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The genetic switches of bone growth

In mammals, only 3% of the genome consists of coding genes which, when transcribed into proteins, ensure the biological functions of the organism and the in-utero development of future individuals. But genes do not function alone. They are controlled by other sequences in the genome, called enhancers, which, like switches, activate or deactivate them as required. A team has now identified and located 2700 enhancers among millions of non-coding genetic sequences that precisely regulate the genes responsible for bone growth. This discovery sheds light on one of the major factors influencing the size of individuals in adulthood, and explains why their failure could be the cause of certain bone malformations.

Flawed genetic switches could be at the origin of malformations or developmental diseases

Embryonic development follows delicate stages: for everything to go well, many genes must coordinate their activity according to a very meticulous scheme and tempo. This precision mechanism sometimes fails, leading to more or less disabling malformations.

A missing genetic switch at the origin of malformations - Communiqués de presse

A missing genetic switch at the origin of malformations - Communiqués de presse
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Missing genetic switch at origin of malformations

UNIGE Scientists have discovered how the absence of a genetic switch can lead to malformations during embryonic development. Fluorescence

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