary and female genitalia . As an foil , Enh13 works by promote the expression of   the   Sry gene by   increase the likeliness of its transcription . Usually , it take in a few different change to have a large event , so it ’s pretty surprising to see   that   Enh13 alone can have a profound upshot on an embryo ’s sex activity .

Enh13 is located in the part of the mouse genome that map directly onto a neighborhood of the human genome , so the scientist expect a similar effect in humans too .

“ Our work also highlights the of import role of what some still refer to as ' detritus ' deoxyribonucleic acid , which makes up 98 pct of our genome . If a single enhancer can have this impact on gender conclusion , other non - coding regions might have likewise drastic effects , ” first authorDr Nitzan Gonen , a postdoctoral investigator at the Francis Crick Institute , tell in astatement .

“ For decade , researchers have look for gene that cause disorders of sexual practice ontogenesis but we have n’t been able to feel the genetic cause for over half of them . Our former bailiwick suggest that many answers could lie down in the non - coding regions , which we will now investigate further . "