Biological Science (7th Edition)
7th Edition
ISBN: 9780134678320
Author: Scott Freeman, Kim Quillin, Lizabeth Allison, Michael Black, Greg Podgorski, Emily Taylor, Jeff Carmichael
Publisher: PEARSON
expand_more
expand_more
format_list_bulleted
Videos
Question
Chapter 21, Problem 15PIAT
Summary Introduction
To review:
A reason for the effectiveness of proteins to induce differentiation in the mouse as well as human iPS (induced pluripotent cells) cells.
Introduction:
The cells that are obtained by dedifferentiating the adult specialized cells are the iPS cells. In the given case, the proteins that were effective in inducing differentiation in the human iPS cells worked similarly in the case of mouse cells also.
Expert Solution & Answer
Want to see the full answer?
Check out a sample textbook solution
Students have asked these similar questions
Your friend can't understand how it is possible to combine a somatic cell from their pet with an oocyte from a different animal and create a clone of their pet. Won't the animal that develops be the offspring of the two animals rather than a clone of the animal that donated the somatic cell? Explain to your friend why this is not the case.
A cultured mouse cell line has a mutation in a gene encoding a ribosomal protein. The mutant protein impairs the fidelity of translation such that incorrect amino acids are incorporated at higher rates than normal during protein synthesis. It also slows the rate of mRNA translation and increases the duration of the cell cycle, i.e., the mutant cells grow and divide more slowly. Researchers noted that these cells express higher levels of chaperone proteins than normal cells. Which of the following is the most likely explanation for the elevated chaperone levels.
Following are the characteristics of organoids, except:
Organoids are in vitro 3D clusters of cells deriving exclusively from primary
tissue or stem cells
Organoids are capable of self-renewal and self-organization.
2D monolayer cultures are much closer to the in vivo situation than the
organoids
Spatially restricted cell-fate decisions contribute to self-organization in
organoids.
Chapter 21 Solutions
Biological Science (7th Edition)
Ch. 21 - 1. What is apoptosis?
a. an experimental technique...Ch. 21 - In adult animals, ______ are a source of...Ch. 21 - 3. What is a homeotic mutant?
a. an individual...Ch. 21 - 4. A tool-kit gene is _________.
Ch. 21 - What is the connection between genetic regulatory...Ch. 21 - Which of the following provides the strongest...Ch. 21 - QUANTITATIVE Imagine a situation in which a...Ch. 21 - 10. PROCESS OF SCIENCE Some stickleback fish...Ch. 21 - Will iPS cells be the cure for diabetes?
Type I...Ch. 21 - 12. If researchers were attempting to stimulate...
Knowledge Booster
Learn more about
Need a deep-dive on the concept behind this application? Look no further. Learn more about this topic, biology and related others by exploring similar questions and additional content below.Similar questions
- Imagine that there are mutations in the CDK genes such that their gene products are nonfunctional. What effect would this mutation have on an immature unspecialized blood cell precursor found in the bone marrow? The cell would not be able to reproduce itself. The cell would complete the cell cycle using cyclins in the absence of CDKS. The cell would be able to replicate its DNA but not translate DNA into RNA. The cell would be able to enter mitosis but not complete it. The cell would still phosphorylate the CDK-associated target proteins, and would do so more quickly.arrow_forwardA cell inherits a mutation in a gene that results in a transcription factor, called NF-kB, constantly being in its active conformation. When active, NF-kB stimulates the expression of cyclins that promote progression of the cell cycle, regardless of other conditions. As a result of this mutation, how would this cell's phenotype be affected by this mutation? A) This cell would have a cancer phenotype B) This cell would grow larger in size, but would never divide C) This cell would likely undergo apoptosis D) This cell would not duplicate its chromosomes .arrow_forwardWhen the gene encoding a certain cellular kinase is deleted, the resulting mutant cells arrest in the cell cycle and do not divide. These mutants can be rescued when a gene encoding an N-terminal GFP fusion of the protein is expressed, but not when a gene encoding a C-terminal GFP fusion is expressed. Which fusion protein is appropriate to use in studying cellular localization and activity? Explain why.arrow_forward
- You are studying Protein X which plays a role in promoting the G1/S phase transition in eukaryotic cells. You design an experiment using wild-type yeast cells to measure the amount of Gene X MRNA and activity levels of Protein X during the cell cycle. The results from your experiment are shown in the graph below. From the data, which of the following could Protein X be? Protein X activity levels Gene X MRNA levels Relative Units G1 G2 M cyclin inhibitor protein O cyclin dependent kinase O Helicase Cyclinarrow_forwardI am confused about how stem cell transplants works. If you put a semi differentiated tadpole nucleus in a denucleated egg cell, it’ll develop into a fully formed tadpole, but if you put a fully differentiated tadpole nucleus, it won’t (because the genes have already been expressed in a way where the cytoplasmic determinants cannot operate to the fullest). Then how come in stem cell transplants, you use adult nucleuses that are already developed and transplant them into the denucleated egg cells?arrow_forwardIn a tissue engineering experiment, stem cells are grown in a circular dish (diameter = 3 cm) with a thin layer of cell culture media covering the cells. It is expected that these cells will differentiate when exposed a new differentiation factor (small molecule) at a surface concentration of 50 ng/cm? During the experiment, 1 ug of the factor is placed at the center of the dish. Assume the diffusivity of the factor in cell culture media is 1 x 10^-5 cm^2/s. A. How long does it take before the cells 1 cm from the center of the dish begin to differentiate? B. Do you expect the cells at the edge of the dish differentiate? Justify your answer with calculations.arrow_forward
