C) As the trait will then pass to others without it and through natural selection will become abundant
Answer:
C
Explanation:
Pluto is not the smallest orbiting body (which includes comets, asteroids, and moons), pluto is the smallest orbiting planet
All planets have an elliptical orbit, not just pluto
Pluto has several moons
Therefore, the right answer is C
1. two copies of the duplicated chromosome are attached at their centromeres before separating
2. chromosomes replicate before cell division
3. chromosome separation begins at the origin of replication on DNA
4. Before separation duplicated chromosomes condense; nuclear envelope fragments permitting chromosome separation
5. replicated chromosomes separate by attaching to some other structural feature of the cell
Explanation:
In the given question, the DNA replication steps of both prokaryotes and eukaryotes are provided in which some are common to both eukaryotes and prokaryotes and some are unique to the prokaryotes and eukaryotes.
<u>Eukaryotes
</u>
1. Option-4 as the nuclear envelope is present in eukaryotes only.
2. Option-1 as centromere allows the kinetochores bind to the centromere which separates the chromosome.
<u>Bacteria
</u>
1. Option-3 as DNA replication process separates the strand of the DNA.
<u>Both
</u>
1. Option-5 as the chromosomes separate by other structures like microtubules
2. Option-2 as genetic material to be passed on to the generation must be replicated.
Answer: B
WHY?
Deletion mutation may cause a shift of base sequence, causing the reading frames for base sequence to change during translation. This may affect the type of amino acid it the original base sequence codes for, resulting in a change in amino acid sequence in the polypeptide translated. Therefore, affecting the whole protein itself. There may be wrong amino acids that prevents vital bonds like disulfide bridges to form, resulting in a huge change in 3 dimensional conformation of the protein. A point mutation may result in a gene sequence being edited. However, only the target sequence is being mutated. The rest of the gene sequences are left untouched. Therefore, the impact is localised. This ensures that even though a few wrong amino acids may be in the polyleptide, most of the bonds that are crucial for the correct 3 dimensional conformation is still present, therefore, lesser defects will be resulted due to point mutation as compared to deletion mutation.
