ChatGPT_Questions1.0 Flashcards

1
Q

What is the central dogma of molecular biology?

A

DNA → RNA → Protein.

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2
Q

What is the primary goal of genome engineering?

A

To modify the genome to study gene function or for therapeutic purposes.

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3
Q

What are the four major ‘-omics’ disciplines?

A

Genomics, Transcriptomics, Proteomics, and Metabolomics.

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4
Q

What is the Kaplan-Meier plot used for?

A

To visualize the survival rate of a population over time.

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5
Q

What are two main roles of homologous recombination?

A

Meiosis and DNA replication.

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6
Q

What technology replaced microarrays for high-throughput genomic studies?

A

Next-Generation Sequencing (NGS).

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7
Q

What is the advantage of Nanopore sequencing over NGS?

A

It can sequence longer DNA fragments and directly sequence RNA.

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8
Q

Define ‘de novo sequencing.’

A

Sequencing a genome without a reference.

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9
Q

What is the function of CpG island methylation?

A

It typically silences gene expression.

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10
Q

What is SNP, and why is it significant?

A

Single Nucleotide Polymorphism; it represents genetic variation and can affect traits or diseases.

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11
Q

What is the polyA tail used for in RNA sequencing?

A

For selecting mRNA by hybridizing with oligo-dT primers.

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12
Q

What is the difference between nascent RNA and total RNA?

A

Nascent RNA represents newly transcribed RNA, while total RNA includes all RNA types in a cell.

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13
Q

What is the purpose of RNA Pol II inhibition in transcriptomics?

A

To assess transcription dynamics by halting elongation.

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14
Q

How do microRNAs regulate gene expression?

A

By binding to mRNAs, leading to degradation or inhibition of translation.

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15
Q

What is the significance of single-cell RNA sequencing?

A

It allows the analysis of gene expression in individual cells.

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16
Q

What is the primary goal of structural biology?

A

To determine how protein structure influences its function.

17
Q

How do proteins recognize specific DNA sequences?

A

Through interactions with the DNA’s major and minor grooves.

18
Q

What is a Holliday junction?

A

A structure formed during homologous recombination.

19
Q

Why is mass spectrometry crucial in structural biology?

A

To determine protein structure and post-translational modifications.

20
Q

Define ‘interactomics.’

A

The study of protein-protein interactions.

21
Q

What are the two main approaches to knock out a gene?

A

Homologous recombination and CRISPR/Cas9.

22
Q

What is the purpose of site-specific recombination systems like Cre/loxP?

A

To create conditional knockouts or insertions.

23
Q

What is the role of guide RNA in CRISPR/Cas9?

A

It directs Cas9 to the target DNA sequence.

24
Q

What does ‘synthetic genome’ mean?

A

A genome entirely synthesized in vitro using techniques like Gibson Assembly.

25
Q

What is a limitation of CRISPR/Cas9?

A

Off-target effects.

26
Q

Why is proteomics considered more complex than genomics?

A

Proteins have multiple isoforms and post-translational modifications.

27
Q

What is the ‘guilt by association’ principle in interactomics?

A

Proteins interacting with the same partners likely share a function.

28
Q

What is the principle of mass spectrometry?

A

Separation of ions by mass-to-charge ratio.

29
Q

How does SILAC work?

A

It uses stable isotope labeling to compare protein expression levels.

30
Q

What is a ubiquitinome?

A

The set of all ubiquitinated proteins in a cell.

31
Q

What is Gibson Assembly?

A

A method for assembling multiple DNA fragments in one reaction.

32
Q

Why are control experiments critical in ChIP-seq?

A

To distinguish specific DNA-protein interactions from background noise.

33
Q

How is gene function tested using knockout mice?

A

By observing phenotypic changes in the absence of the target gene.

34
Q

What is the advantage of using high-throughput sequencing?

A

It generates large amounts of data quickly and cost-effectively.

35
Q

Define ‘conditional knockout.’

A

Gene inactivation in specific tissues or at specific times.