Research Report 1 James Elliott Spring 2016
Article Reported:
Magidson V, He J, Ault JG, O’Connell CB, Yang N, Tikhonenko I, McEwen BF, Sui H, Khodjakov A. 2016. Unattached kinetochores rather than intrakinetochore tension arrest mitosis in taxol-treated cells. J Cell Biol. 212 (3): 307-319. Accessed 8 Feb 2016. doi: 10.1083/jcb.201412139
I. Paper Review
A. Background and Key Question
This article was about a study performed by scientists looking to investigate the mechanism of how Taxol interrupts the cell cycle. The interval often referred to as the spindle apparatus checkpoint is without a doubt the time frame where Taxol acts, as it is an antimicrotubule drug that is cell cycle specific. It is understood that the structure
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To make the specimen compatible with both forms of advanced microscopy, they sufficiently prepared samples by coupling the specimen with a fluorescence that was also conductive. This technique was accomplished with the FlouroNanogold label, which contains gold nanoparticles covalently bonded to a fluorescence label. That way, the LM worked as well as the EM for the same set of kinetochores that were being studied. The Hec1 protein was stained in this case because this protein naturally delineates the structures to be studied.
C. Describe One Specific Result
The orientation between the kinetochores with respect to centromeres (kTilt) was of a larger degree in the Taxol treated cells in comparison to the cells progressing through metaphase normally. There was a 16° increase from 10° to 26° when cells were treated with Taxol.
D. What are the major conclusions/implications of this work?
This was a multifaceted study that simply is not given justice by my review that is limited to two pages. Through this study, the scientists believed that the data validated that kinetochores are significantly influenced by the Taxol treatment. This interpretation was inferred from the results in differences in Delta (distance between Hec1 and CenpT labels within kinetochores), cTilt (angle of centromeres from the spindles), and kTilt (angle of the kinetochores with respect to centromeres). One of these results was described above in
In most eukaryotes, the nuclear envelope that separates the DNA from the cytoplasm disassembles. The chromosomes align themselves in a line spanning the cell. As the cell elongates, corresponding sister chromosomes are pulled toward opposite ends.
2. In which phases of mitosis are sister chromatids visible, and attached to each other at the centromere?
Without cell division and the cell cycle nearly all life would fail to exist. Cell division allows an organism to not only replace its own cells but to create offspring. The cell cycle consists of two main parts: interphase and mitotic phase. Within these two phases the processes can be broken down into further categories. Interphase can be broken down into three subphases that are the necessary preparations the cell makes in order to be ready to divide during mitosis. For this lab we looked mainly at the mitotic phase because of its fascinating and rapid changes to the cell. The cell types we looked at were prepared slides of whitefish and onion root tip.
The cell cycle is a series of stages that occurs when a new cells makes the division from the parent cell to two daughter cells. This is a stage in cellular reproduction. The cell cycle consists of three phases, interphase, mitosis, and cytokinesis. During Interphase, a cell will continue to perform its functions as usual. The time frame for Interphase varies; while an embryonic cell will take just a few hours to complete the cycle, a stem cell from an adult can take 24 hours (Mader, Windelspecht, 2015). After the interphase stage completes itself, a complete nuclear division happens and mitosis occurs. During the stage of mitosis, the daughter cells will receive the same amounts of the contents of the parent cell. Throughout the last stage, in the cytoplasm there is a division known as Cytokinesis (Mader, Windelspecht, 2015). Cytokinesis occurs differently in plant cells than it does in animal cells, as the cell wall around the plant prevents the process from happening the same way. Instead, a new plasma membrane and cell walls are built are built between the daughter cells. However, in animal cells a single cell will become two (Mader, Windelspecht, 2015).
A key characteristic of cancer cells is that they are no longer constrained by the standard cell cycle controls that normally coordinate cell division activity. Consequently the timing of mitosis in cancer cells is altered. You may
The phase in mitosis which chromatin begins to coil and the mitotic spindle begins to form.
The cell cycle has four main stages. The cell cycle is the regular pattern of growth. The four stages consist of Gap 1 (G1), Synthesis (S), Gap 2 (G2), and Mitosis (M). Gap 1, consists of a cell that carries its normal functions. Calls also increase in size, and the organelles increase in number. A cell will spend the most time in this phase. But it also depends on the cell type to see how long it will spend in this phase. During this phase the cell has to pass a critical checkpoint before it can continue into the (S) stage, also called the Synthesis stage. It would be dangerous for a cell to keep dividing if the certain conditions were not met. The cells in this stage also need signals from the other cells to tell the if division is needed. Now the next stage is the Synthesis stage. During this phase the cell makes a copy of it’s nuclear DNA. By the end of the (S) phase DNA appears grainy in photos and the cell nucleus contains two complete sets of DNA. Gap 2, is the third stage of the cell cycle. The cells continue doing there thing and more growth occurs. This phase is like the checkpoint, everything in the cell has to be going right for the cell to be able to enter mitosis.
