Molecular Basis of Inheritance Questions and Answers

In "the repressillator" (also known as "the represilator"), gene A is the Lac repressor. What should occur if cells containing the repressillator were continually maintained in very high (and excess) levels of allolactose?
The expression of B will be the opposite of the expression of C, but the expression will oscillate at long intervals.
The expression of B will always be high and the expression of C will always be low.
The oscillations of all proteins will occur with increasing amplitude.
The expression of B will be the opposite of the expression of C, but the expression will oscillate at short intervals.
Biology
Molecular Basis of Inheritance
In "the repressillator" (also known as "the represilator"), gene A is the Lac repressor. What should occur if cells containing the repressillator were continually maintained in very high (and excess) levels of allolactose? The expression of B will be the opposite of the expression of C, but the expression will oscillate at long intervals. The expression of B will always be high and the expression of C will always be low. The oscillations of all proteins will occur with increasing amplitude. The expression of B will be the opposite of the expression of C, but the expression will oscillate at short intervals.
A proteasome inhibitor will...
decrease the number of multiubiquitylated proteins.
decrease the number of polyubiquitylated proteins.
increase the number of multiubiquitylated proteins.
increase the number of polyubiquitylated proteins.
Biology
Molecular Basis of Inheritance
A proteasome inhibitor will... decrease the number of multiubiquitylated proteins. decrease the number of polyubiquitylated proteins. increase the number of multiubiquitylated proteins. increase the number of polyubiquitylated proteins.
-hort tandem repeats are inherited from parents. The mother has 8 repeats of the TPOX STR on
one chromosome and 6 repeats of the TPOX STR on the other chromosome (alleles are 8,6) and
he father is homozygous with 5 repeats of the TPOX STR on both chromosomes (alleles are 5,5).
What alleles could the son could have for the TPOX STR?
8, 6 only
5,5 only
8, 6 and 5, 5
8, 5 and 6, 5
Biology
Molecular Basis of Inheritance
-hort tandem repeats are inherited from parents. The mother has 8 repeats of the TPOX STR on one chromosome and 6 repeats of the TPOX STR on the other chromosome (alleles are 8,6) and he father is homozygous with 5 repeats of the TPOX STR on both chromosomes (alleles are 5,5). What alleles could the son could have for the TPOX STR? 8, 6 only 5,5 only 8, 6 and 5, 5 8, 5 and 6, 5
Why does adding SDS and potassium acetate, followed by centrifugation precipitate the proteins and chromosomal DNA out of solution? Why does the RNA not precipitate out? 
This is for an RNA isolation & electrophoresis lab. Below is the explanation given in the lab manual: 
Detergents lyse membranes: SDS Cell membranes are composed of lipids and proteins rich in hydrophobic residues. SDS (sodium dodecyl sulfate) is a strong ionic detergent that solubilizes the plasma membrane. (Remember that in this protocol, E. coli, a prokaryote, is the source of RNA. Prokaryotes have cell walls which we need to break with lysozyme, but they do not have membrane bound organelles-meaning they do not have a nucleus-so we will need to separate the DNA from the RNA). In addition, SDS is also a strong protein denaturant as you learned when you isolated eukaryotic DNA in BIO130. In this protocol we use SDS plus potassium acetate to remove protein and other cellular constituents (discussed below under "Selective precipitation by SDS and potassium acetate"). 
Potassium acetate and SDS selectively precipitate protein and cell debris Sodium dodecyl sulphate is very soluble in water, while potassium dodecyl sulphate is very insoluble. In this procedure, we add potassium ions (potassium acetate), which form ionic bonds to produce insoluble potassium dodecyl sulphate. All of the molecules previously bound to SDS now precipitate from solution with the insoluble potassium dodecyl sulphate. By centrifuging this mixture, you remove most proteins, unbroken cells and fragments of cells, as well as most of the large, chromosomal DNA, which becomes trapped in the precipitate. Only very soluble molecules, such as RNA, small DNAs, and small salts remain in solution.
