The amino acids coded triplets in the 3' to 5' strand on the normalp53 gene of chromosome 13 are lysine, leucine, Glutamine, stop codons.
Explanation:
mRNA is formed by the transcription of DNA strand coding for a gene.
Any mutation in the DNA sequence even a difference of base pair would cause formation of different amino acids and hence altered protein.
The amino acid is formed in the step of translation where codes are read by tRNA on the mRNA strand and correct nucleotide is brought to growing polypeptide chain.
In transcription 3' to 5' strand acts a template strand. The amino acids on the p53 gene of chromosome 17 is
3'TTT AAC GTC ATC 5' Gene sequence
5' AAA UUG CAG UAG 3' mRNA
lysine, leucine, Glutamine, stop
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Answer:
Please find the explanation below
Explanation:
Deoxyribosenucleic acid, commonly called DNA is the stored form of genetic material in living cells. It contains the information needed by an organism to survive. A segment of the DNA that encodes the necessary information needed to produce a particular protein that determines a trait is called GENE.
The DNA consists of long polynucleotide chains, hence, due to Its length, it cannot git into the cell. The cell then devises a means by wrapping the long strands of DNA around certain proteins called HISTONES. This initially forms a NUCLEOSOME structure, then continuous wrapping around histones and condensation forms the visible CHROMOSOME structure.
Now, the CHROMOSOME contains the DNA molecule, which contains protein-coding segments called GENES. The information contained on the gene is used to produce a protein that is responsible for a particular TRAIT in the organism.
Answer:
cause cells to shrink due to an increase in the osmolarity of extracellular fluid.
Explanation:
Normovolemic describes the situation in which a living organism maintains a normal volume or amount of blood in the body.
A hyperosmotic solution can be defined as a solution having an increased level of osmotic pressure. Thus, when there's a greater amount of solute with respect to another solution in a membrane with close similarities, it is known as hyperosmotic solution.
Basically, hyperosmotic solution gives rise to higher difference between solutes and similar solutions.
Hence, when a normovolemic person consumes a large quantity of a hyperosmotic solution, it will cause cells to shrink due to an increase in the osmolarity of extracellular fluid i.e the total number of solute particles with respect to the concentration of a solution (Osm/L).
A kitten born will have genotype different from sister because the concentration of gene expressed is different in all kittens as it is a phenomenon of codominance.
Explanation:
The moo cat is black and white bicolour cat.
The cat has white colour fur which is combined with some other colour as black.
White colour in cat has white spotting gene that prevents the patches over cat's body.
SS genotype results in large concentration of white colour.
Ss results in medium concentration of white colour.
ss results in black or other dark colurs with very meager or no white colour on skin.
The resultant colour appearance of skin in cats is due to codominance. The colour of the skin depends on the concentration of gene and protein expressed. So, the sister moo cats can have diffrent genotype and different level of white colour patches on the skin and genotype of SS,Ss or ss can be there in sister kittens.
