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 14, Problem 25P
Summary Introduction

a.

To determine:

The reason due to which same symptoms appear from mutations in a mitochondrial gene and a nuclear gene.

Introduction:

It is given that Leigh syndrome is characterized by psychomotor regression. This means the progressive loss of mental and movement abilities.

Summary Introduction

b.

To determine:

Whether the given pedigree gives enough evidence to distinguish between the possibilities that Leigh syndrome in the family is due to a mutation in a mitochondrial gene or a nuclear gene.

Introduction:

It is known that nuclear gene codes for the majority of the proteins that are required for the gene expression in mitochondria and chloroplast in all organisms.

Summary Introduction

c.

To determine:

The practical way in which it would be helpful to members of the given family to distinguish between the two possible modes of inheritance.

Introduction:

Mitochondria has its own DNA that replicates independently of the nuclear genome. The cooperation between an organelle and the nucleus is required for the proper functioning of an organism.

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Mitochondrial mutations; Author: Useful Genetics;https://www.youtube.com/watch?v=GvgXe-3RJeU;License: CC-BY