Final Exam More Review Questions Flashcards
Part of your blood type is determined by the gene that codes for the ABO blood groups. Within the ABO blood group, A and B are codominant with each other and O is recessive to both A and B. A mother with type O blood has a child with a father with type AB blood. Which of the following is false, based on this information?
a
The mother is homozygous recessive
b
This combination of parents cannot produce children with the AB blood type
c
This combination of parents cannot produce children with the O blood type
d
Approximately 50% of their children will have type A blood
a
The mother is homozygous recessive
b
This combination of parents cannot produce children with the AB blood type
c
This combination of parents cannot produce children with the O blood type
d
Approximately 50% of their children will have type A blood
A couple has just found out that they are going to have a male child. The mother has hemophilia; the father does not have hemophilia. If they know that the child will be male, what is the chance that their male child will develop hemophilia (the hemophilia allele is recessive and found on the X chromosome)?
a
0%
b
25%
c
50%
d
75%
e
100%
e
100%
Though it is a common example of a recessive genetic disorder, phenylketonuria (PKU) is also an example of another genetics concept that we discussed in this course. Individuals with PKU that do not control their intake of phenylalanine show a wide variety of symptoms due to the buildup of phenylalanine and its byproducts in their systems. These symptoms include hyperactivity, light pigmentation, and delayed development. Based on this information, PKU is an example of:
a
epistasis
b
plieotropy
c
mitochondrial inheritance
d
polygenic inheritance
e
linked genes
b
plieotropy
Your neighbor has planted a bed of pink snapdragons in his yard. As the growing season progresses, he notices that some white and red snapdragons are popping up in what was supposed to be a bed of pink flowers. Explain to him the reason that this is happening, knowing that pink is the phenotype coded for by a heterozygous genotype in the flower color of snapdragons.
This color gene is inherited through incomplete dominance. The heterozygous pink flowers have one copy of the red color allele and one copy of the white color allele, either of which they can pass to their offspring, resulting in red or white offspring when homozygous
Usually, evolution by natural selection eliminates alleles that kill individuals of a species. Nonetheless, some lethal genetic diseases exist in humans - cystic fibrosis, sickle cell anemia, Huntington, to name a few. Why do these genetic disorders persist in human population, despite being lethal to individuals with the disorder? In your answer, consider recessively inherited diseases separately from dominantly inherited diseases.
Dominant diseases can persist if they have their effects after most individuals would have already reproduced. Recessive disorders can persist in carriers/heterozygotes with little to no harm to individuals that carry them. Sometimes, heterozygotes are even at an advantage over those who do not carry the recessive disease allele, as seen in individuals who are heterozygous for sickle cell being resistant to malaria
Given the DNA sequence:
TAC-GTA-CCA-AAA-TTT-ATA-ATT
a) What is the corresponding RNA sequence?
b) What is the sequence of amino acids in the protein?
a) AUG-CAU-GGU-UUU-AAA-UAU-UAA b) Met-His-Gly-Phe-Lys-Tyr
PCR is a common laboratory technique that is used to create many copies of a DNA sequence. Imagine that you are trying to perform PCR in your lab, but your thermocycler is not working. The thermocycler raises and lowers the temperature for each cycle of a PCR reaction. Given that the function of raising and lowering the temperature is to separate the DNA strands, which of the following enzymes might you add as a substitute for the temperature change?
a
Helicase
b
Telomerase
c
Primase
d
Topoisomerase
e
Ligase
a
Helicase
A single fat cell can produce two different proteins (one longer and one slightly shorter amino acid sequence) from the same gene at different times during development. The best explanation for this out of the following is the process of:
a
heterozygosity
b
semiconservative replication
c
epigenetics
d
alternative mRNA splicing
e
wobble pairing
d
alternative mRNA splicing
You injected some mRNAs into the cytoplasm of a yeast cell in order to force the yeast cell to make the protein coded for by the mRNA. Nonetheless, you mistakenly assumed that yeast are prokaryotes (when they are actually eukaryotic), so you did not think to add 5’ caps and poly(A) tails to the mRNAs. Assuming you did everything else correctly, which of the following is a likely consequence of your mistake?
