The following statements are made to describe the biosynthetic pathway of IAA;

a)  IPA pathway involves a deamination reaction to form IPA, followed by a decarboxylation reaction to form indole-3-acetaldehyde (IAld) and then oxidized to IAA by a specific dehydrogenase

b) IAN pathway is similar to the IPA pathway, except that the order of the deamination and decarboxylation reactions is reversed, and different enzymes are involved

c) IAM pathway  involves the two enzymes  tryptophan monooxygenase and IAM hydrolase

d) In the IAN pathway, tryptophan is first converted to indole-3-acetaldoxime and then to indole-3-acetonitrile. The enzyme that converts IAN to IAA is called nitrilase

Which of the following is the correct  statements  of about the biosynthesis of  IAA?

#Question id: 5807

#Unit 8. Inheritance Biology

Which of the following would be an example of a germline mutation?

#Question id: 5806

#Unit 8. Inheritance Biology

Which of these is NOT a mechanism by which a chromosome rearrangement could affect gene function?

#Question id: 5805

#Unit 8. Inheritance Biology

In Himalayan rabbits, the ears, feet, and muzzle are pigmented while the rest of the body is white. This is because they express an enzyme variant that is ineffective at body temperature but functions at the lower temperatures experienced by cells of the extremities. This is an example of:

#Question id: 5804

#Unit 8. Inheritance Biology

The gene that is mutated in cases of cystic fibrosis encodes an ion transporter protein normally expressed in the respiratory and digestive tracts along with other locations. Individuals homozygous for the most common mutation in this gene (ΔF508) died at very early ages prior to the advent of advanced medical intervention. Despite this, the mutation exists at relatively high frequency in populations of European descent. One potential explanation is that heterozygotes for such mutations may be relatively immune to the lethal effects of diseases such as typhoid fever. Which statement below is most accurate?

#Question id: 5803

#Unit 8. Inheritance Biology

The mutation which causes sickle cell anemia in humans:

#Question id: 5802

#Unit 8. Inheritance Biology

A wild type allele: