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D1.1 SL DNA Replication

Authored by Nadine Handoyo

Biology

12th Grade

Used 2+ times

D1.1 SL DNA Replication
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21 questions

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1.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What is the primary purpose of DNA replication?

To repair damaged tissues in the body.

To synthesize proteins for cell function.

The primary purpose of DNA replication is to ensure accurate transmission of genetic information to daughter cells.

To produce energy for cellular processes.

Answer explanation

The primary purpose of DNA replication is to ensure accurate transmission of genetic information to daughter cells, allowing for proper cell division and maintenance of genetic continuity.

2.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

Explain the semi-conservative nature of DNA replication.

DNA replication is semi-conservative because each new DNA molecule contains one original strand and one new strand.

Each new DNA molecule consists of two original strands.

DNA replication is conservative, with both strands being newly synthesized.

DNA replication involves the complete breakdown of the original DNA strand.

Answer explanation

DNA replication is semi-conservative because each new DNA molecule contains one original strand and one new strand. This ensures genetic continuity, as half of the original DNA is preserved in each new molecule.

3.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

How does complementary base pairing contribute to DNA replication accuracy?

Complementary base pairing has no effect on DNA replication accuracy.

Complementary base pairing decreases DNA replication accuracy by allowing random base pairing.

Complementary base pairing increases DNA replication accuracy by ensuring specific base pairing and enabling error correction.

Complementary base pairing only affects RNA synthesis, not DNA replication.

Answer explanation

Complementary base pairing increases DNA replication accuracy by ensuring that adenine pairs with thymine and cytosine pairs with guanine, which minimizes errors. Additionally, it allows for error correction mechanisms to fix mismatches.

4.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What role does helicase play in DNA replication?

Helicase synthesizes new DNA strands.

Helicase repairs DNA damage.

Helicase unwinds the DNA strands.

Helicase transports DNA to the nucleus.

Answer explanation

Helicase unwinds the DNA strands by breaking the hydrogen bonds between the base pairs, allowing the replication machinery to access the single strands for synthesis. This is crucial for accurate DNA replication.

5.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

Describe the function of DNA polymerase during DNA replication.

DNA polymerase removes RNA primers from the DNA strand.

DNA polymerase repairs damaged DNA strands.

DNA polymerase unwinds the DNA double helix.

DNA polymerase synthesizes new DNA strands by adding nucleotides complementary to the template strand.

Answer explanation

DNA polymerase is essential for DNA replication as it synthesizes new DNA strands by adding nucleotides that are complementary to the template strand, ensuring accurate duplication of genetic information.

6.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What are the key steps involved in the polymerase chain reaction (PCR)?

Denaturation, Annealing, Extension

Separation, Binding, Synthesis

Initiation, Elongation, Termination

Replication, Transcription, Translation

Answer explanation

The key steps in PCR are Denaturation (separating DNA strands), Annealing (binding primers to the target sequence), and Extension (synthesizing new DNA strands). This process amplifies specific DNA segments effectively.

7.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

How do temperature changes affect the PCR process?

PCR requires a constant temperature throughout the process.

Temperature changes have no effect on PCR.

Temperature changes are essential for denaturation, annealing, and extension in PCR.

Higher temperatures are only needed for the final product stabilization.

Answer explanation

Temperature changes are crucial in PCR as they facilitate the three main steps: denaturation (separating DNA strands), annealing (binding primers), and extension (synthesizing new DNA). Without these changes, PCR cannot occur.

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