<span>also supports and protects and shapes a plant cell and also regulates what moves into the cell can help support the entire plant. What similarities do the mitochondria and chloroplasts share? Both membrane bound organelles have their own DNA and help make energy available to the cell.</span>
Answer:
Cystic fibrosis mutation is recessive to normal allele because only one functional or normal allele is enough to produce a functional protein. So, if mutation is present in one allele then also, a normal protein can be made from normal allele. The presence of normal protein prevents the expression of disease.
In addition, mutated allele only results in the loss of function of protein which can be compensated by the expression of normal allele. It does not add any toxic effect to the protein. Consequently, the disease is inherited in autosomal recessive fashion.
In contrast, Huntington mutation not only alters the structure of the functional protein but also adds toxicity to it. The altered protein is enable to interact with 100s of other proteins and inhibit or decrease their function. So, if only one allele is present then also, the mutated protein will be produced and it will result in the phenotype. Consequently, it is inherited as autosomal dominant fashion.
Answer:
If it is still maintained in the human population, hemoglobin Lepore must be selected for in evolution.
Color blindness is a recessive x-linked trait in humans. In a family where the mother is color-blind, and the father is normal, the probability of their having a color-blind son is 100%.
Color blindness is a recessive x chromosome liked recessive disease which is more prone in males than in females. As the mother is color-blind she has both the alleles of colorblindness while the father is normal with both x chromosome and y chromosome normal.
So if the parents have a boy, he will always receive an x chromosome with colorblindness gene from the mother and a normal y chromosome from the father always. Thus, the probability of having a colorblind boy will be 100%.
To know more about colorblindness refer to the link below
brainly.com/question/2094919
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Answer:
PROMOTER is a DNA sequence where RNA polymerase binds and begins the process of transcription. ENHANCER is a D N A sequence that binds regulatory proteins that interact with promoter-bound proteins to activate transcription.
Explanation:
