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CRISPR technology development Trivia Questions

How much do you really know about CRISPR technology development? Below are 8 true or false statements. Click each one to reveal the answer and explanation.

1.

Jennifer Doudna and Emmanuelle Charpentier won the Nobel Prize in Chemistry for CRISPR in 2020.

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Easy
✓ TRUE

They received the 2020 Nobel Prize for developing the CRISPR-Cas9 gene-editing method, a revolutionary breakthrough.

2.

CRISPR technology was inspired by how bacteria store viral DNA for future defense.

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Easy
✓ TRUE

Bacteria capture viral DNA snippets into CRISPR arrays, using them like a genetic memory to guide Cas enzymes against reinfection.

3.

CRISPR was first discovered as a bacterial immune system in E. coli in 1987.

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Medium
✗ FALSE

CRISPR repeats were first observed in 1987 by Yoshizumi Ishino, but their function as a bacterial immune system was only identified years later. Thus, the statement falsely attributes the immune system discovery to 1987.

4.

CRISPR-Cas9 was originally adapted from a fungal genome editing system.

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Medium
✗ FALSE

CRISPR-Cas9 comes from a bacterial immune system (Streptococcus pyogenes), not a fungal system.

5.

CRISPR always creates permanent changes to the genome that cannot be reversed.

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Medium
✗ FALSE

CRISPR includes non-cutting versions like CRISPRi (temporary gene silencing) and epigenetic editors (reversible modifications), so it does not always create permanent, irreversible changes.

6.

The first human CRISPR trial targeted sickle cell disease using fetal hemoglobin reactivation.

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Hard
✗ FALSE

The first human CRISPR trial was in 2016 for lung cancer, not sickle cell disease. The sickle cell trial using fetal hemoglobin reactivation began later, in 2019.

7.

The first CRISPR-based COVID-19 diagnostic test was approved in the U.S. in 2020.

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Hard
✓ TRUE

Sherlock Biosciences’ CRISPR-based test received FDA emergency use authorization in May 2020 for rapid SARS-CoV-2 detection.

8.

CRISPR can only edit DNA, not RNA, in any living cell.

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Hard
✗ FALSE

CRISPR systems like Cas13 can target and edit RNA, enabling applications like viral RNA degradation without altering DNA.

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