Physicist cracks women's random but always lucky choice of X chromosomeJune 13, 2007A University of Warwick physicist has uncovered how female cells are able to choose randomly between their two X chromosomes and why that choice is always lucky. Human males have both a X and a Y chromosome but females have two X chromosomes. This means that in an early stage in the development of a woman's fertilised egg the cells need to silence one of those two X chromosomes. This process is crucial to survival and problems with the process are related to serious genetic diseases. Both X chromosomes in a cell have a suicide gene called XIST which, if activated, seals the chromosome behind a barrier of RNA preventing the activation of any other gene. Researchers believe that this suicide gene can be itself blocked by a plug of proteins forming on top of its specific location on the chromosome but they had little idea as to why this should happen randomly to one X chromosome's gene and not the other.
Scientists are extremely uncomfortable with this randomness and have sought a clear scientific reason as to why one X chromosome was switched off rather than the other. The observations also seem to run counter to the usual idea that the biological mechanisms evolve in ways that allow a "best" choice to be made between things rather than a random one. Now researchers led by University of Warwick physicist Dr Mario Nicodemi have explained how this randomness occurs and why that it is beneficial. This will help understand the problems of a small number of women who unusually don't have a completely random distribution of X chromosomes but the explanation may have much wider implications as at least 10% of our genes may behave in similar ways as mechanism that "chooses" between X chromosomes. Examples of this range from the immune system to our olfactory apparatus. Coming at the problem from the perspective of a physicist Dr Nicodemi has found an explanation for the random selection based on thermodynamics. Research has already shown that at the key moment in this process both X chromosomes are brought close together within the cell. The Warwick researcher paper says that what happens next is that material for a "protein plug" then begins to gather around both of the XIST suicide genes on each X Chromosome. This starts a race between the two build ups of protein. Inevitably one of these two nascent protein plugs narrowly wins that race and reaches an energy state in which it can pull together all the material building up in both plugs into a single protein plug. That single plug then closes off one of the XIST suicide genes allowing its host X chromosome to continue to operate. However the other XIST suicide gene is now freed to activate and shuts down its X chromosome. Since putting forward this explanation researchers in Harvard have observed actual plugs of protein shutting down X chromosome XIST genes in a manner giving further confirmation to Dr Nicodemi's research. So the randomness is explained but what about researchers' other concerns? Dr Nicodemi believes the randomness actually does give an evolutionary advantage. The mechanism means equal numbers of both the maternal and paternal X chromosome are preserved in the gene pool and the resultant population thus has more chance of surviving any biological threat targeted at a single version of the X chromosome. University of Warwick | |||||||||||||||||||||
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Related Chromosome Current Events and Chromosome News Articles M.I.N.D. Institute researchers call for fragile X testing throughout the lifespan Writing in this week's Journal of the American Medical Association, UC Davis M.I.N.D. Institute researchers urge physicians to test for mutations of the fragile X gene in patients of all ages. Researchers Shed Light on Evolution of Gene Regulation Scientists at Penn State have shed light on some of the processes that regulate genes -- such as the processes that ensure that proteins are produced at the correct time, place, and amount in an organism -- and they also have shed light on the evolution of the DNA regions that regulate genes. Med school discovery could lead to better cancer diagnosis, drugs A Florida State University College of Medicine research team led by Yanchang Wang has discovered an important new layer of regulation in the cell division cycle, which could lead to a greater understanding of the way cancer begins. Two From One-Pitt Research Maps Out Evolution of Genders From Hermaphroditic Ancestors Research from the University of Pittsburgh published in the Nov. 20 edition of "Heredity" could finally provide evidence of the first stages of the evolution of separate sexes, a theory that holds that males and females developed from hermaphroditic ancestors. ADHD medications do not cause genetic damage in children In contrast to recent findings, two of the most common medications used to treat attention deficit hyperactivity disorder (ADHD) do not appear to cause genetic damage in children who take them as prescribed, according to a new study by researchers at the National Institutes of Health (NIH) and Duke University Medical Center. Scientists exploring new compounds to target muscular dystrophy Scientists have identified a promising set of new compounds in the fight against muscular dystrophy. Microarray analysis improves prenatal diagnosis A "chip" or array that can quickly detect disorders such as Down syndrome or other diseases associated with chromosomal abnormalities proved an effective tool in prenatal diagnosis in a series of 300 cases at Baylor College of Medicine, said researchers in a report that appears in the current issue of the journal Prenatal Diagnosis. Case Western Reserve University uncovers genetic basis for some birth defects A multidisciplinary research team at Case Western Reserve University led by Gary Landreth, Ph.D., a professor in the School of Medicine's Department of Neurosciences, has uncovered a common genetic pathway for a number of birth defects that affect the development of the heart and head. Abnormal development of the jaw, palate, brain and heart are relatively common congenital defects and frequently arise due to genetic errors that affect a key developmental pathway. Researchers use chemical from medicinal plants to fight HIV Like other kinds of cells, immune cells lose the ability to divide as they age because a part of their chromosomes known as a telomere becomes progressively shorter with cell division. As a result, the cell changes in many ways, and its disease fighting ability is compromised. Yale researchers unravel mystery of brain aneurysms Yale researchers have taken the first critical steps in unraveling the mysteries of brain aneurysms, the often fatal rupturing of blood vessels that afflicts 500,000 people worldwide each year and nearly killed Vice President-elect Joseph Biden two decades ago. More Chromosome Current Events and Chromosome News Articles |
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