Biology
Molecular Basis of Inheritance
Why does adding SDS and potassium acetate, followed by centrifugation precipitate the proteins and chromosomal DNA out of solution? Why does the RNA not precipitate out? This is for an RNA isolation & electrophoresis lab. Below is the explanation given in the lab manual: Detergents lyse membranes: SDS Cell membranes are composed of lipids and proteins rich in hydrophobic residues. SDS (sodium dodecyl sulfate) is a strong ionic detergent that solubilizes the plasma membrane. (Remember that in this protocol, E. coli, a prokaryote, is the source of RNA. Prokaryotes have cell walls which we need to break with lysozyme, but they do not have membrane bound organelles-meaning they do not have a nucleus-so we will need to separate the DNA from the RNA). In addition, SDS is also a strong protein denaturant as you learned when you isolated eukaryotic DNA in BIO130. In this protocol we use SDS plus potassium acetate to remove protein and other cellular constituents (discussed below under "Selective precipitation by SDS and potassium acetate"). Potassium acetate and SDS selectively precipitate protein and cell debris Sodium dodecyl sulphate is very soluble in water, while potassium dodecyl sulphate is very insoluble. In this procedure, we add potassium ions (potassium acetate), which form ionic bonds to produce insoluble potassium dodecyl sulphate. All of the molecules previously bound to SDS now precipitate from solution with the insoluble potassium dodecyl sulphate. By centrifuging this mixture, you remove most proteins, unbroken cells and fragments of cells, as well as most of the large, chromosomal DNA, which becomes trapped in the precipitate. Only very soluble molecules, such as RNA, small DNAs, and small salts remain in solution.
Dr. Stevens is examining the DNA sequences of a group of mice. He notices that in one of the mice, one nucleotide pair is substituted with another in the part of the DNA sequence that codes for fur color. However, despite the substitution, the mouse still has the same fur color as the other mice with the correct DNA sequence. Why
doesn't the substitution of nucleotides in the mouse change its phenotype, or physical characteristics?
A. The mouse has a completely different DNA sequence than the other mice.
B. The substituted nucleotide has the same directions as the original nucleotide.
C. DNA sequences don't determine the color of a mouse's fur.
D. Substitutions in the nucleotides of a mouse's DNA never affect their phenotypes.
Biology
Molecular Basis of Inheritance
Dr. Stevens is examining the DNA sequences of a group of mice. He notices that in one of the mice, one nucleotide pair is substituted with another in the part of the DNA sequence that codes for fur color. However, despite the substitution, the mouse still has the same fur color as the other mice with the correct DNA sequence. Why doesn't the substitution of nucleotides in the mouse change its phenotype, or physical characteristics? A. The mouse has a completely different DNA sequence than the other mice. B. The substituted nucleotide has the same directions as the original nucleotide. C. DNA sequences don't determine the color of a mouse's fur. D. Substitutions in the nucleotides of a mouse's DNA never affect their phenotypes.
Chargaff's rule explains how the nitrogenous bases in DNA pair in complementary patterns. Adenine always pairs with thymine, and guanine always pairs with cytosine in order to maintain the same size of the base pairs throughout the DNA strands. 
BASED ON THIS ANSWER CREATE MULTIPLE CHOICE QUESTION
Biology
Molecular Basis of Inheritance
Chargaff's rule explains how the nitrogenous bases in DNA pair in complementary patterns. Adenine always pairs with thymine, and guanine always pairs with cytosine in order to maintain the same size of the base pairs throughout the DNA strands. BASED ON THIS ANSWER CREATE MULTIPLE CHOICE QUESTION
Which technique would be MOST useful in determining the father of a child in a paternity suit?
