Genetics: From Genes to Genomes, 5th edition
Genetics: From Genes to Genomes, 5th edition
5th Edition
ISBN: 9780073525310
Author: Leland H. Hartwell, Michael L. Goldberg, Janice A. Fischer, Leroy Hood, Charles F. Aquadro
Publisher: McGraw-Hill Education
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Chapter 19, Problem 18P
Summary Introduction

a.

To determine:

Whether the given proteins in the question act as a proto-oncogene or a tumor-suppressor gene.

Introduction:

The proto-oncogene is a normal gene that promotes cell growth. When a proto-oncogene undergoes a dominant mutation like a gain of function mutation, this gene becomes an oncogene. Tumor-Suppressor genes are normal genes that are responsible for inhibiting the cell proliferation and development of a tumor.

Summary Introduction

b.

To determine:

The effect of the addition of a phosphate group to the phosphatase by kinase A in the given problem.

Introduction:

Phosphatase enzymes are the enzymes responsible for removing phosphates from proteins.

Summary Introduction

c.

To determine:

Whether the phosphatase gene is likely to be a proto-oncogene or a tumor-suppressor gene or neither.

Introduction:

A normal proto-oncogene promotes cell proliferation. A normal tumor-suppressor gene inhibits cell proliferation.

Summary Introduction

d.

To determine:

Whether the listed mutations would lead to excessive cell growth or decreased cell growth if the cell were either homozygous for the mutation, or heterozygous for the mutation and a wild-type allele.

Introduction:

When a tumor suppressor gene undergoes loss of function mutation, it will result in cell proliferation. When a proto-oncogene undergoes gain of function mutation, it will cause cell proliferation. A null mutation makes a gene non-functional.

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A sample of blood was taken from the above individual and prepared for haemoglobin analysis. However, when water was added the cells did not lyse and looked normal in size and shape. The technician suspected that they had may have made an error in the protocol – what is the most likely explanation?   The cell membranes are more resistant than normal.   An isotonic solution had been added instead of water.   A solution of 0.1 M NaCl had been added instead of water.   Not enough water had been added to the red blood cell pellet.   The man had sickle-cell anaemia.
A sample of blood was taken from the above individual and prepared for haemoglobin analysis. However, when water was added the cells did not lyse and looked normal in size and shape. The technician suspected that they had may have made an error in the protocol – what is the most likely explanation?   The cell membranes are more resistant than normal.   An isotonic solution had been added instead of water.   A solution of 0.1 M NaCl had been added instead of water.   Not enough water had been added to the red blood cell pellet.   The man had sickle-cell anaemia.
With reference to their absorption spectra of the oxy haemoglobin intact line) and deoxyhemoglobin (broken line) shown in Figure 2 below, how would you best explain the reason why there are differences in the major peaks of the spectra? Figure 2. SPECTRA OF OXYGENATED AND DEOXYGENATED HAEMOGLOBIN OBTAINED WITH THE RECORDING SPECTROPHOTOMETER 1.4 Abs < 0.8 06 0.4 400 420 440 460 480 500 520 540 560 580 600 nm 1. The difference in the spectra is due to a pH change in the deoxy-haemoglobin due to uptake of CO2- 2. There is more oxygen-carrying plasma in the oxy-haemoglobin sample. 3. The change in Mr due to oxygen binding causes the oxy haemoglobin to have a higher absorbance peak. 4. Oxy-haemoglobin is contaminated by carbaminohemoglobin, and therefore has a higher absorbance peak 5. Oxy-haemoglobin absorbs more light of blue wavelengths and less of red wavelengths than deoxy-haemoglobin
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