- In the mRNA; A will be complementary to U
- In tRNA; U will be complementary to A
The mutation does not affect the structure of the protein and is called a silent mutation.
<h3>What is a mutation?</h3>
A mutation is a change that occurs in the sequence of nucleotides of a gene.
The mutation that changes the base G in the DNA to A will result in the following corresponding changes in the mRNA and tRNA:
- In the mRNA; A will be complementary to U
- In tRNA; U will be complementary to A
The mutation does not result in any changes since the amino acid coded for by the mRNA has more than one codon coding for it.
This type of mutation is called a silent mutation.
In conclusion, some mutations occurring in genes have no effect on the proteins the gene codes for.
Learn more about mutations at: brainly.com/question/14455966
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Very interesting problem!
On first reading, it sounded impossible. Tom has normal vision, and there are no male carriers for x-linked recessive disorders. So the daughter can at best (or worst) be carrier of the disorder.
We are told that the daughter has the disorder, but the daughter can only be a carrier with genotype XBXb.
We are also told that Turner Syndrome, which is a disorder related to the x-chromosome. Half of those affected have one of the x-chromosomes missing (monosomy), and some others have some cells with missing or deformed x-chromosomes (mosaicism). Under these circumstances where the normal chromosome is missing, the X-linked recessive Xb allele will be expressed, hence even a carrier can express the red-green colour-blindness.
From the pedigree chart, we can deduce that the colour-blindness must be inherited from Jill, the mother. Tom with normal vision cannot be a carrier because X-linked recessive disorders do not have male carriers.
The daughter's colour-blindness is derived from two sources,
1. inherited Xb allele from mother Jill
2. Turner syndrome that allowed the single allele to express colour-blindness.
Answer:
distruptions of temperature, precipitation and winds are caused by patterns that shift back and forth irreguraly every 2 - 7 years
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If I am correct
Part One: Fatty Acids
Part Two: a decrease in the rate of lipid breakdown
I hope this helped! :D
Answer:
Explanation:
When cell divides, the DNA will replicate in the parent cell or make copies of itself and this will make the chromatics to split or divide in order to create a new cell or daughter cell which contain the exact same DNA. The daughter cell then pass these DNA to subsequent generations, when it also undergo cell division and the dna is been replicated