A. DNA Fingerprinting
B. Polymerase chain reaction
C. Computer generated parental punnett square
D. Karyotype of father and child
Biology
Molecular Basis of Inheritance
Which technique would be MOST useful in determining the father of a child in a paternity suit? A. DNA Fingerprinting B. Polymerase chain reaction C. Computer generated parental punnett square D. Karyotype of father and child
During the process of replication, a molecule of DNA unzips, forming two single strands. What makes up each individual strand of DNA?
A. nitrogenous bases attached to a sugar-phosphate backbone
B. paired thymine and guanine bases
C. paired adenine and uracil bases
D. sugar groups attached to individual amino acids
Biology
Molecular Basis of Inheritance
During the process of replication, a molecule of DNA unzips, forming two single strands. What makes up each individual strand of DNA? A. nitrogenous bases attached to a sugar-phosphate backbone B. paired thymine and guanine bases C. paired adenine and uracil bases D. sugar groups attached to individual amino acids
The diagram below illustrates a process that can occur during cell division and results in an alteration in the composition of a chromosome. Each letter in the diagram represents a specific gene on the chromosome.
The diagram shows that a section of the chromosome was broken out and reinserted backwards. This is known as
A. Chromosomal Translocation
B. Chromosomal Insertion
C. Chromosomal Deletion
D. Chromosomal Inversion
Biology
Molecular Basis of Inheritance
The diagram below illustrates a process that can occur during cell division and results in an alteration in the composition of a chromosome. Each letter in the diagram represents a specific gene on the chromosome. The diagram shows that a section of the chromosome was broken out and reinserted backwards. This is known as A. Chromosomal Translocation B. Chromosomal Insertion C. Chromosomal Deletion D. Chromosomal Inversion
Which option below illustrates the DNA "Base Pairing Rule"?
G-C and A-T
Jack and Jill
G-C and A-U
Biology
Molecular Basis of Inheritance
Which option below illustrates the DNA "Base Pairing Rule"? G-C and A-T Jack and Jill G-C and A-U
(8.3) Thirty-three percent of sea urchin DNA is composed of the nitrogenous base adenine (A). According to Erwin Chargaff, what
percent of the DNA is composed of guanine (G)?
a 17%
b 66%
c 33%
d 8%
Biology
Molecular Basis of Inheritance
(8.3) Thirty-three percent of sea urchin DNA is composed of the nitrogenous base adenine (A). According to Erwin Chargaff, what percent of the DNA is composed of guanine (G)? a 17% b 66% c 33% d 8%
In a DNA double helix, a region along one strand of DNA has the following sequence:
5'- GCCTAATC-3'
What is the complementary sequence?
A. 3'-GCCTAATC-5'
B. 5'-CGGAUUAG-3'
C. 5'-CGGATTAG-3'
D. 3'-CGGATTAG-5'
Biology
Molecular Basis of Inheritance
In a DNA double helix, a region along one strand of DNA has the following sequence: 5'- GCCTAATC-3' What is the complementary sequence? A. 3'-GCCTAATC-5' B. 5'-CGGAUUAG-3' C. 5'-CGGATTAG-3' D. 3'-CGGATTAG-5'
If double stranded DNA has 14% G (guanine), what percent A (adenine), T (thymine) and C (cytosine) would you expect?
A. A = 14%, T = 36 % and C=36%
B. C=14%, A= 36% and T=36%
C. A= 14%, T=14% and C= 14%
D. A 14%, T=36% and C=14%
Biology
Molecular Basis of Inheritance
If double stranded DNA has 14% G (guanine), what percent A (adenine), T (thymine) and C (cytosine) would you expect? A. A = 14%, T = 36 % and C=36% B. C=14%, A= 36% and T=36% C. A= 14%, T=14% and C= 14% D. A 14%, T=36% and C=14%
(8.2) Watson and Crick published a paper that shows DNA was a double helix made of complementary strands. Which means that if one strand is CTATGT, the other
strand would be
a GATACA
b CTATGT
c GATCCA
Biology
Molecular Basis of Inheritance
(8.2) Watson and Crick published a paper that shows DNA was a double helix made of complementary strands. Which means that if one strand is CTATGT, the other strand would be a GATACA b CTATGT c GATCCA
Which of the following statements explains the relationship that is most similar to the relationship between genes and chromosomes? 