a
tRNA would not have the right anti-codons to bind to this mRNA
b
The introns would not be removed from this mRNA
c
RNA polymerase would not easily bind to this mRNA
d
The rate of translation of this mRNA would be slower than if you had not made this mistake
e
Transcription of the gene would occur at a slower rate than normal
d
The rate of translation of this mRNA would be slower than if you had not made this mistake
A specific archaeon species is discovered that has a different gene expression pattern than most organisms. Instead of the codon UUU coding for the amino acid phenylalanine, UUU codes for valine in this species. That is, every time there is a UUU in the mRNA of this species, a valine is added to the protein instead of the more normal phenylalanine being added. Which of the following genes is likely mutated in this archaeon species?
a
a gene coding for a sgRNA
b
a gene coding for part of the large ribosomal subunit
c
a gene coding for an aminoacyl-tRNA synthetase
d
a gene coding for a transcription factor
e
a gene coding for RNA polymerase
c
a gene coding for an aminoacyl-tRNA synthetase
Given the DNA sequence: TAC-AGC-GCA-CCC-AAA-GAA-ACC-ATT
which of the following mutations would no effect on the amino acid sequence of the protein produced from this gene?
a
A mutation that changed the first A in the DNA to a T
b
A mutation that deleted the second A in the DNA sequence
c
A mutation that changed the last A in the DNA sequence to a G
d
A mutation that changed the last C into a T in the DNA sequence
e
A mutation that changed the second C in the DNA sequence to a G
e
A mutation that changed the second C in the DNA sequence to a G
which of the following are true of mutations
a
Only mutations that affect the sperm and egg can be passed on to the next generation
b
Additions or subtractions of nucleotides in a gene sequence are more likely to cause a loss-of-function of the protein produced by that gene than are mutations that substitute one nucleotide for another
c
Though mutations can be good, bad, or neutral for the individual that they occur in, they are important in the context of evolution because they create new variation
d
Though an incorrect nucleotide is sometimes added during DNA synthesis, DNA polymerase often corrects its own mistakes before continuing to add more nucleotides
a
Only mutations that affect the sperm and egg can be passed on to the next generation
b
Additions or subtractions of nucleotides in a gene sequence are more likely to cause a loss-of-function of the protein produced by that gene than are mutations that substitute one nucleotide for another
c
Though mutations can be good, bad, or neutral for the individual that they occur in, they are important in the context of evolution because they create new variation
d
Though an incorrect nucleotide is sometimes added during DNA synthesis, DNA polymerase often corrects its own mistakes before continuing to add more nucleotides
Imagine you are trying to insert a prokaryotic gene into a eukaryotic organism. You know that you need the nucleotide sequence encoding the gene itself. Based on what you know of transcription and translation, which out of the following would you also need to add to the sequence in order for the gene to be expressed correctly in a eukaryote?
a
a eukaryotic promotor sequence
b
introns
c
-35 and -10 boxes
d
sequences to code for prokaryotic tRNAs
e
sequences to code for the sigma protein
a
a eukaryotic promotor sequence
Imagine that you’ve discovered a mutant eukaryotic line of cells whose histone proteins have more negatively charged amino acids in them than are present in normal histone proteins. In these mutants, you would expect:
a
This would increase gene expression because histone proteins would associate more closely with DNA
b
This would decrease gene expression because histone proteins would associate more closely with DNA
c
This would increase gene expression because histone proteins would associate less closely with DNA
d
This would decrease gene expression because histone proteins would associate less closely with DNA
c
This would increase gene expression because histone proteins would associate less closely with DNA
You isolate a mutant eukaryotic cell that can’t produce the RISC protein, so they are unable to use RNA interference to control gene expression. Which of the following would be an effect of this mutation, in comparison with a normal eukaryotic cell?
a
Fewer proteins would be made in the cell
b
Fewer transcription factors would be needed to activate transcription of genes
c
There would be more mRNA molecules in the cell
d
The chromatin would be significantly less condensed
e
Less alternative RNA splicing would occur in the cell
c
There would be more mRNA molecules in the cell