Below we are comparing two alleles: wildtype (functional) and mutant (not functional). Normally, p53 can bind to DNA and detect damage. Here we are considering a heterozygote: one wildtype allele, one mutant allele. DNA DNA Consider two phenotypes: 1. Binding to DNA 2. Cancer risk. For each phenotype level, would the wildtype or mutant allele be considered dominant (or is neither allele dominant)? Explain.

Human Anatomy & Physiology (11th Edition)
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Chapter1: The Human Body: An Orientation
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7. Consider p53. The p53 gene codes for a protein
(single circle below). Protein monomers form
dimers (two circles attached). Two dimers come
together to form the functional p53. This triggers
other pathways that can result in either repair of
the damage, or cell death. In this way, p53 is
sometime called the "guardian of the genome"
because the function of p53 reduces mutation. If
damage is not detected, it can lead to an
increase in the frequency of mutation, which can
have negative impacts such as increased cancer
risk. The reason for this is that, over time, if
mutations occur that result in more, unregulated
cell division, that is a cancerous phenotype.
In a heterozygote (+/m)
Wild type
Dimers
Mutant
Not functional
Funçtjonal
Below we are comparing two alleles: wildtype
(functional) and mutant (not functional). Normally,
p53 can bind to DNA and detect damage. Here
we are considering a heterozygote: one wildtype allele, one mutant allele.
DNA
DNA
Consider two phenotypes:
1. Binding to DNA
2. Cancer risk.
For each phenotype level, would the wildtype or mutant allele be considered dominant (or
is neither allele dominant)? Explain.
Transcribed Image Text:7. Consider p53. The p53 gene codes for a protein (single circle below). Protein monomers form dimers (two circles attached). Two dimers come together to form the functional p53. This triggers other pathways that can result in either repair of the damage, or cell death. In this way, p53 is sometime called the "guardian of the genome" because the function of p53 reduces mutation. If damage is not detected, it can lead to an increase in the frequency of mutation, which can have negative impacts such as increased cancer risk. The reason for this is that, over time, if mutations occur that result in more, unregulated cell division, that is a cancerous phenotype. In a heterozygote (+/m) Wild type Dimers Mutant Not functional Funçtjonal Below we are comparing two alleles: wildtype (functional) and mutant (not functional). Normally, p53 can bind to DNA and detect damage. Here we are considering a heterozygote: one wildtype allele, one mutant allele. DNA DNA Consider two phenotypes: 1. Binding to DNA 2. Cancer risk. For each phenotype level, would the wildtype or mutant allele be considered dominant (or is neither allele dominant)? Explain.
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