Let's say that an experiment had no disruption to kinetochores and you are able to inactivate the CDC 14 phosphatase, which acts to remove phosphate groups from substrates that were previously phosphorylated by active MPF. What effect, if any, would this have on (i) the duration (length) of the mitotic phase, (ii) the timing of cyclin B’s appearance or disappearance, and (iii) the period of time for which MPF is active? Briefly explain your reasoning

Let's say that an experiment had no disruption to kinetochores and you are able to inactivate the CDC 14 phosphatase, which acts to remove phosphate groups from substrates that were previously phosphorylated by active MPF. What effect, if any, would this have on (i) the duration (length) of the mitotic phase, (ii) the timing of cyclin B’s appearance or disappearance, and (iii) the period of time for which MPF is active? Briefly explain your reasoning

Biology 2e

2nd Edition

ISBN:9781947172517

Author:Matthew Douglas, Jung Choi, Mary Ann Clark

Publisher:Matthew Douglas, Jung Choi, Mary Ann Clark

Chapter10: Cell Reproduction

Section: Chapter Questions

Problem 45CTQ: Describe how the duplicated bacterial chromosomes are distributed into new daughter cells without...

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Explain why we can say that M-phase of the cell-cycle is triggered by a positive feedback loop. a) What would the consequences be if cohesins were working normally but condensins were not? and b) what stage of the cell cycle would this cause problems in? Why is it important for the centrosome to duplicate during G1-G2 (interphase) before M phase? The kinetochores serve as a link between the sister chromatids and the microtubules attached to the mitotic spindle. a) How are microtubules still able to exhibit dynamic instability after they are bound to the sister chromatids and b) why is this important to mitosis? As the name suggests, the Anaphase-promoting-complex (APC), promotes the 4th phase of mitosis by separating the sister chromatids so they can travel to separate poles of the cell, and prevents them from being re-zipped together. Describe how APC does these two things (Hint: one involves M-cyclin and the other involves…
Let's say that an experiment resulted in the production of several unattached kinetochores. What effect, if any, would this have on (i) the duration (length) of the mitotic phase, (ii) the timing of cyclin B’s appearance or disappearance, and (iii) the period of time for which MPF is active? Briefly explain your reasoning.
Kinetochores control the transition from metaphase to anaphase. Why is this statement true? Question 7 options: a) Anaphase will only begin after the M checkpoint where all the kinetochores and mitotic spindle have correctly attached. b) Anaphase will only begin after the M checkpoint where all the mitotic spindle have correctly formed. c) Kinetochores bind to microtubules in monotelic attachment to the sister chromatids. d) Kinetochores bind to microtubules in syntelic attachment to the sister chromatids. e) Kinetochores will halt at the M checkpoint to weaken the mitotic spindle formation, which is the event that initiates anaphase.
A small amount if cytoplasm isolated from a mitotic cell is injected into an unfertilized frog oocyte, causing the oocyte to enter M phase. A sample of the injected cytoplasm is then taken and injected into a second oocyte, causing this cell also to enter the M phase. this process is repeated many times until essentially, none of the original protein samples remains, and yet, cytoplasm taken from the last in the series on injected oocytes is still able to trigger entry into the M phase with undiminished efficiency. Explain this remarkable observation.
A mitotic spindle is a structure formed in [Select] [Select] types of microtubules. [Select] while [Select] located at opposite ends of the cell. Within each of these are 3 cells that consists of a mitosis. Finally, without [Select] connection between the two spindle poles. microtubules help position each spindle, microtubules help to pull sister chromatids apart during microtubules, there would be no
Question 1) which cytoskeleton supports the cilia in moving mucous laden with foreign particles? Question 2) What will happen in a cell if the DNA ligase gene is mutated Question 3) Describe how is prophase mitosis different from prophase of meiosis I? Question 4) What happens to acetylcholine after it evoked activation of nicotinic acteylcholine receptors in the neuromusclar function?
Describe how the duplicated bacterial chromosomes are distributed into new daughter cells without the direction of the mitotic spindle.
If you expose a culture of human cells (for example,HeLa cells) to 3H-thymidine during S phase, howwould the radioactivity be distributed over a pair ofhomologous chromosomes at metaphase? Would theradioactivity be in (a) one chromatid of one homolog,(b) both chromatids of one homolog, (c) one chromatid each of both homologs, (d) both chromatids ofboth homologs, or (e) some other pattern? Choose thecorrect answer and explain your reasoning.
Asymmetric cell division often relies on cytoskeletal elements to generate or maintain the asymmetric distribution of cellular factors. In S. cerevisiae, what factor is localized to the bud by myosin motors? In Drosophila neuroblasts, what factors are localized apically by microtubules?
If chemical signals in the cytoplasm control the progression of a cell to the M phase of the cell cycle, then fusion of a cell in G1 with a cell in early M phase would most likely result in the (A) replication of chromosomes only in the G1 cell (B) exiting of both cells from the cell cycle and into the G0 phase (C) condensation of chromatin in preparation of nuclear division in both cells (D) transfer of organelles from the G1 cell to the cell in the M phase Please select the correct option. For the incorrect options, please explain why each one is incorrect. Thank you.
What are the functionalroles of the mitotic spindle in an animal cell? Explain how thesefunctions are related to the three types of microtubules: aster, polar,and kinetochore microtubules.
One change observed at the centrosomes early in mitosis is an increase in the number of γ-TURCcomplexes (which contain γ-tubulin.).How does the presence of γ-tubulin affect the balance between microtubule assembly & disassembly? Why might having more of it present in the centrosomal region be beneficial in the spindle assembly process?