BIOLOGY
BIOLOGY
12th Edition
ISBN: 9781260169614
Author: Raven
Publisher: RENT MCG
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Chapter 52, Problem 1DA

Data analysis Two different genes have mutant alleles that cause this spotting phenotype. One gene encodes a signaling molecule. What Is the likely function of the other gene product?

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Summary Introduction

To determine: The function of other gene product in spotting phenotype, if one gene encodes a signaling molecule.

Introduction: A mutation can be defined as a sudden change that occurs in the DNA sequence, during DNA replication. It can also be caused by exposure to specific chemicals or radiation. Mutation contributes to genetic variability.

Explanation of Solution

Neural crest cell under the surface of ectoderm differentiates into pigment cells of the skin. Survival and migration of these cellsare affected by a mutation in genes leads to white spotting in the skin. Two different genes have a mutant allele that causes the spotting phenotype in humans and mice. One gene act as a signaling molecule then the other is likely to be a receptor for the molecule.

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4e. You also study the expression of 3 different mutants for this gene. For each mutant answer the following: Does this mutation change the sequence of the protein produced? Why or why not? If it does change the sequence of protein be sure to write out the new sequence. If it does not change the protein sequence, what effect (if any) would you expect it to have on expression of the gene? 1 20 ORI 40 60 5'..TTCGAGCTCTCGTCGTCGAGATACGCGATGATATTACTGGTAATATGGGGATGCACTATC...3’ 3'...AAGCTCGAGAGCAGCAGCTCTATGCGCTACTATAATGACCATTATACCCCTACGTGATAG...5’ promoter i. Mutant A has a single base pair substitution with the T/A being replaced with C/G base pair at position 35 (position denoted by the * in the sequence above). ii. Mutant B has a 2 G/C pairs inserted between position 19 and 20 (position denoted by the ^ in the sequence above).
Please help me with the question below - it is based on Cellular Biology.
Star eye A peculiar eye condition known as "star” is manifested as a dominant gene in Drosophila. Its recessive allele R* produces the normal eye of wild type. The expression of R can be suppressed by the dominant allele of another locus, Ru-R. Ru-R*, as the recessive allele of the said locus, has no inhibitory effect on R*.   When a normal-eyed male of genotype Ru-R Ru-R RR is crossed to a homozygous wild-type female of genotype Ru-R* Ru-R* R*R*, what phenotypic ratio is expected in the F2?
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