According to the ABC model of flower development in Arabidopsis, three classes of organ identity genes— designated A, B, and C— are required to specify the identity of floral organs in each whorl of a flower. If wild type Arabidopsis were transformed with a chimeric gene composed of a C class promoter fused to a B class coding sequence, which of the following arrangements   (outer to inner) would be predicted?

#Question id: 4765

#SCPH01 Biochemistry

The recessive mutant allele that causes cystic fibrosis is much more frequent in Caucasians population than in other world populations. Some scientists believe heterozygotes must have had a survival advantage during plagues such as cholera that occasionally swept through this population. What concept does this illustrate?

#Question id: 4765

#SCPH12 I Genetics

The recessive mutant allele that causes cystic fibrosis is much more frequent in Caucasians population than in other world populations. Some scientists believe heterozygotes must have had a survival advantage during plagues such as cholera that occasionally swept through this population. What concept does this illustrate?

#Question id: 4766

#SCPH01 Biochemistry

In soybeans, resistance to sudden death syndrome (SDS) is inherited as a dominant condition. In some cases, individuals that are not resistant to SDS (but whose parents were) can pass the trait on to their progeny. This is an example of which of the following?

#Question id: 4766

#SCPH12 I Genetics

In soybeans, resistance to sudden death syndrome (SDS) is inherited as a dominant condition. In some cases, individuals that are not resistant to SDS (but whose parents were) can pass the trait on to their progeny. This is an example of which of the following?

#Question id: 4767

#SCPH01 Biochemistry

Neurofibromatosis is a condition in humans which is generally inherited in a dominant fashion. Assuming this disorder is 90% penetrant, what is the chance that a single child born to a father with neurofibromatosis and a mother known not to carry the mutation will have the disorder?

#Question id: 4767

#SCPH12 I Genetics

Neurofibromatosis is a condition in humans which is generally inherited in a dominant fashion. Assuming this disorder is 90% penetrant, what is the chance that a single child born to a father with neurofibromatosis and a mother known not to carry the mutation will have the disorder?