Directions for building a structure
Stairs going to the second floor
Sails that powers the boat
Fur covering a polar bear
Biology
Molecular Basis of Inheritance
Which of the following statements explains the relationship that is most similar to the relationship between genes and chromosomes? Directions for building a structure Stairs going to the second floor Sails that powers the boat Fur covering a polar bear
Select all of the following genotypes that is/are homozygous?
A ZZ
B ZZ
c Aa
D AA
E aa
F ZZ
Biology
Molecular Basis of Inheritance
Select all of the following genotypes that is/are homozygous? A ZZ B ZZ c Aa D AA E aa F ZZ
Q2A: Knowing how the ara operon is being regulated when only Arabinose is present, which of
the following conclusions can you make based on your results? Select all that apply (2 marks).
(a) The fluorescence intensity increases as the concentration of Arabinose increases. This
results from high transcription of pGLO plasmid DNA.
(b) Glucose concentration does not affect RNAP binding to the PBAD promoter.
(c) The low level of fluorescence in AOGO suggests that the change in fluorescence is caused
by the Arabinose treatment.
(d) If glucose was present, there will be high transcription.
Biology
Molecular Basis of Inheritance
Q2A: Knowing how the ara operon is being regulated when only Arabinose is present, which of the following conclusions can you make based on your results? Select all that apply (2 marks). (a) The fluorescence intensity increases as the concentration of Arabinose increases. This results from high transcription of pGLO plasmid DNA. (b) Glucose concentration does not affect RNAP binding to the PBAD promoter. (c) The low level of fluorescence in AOGO suggests that the change in fluorescence is caused by the Arabinose treatment. (d) If glucose was present, there will be high transcription.
Zoe is a healthy young woman who is researching her ancestry. She sent a DNA sample to a company to have her genes analyzed. The results show
that a large percentage of her ancestors came from an area of South America bordering the equator. Her results also revealed that she carried the
Sickle Cell Trait. How will having the Sickle Cell Trait influence Zoe's future health status?
Multiple Choice
Zoe's bone marrow will start to make fragile, sickle-shaped erythrocytes.
Zoe start to experi regular periods of fatigue, dizziness, pale skin, and lightheadedness.
The rate of destruction of Zoe's erythrocytes will be faster than her body's ability to make new erythrocytes.
Zoe will be healthy and not experience any type of adverse effects from having the Sickle Cell Trait.
Biology
Molecular Basis of Inheritance
Zoe is a healthy young woman who is researching her ancestry. She sent a DNA sample to a company to have her genes analyzed. The results show that a large percentage of her ancestors came from an area of South America bordering the equator. Her results also revealed that she carried the Sickle Cell Trait. How will having the Sickle Cell Trait influence Zoe's future health status? Multiple Choice Zoe's bone marrow will start to make fragile, sickle-shaped erythrocytes. Zoe start to experi regular periods of fatigue, dizziness, pale skin, and lightheadedness. The rate of destruction of Zoe's erythrocytes will be faster than her body's ability to make new erythrocytes. Zoe will be healthy and not experience any type of adverse effects from having the Sickle Cell Trait.
Due to gene interactions, pigment in mouse fur is only produced when the W allele is present. Individuals of the ww genotype
are white. If color is present, it may be determined by the A, a alleles. AA or Aa results in agouti color, while ad results in black
coats.
a) What F1 genotypic and phenotypic ratios are obtained from a Pgen cross between AAWW and aaww mice?
b) What phenotypic ratios would be expected in the F2 generation of the above Pgen cross?
Biology
Molecular Basis of Inheritance
Due to gene interactions, pigment in mouse fur is only produced when the W allele is present. Individuals of the ww genotype are white. If color is present, it may be determined by the A, a alleles. AA or Aa results in agouti color, while ad results in black coats. a) What F1 genotypic and phenotypic ratios are obtained from a Pgen cross between AAWW and aaww mice? b) What phenotypic ratios would be expected in the F2 generation of the above Pgen cross?
