Genetics: Analysis and Principles
Genetics: Analysis and Principles
6th Edition
ISBN: 9781259616020
Author: Robert J. Brooker Professor Dr.
Publisher: McGraw-Hill Education
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Chapter 22, Problem 7EQ
Summary Introduction

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Reverse genetics is the opposite of conventional genetic study of gene function.

Introduction:

The conventional study of gene function includes identification of gene because of an altered phenotype. In reverse genetics, the gene is identified before its phenotypic effect is observed. Gene knockout is a technique by which the function of a specific gene is eliminated in an organism.

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In the study of plants and animals, it is relatively common forresearchers to identify a gene using molecular techniques withoutknowing the function of the gene. In the case of mice, the functionof the gene can be investigated by making a gene knockout. Aknockout that causes a phenotypic change in the mouse may providean important clue regarding the function of a gene. For example,a gene knockout that produced an albino mouse would indicate that the knocked-out gene probably plays a role in pigment formation. The experimental strategy of first identifying a gene based on its molecular properties and then investigating its function by making a knockout is called reverse genetics. Explain how this approach is opposite to (or the reverse of) the conventional way that geneticists study the function of genes.
You are interested in studying a novel gene that appears to be involved in cancer. There is no information about the function of this gene. What would you do to obtain the cDNA for this gene? How would you express this gene and what expression systems might you utilize to study its function and why? How would determine the subcellular localization of this gene in eukaryotic cells? What are alternative methods in case one doesn't work? How would you purify and determine the 3-dimensional structure of this protein?
During experimental RNAi, how does the researcher affect expression of a target gene? Group of answer choices Inject custom, lab-made double-stranded RNA into the specimen that will be targeted by the cell's existing Dicer to create siRNA complementary to the target gene's transcript. Inject lab-made Dicer proteins into the specimen which will cut up the target gene's transcript. Inject custom, lab-made siRNAs complementary to the target gene's transcript.

Chapter 22 Solutions

Genetics: Analysis and Principles

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