Answer:
False
Explanation:
Mendel realized that the F2 had a phenotypic ratio 3:1, meaning 3/4 = 75% were yellow and 1/4 = 25% green.
Mendel observed that the F1 expressed only one of the alternative variants (in this case, only yellow seeds appeared), while the other variant (green) disappeared. Mendel named dominant the expressed variant. Mendel allowed auto pollination and observed that in the second generation, F2, the other disappeared variant reappeared. Both alternative variants were present in the F2. Mendel named recessive the second alternative variant.
Mendel thought that hereditary traits determined by discrete factors were the possible explication for these phenotypes. These factors should have been present in the F1 in pairs. One of them came from one parental plant, and the other factor came from the other plant. These factors then separated again when sex cells were produced, giving two types of gametes, each with only one factor.
Mendel concluded that each individual (plant) has a pair of factors (alleles), one for each trait (yellow and green) and that the pair separates (segregates) during the formation of the gametes. This conclusion is known as the segregation principle (First Mendels´ Low).
The correct answer is the ship beagle I think I spelled that right
Answer:
Having a repetitive enzyme system would allow more than one enzyme to catalyze a particular reaction. If one of the types of enzyme is not able to perform its function due to temperature or any other factor, then another kind of enzyme would be able to catalyze the reaction. Hence, having repetitive enzyme systems is very effective in carrying out the metabolic functions of the body even when conditions are not favourable.
Based on the above information, the mutation type is frameshift mutation.
It is a genetic mutation caused by indels of various nucleotides in a DNA succession that is not detachable by three. The additions and erasures cause an adjustment in the length of a quality, which causes a movement in the codon perusing outline. A frameshift mutation happens when a protein is radically modified as a result of an addition or an erasure. Tay-Sachs illness is a human issue caused by a frameshift change.