You want to search for latent prints on a styrofoam cup. What type of fingerprint processing will you use? *
Ninhydrin
Super glue / Cyanoacrylate
Amido Black
Black or Magnetic Fingerprint Powder
Biology
Molecular Basis of Inheritance
You want to search for latent prints on a styrofoam cup. What type of fingerprint processing will you use? * Ninhydrin Super glue / Cyanoacrylate Amido Black Black or Magnetic Fingerprint Powder
Helicases are proteins that "unzip" double stranded DNA to produce two, unbound single-strands of DNA. Some helicases initially bind to double-stranded DNA, while other helicases initially bind to single-stranded DNA and then unzip the double-stranded DNA in front of them. Viruses are particularly dependent on helicases for viral replication. What features in DNA would be recognized by each of these two classes of helicases that would allow them to be specific?
Biology
Molecular Basis of Inheritance
Helicases are proteins that "unzip" double stranded DNA to produce two, unbound single-strands of DNA. Some helicases initially bind to double-stranded DNA, while other helicases initially bind to single-stranded DNA and then unzip the double-stranded DNA in front of them. Viruses are particularly dependent on helicases for viral replication. What features in DNA would be recognized by each of these two classes of helicases that would allow them to be specific?
Why is cancer growth dependent on an increased number of blood vessels?
a) All options are correct
b) To shield the tumor from immune cells
c) To increase the tumor's stability
d) To supply the tumor with oxygen and nutrients
Biology
Molecular Basis of Inheritance
Why is cancer growth dependent on an increased number of blood vessels? a) All options are correct b) To shield the tumor from immune cells c) To increase the tumor's stability d) To supply the tumor with oxygen and nutrients
Vocab: match the definition or description to the correct pattern of genetics.
Column A
.Show changes in chromosomes such as
Down syndrome
Human skin color and eye color
both traits are fully and separately
expressed
Blending the ingredients of a fruit
smoothie
Column B
a. codominance
b. incomplete dominance
c. polygenic traits
d. multiple alleles
e. pedigree
f. karyotype
Biology
Molecular Basis of Inheritance
Vocab: match the definition or description to the correct pattern of genetics. Column A .Show changes in chromosomes such as Down syndrome Human skin color and eye color both traits are fully and separately expressed Blending the ingredients of a fruit smoothie Column B a. codominance b. incomplete dominance c. polygenic traits d. multiple alleles e. pedigree f. karyotype
Which technique would you use to separate proteins by charge?
a) Size exclusion chromatography
b) PCR
c) Sonication
d) lon exchange chromatography
Biology
Molecular Basis of Inheritance
Which technique would you use to separate proteins by charge? a) Size exclusion chromatography b) PCR c) Sonication d) lon exchange chromatography
What does it usually mean when an actin filament has an ATP cap?
The actin filament has actin covalently bound to ATP via a phosphodiester bond at
the plus end.
The actin filament has additional ATP molecules added onto its actin-ATP units at
the plus end to stabilize the filament and prevent dynamic instability.
The actin filament has additional ATP molecules added onto its actin-ATP units at
the plus end to stabilize the filament and prevent treadmilling.
The actin filament has actin bound to ATP at the plus end.
Biology
Molecular Basis of Inheritance
What does it usually mean when an actin filament has an ATP cap? The actin filament has actin covalently bound to ATP via a phosphodiester bond at the plus end. The actin filament has additional ATP molecules added onto its actin-ATP units at the plus end to stabilize the filament and prevent dynamic instability. The actin filament has additional ATP molecules added onto its actin-ATP units at the plus end to stabilize the filament and prevent treadmilling. The actin filament has actin bound to ATP at the plus end.
