Answer:
Explanation:
Sister chromatids are regarded as replicated chromosomes. Sister chromatids are two identical copies of chromosomes held at the centromere that are formed as a result of replication. They are identical in the sense that they contain same alleles/gene sequence of the same genes.
Homologous chromosomes, on the other hand, are similar (in length, centromere position) but non-identical chromosomes. Homologous are non-identical in the sense that they may contain different alleles of a gene and are received from each parent. homologous chromosome contain four chromatids; two of which are sister chromatids and non-sister to the other two.
Both undergo meiosis where homologous chromosomes separate in meiosis I while sister chromatids separate in meiosis II but only sister chromatids undergo mitosis.
B . its a 50 50 chance because the traits are stronger
The correct answer is the last statement.
If the regulatory serine is mutated to alanine, then acetyl-CoA carboxylase will get activated spontaneously and will produce malonyl-CoA. The increased concentrations of malonyl-CoA will obstruct the oxidation of fatty acids by preventing the entry of fatty acids into the mitochondria.
It is because the AMP-activated protein kinase phosphorylates the serine residues of acetyl-CoA carboxylase to inactivate it. If a mutation occurs in such residues, then the AMPL cannot phosphorylate acetyl-CoA carboxylase and this enzyme will get activated spontaneously.
In such a situation, there will be more than sufficient production of malonyl-CoA, which will inhibit the admittance of more fatty acid getting inside the mitochondria; this will indirectly prevent the oxidation of fatty acids.
