Cyclin proteins fluctuate in level during the different stages of the cell cycle (except for Cyclin D). For example, Cyclin E regulates the entry into S phase. The expression of the cyclin E gene increases, which leads to higher Cyclin E protein levels in the cell. After the cell passes S phase, Cyclin E protein is actively destroyed by ubiquitination. 

When Cyclins are bound to Cdks, they can regulate the activity of proteins that regulate processes like replication and microtubule formation; however, of the cellular processes listed, blocking ubiquitination would be the only process that would directly interfere with cyclins' role to regulate the cell cycle as cyclin proteins need to be destroyed at the correct time to allow the cell cycle to progress.

Kinases are proteins that phosphorylate their substrates, often activating these substrates. In the context of cell cycle progression, cyclins interact with cyclin-dependent kinases (CDKs) and activate the CDK kinase domain to phosphorylate substrates and promote cell cycle progression. CDK inhibitors interact with CDKs to inhibit the CDK kinase domain from phosphorylating substrates. 

The correct answer is prometaphase, in which the nuclear membrane dissolves and the microtubules attach to the centromeres. Interphase occurs before mitosis begins, and includes S phase, where the chromosomes are duplicated. In anaphase, the chromosome duplicates are separated by the microtubules. In telophase, cell division begins with the newly separated chromosome copies.

The correct answer is myosin and actin filaments. Myosin hydrolyzes adenosine triphosphate (ATP) and moves along the actin filaments previously assembled at the cell cortex, constricting the actin and the plasma membrane. Lamin is found in the nucleus and gives structural support to the nuclear membrane. Tubulin and microtubules are components of the cell cytoskeleton. 

DNA ligase is an enzyme used to link DNA via the formation of a phosphodiester bond. During lagging strand synthesis, DNA ligase connects the okazaki fragments. Without this enzyme functioning properly, the lagging strand would not be completed.

This question is a little tricky and depends entirely on the definition of when something is officially a chromosome. A sister chromatid is not officially considered a chromosome until being separated from its partner.

During metaphase I, the homologous chromosomes have yet to separate, so ploidy is still 2n (diploid). Statement IV is false.

During telophase I, the homologous chromosomes have separated and the nuclear envelopes have reformed, effectively forming two haploid nuclei during telophase I. Statement I is true.

During metaphase II, the sister chromatids are still attached, so the cells are still haploid. Statement II is true.

During anaphase II, however, immediately after the sister chromatids are separated they are now considered individual chromosomes. This effectively increases ploidy back to 2n until the nuclear envelopes reform. Statement III is false.

For this question it is important to know the distinction between the genetic material being separated in meiosis I versus meiosis II. During meiosis I homologous chromosomes are separated, and during meiosis II sister chromatids are separated. Reduction of ploidy therefore occurs during telophase I, after the nuclear envelope reforms (due to the segregation of homologous chromosomes). During anaphase I there are technically still 46 chromosomes in the cell, even though each contains two sister chromatids and have been pulled to different regions of the cell. The total amount of genetic material has not changed.

Note that during anaphase of meiosis II ploidy is also at 46 chromosomes. At this point, sister chromatids have been separated from each of the 23 chromosomes present, resulting in 46 separate genetic units. The cell is still considered haploid, since the homologous chromosomes are not present.

Meiosis has many key differences from mitosis, despite the fact that both are used to divide a parent cell into daughter cells. One of the main differences is that meiosis involves the separation of homologous chromosomes, which halves the chromosome number in the daughter cells. This event does not take place in mitosis, because both daughter cells are are still diploid following division. 

Meiosis results in genetically unique daughter cells due to the event of crossing over and the phenomenon of independent assortment. Crossing over takes place during prophase I when the homologous chromosomes come in contact with each other to form tetrads.

During anaphase I, spindle fibers form and homologous chromosomes (each consisting of two chromatids) move toward opposite poles of the cell. During anaphase II, sister chromatids separate at their centromeres and are pulled toward opposite poles of the cell. Synapsis happens during prophase I, not anaphase I, as chromosomes condense and homologs align.