Microbiology: An Evolving Science (Fourth Edition)
Microbiology: An Evolving Science (Fourth Edition)
4th Edition
ISBN: 9780393615098
Author: John W. Foster, Joan L. Slonczewski
Publisher: W. W. Norton & Company
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Chapter 8, Problem 3RQ
Summary Introduction

 

To review:

The difference between a pair of orthologous genes and a pair of paralogous genes.

Introduction:

A gene is defined as the region of deoxyribonucleic acid (DNA) that is expressed in the form of ribonucleic acid (RNA) or a polypeptide. The complete set of genes of a particular individual is called the genome. Closely related individuals share similar genome. The genes that arise from the common DNA ancestral sequence are called homologous genes. There are two types of homologous genes, orthologous genes and paralogous genes.

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A) Distinguish between the general concept of a gene and the specific concept of an allele at the level of the DNA. B) Strictly speaking, do identical twins have identical phenotypes? Explain.
A hereditary disease is inherited as an autosomal recessive trait. The wild-type allele of the disease gene produces a mature  mRNA that is 1250 nucleotides (nt) long. Molecular analysis shows that the mature mRNA consists of four exons that measure 400 nt (exon 1), 320 nt (exon 2), 230 nt (exon 3), and 300 nt (exon 4). A mother and father with two healthy children and two children with the disease have northern blot analysis performed. The results of the northern blot for each family member are shown below.  a) Identify the genotype of each family member, using the size of mRNAs to indicate each allele. (For example, a person who is homozygous wild type is 1250/1250).  b) Based on your analysis, what is the most likely molecular abnormality causing the disease allele?
Name four mobile genetic elements.
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