For a human offspring to express a paternal mitochondrial gene, the individual must have inherited a mitochondrion from the sperm this is called paternal leakage.
<h3>What is mitochondrial diseases ?</h3>
A disease that develops when cellular energy production systems are broken.
The mitochondria's inability to fully burn nutrients and oxygen to produce energy, which is necessary for healthy cell function, is a common factor across mitochondrial disorders. It's frequently inherited.
Muscle weakness, developmental delays, and poor growth are possible symptoms. Although there is no cure, symptoms can be managed with medicine and physical therapy.
<h3>Causes of mitochondrial myopathies</h3>
Genetic mutations lead to mitochondrial disorders. Proteins are made according to instructions provided by genes, and the genes causing mitochondrial illness typically produce proteins that function inside mitochondria.
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Choice A is false. RNA uses the 5 carbon sugar Ribose
In order to test the presence of starch, one has to treat with iodine. If the food turns blue-black in color, it is an indication of the presence of the starch.
Given what we know, we can confirm that If a single protein carries out multiple functions, then each function may be carried out by a specific region of the protein called a domain.
<h3>What is a domain in proteins?</h3>
This is one of the many parts that make up a protein. This is what we can call the most independent parts of a protein given that they are each self-stabilizing and form their own three-dimensional structures. Each domain of a protein is considered a functional group, and therefore a single protein can carry out multiple functions.
Therefore, we can confirm that for a protein like the one described in the question, the multiple functions being carried out can be explained by the presence of the domain regions of the protein.
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