Answer:
1. Chromatin condense into chromosomes.
4. Homologous chromosomes pair up (formation of tetrads).
5. Homologous chromosomes separate and move to poles.
2. Sister chromatids separate.
3. Chromosomes unravel in to chromatin.
Explanation:
This question portrays the process of meiosis in a cell. The ordered sequence of events in the options are:
1. Chromatin condense into chromosomes - This process occurs in the Prophase stage. Prior to the cell division, the nuclear material is found as Chromatin material. This Chromatin material then undergoes condensation to form visible chromosomes.
4. Homologous chromosomes pair up (formation of tetrads) - This process also occurs during the Prophase stage of meiosis I. In this stage, homologous chromosomes (similar but non-identical chromosomes received from each parent) are paired up side by side to form a structure known as TETRAD or BIVALENT.
5. Homologous chromosomes separate and move to poles - This process characterizes the Anaphase stage of meiosis I. Homologous chromosomes are pulled apart to opposite poles of the cell by spindle microtubules.
2. Sister chromatids separate - After meiosis I, meiosis II involving sister chromatids instead of homologous chromosomes follows. In the Anaphase stage of meiosis II specifically, sister chromatids are pulled apart towards opposite poles of the cell.
3. Chromosomes unravel in to chromatin - After the whole division process i.e. karyokinesis (division of the nuclear material), the chromosomes begin to unravel to form the CHROMATIN threads once again. This process occurs in the Telophase stage of meiosis.
The statement which best explains why carbon is present in so many kinds of molecules is because <u>it can form four covalent bonds.
<em /></u>It isn't rare on Earth, so A is incorrect. It has valence electrons, so C is incorrect. It cannot become an ion, so D is incorrect.<u>
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Answer:
The Cardiovascular System
Explanation:
The respiratory system draws air into the lungs. Oxygen diffuses through the walls of the alveoli and across the walls of the capillaries where it enteres the bloodstream. The oxygen molecules are picked up by red blood cells, which are pumped through the blood vessels by the action of the heart. As the red blood cells carrying oxygen pass through capillaries near the cells, oxygen diffuses into the cells.
Answer/Explanation:
DNA polymerase is the enzyme responsible for replicating DNA. It is hugely important that is performs its functions accurately, as if incorrect bases are incorporated this can lead to mutations that disrupt the structure and function of genes. It adds nucleotides in a 5' - 3' direction only.
DNA polymerase III also has high processivity, which means that for every time it binds DNA, it is able to add many bases before it becomes dissociated.
A. DNA polymerase avoids the incorporation of improperly paired nucleotides in two ways:
- The first way depends on the structure of the enzyme. If the nucleotide that the enzyme is in the process of adding is not complementary to the template, then the nucleotide will not align with the template, and thus it is more inefficient to add. This inefficiency means the nucleotide is more likely to leave the active site before it is added, and DNA polymerase can replace it with the correct nucleotide.
- It also has proofreading capabilities. This means, when an incorrect base is added, it recognises the error and can fix this. It can do this because it possesses 3'-5' exonuclease activity. That means, it can chop out incorrectly added bases.
B. Ribonucleotides are the nucleotides that are incorporated into a growing RNA molecule. They are different from deoxyribonucleotides because of the differences in the sugar backbone (ribose vs deoxyribose). Their incorporation would disrupt the structure and function of the DNA, leading to problems with transcription and replication.
DNA polymerase avoids incorporating these nucleotides primarily because of the structure of the enzyme. Ribonucleotides cannot fit into the active site of DNA polymerase due to what is called a "steric filter" or "steric gate". This gate/filter function is performed by specific amino acid residues which usually have a bulky side chain and thus block the incorporation of the 2'OH of the ribose sugar (which is lacking in the deoxyribose sugar)
