<span>Explanation: Oxygen is the more electro-negative of the atoms in the water molecule, so it tends to pull the 'shared' electron more to itself. Thus, the oxygen atom has a greater time-share of all electrons, and therefore the hydrogen atoms are more positive for a partial lack of electrons</span>
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the doe did not eat
Explanation:
it should be did the doe not eat
no the dog did not eat
Answer: c. maybe, depending on specific traits at organism in cellular levels of both animals
Explanation:
Evolutionary history has to do with the processes through which living organisms evolve from their ancestors to their present generations.
It's quite possible for the fruit fly and the fruit bat to share a common ancestor based on their evolutionary history depending on specific traits at the organism and cellular levels of both animals.
Therefore, the correct option is C.
Answer:
1. The difference between the normal hemoglobin protein DNA sequence and the sickle cell hemoglobin DNA sequence is a base to base shift, in this case adenine (GAG) to thymine (GTG).
2. The difference affects the amino acid sequence of the protein by replacing glutamic acid (Glu) with valine (Val).
Explanation:
In sickle cell anemia, a change in the DNA nucleotide sequence is observed, where adenine is substituted by thymine, whose expression is the change in the amino acid sequence of globine β, incorporating valine instead of glutamic acid. This represents a molecular mutation - point mutation - by subtitution, which corresponds to missense mutation.
<u>Normal hemoglobin protein in a RBC</u>
DNA CTG ACT CCT GAG GAG AAG TCT
Amino acids Leu Thr Pro Glu Glu Lys Ser
<u>Sickle cell hemoglobin protein in a RBC</u>
DNA CTG ACT CCT <em>GTG</em> GAG AAG TCT
Amino acids Leu Thr Pro <em>Val</em> Glu Lys Ser
When GAG is transcribed to mRNA, the CUC codon is obtained, which codes for glutamic acid. Thymine substitution causes the DNA sequence to change to GTG, which is transcribed as CAC, the codon that encodes the amino acid valine. The <u>change from glutamic acid to valine in β-globin causes an altered hemoglobin, giving the abnormal erythrocytes observed in sickle cell disease</u>.
