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41. The non-template strand of a gene is also frequently referred to in molecular biology as the

A. Antisense strand
B. Coding or sense strand
C. Primer strand
D. Okazaki fragment

The non-template strand matches the mRNA transcript sequence exactly (except that DNA has T where RNA has U), earning it the name "coding strand."

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The nucleosome is the primary structural unit of chromatin, packing a 147-base-pair segment of DNA around a histone octamer core.

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39. The occurrence of a mutation where a single nucleotide is inserted or deleted within the coding region of a gene leads to a

A. Missense mutation
B. Frameshift mutation
C. Silent mutation
D. Transversion mutation

Inserting or deleting a base shifts the triplet reading frame downstream, completely altering the remaining amino acid sequence.

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38. The chemical reason why the DNA molecule behaves fundamentally as an acid in cellular solutions is the presence of

A. Alkaline purine rings
B. Highly ionized phosphate groups in the backbone
C. Hydroxyl groups on the deoxyribose sugars
D. Volatile hydrogen bonds between the strands

Each phosphate group in the backbone retains a negative charge at physiological pH by releasing a hydrogen ion (H+), acting as an acid.

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By convention, the coding strand is written 5' to 3' because the ribosome reads mRNA 5' to 3' to build a protein from its N- to C-terminus.

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The B-DNA helix has a pitch of 3.4 nm and a base-pair step of 0.34 nm, accommodating roughly 10 base pairs per full turn.

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Exons are the coding segments of a gene that remain in the mature mRNA transcript after splicing, carrying the blueprint for translation.

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34. The chemical link that anchors a nitrogenous base to the 1′ carbon of the deoxyribose sugar ring is an

A. N-glycosidic bond
B. Phosphodiester bond
C. Peptide bond
D. Anhydride bond

An N-glycosidic bond connects the 1' carbon of the pentose sugar to the nitrogen atom at position 1 in pyrimidines or position 9 in purines.

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Pleiotropy happens when a single gene codes for a protein used in multiple tissues, meaning a mutation can cause widespread symptoms.

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32. The physical explanation for why the two strands of a DNA molecule can separate easily during replication and transcription is that

A. The backbones are made of weak ionic bonds
B. The strands are held together horizontally by weak hydrogen bonds
C. The molecule is wrapped tightly around nuclear lipids
D. Enzymes cut the covalent bonds of the sugar rings

Hydrogen bonds are weak non-covalent interactions, allowing the twin strands to unzip easily when driven by specialized enzymes.

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31. The dynamic process where a single point mutation within a gene changes a codon to specify a different amino acid is termed a

A. Nonsense mutation
B. Missense mutation
C. Silent mutation
D. Frameshift mutation

A missense mutation alters a single nucleotide, changing a codon so that it incorporates a different amino acid into the protein.

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The promoter is a specific upstream nucleotide sequence that signals the transcription machinery where to start making RNA.

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29. The structural layout where the hydrophilic sugar-phosphate backbones face the outside and the hydrophobic bases face the inside shows that DNA is

A. Soluble and stable in the aqueous nuclear environment
B. Insoluble in water and restricted to lipid membranes
C. Unstable and prone to spontaneous breakdown
D. Highly acidic throughout its inner core

Placing the charged, polar groups on the outside allows DNA to interact favorably with the watery environment of the nucleoplasm.

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28. The molecular feature that prevents the human gene for insulin from being translated accurately inside a bacterial cell without prior modification is the

A. Difference in the universal genetic code
B. Presence of introns within the human genomic DNA sequence
C. Inability of bacteria to form peptide bonds
D. Complete absence of ribosomes in prokaryotes

Human genes contain introns, which bacteria cannot slice out because they lack spliceosomes, leading to a flawed, non-functional protein.

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27. The presence of a hydroxyl group (-OH) exclusively at the 3′ carbon of the deoxyribose sugar is functionally vital during DNA replication because it

A. Acts as the mandatory nucleophile required to attach the next incoming nucleotide
B. Binds directly to the nitrogenous base of the opposing strand
C. Stabilizes the major groove of the double helix
D. Triggers the destruction of the template strand

DNA polymerases require a free 3'-OH group to form a phosphodiester bond with the 5' phosphate group of an incoming dNTP.

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Transcription generates an RNA transcript that is complementary and anti-parallel to the DNA template strand, swapping thymine for uracil.

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Introns are intervening, non-translated sequences within a gene that are transcribed into pre-mRNA but removed by splicing.

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24. An increase in the collective ratio of G-C base pairs relative to A-T base pairs within a DNA fragment results in

A. A lower melting temperature (Tm​) due to weak bonds
B. A higher melting temperature (Tm​) due to triple hydrogen bonding
C. Spontaneous conversion of the helix into a linear RNA molecule
D. The immediate exclusion of all histone proteins

G-C pairs are linked by three hydrogen bonds, which require more thermal energy to disrupt than the two hydrogen bonds holding A-T pairs together.

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23. The average distance separating two adjacent, vertically stacked nucleotide base pairs in the B-DNA model is

A. 3.4 nanometers
B. 0.34 nanometers
C. 2.0 nanometers
D. 0.11 nanometers

With 10 base pairs per complete helical turn of 3.4 nm, the step distance between consecutive base pairs is 3.4/10=0.34 nm.

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