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Test #3 Key

 

1. B

2. E

3. A or C

4. C

5. B

6. D

7. C

8. C

9. B

10. B

11. A

12. C

13. D

14. C

15. A

16. B

17. D

18. C

19. D

20. D


Test #3 short answer section

 

1. What is the most likely result … (3 pts)

 

Frame shift (2)

Missense (2)

Nonsense translation past deletion (3)

Early termination of translation (2)

No effect – homologous gene will express (3)

Decrease/50% expression of protein product (3)

Defective protein/enzyme (3)

 

2. Given a family with the gene for hemophilia:  Mom is a carrier, Dad expresses the trait.  They have one daughter, one son.  What are the odds for:

 

The son expressing?  _50% or .5  or  1:1  or  1/2_____________

 

The daughter expressing? __same as above____________(1 pt each)

 

3. Deaf-mutism:  given the genes for deaf-mutism are recessive, explain how a deaf-mute mom and a deaf-mute dad can have normal children. Be specific re: genotypes. (3 pts)          Note hint in the language…genes ARE

 

This is a TWO GENE trait (*not* two alleles!).

If either gene is homozygous recessive, person is deaf-mute.

 

Here father is homozygous recessive for one gene, homozygous dominant for the other.  Mother is homozygous dominant for the first gene, homozygous recessive for the other.   ddEE x DDee

 

Children are all fully heterozygous (DdEe), thus don’t express.

 

See web link!

 

4.Give a specific example of temporal gene regulation in a eukaryotic system. (2 pts)

 

Temporal = time regulated, as in something happens at a particular time in the organism’s life.

Beta and gamma hemoglobin activation in fetus; also apoptosis of inter-digit flesh

 

5.  Questions about Translation:

 

What is main chemical energy source for translation?  ____GTP______(1 pt)

 

What components are necessary for assembling “loaded” tRNA’s for use in translation?  Be specific. (2 pts) [half point each]

 

Aminoacyl-tRNA synthetase (1 of 20) or specific assembly enzyme

Proper amino acid

Proper tRNA

ATP

 

What are the components necessary for translation initiation, listed in order of use?(3 pts) (half point each, final half point for 1st and last in proper place)

 

Must begin with mRNA

 

Then, in no particular order…

 

Initiation factor(s)

Charged (“loaded”) tRNA [for Methionine] [for AUG codon] [with UAC anticodon]

GTP

Small ribosomal subunit

 

Must end with large ribosomal subunit

 

 

 

 

 

 

 


6. Pedigree questions: The following pedigrees represent phenotypes displayed by parents and their offspring.  Answer the possibility Yes or No, and give a 10 word or less explanation proving your choice. (2 pts each; no credit for just yes/no answers)

 

Pedigree 1

 

 

 

Yes/No?

NO ______     Could this trait be inherited as a simple autosomal recessive?

                  Reason:  No dominant gene in parents  or

                              Son’s don’t express recessive

 

 Yes______     Could this trait be inherited as a simple autosomal dominant?

                  Reason:  Parents both heterozygous                                   

 

Yes______      Could this trait be inherited as a simple X-linked dominant?

                  Reason:   Mom heterozygous                                     

 

Pedigree 2

 

 

 

 

Yes/No?

 Yes______     Could this trait be inherited as a simple autosomal recessive?

                  Reason:    Mom heterozygous                                    

 

 Yes______     Could this trait be inherited as a simple autosomal dominant?

                  Reason:     Dad heterozygous                                               

 

Yes______      Could this trait be inherited as a simple X-linked recessive?

                  Reason:     Mom heterozygous                                                                                                                                  

 

NO______      Could this trait be inherited as mitochondria associated?

                  Reason:    Mom doesn’t express or all children don’t express                                              

 

 

 

Test #3 essay questions:

Essay:  compare the Mendelian and molecular genetic explanations for the phenotype and genotype expressions of PKU.  Be sure to include organismal and biochemical effects. (12 pts)  A diagram might be helpful. 

**See web link for diagrams

Phenotype – retardation – genotype: acts as Mendelian recessive gene, 1:3 ratio for heterozygous parent cross  (4pts)

Protein (enzyme) production – same level for homozygous normal, heterozygous, homozygous affected (4 pts)

Enzyme activity is incomplete dominant –

          Homo normal – 100%

          Hetero – 50%

          Homo affected – 0%     (4pts)

Enzyme quality is co-dominant

          Homo normal – 100% good

          Hetero – 50% good, 50% bad

          Homo affected – 100% bad          (4 pts)

 

2. Discuss the Griffith’s experiment and the meaning of his unexpected dead mice.  Be sure your discussion uses only the concepts understood at the time of the experiment! [1920’s] (8 pts)  A simple diagram might be helpful.

 

Smooth bacteria – dead mouse

Rough bacteria – live mouse

Heat killed smooth bacteria – live mouse            (2 pts)

 

Heat killed smooth + rough live bacteria – dead mouse          (2 pts)

Recovered live smooth bacteria from dead mouse (2 pts)

 

“Transforming factor”  (1 pt) in heat-killed smooth

changed non-virulent rough into virulent smooth          (4 pts)

 

Use the words/phrases:      DNA, Nucleic Acid, Nucleus, Chromosome        (-1 pt)