In the article from ScienceDaily, UIC researchers, led by co-investigators Alexander Mankin and Nora Vazquez-Laslop discovered that a natural product from honeybees, Api137, is an inhibitor of translation termination. Antibiotics are known to kill bacteria by targeting ribosomes. However, Api137 interferes with different stages of translation when DNA is to be translated to proteins. This is significant because no new antibiotics have been discovered in 30 years and many bacteria are becoming resistant which is a major concern in public health. About 2 million people each year become infected with bacteria that is resistant to antibiotics, and about 23,000 of them die. This discovery can help create many new drugs to fight bacteria.
Showing posts with label DNA translation. Show all posts
Showing posts with label DNA translation. Show all posts
Saturday, September 9, 2017
Friday, December 2, 2016
Taking a Closer look at Huntington's Disease
Huntington’s Disease is a hereditary disorder that results in the death of nerve cells in the brain. Individuals with this disease begin to show symptoms around the ages of 30 and 40. They show loss of cognition or ability to think. It
occurs when a faulty gene disrupts DNA translation. It also decreases the
ability to produce the Huntington protein, which leads to the cell not
functioning properly.
Many scientists believe that it is caused when nerve cells
in the brain are destroyed. In order to
find out what mainly affects motor function as a result of this disease,
scientists found in a previous study that the early form of Huntington’s
disease caused the skeletal muscles to have defects in the later stages. In addition,
they also found that the protein called CIC-1 decreased in function because
chloride ions were carried into the cells. This is the leading factor to why
DNA translation became faulty for making the CIC-1 protein. The faulty
translation is what could be the cause of the physical movements due to Huntington’s disease.
Although they found out what causes the cell to malfunction,
that study did not aid in finding out whether the defect in protein code was
only because the death of nerve cells or if it changes as the disease
progressed. For this, they conducted a new study where they looked at healthy, wild type mice. They studied what happened during DNA translation to make the CIC-1 protein when the disease develops and also as it progresses. More specifically, they wanted to find out what happened to the messenger RNA as it carried the code for CIC-1 protein. They found that in both the young control mice and the Huntington's mice there was a defect in the encoding process for messenger RNA for CIC-1 protein. Although this was the case, they found something very interesting. They found out that as the healthy mice aged, the defect corrected itself to produce the functional CIC-1. The scientists discovered that Myosin was expressed in the muscles of newborn mice. Myosin, a motor protein was also found to be expressed in the mice with adult- onset Huntington's disease. From this study, they concluded that Huntington's disease causes disturbance in the muscles as well as brain tissue but changes over a period of time. Learning that this disease effects the skeletal muscles rather than just brain tissue and varies over time, will lead to increased help in patient care.
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