Mitosis is one of two main methods of cell replication, the other being meiosis. It is “the simple duplication of a cell and all of its parts” resulting from the splitting of a cell. The ‘parent’ or original cell splits, duplicating its DNA (packaged in chromosomes) producing two ‘daughter’ or new cells with the same genetic code. There are four stages of mitosis; Prophase, Metaphase, Anaphase and Telophase. Interphase is not an official phase of mitosis as the cell is at ‘rest’ and not being divided during this phase. It is often called one of the phases of mitosis as it is one of the stages in the life cycle of a cell; however it is not a phase of mitosis due to the fact that no division takes place.
This division of the nucleus is called mitosis. Another part of cell division is cytokinesis, where the cytoplasm divides and the cell becomes two cells. The first steps in cell division begin with mitosis, and mitosis is divided into five different stages which include: prophase, prometaphase, metaphase, anaphase, and telophase. (pg. 571) Prophase is the first step in mitosis. During prophase the chromosomes become compact together. The centrisomes begin to form the mitotic spindle. Prometaphase is the next step in cell division, which the nuclear envelope breaks apart and the paired chromatids connect. (pg. 572) Then the chromatids connect with spindle microtubules to form kinetochores and migrate to the poles of the cell. In metaphase the chromosomes line up in the middle of the cell. (pg. 573) The next step in mitosis is anaphase, which is where the chromatids of each chromosome separate at the centromere and are pulled to opposite ends. The last step in mitosis is telophase. During telophase the spindle fibers disassembled and the chromosomes uncoil into chromatin. At this point the cell enters into cytokinesis. (pg. 574) During cytokinesis the cytoplasm splits along the cleavage furrow. (pg 578) In plant cells, during cytokinesis a cell wall must be formed. Vesicles migrate toward the center and form a cell plate, which becomes the cell wall. (pg.580) In either a plant cell or animal cell, at this
In the article, “Mitosis and Cancer,” it talks about how cancer is formed and how the spread of cancer cells can be slowed down. Cancer is essentially a disease that causes an abnormal growth of cells. In mitosis, there are certain checkpoints that a cell must pass before dividing. With cancer, the checkpoints are ignored and continue to grow rapidly.
A mitotic inhibitor is a drug inhibiting mitosis or cell division. Mitotic inhibitors are widely used in cancer treatment, because cancer cells can grow and eventually spread through the body via continuous mitotic division.
The microtubule ultimately forms when the GTP bound to the β-tubulin is hydrolyzed (Agard et al., 2008). Microtubules possess the property of dynamic instability, which refers to extended periods of shortening that result in a period of growth. Dynamic instability also refers to the opposite situation involving a span of extended growth, followed by a period of shortening. This shortening period is commonly known as catastrophe (Cassimeris et al., 2005). Dynamic instability is essential to cell movement, cell signaling, and mitotic chromosome separation (Cabral et al.,
The cell cycle is composed of two major stages called interphase and mitosis. Interphase takes the most of the time in the cell cycle; interphase can be divided into G1, S and G2 phase. There is also a phase called G0, which is a stage in which the cells do not divide anymore even if cells need to be repaired. During the G1 phase, the cell grows and performs activities. In the S phase, cells replicates DNA; replicating DNA is very important because if the two daughter cells can’t be inherited the identical DNA from the parent cell, they won’t function out well and eventually die. During the G2 phase, which is the last phase of interphase, the cell keeps growing and prepares for division. The cell checks the DNA for damage and prepares for mitosis by producing the proteins needed during cell division. Then, the cell splits the content and the membrane during mitosis and cytokinesis. Cancer is a set of diseases that are characterized by uncontrolled, abnormal growth of cells caused by
As described, chemotherapy aims to prevent or slow the growth of cancerous cells. The complex function of chemotherapy is directly related to cell division, or mitosis. To begin, the body’s immune
Elongation of the GUF deletion seems indicative that the loss of YKL222C's function has adversely affected the ability of the cell to maintain its shape under stress. The fact that many of the tests performed prior to the experiment seemed to show nuclear localization means that