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Thursday 29 September 2016 Instagram
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Down's signs "seen in stem cells"

Down's signs "seen in stem cells"

Scientists investigating the mechanisms of Down's syndrome have revealed the earliest developmental changes in embryonic stem cells caused by an extra copy of human chromosome 21 – the aberrant inheritance of which results in the condition.

Lead by Dean Nizetic, professor of cellular and molecular biology at Barts and The London School of Medicine and Dentistry, the team utilised embryonic stem cells from a previously genetically engineered species of mice carrying a copy of human chromosome 21.

They discovered that extra chromosome 21 – a genetic state known as trisomy 21 – disturbs a key regulating gene called NRSF or REST, which in turn disturbs the cascade of other genes that control normal development at the embryonic stem cell stage. Furthermore, they identified one gene (DYRK1A) on human chromosome 21, whose overdose in trisomy (DS) is responsible for the observed effects.

Professor Nizetic, calling for further research into the components of the disturbed cascade he and his team have revealed, said: "We hope that further research might lead to clues for the design of new therapeutic approaches tackling developmental delay, mental retardation, aging and regeneration of brain cells, and Alzheimer's disease. In other words, we hope our work will open new routes to tackle the genetics of these health disorders, approaching them from the 'back entrance', as dominant component-symptoms of Down's syndrome."

Down's syndrome belongs to the group of conditions called"aneuploidies", defined by an abnormal loss or gain of geneticmaterial, ie, fragments of chromosomes or whole chromosomes.Aneuploidies cause congenital anomalies that are a prime cause ofinfant death in Europe and the USA, and are currently on the increasewith advancing maternal age in European countries.

The number of people with Down's syndrome in Europe exceeds half amillion. The condition is more common than muscular dystrophy andcystic fibrosis, but the development of new therapeutic concepts ishindered by the fact that unlike muscular dystrophy and cysticfibrosis, where a single mutated gene causing the disease is known, theentire human chromosome 21 (containing around 300 genes) still has tobe dissected into individual gene-dose contributions to the symptoms.

Their study is published in the American Journal of Human Genetics.

American Journal of Human Genetics

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