Answer:
Enhancer sequence.
Explanation:
Enhancers may be defined as the transcription factors that are used to enhance or increase the activity of the gene. Enhancers bind with the transcription factors to regulate and increase its expression.
The mutation in the enhancers decrease the transcription of of the other gene. These sequences lies far away from the transcription site but still known to increase the rate of transcription. Hence, the mutation has been done in the enhancer sequences.
Thus, the correct answer is option (b).
The correct answer is:
A. begin with the breakdown of glucose in glycolysis.
Explanation:
They both begin with a sequence of reactions known as glycolysis, which breaks glucose particles into smaller pyruvate molecules. They are also related in that through both processes, ATP is generated for the cell to use. Glycolysis is the metabolic pathway that transforms glucose C6H12O6, into pyruvate, CH3COCOO− + H+. The free energy delivered in this process is applied to form the high-energy molecules ATP and NADH .
1 is C - see first attachment. Genotypes with Y's represent males, and big R represents red eyes, while little r represents white eyes. For example XRxr is a heterozygous (red-eyed) female, and XrYr is a homozygous white-eyed male.
2 is B because the absence of functional proteins and some ribosomes due to the mRNA strand is not as detrimental as the loss of the entire cell.
3 is B. (The insertion of 3 base pairs into a genetic sequence is the length of a single codon, meaning that only one amino acid in the entire polypeptide was added)
Answer:
A point mutation is a type of mutation in DNA or RNA, the cell’s genetic material.
Explanation:
DNA and RNA are made up of many nucleotides. There are five different molecules that can make up nitrogenous bases on nucleotides: cytosine, guanine, adenine, thymine (in DNA) and uracil (in RNA), abbreviated C, G, A, T, and U.
Answer:
A recessive autosomal allele is a heterozygous pair.
Explanation:
they have one mutated gene (recessive gene) and one normal gene (dominant gene) for the condition.
I would say you're best choice is E or F, but I can't remember right now. Its been a bit since my gene mutation module. Sorry I can't help more!
