Mrna,amino acids,type of mutation
1 answer:
Answer:
mRNA: 3' AUG-AAU-GCU-GCC-GGU-GA-5'
amino acids : methionine, asparagine, alanine, arginine, proline
type of mutation: deletion, missense
Explanation:
The mRNA sequence is complementary to the DNA sequence. A always pairs with T, C always pairs with G. Except this is an RNA sequence not a DNA sequence, so T is replaced with U.
The mRNA sequence is translated into an amino acid sequence based on the triplet code. The triplet code for this sequence is shown in the attached picture. Each triplet signifies a specific amino acid. The codon can be identified from the table and placed in sequence. We can see that the new DNA strand has caused a new amino acid sequence. It has also left us with an incomplete sequence, as GA cannot signify an amino acid.
The type of mutation is a single base deletion. We can see that the base C is missing from the 9th amino acid in the original strand. As you can see, this has an ongoing affect on all the bases in the rest of the sequence, as it changes the way the sequence is organised into codons. This results in a missense mutation.
You might be interested in
Answer:
SER, they are capable of synthesizing testosterone of Adrenocortical cells.
Explanation:
Adrenal smooth microsomal cells are enriched in smooth endoplasmic reticulum SER, membranes of which contain high levels of translocation apparatus and oligosaccharyltransferase complex proteins. STEROID-SECRETING CELLS are characterized by abundant smooth endoplasmic reticulum (SER). These cells synthesize cholesterol as a precursor for steroid hormones or take up this substrate from plasma lipoproteins. Many of the enzymes for sterol and steroid synthesis are localized in the smooth-surfaced endoplasmic reticulum. This organelle is particularly prominent in cells of the inner zones of the adrenal and fluctuates in amount and configuration in response to hormonal stimulation and sterol levels.