- Human cells are highly resistant to transformation. Experiments have shown that 5 regulatory circuits (pathways) have to be altered before human cells can grow as tumor cells in immunocompromised mice. State each of these circuits. Explain how the alteration of the protein of that particular circuit leads to uncontrolled growth. the mitogenic signaling pathway controlled by Ras. the cell cycle checkpoint controlled by pRb. the alarm pathway controlled by p53. the telomere maintenance pathway controlled by hTERT. the signaling pathways are controlled by protein phosphatase 2A, which modulates the activity of the mTOR, Myc, β-catenin, and PKB/ Akt signaling proteins.arrow_forwardSince all cells contain the same number of chromosomes and the overall same/similar genome how would the genome in a nerve cell work differently than the genome of a muscle cell? In other words what epigenetic processes cause these differences between cell types at the molecular levelarrow_forwardDescribe how Ras and p53 can alter the simplified genetic pathway controlling cell division shown below. For each of the two genes, would uncontrolled cell division result from a loss-of-function or a gain-of-function mutation? growth factors - receptors - cyclins - cyclin-dependent kinases - cell divisionarrow_forward
- (46) A mutated form of protein pox is found in patients with squamous cell carcinoma. In vitro studies show that the normal p5x molecule binds to DNA, and neoplastic cells accumulate in the G0 phase of the cell cycle. In contrast, the mutated form of p5x does not bind to DNA. These finding are most characteristics of which of the following? (A) Growht factor receptors (B) GTP-binding protein (C) Nonreceptor tyrosine kinases (D) Oncogene proteins (E) Tumor suppressor gene proteinsarrow_forwardA lab wants to convert a skin cell back into an embryonic stem cell (to create what is known as an induced pluripotent stem cell). They transform a set of transcription factors into the skin cell in hopes of accomplishing this. Discussion Question 1: Once you have transformed these factors into your skin cell, how might you identify your induced pluripotent stem cells? List three characteristics you could look for.arrow_forwardOverexpression of the Myc protein is a common feature of many types of cancer cells, contributing to their excessive cell growth and proliferation. By contrast, when Myc is overexpressed in most normal cells, the result is not excessive proliferation, but cell-cycle arrest or apoptosis.Which one of the following statements provides the most likely explanation for why overexpression of Myc can have such different outcomes in normal cells and in cancer cells? A. Normal cells contain checks and balances that prevent Myc-induced proliferation. B. In normal cells, Myc protein acts as a mediator in cell-cycle arrest and apoptosis. C. The target protein for Myc-induced proliferation is missing from most normal cells. D. In normal cells, when Myc is overexpressed, the excess Myc protein precipitates.arrow_forward
arrow_back_ios
SEE MORE QUESTIONS
arrow_forward_ios
Recommended textbooks for you
Human Anatomy & Physiology (11th Edition)BiologyISBN:9780134580999Author:Elaine N. Marieb, Katja N. HoehnPublisher:PEARSON
Biology 2eBiologyISBN:9781947172517Author:Matthew Douglas, Jung Choi, Mary Ann ClarkPublisher:OpenStax
Anatomy & PhysiologyBiologyISBN:9781259398629Author:McKinley, Michael P., O'loughlin, Valerie Dean, Bidle, Theresa StouterPublisher:Mcgraw Hill Education,
Molecular Biology of the Cell (Sixth Edition)BiologyISBN:9780815344322Author:Bruce Alberts, Alexander D. Johnson, Julian Lewis, David Morgan, Martin Raff, Keith Roberts, Peter WalterPublisher:W. W. Norton & Company
Laboratory Manual For Human Anatomy & PhysiologyBiologyISBN:9781260159363Author:Martin, Terry R., Prentice-craver, CynthiaPublisher:McGraw-Hill Publishing Co.
Inquiry Into Life (16th Edition)BiologyISBN:9781260231700Author:Sylvia S. Mader, Michael WindelspechtPublisher:McGraw Hill Education
Human Anatomy & Physiology (11th Edition)
Biology
ISBN:9780134580999
Author:Elaine N. Marieb, Katja N. Hoehn
Publisher:PEARSON
Biology 2e
Biology
ISBN:9781947172517
Author:Matthew Douglas, Jung Choi, Mary Ann Clark
Publisher:OpenStax
Anatomy & Physiology
Biology
ISBN:9781259398629
Author:McKinley, Michael P., O'loughlin, Valerie Dean, Bidle, Theresa Stouter
Publisher:Mcgraw Hill Education,
Molecular Biology of the Cell (Sixth Edition)
Biology
ISBN:9780815344322
Author:Bruce Alberts, Alexander D. Johnson, Julian Lewis, David Morgan, Martin Raff, Keith Roberts, Peter Walter
Publisher:W. W. Norton & Company
Laboratory Manual For Human Anatomy & Physiology
Biology
ISBN:9781260159363
Author:Martin, Terry R., Prentice-craver, Cynthia
Publisher:McGraw-Hill Publishing Co.
Inquiry Into Life (16th Edition)
Biology
ISBN:9781260231700
Author:Sylvia S. Mader, Michael Windelspecht
Publisher:McGraw Hill Education
Cell Differentiation | Genetics | Biology | FuseSchool; Author: FuseSchool - Global Education;https://www.youtube.com/watch?v=gwAz_BtVuLA;License: Standard YouTube License, CC-BY