What role did genetic linkage play in ultimately identifying the gene for cystic fibrosis?
QUESTION-1
ANSWER
CYSTIC FIBROSIS
The symptoms of Cystic fibrosis-
The role genetic linkage play in ultimately identifying the gene for cystic fibrosis-
Cystic Fibrosis is primarily caused by genetic mutations that take place in the cystic fibrosis transmembrane conductance regulator, commonly referred to as the CFTR gene.
The CFTR gene has a role to play in the production of CFTR proteins.
When these CFTR proteins function as they should, this regulates the usual transport of the salt and fluids to and fro from the cells.
In order to develop cystic fibrosis, the child has to inherit both mutated copies of this CFTR gene, one from each parent.
CFTR modulators are used to treat Cystic fibrosis.
We can clone cystic fibrosis gene by positional cloning: on the basis of map location.CF was the first genetic disorder elucidated strictly by positional cloning.
Cystic fibrosis used genetic mapping to determine where the CFTR gene was located in order to identify and treat them.
GOOD LUCK.
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