Answer:
Myocardium
The Heart itself. The nearest organ is the blood supplied to the Myocardium (Heart muscle) by the Heart pumping oxygenated blood through the Coronary Arteries.
Answer:
Repair mechanism for base cleavage (BER)
Explanation:
Repair by base cleavage (BER)
The altered bases are specifically recognized by glycosylases and removed, generating an AP site. The hole is filled by a DNA polymerase that takes the healthy strand as a template. This system arises not only by exposure to external agents, but also by the cell's own activity.
In case of damage in more than one nucleotide, repair by nucleotide excision (NER) is performed.
Nucleotide excision repair (NER)
The damaged area is recognized by UvrA and B, then A and B separate and UvrC enters which forms a complex with endonuclease activity with B. This enzyme cuts the T-dimer and the gap is filled by a DNA polymerase. There is also the TC-NER system (transcription-coupled nucleotide repair system). The alteration of these mechanisms gives rise to diseases such as: Xeroderma pigmentosum, Trichotiodystrophy or Cockayne Syndrome
The amount of glucose in each ml of their blood will be 0.00138 g.
<h3>Blood glucose concentration</h3>
The concentration of glucose in the person's blood is 1.38%.
This means that there is 1.38 g of sugar per Liter of blood.
1 Liter of blood contains 1.38 g of glucose, and there is 1000 mL in 1 Liter of blood.
1000 mL contains 1.38 g
1 ml contains = 1.38 x 1 / 1000 = 0.00138 g
This means 0.00138 g of glucose will be present in every 1 mL of the person's blood.
More on blood glucose can be found here: brainly.com/question/8394646
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Answer:
The correct answer is: C. third nucleotide position.
Explanation:
- Genes located on the chromosomes encodes for proteins.
- A Gene is made up of a Deoxyribonucleotide (DNA) sequence which is transcribed into the messenger Ribonucleotide (mRNA) sequence by the help of RNA polymerase.
- This mRNA sequence is further translated into the amino acid sequence, that folds to form the functional protein, by the help of the Ribosome.
- The Ribosome reads the mRNA sequence in the form of triplets (three nucleotide together) and each such triplet nucleotide codes for an amino acid.
- Each such triplet nucleotide is known as a Codon.
- The Genetic Code is a table which represents the amino acid encoded by each codon.
- However, the Genetic Code is degenerate in nature. This means that one amino acid can be coded by more than one codon.
- This is because, among the the three nucleotide positions in a codon only the first two determine the specificity of the amino acid while the third nucleotide, also called the wobble nucleotide, is not specific. Presence of any nucleotide in the third position of the codon will not alter the amino acid encoded by the codon.
- In the given question, organisms producing homologous protein have similar amino acid sequence but they vary in the corresponding nucleotide sequence of the gene which codes for the homologous protein.
- This is because at the nucleotide level the variation lies in the wobble nucleotide position that occupies the third position in the codon.
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