Genetic Analysis: An Integrated Approach (2nd Edition)
Genetic Analysis: An Integrated Approach (2nd Edition)
2nd Edition
ISBN: 9780321948908
Author: Mark F. Sanders, John L. Bowman
Publisher: PEARSON
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Chapter 10, Problem 6P
Summary Introduction

To analyze:

Analyzing the single amino acid substitution in the given β- globin mutant with the help of wild type β- globin form, determine the wild type template DNA sequences and the template sequence for each mutant.

β- globin form Position Amino acid
βA (wild- type) 7 Glu
Siriraj 7 Lys
San Jose 7 Gly
βA (wild- type) 58 Pro
Ziguinchor 58 Arg
βA (wild- type) 145 Try
Bethesda 145 His
Fort Gordon 145 Asp

Codon table

Genetic Analysis: An Integrated Approach (2nd Edition), Chapter 10, Problem 6P

Introduction:

The word base substitution refers to the exchange of one base pair with another. Base substitution mutation in the triplet codon can result in the synthesis of the wrong amino acid thereby changing the protein structure or function.

Many hereditary anemic conditions arise due to base substitution mutation in the wild type template strand of β- globin which leads to the incorporation of a wrong base pair in the codonthus causing a change in the β- globin function ( Mutant β- globin form).

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You have discovered a family with a new genetic form of anemia. The DNA sequences at the 5’ end of the non-template strand of the normal and mutant DNA encoding the alpha subunit of hemoglobin are given below: Normal 5’-ACGTTATGCCGTACTGCCAGCTAACTGCTAAAGAACAATTA…..-3’ Mutant 5’-ACGTTATGCCCGTACTGCCAGCTAACTGCTAAAGAACAATTA….-3’ What are the amino acid sequences of the normal and mutantpolypeptides? What are the codons in the translated portion of the mRNA transcribed from the normal and mutant genes? What type of mutation is present in the mutant hemoglobin gene?
Shown below are two homologous lengths of the alpha and betachains of human hemoglobin. Consult a genetic code dictionary and determine how many amino acid substitutionsmay have occurred as a result of a single nucleotidesubstitution. For any that cannot occur as a result of a singlechange, determine the minimal mutational distance. Alpha: ala val ala his val asp asp met proBeta: gly leu ala his leu asp asn leu lys
In the human genome for the beta chain of haemoglobin (the oxygen-carrying protein in the red blood cells), the first 30 nucleotide in the amino acid coding region is represented by the sequence  3'-TACCACGTGGACTGAGGACTCCTCTTCAGA-5'
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