Answer:
The type of mutation responsible for changing a base in the mRNA strand, without changing the coding aminoacid or protein, is called a <u>silent</u> mutation.
Explanation:
In a silent mutation occurs the change of a nitrogenous base in one of the codons that encodes an aminoacid, without changing the aminoacid or altering the structure or function of the protein to be synthesized.
In this type of mutations the change of the base does not mean the change of the aminoacid, because some aminoacids can be coded with more than one codon. In the case of Leucine, the codons that encode it are CUU, CUC, CUG or CUA, so even if a base changes, the final protein will be the correct one.
For the other options:
- <u><em>Missense</em></u><em>: the change of the base in the DNA chain implies the change of the codon in the mRNA and of the encoded aminoacid, in that way a structural and functional alteration of the synthesized protein occurs. </em>
- <u><em>Nonsense</em></u><em>: the change in the nitrogenous base in the DNA leads to the coding of a termination codon, so that the protein is ultimately incomplete.</em>
- <u><em>Insertion</em></u><em>: in this case there is the addition of more nitrogenous bases to the DNA chain, with respect to the original one.</em>
<span>bones and footprints preserved in stone are examples of fossils. Fossils hardened animal remains such as shells, bones, and teeth.</span> That is the best i can come up with. Hope it helps any.
I believe he is looking for an allele
An allele is a variant form of a gene. Some genes have a variety of different forms, which are located at the same position, or genetic locus, on a chromosomes. Humans are called diploid organisms because they have two alleles at each genetic locus, with one allele inherited from each parent.
