Genetics
Published March 2018
www.BioInteractive.org
Page 1 of 3
Activity
Student
Handout
Central Dogma Card Sorting Activity
INTRODUCTION
Hemophilia is a rare genetic disorder in which the blood does not clot properly because it lacks sufficient blood-
clotting proteins. The disease is caused by mutations in a gene on the X chromosome. Because males typically
have only one X chromosome, to inherit the disease, they only need to inherit one copy of the mutated gene,
whereas females with two copies of the X chromosome must inherit two copies of the mutated gene. Symptoms
of the disease vary but generally include excessive internal and external bleeding. Currently, there is no long-
term cure, and many patients receive infusions of blood-clotting proteins. Because the disease is caused by
mutations in the DNA, scientists think that they could someday treat it by intervening in the steps that occur
from DNA to protein production. This flow of information represents the way most genes are expressed in
eukaryotic cells and is also referred to as the central dogma of molecular biology. How would knowledge of the
central dogma help find a treatment for hemophilia?
Working in small groups or alone, you will place cards with drawings of cellular molecules in the order in which
the steps occur in eukaryotic gene expression, labeling all names and molecules as instructed. Then, answer the
questions that your instructor assigns.
QUESTIONS
1. A genotype is the complete genetic makeup of an individual, whereas a phenotype is all observable
characteristics of the individual. Because genes direct the production of proteins and proteins are
responsible for an individual’s observable characteristics, genotypes control phenotypes.
The final card in the series shows a mature protein. Proteins can play several different cellular functions, as
shown in the figure below. Using prior knowledge, describe a specific role each type of protein performs for the
cell and provide an example of an actual protein (e.g., lactase). Write your answer next to each picture.
Central Dogma Card Sorting Activity
Genetics
Published March 2018
www.BioInteractive.org
Page 2 of 3
Activity
Student Handout
Questions 2-4 present different disease scenarios. For each one you are asked to identify a way to treat the
disease by targeting a specific molecule or step in the central dogma pathway. Refer to your cards as you
think of an answer and make sure you pick a different approach for each disease.
2. Cystic fibrosis is a devastating illness that affects the lungs, pancreas, and intestines. In 1989, researchers
discovered that the disease is caused by a mutation in a gene that produces a protein that channels chloride
across cellular membranes. People with two copies (or alleles) of the mutated gene have a buildup of mucus
in the lungs, intestines, and other organs due to nonfunctioning or absent channel proteins. Suggest two
ways you could intervene to treat the disease by targeting the DNA molecule and justify why each approach
could be effective.
3. Like cystic fibrosis, sickle cell anemia is an autosomal recessive condition. It can be caused by mutations in
the gene for β-globin (HBB). HBB is one of the two subunits of adult hemoglobin, the protein that carries
oxygen in red blood cells. People who inherit two copies of the mutation produce abnormal hemoglobin,
and their tissues are starved of oxygen. One interesting finding is that some individuals with HBB mutations
do not have sickle cell anemia because they have another mutation that allows them to produce fetal
hemoglobin throughout their lives. Fetal hemoglobin production is normally turned off after birth. Based on
this knowledge, suggest two ways you could treat sickle cell anemia by targeting the transcription step of
the fetal hemoglobin gene and justify why each approach might be effective.
Central Dogma Card Sorting Activity
Genetics
Published March 2018
www.BioInteractive.org
Page 3 of 3
Activity
Student Handout
4. Another disease caused by a mutation in a single gene is Huntingtons disease (HD), an autosomal dominant
condition. It is caused by mutations in a gene required for normal nerve cell function. The mutations cause
abnormal proteins to be produced which sticktogether and accumulate in nerve cells, eventually
interfering with normal cell operations. Suggest two ways you could treat the disease by targeting the
translation step for the HD protein and justify why each approach might be effective.
5. (Optional) For any genetic disease, several approaches for treating it at different steps of gene expression
could work. Complete the Click & Learn “Central Dogma and Genetic Medicine
,” paying particular attention
to the genetic medicines that have been developed or are in development for the diseases above. Were the
approaches you identified in this activity like the ones in the interactive? If so, how were they similar? If not,
how did they differ?
6. Consider hemophilia again. Identify two ways the researcher could design an intervention to treat
hemophilia, provide a brief explanation of each, and justify why each approach might be effective.