Yes it can !!!!!!!!!!!!!!! just did that got it right
Answer:
The correct answer will be option-formation of heterochromatin
Explanation:
Methylation of DNA is the epigenetic mechanism which controls the expression of a gene by adding a methyl group to the cytosine bases in eukaryotic DNA.
The methylation of DNA converts the cytosine residues to the 5-methylcytosine catalysed by DNA methyltransferase enzyme. This results in the silencing of the gene and transcription get switched off.
Studies have shown that DNA methylation is involved in the formation and maintenance of the heterochromatin structure which is the condensed form of the chromatin in which transcription is switched off.
Thus, the formation of heterochromatin is the correct answer.
Answer:
The function of biomolecule inside our body system fully depends on the structure of that biomolecule.It is because the functional groups that participate in a chemical or biochemical reactions are arranged in a specific array in the structure of that biomolecule or macromolecule.
Explanation:
a enzyme structure/catalysis Enzymes are proteinecious in nature.Enzyme contain various amino acids in its active site such as histidine,serine,glutamic acid etc The amino acids of the active site of that enzyme interact with the substrate resulting in the formation of the product.
b mRNA structure/protein synthesis mRNA or messenger RNA consist of nucleotide sequence.The 3 concequetive nucleotides of an mRNA is termed as codons.Each codon codes for specific amino acid.The so formed amino acid linked with the adjacent amino acid by peptide linkage.
c cell membrane structure and signal transduction cell membrane contain various surface protein that act as receptor to detect signals by binding with signaling molecule during signal transduction process.
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❖ B. Punnet Square is a chart used to show the possible outcomes of allele combinations that parents can pass on to their offspring.
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An example of a missense mutation in a protein-encoding gene would most likely be a neutral mutation is option B: replacement of a polar amino acid with another polar amino acid at the protein's surface.
A frequent and well-known example of a missense mutation is the blood condition sickle-cell anemia. Missense mutations exist in the DNA at a single location in sickle-cell anemia patients. A different amino acid is required in this missense mutation, which also alters the overall structure of the protein. Similarly, replacement of a polar amino acid by another polar Ami no acid at the protein's surface is a missense mutation causing change in a single site.
A neutral mutation is one whose fixation is unrelated to natural selection. Therefore, the independence of a mutation's fixation from natural selection can be used to define the selective neutrality of a mutation.
To know more about mutations, refer to the following link:
brainly.com/question/20407521
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Complete question is:
Which example of a missense mutation in a protein-encoding gene would most likely be a neutral mutation?
a) Replacement of a polar amino acid with a nonpolar amino acid at the protein's outer surface
b) Replacement of a polar amino acid with another polar amino acid at the protein's surface
c) Replacement of a polar amino acid with another polar amino acid in the protein's interior
d) Replacement of a polar amino acid with a nonpolar amino acid in the protein's interior