Recombination within which type of inversion heterozygote results in a dicentric
chromosome? Why does a dicentric chromosome not form in the other type of inversion
heterozygote. You must explain in enough detail to tell me you know what you're talking about.
Biology
Molecular Basis of Inheritance
Recombination within which type of inversion heterozygote results in a dicentric chromosome? Why does a dicentric chromosome not form in the other type of inversion heterozygote. You must explain in enough detail to tell me you know what you're talking about.
Which statement below about nucleotides is TRUE?
Base pairing occurs between the 5' and 3' carbons of the sugar in a nucleotide.
A deoxynucleotide triphosphate (dNTP) consists of three DNA nucleotides attached together.
In a nucleotide, the base is either deoxyribose (in DNA) or ribose (in RNA).
A nucleotide is composed of a nitrogenous base, a sugar, and a phosphate group.
Biology
Molecular Basis of Inheritance
Which statement below about nucleotides is TRUE? Base pairing occurs between the 5' and 3' carbons of the sugar in a nucleotide. A deoxynucleotide triphosphate (dNTP) consists of three DNA nucleotides attached together. In a nucleotide, the base is either deoxyribose (in DNA) or ribose (in RNA). A nucleotide is composed of a nitrogenous base, a sugar, and a phosphate group.
You are in the lab and you are working with a single neuron (Good job, you neuroscientist!). You expose the dendrites to some neurotransmitters and detect some depolarization in the cell body. However, you observe no action potential. What should you do differently to see an action potential?
Expose the axon hillock to the neurotransmitters.
Get a new neuron. This one is busted.
Increase the concentration of neurotransmitter given.
Add more chloride ions to the extracellular fluid.
Biology
Molecular Basis of Inheritance
You are in the lab and you are working with a single neuron (Good job, you neuroscientist!). You expose the dendrites to some neurotransmitters and detect some depolarization in the cell body. However, you observe no action potential. What should you do differently to see an action potential? Expose the axon hillock to the neurotransmitters. Get a new neuron. This one is busted. Increase the concentration of neurotransmitter given. Add more chloride ions to the extracellular fluid.
Which of the following statements is
correct for a transmembrane protein
being translated by an ER-bound
ribosome?
There must be a nuclear localization
signal.
There must be multiple start-transfer
sequences.
There must be an N-terminal signal
sequence.
There must be an N-terminal or internal
signal sequence.
Biology
Molecular Basis of Inheritance
Which of the following statements is correct for a transmembrane protein being translated by an ER-bound ribosome? There must be a nuclear localization signal. There must be multiple start-transfer sequences. There must be an N-terminal signal sequence. There must be an N-terminal or internal signal sequence.
The Repressor protein...
A. attaches to the operator region and blocks GFP gene transcription
B. is inactivated by the sugar arabinose
C. is activated by the sugar arabinose
D. attaches to the promoter of the GFP gene and blocks transcription
A and B
Biology
Molecular Basis of Inheritance
The Repressor protein... A. attaches to the operator region and blocks GFP gene transcription B. is inactivated by the sugar arabinose C. is activated by the sugar arabinose D. attaches to the promoter of the GFP gene and blocks transcription A and B
Which of the following is known as the "translator molecule"?
ribosome
mRNA
amino acid
tRNA
DNA
Biology
Molecular Basis of Inheritance
Which of the following is known as the "translator molecule"? ribosome mRNA amino acid tRNA DNA
Match the statements in the left with the type of gene transfer in the right.
