Gene linked to birth defects identifiedMay 31st, 2010 - 3:09 pm ICT by ANI
London, May 31 (ANI): An international team of scientists has identified a gene linked to birth defects.
The work, co-led by geneticists at the University of Leeds, together with colleagues from institutes and universities in Paris, Rome and San Diego, has appeared in the journal Nature Genetics.
The findings should allow couples at risk of conceiving babies with the profoundly disabling Meckel-Gruber and Joubert syndromes to be identified beforehand through genetic screening.
The research, which demonstrates how the disease gene stops cells’ finger-like antennae or ‘cilia’ from detecting and relaying information, may ultimately lead to treatments for more common related disorders, such as spina bifida and polycystic kidney disease.
University of Leeds researcher Professor Colin A. Johnson, said: “By understanding the science behind this relatively rare condition, we can gain insight into other developmental conditions that are less serious but far more frequent.
“Spina bifida, for example, is one of the most common birth defects, affecting in one in every 1000 children.”
Meckel-Gruber syndrome and Joubert syndrome are part of a wider family of disorders known as ‘ciliopathies’ - so called because the cilia are not working as they should and do not respond properly to signals.
This lack of communication can prevent the neural tube from developing correctly in growing embryos, leading to abnormalities in the brain.
Affected embryos can also develop abnormalities in the eyes, extra fingers or toes, and multiple cysts in their kidneys. These defects are often only picked up on a 12 week ultrasound scan.
To find the gene responsible for Meckel-Gruber and Joubert syndromes, the researchers examined DNA from families with a history of the disorder, from skin cells donated by patients, and from cells grown in the laboratory.
They also studied zebrafish, which have very visible embryos.
The work identified a previously unknown gene - TMEM216 - as a cause of Meckel-Gruber and Joubert syndromes.
They also showed that the faulty TMEM216 gene stopped cells from making a protein that is needed for signalling.
Because Meckel-Gruber and Joubert syndromes are recessive genetic disorders, only couples who both have a copy of the disease gene are at risk of conceiving babies with these birth defects.
The condition is more common in certain close-knit populations where the gene has been passed down from generation to generation. These include families of Ashkenazi Jewish origin.
Prof Johnson said: “Accurate genetic testing for TMEM216 will be particularly important for families throughout the world that have a history of ciliopathies caused by mutations to this gene.
“Now that we have identified a gene that causes Meckel-Gruber syndrome and Joubert syndrome, the role of particular signalling pathways whilst the embryo is developing can also be more clearly understood,” he added. (ANI)
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Tags: cilia, common birth defects, disease gene, genetic screening, geneticists, joubert syndrome, journal nature genetics, kidney disease, lack of communication, meckel gruber, neural tube, paris rome, professor colin, rare condition, researcher professor, skin cells, ultrasound scan, universities in paris, university of leeds, zebrafish