4. The forward primer used in this experiment incorporates part of the HaeIII recognition site, GGCC. How is this different from the sequence of the human TAS2R38 gene? What characteristic of the PCR reaction allows the primer sequence to "override" the natural gene sequence? Draw a diagram to support your contention. The HaeIII recognition site is GGCC, and the forward primer used in the experiment incorporating part of this recognition site means that the primer sequence has a region similar to GGCC. In the context of the human TAS2R38 gene, the natural gene sequence may not perfectly match the primer sequence. The characteristic of the PCR reaction that allows the primer sequence to "override" the natural gene sequence is the ability of DNA polymerase to extend from the primers during DNA amplification. During PCR, the DNA polymerase enzyme synthesizes a new DNA strand using the template DNA and the primers as starting points. If the primer sequence is similar to the target gene's sequence, the polymerase will initiate synthesis at the primer and extend along the template. This allows for selective amplification of the region between the primers. In this case, even if the natural gene sequence does not perfectly match the primer sequence, the DNA polymerase can still initiate synthesis at the primer's binding site and extend along the target gene. This ability of the primer to bind to a region with partial similarity and initiate DNA synthesis is a key feature of PCR.

Human Heredity: Principles and Issues (MindTap Course List)
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Chapter13: An Introduction To Genetic Technology
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Problem 20QP: Analyzing Cloned Sequences A base change (A to T) is the mutational event that created the mutant...
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4. The forward primer used in this experiment incorporates part of the HaeIII recognition
site, GGCC. How is this different from the sequence of the human TAS2R38 gene? What
characteristic of the PCR reaction allows the primer sequence to "override" the natural
gene sequence? Draw a diagram to support your contention.
The HaeIII recognition site is GGCC, and the forward primer used in the experiment
incorporating part of this recognition site means that the primer sequence has a region similar to
GGCC. In the context of the human TAS2R38 gene, the natural gene sequence may not
perfectly match the primer sequence. The characteristic of the PCR reaction that allows the
primer sequence to "override" the natural gene sequence is the ability of DNA polymerase to
extend from the primers during DNA amplification.
During PCR, the DNA polymerase enzyme synthesizes a new DNA strand using the template
DNA and the primers as starting points. If the primer sequence is similar to the target gene's
sequence, the polymerase will initiate synthesis at the primer and extend along the template. This
allows for selective amplification of the region between the primers.
In this case, even if the natural gene sequence does not perfectly match the primer sequence, the
DNA polymerase can still initiate synthesis at the primer's binding site and extend along the
target gene. This ability of the primer to bind to a region with partial similarity and initiate DNA
synthesis is a key feature of PCR.
Transcribed Image Text:4. The forward primer used in this experiment incorporates part of the HaeIII recognition site, GGCC. How is this different from the sequence of the human TAS2R38 gene? What characteristic of the PCR reaction allows the primer sequence to "override" the natural gene sequence? Draw a diagram to support your contention. The HaeIII recognition site is GGCC, and the forward primer used in the experiment incorporating part of this recognition site means that the primer sequence has a region similar to GGCC. In the context of the human TAS2R38 gene, the natural gene sequence may not perfectly match the primer sequence. The characteristic of the PCR reaction that allows the primer sequence to "override" the natural gene sequence is the ability of DNA polymerase to extend from the primers during DNA amplification. During PCR, the DNA polymerase enzyme synthesizes a new DNA strand using the template DNA and the primers as starting points. If the primer sequence is similar to the target gene's sequence, the polymerase will initiate synthesis at the primer and extend along the template. This allows for selective amplification of the region between the primers. In this case, even if the natural gene sequence does not perfectly match the primer sequence, the DNA polymerase can still initiate synthesis at the primer's binding site and extend along the target gene. This ability of the primer to bind to a region with partial similarity and initiate DNA synthesis is a key feature of PCR.
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