Gene transfer between cells of different generation
Gene transfer as a plasmid between two Gram-negative bacteria connected though pilus
Gene transfer between two bacteria mediated by a bacteriophage
Gene transfer between two bacteria mediated by naked DNA in solution
Introduction of a plasmid containing the human insulin gene in Escherichia coli
Biology
Molecular Basis of Inheritance
Match the statements in the left with the type of gene transfer in the right. Gene transfer between cells of different generation Gene transfer as a plasmid between two Gram-negative bacteria connected though pilus Gene transfer between two bacteria mediated by a bacteriophage Gene transfer between two bacteria mediated by naked DNA in solution Introduction of a plasmid containing the human insulin gene in Escherichia coli
Recombinant E. coli that contain the plasmid PGLO will only glow in a medium containing...
ampicillin
repressor
GFP gene
arabinose
all of the above
Biology
Molecular Basis of Inheritance
Recombinant E. coli that contain the plasmid PGLO will only glow in a medium containing... ampicillin repressor GFP gene arabinose all of the above
Which of the following statements is FALSE?
a. A prophage is phage DNA inserted into a bacterial chromosome.
b. A prophage can "pop" out of the chromosome.
c. A prophage may result in new properties of the host cell.
d. A prophage is phage RNA inserted into a bacterial chromosome.
Biology
Molecular Basis of Inheritance
Which of the following statements is FALSE? a. A prophage is phage DNA inserted into a bacterial chromosome. b. A prophage can "pop" out of the chromosome. c. A prophage may result in new properties of the host cell. d. A prophage is phage RNA inserted into a bacterial chromosome.
A frame-shift mutation can generate:
A. A non-functional protein
B. A longer mutated protein
C. A shorter protein
D. A mutated protein with a different 3D shape
E. All of the above
I select this option because...
Biology
Molecular Basis of Inheritance
A frame-shift mutation can generate: A. A non-functional protein B. A longer mutated protein C. A shorter protein D. A mutated protein with a different 3D shape E. All of the above I select this option because...
Which one of these statements is correct? Read VERY carefully
A. During transcription, all the DNA molecule is transcribed to one mRNA
B. Ribosomes start translation at the AUG codon in the tRNA
C. Ribosomes always translate all the nucleotides in the mRNA into proteins
D. The mechanism of DNA replication is conservative
E. All these statements are false
Biology
Molecular Basis of Inheritance
Which one of these statements is correct? Read VERY carefully A. During transcription, all the DNA molecule is transcribed to one mRNA B. Ribosomes start translation at the AUG codon in the tRNA C. Ribosomes always translate all the nucleotides in the mRNA into proteins D. The mechanism of DNA replication is conservative E. All these statements are false
If a mutation happens in the DNA that changes the T at base 10 to a C:
a) What would be the mutated sequence of nucleotides in the corresponding codon in the mRNA and the anticodon in the tRNA?
mRNA codon: Changes from__.
tRNA anticodon: Changes from
b) What is the effect of this mutation on the sequence of amino acids in a protein? Be very specific and explain WHY changes or does not change
Biology
Molecular Basis of Inheritance
If a mutation happens in the DNA that changes the T at base 10 to a C: a) What would be the mutated sequence of nucleotides in the corresponding codon in the mRNA and the anticodon in the tRNA? mRNA codon: Changes from__. tRNA anticodon: Changes from b) What is the effect of this mutation on the sequence of amino acids in a protein? Be very specific and explain WHY changes or does not change
What is/are required for the RNA poltmerase to be able to transcribe the 3 inducible enzymes in the Lac Operon?
A. Lactose should be present
B. Glucose should be absent
C. Glucose should be present
A and B
A and C
Biology
Molecular Basis of Inheritance
What is/are required for the RNA poltmerase to be able to transcribe the 3 inducible enzymes in the Lac Operon? A. Lactose should be present B. Glucose should be absent C. Glucose should be present A and B A and C
While in the Inducible Operon the repressor is synthesized already in active form (i.e. ready to bind to the operator), in the Repressible Operon the repressor is synthesized in an inactive form (i.e. unable to bind to the operator unless the "correpresor tryptophan is present too). 
