Exam 1 review Flashcards

1
Q

An insertion mutation added two nucleotides to a gene’s ORF causing a frameshift that alters the amino acid sequence and causes a complete functional loss. What mechanism(s) is(are) capable of restoring function to the gene product?

A

Second-site reversion, true reversion and back mutation

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2
Q

protein can serve as a template for RNA synthesis

A

Flase

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3
Q

Holiday Junction resolution can produce different patterns of recombinant and/or parental chromatids. Which type of Holiday Junction resolution (vertical or horizontal) would account for diagram B ?

A

Vertical

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4
Q

Which feature of higher eukaryote (would include humans) increases the diversity of peptide products produced from its genome?

A

RNA processing

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5
Q

An enzyme that cleaves a polynucleotide chain somewhere in the middle without sequence requirement is:

A

an endonuclease

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6
Q

Transcription in a bacterium occurs in the nucleus

A

False

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7
Q

The components of a nucleotide are:

A

a nitrogenous base, a pentose sugar and a phosphate group and a nucleoside and phosphate group

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8
Q

A mutation in a gene’s sequence that prevents its ability to be transcribed is acting in trans.

A

False

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9
Q

A reading frame that has frequent termination codons is called an “alternative reading frame”

A

False

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10
Q

Nitrogenous bases are at the ends of a polynucleotide chain.

A

False

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11
Q

A mutation in a coding gene causes the protein product to prematurely terminate translation by changing a single nucleotide so that a stop codon is generated. This type of mutation is an example of a(an):

A

nonsense mutation

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12
Q

The 3’ to 5’ phosphate linkage is an example of a (an):

A

covalent bond

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13
Q

A missense mutation results in an amino acid substitution in the peptide product.

A

True

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14
Q

DNA polymerase adds nucleotides to the 3’ end of a polynucleotide chain.

A

True

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15
Q

A mutant phenotype is observed in 1/4 of the offspring from a breeding pair of phenotypically wildtype toads. We can deduce that:

A

The parents are heterozygous for the phenotype causing allele, and the trait is recessive.

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16
Q

The Belgium Blue Bull is the result of a single gene disruption. Which statements are false about the mutation or gene product?

A

The mutation is gain-of-function affecting the myostatin gene, and Myostatin functions normally in the mutant.

17
Q

A and T pair with two hydrogen bonds whereas G and C base pair with three hydrogen bonds.

18
Q

Mutant alleles in the same cistron must have the same sequence.

19
Q

Which types of mutation will definitely cause a change in the peptide sequence of a gene product?

A

frameshift mutation in the coding sequence, missense mutation, and indel in the coding sequence

20
Q

What genomic features can affect a DNA fingerprint?

A

Indels, Transition mutations, Presence of repetitive DNA sequence, Single nucleotide polymorphisms, and Absence of repetitive DNA sequence

21
Q

Which diagram and proposed cleavage sites (dotted line(s)) would produce four recombinant strands in the resulting chromatids?

A. vertical B. Horizontal

22
Q

A mutation that changes the sequence from ATCTGCTGA to ATCTCTGA is an example of:

23
Q

In a hypothetical situation a gene is mutated by the insertion of 11 nucleotides in the open reading frame. A subsequent mutation deletes the 11 nucleotides inserted in the first mutation. Therefore, the second mutation is an example of a(an):

A

true reversion

24
Q

Alternative splicing is most common in simple eukaryotes like yeast.

25
A paternal allele and maternal allele are part of different cistrons, therefore if an animal that is homozygous for the paternal allele is breed with an animal homozygous for the maternal allele the outcome would be:
Complementation
26
In eukaryotes, what is true about mature mRNA?
introns have been spliced out
27
DNA from the nucleus of a frog embryo was isolated and biochemical analysis showed that 26% of nucleotide bases were guanine what proportions of other bases would you expect to find?
26% Cytosine; 24% Adenine; 24% Thymine
28
A geneticist working with mice isolated several mutant mice that exhibited a grey coat color instead of the wildtype white coat. When a grey mouse was breed with a white mouse all of the offspring were grey. What does this tell us about the mutation that is causing the grey coat?
The grey coat is a product of a dominant mutation.