True 
False
Biology
Molecular Basis of Inheritance
While in the Inducible Operon the repressor is synthesized already in active form (i.e. ready to bind to the operator), in the Repressible Operon the repressor is synthesized in an inactive form (i.e. unable to bind to the operator unless the "correpresor tryptophan is present too). True False
Transcription starts at any site on a DNA molecule
 True
 False
Biology
Molecular Basis of Inheritance
Transcription starts at any site on a DNA molecule True False
4. Why the mechanism of DNA synthesis is different between the two strands of DNA?
A Because the genetic code is degenerate
B. Because the strands of DNA are antiparallel
C. Because the strands are antiparallel and DNA polymerase can only synthesize DNA from 5' to 3¹
D. Because the strands are antiparallel and DNA polymerase can only synthesize DNA from 3 to 5'
E. Because DNA replication is semi-conservative
Biology
Molecular Basis of Inheritance
4. Why the mechanism of DNA synthesis is different between the two strands of DNA? A Because the genetic code is degenerate B. Because the strands of DNA are antiparallel C. Because the strands are antiparallel and DNA polymerase can only synthesize DNA from 5' to 3¹ D. Because the strands are antiparallel and DNA polymerase can only synthesize DNA from 3 to 5' E. Because DNA replication is semi-conservative
The anticodon is the 3 nucleotides in the tRNA that bind to the codon (3 nucleotides) in the mRNA
True
False
Biology
Molecular Basis of Inheritance
The anticodon is the 3 nucleotides in the tRNA that bind to the codon (3 nucleotides) in the mRNA True False
Translation ends when ribosomes "read" any of the three nonsense codons on the sequence of the tRNA that is being translated
True
False
Biology
Molecular Basis of Inheritance
Translation ends when ribosomes "read" any of the three nonsense codons on the sequence of the tRNA that is being translated True False
A mutation is a permanent change in the nucleotide sequence of RNA
O True
O False
Biology
Molecular Basis of Inheritance
A mutation is a permanent change in the nucleotide sequence of RNA O True O False
In bacteria, certain mutations result in resistance to antibiotics
O True
O False
Biology
Molecular Basis of Inheritance
In bacteria, certain mutations result in resistance to antibiotics O True O False
There has been an explosion of interest in small noncoding RNAs in plant, animal, and other genomes. Why were these small RNAs not identified and studied in earlier decades?
Biology
Molecular Basis of Inheritance
There has been an explosion of interest in small noncoding RNAs in plant, animal, and other genomes. Why were these small RNAs not identified and studied in earlier decades?
Robertsonian translocations occur between__ chromosomes:
a. Telocentric
b. Submetacentric
c. Metacentric
d. None of the given choices
Biology
Molecular Basis of Inheritance
Robertsonian translocations occur between__ chromosomes: a. Telocentric b. Submetacentric c. Metacentric d. None of the given choices
Is its inheritance sex-linked or autosomal?
The inheritance of the disorder is sex-linked because it is encoded by Y-linked genes.
The inheritance of the disorder is sex-linked because it is seen only in boys.
The inheritance of the disorder is autosomal because sick children are born to apparently unaffected parents.
The inheritance of the disorder cannot be determined as sex-linked or autosomal.
Biology
Molecular Basis of Inheritance
Is its inheritance sex-linked or autosomal? The inheritance of the disorder is sex-linked because it is encoded by Y-linked genes. The inheritance of the disorder is sex-linked because it is seen only in boys. The inheritance of the disorder is autosomal because sick children are born to apparently unaffected parents. The inheritance of the disorder cannot be determined as sex-linked or autosomal.
A plant X is grown under certain conditions and the seeds have been supplied. How would one check for its totipotent character? Critically discuss each step and include diagrams, wherever necessary.
Biology
Molecular Basis of Inheritance
A plant X is grown under certain conditions and the seeds have been supplied. How would one check for its totipotent character? Critically discuss each step and include diagrams, wherever necessary.
Did purified rCptA show the same major band as CptA?
No, rCptA is bigger.
Yes, the size of the major band was unaffected.
No, rCptA is smaller.
Biology
Molecular Basis of Inheritance
Did purified rCptA show the same major band as CptA? No, rCptA is bigger. Yes, the size of the major band was unaffected. No, rCptA is smaller.