Unit 6: Cellular Control Flashcards

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1
Q

How do cells control gene expression, and why is this important in multicellular organisms?

A

Cells control gene expression to produce specific proteins only when needed, conserving resources.
• In multicellular organisms, gene expression differences allow cells with identical DNA to specialize into various types (e.g., muscle or nerve cells).
• Control of gene expression happens at multiple levels: transcriptional, post-transcriptional, translational, and post-translational.

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2
Q

What is transcriptional regulation and how does it affect gene expression?

A

• Transcriptional regulation involves controlling whether a gene is transcribed into mRNA.
• It is primarily controlled by transcription factors that bind to DNA, either promoting or inhibiting the binding of RNA polymerase to initiate transcription.
• This level of regulation is crucial for determining which genes are active in a cell.

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3
Q

What are transcription factors and how do they influence gene transcription?

A

Transcription factors are proteins that bind to specific DNA sequences to control gene transcription.
• Activators increase transcription by aiding RNA polymerase binding.
• Repressors inhibit transcription by blocking RNA polymerase.
• Through these proteins, cells can fine-tune gene expression levels for specific cellular needs.

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4
Q

Define an operon and its components, explaining its role in prokaryotic gene regulation.

A

An operon is a cluster of genes in prokaryotes controlled as a single unit, ensuring efficient regulation.
• Components include:
• Promoter: Site for RNA polymerase binding.
• Operator: Site for repressor binding, controlling access to structural genes.
• Structural Genes: Encode proteins needed for specific cellular functions.
• This coordinated system allows the cell to activate or deactivate multiple genes simultaneously.

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5
Q

Describe the lac operon in E. coli and how it regulates lactose metabolism.

A

The lac operon controls genes (lacZ, lacY, lacA) for lactose processing.
• Without Lactose: The lac repressor binds to the operator, blocking transcription.
• With Lactose: Lactose binds to the repressor, changing its shape so it can’t bind the operator, allowing transcription.
• This regulation conserves energy by producing lactose-metabolizing enzymes only when lactose is present.

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6
Q

Explain the role of the lac repressor and operator in the lac operon.

A

Lac Repressor: A protein that binds to the operator in the lac operon, preventing transcription when lactose is absent.
• Operator: A DNA segment where the repressor binds, controlling access of RNA polymerase to structural genes.
• When lactose is available, it binds to the repressor, causing it to detach from the operator, allowing gene transcription to proceed.

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7
Q

What is post-transcriptional regulation, and how does it modify mRNA?

A

Post-transcriptional regulation occurs after mRNA is synthesized from DNA.
• Modifications include splicing, adding a 5’ cap, a poly-A tail, and mRNA editing.
• These changes can affect mRNA stability, translation efficiency, and the eventual protein product, adding flexibility to gene expression.

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8
Q

What is mRNA splicing, and why is it important in eukaryotic cells?

A

• mRNA Splicing: The process of removing non-coding regions (introns) and joining coding regions (exons) in mRNA.
• Splicing creates mature mRNA that can be translated into protein.
• This allows a single gene to produce different protein products through alternative splicing, increasing protein diversity.

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9
Q

What is mRNA editing and how does it contribute to protein diversity?

A

• mRNA editing involves adding, deleting, or altering specific nucleotides in the mRNA sequence.
• This can change the amino acid sequence of the resulting protein, allowing different protein variants from the same gene.
• mRNA editing enables cells to adapt protein functions without altering the original DNA, enhancing flexibility.

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10
Q

Describe cAMP’s role in gene expression regulation at the post-translational level.

A

• cAMP (cyclic AMP) acts as a secondary messenger that regulates proteins after they are synthesized.
• It binds to and activates protein kinase A (PKA), which then modifies target proteins.
• Through these changes, cAMP influences various cellular processes, including metabolism and gene expression.

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11
Q

Explain how cAMP activates protein kinase A (PKA) and the effects on target proteins.

A

cAMP binds to the regulatory subunits of PKA, causing them to release the catalytic subunits.
• The catalytic subunits become active and phosphorylate target proteins, altering their function.
• Phosphorylation can activate or deactivate enzymes, impacting cellular pathways post-translationally.

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12
Q

Summarize the role of transcriptional, post-transcriptional, and post-translational regulation in controlling gene expression.

A

• Transcriptional: Regulates the initiation of mRNA synthesis via transcription factors and operons (e.g., lac operon in E. coli).
• Post-Transcriptional: Involves mRNA splicing, editing, and stability modifications to control the mRNA’s translation potential.
• Post-Translational: Modifies proteins after translation (e.g., phosphorylation by PKA), adjusting protein function and activity.

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13
Q

Why is multilevel regulation of gene expression important for cellular function?

A

• Multilevel regulation ensures precise control over which proteins are produced, when, and in what amounts.
• It allows cells to adapt to environmental changes, conserve energy, and maintain specific functions based on their type.
• Such regulation is vital for processes like cell differentiation, response to signals, and efficient resource management in both prokaryotic and eukaryotic organisms.

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14
Q

How do some genes control the development of body plans in organisms?

A

Body Plan Genes direct the overall structure of an organism, determining the positioning and shape of body parts.
• Genes like homeobox genes (in animals) and homeotic genes (in plants) play key roles by controlling patterns of development.
• These genes are highly conserved, meaning they are similar across many species, indicating their critical role in body structure formation.

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15
Q

What are homeobox genes and how do they influence development?

A

• Homeobox Genes: A group of regulatory genes with a DNA sequence (homeobox) that encodes transcription factors.
• These transcription factors bind to DNA and activate other genes that control body structure formation during development.
• Homeobox genes are essential for determining the positioning of limbs, organs, and other body parts, ensuring a correct body plan.

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16
Q

What role does apoptosis play in the development of body plans?

A

Apoptosis is programmed cell death, crucial for normal development by removing cells no longer needed.
• It shapes structures (e.g., removing webbing between fingers) and removes damaged or unneeded cells to prevent potential harm.
• During development, apoptosis helps refine body parts by breaking down specific cells, contributing to organism shape and function.

17
Q

Describe the process of apoptosis and the steps involved.

A

Apoptosis is a controlled sequence of events:
1. Cells shrink and their contents break down.
2. DNA and proteins degrade, and the cell membrane starts to bleb (form bubble-like protrusions).
3. Cell components are enclosed in vesicles for phagocytosis (cell “eating”).
• This efficient breakdown prevents inflammation and damage to surrounding tissues, allowing clean removal of unnecessary cells.

18
Q

How does apoptosis help maintain balance in cell populations?

A

Apoptosis controls cell numbers by balancing cell production (mitosis) and cell death.
• Cells die via apoptosis as needed, preventing overgrowth, managing tissue shape, and removing potentially harmful cells.
• It is essential for processes such as immune system regulation, tissue renewal, and embryonic development.

19
Q

Explain the connection between apoptosis and the cell cycle, and how they respond to external stimuli.

A

Genes that regulate apoptosis and cell cycle progression respond to signals like DNA damage or stress.
• When DNA is damaged, cells may initiate apoptosis to prevent the spread of mutations.
• External stimuli, such as infection or cellular stress, can trigger apoptosis as a protective mechanism to eliminate compromised cells.

20
Q

What are mutations and how do they affect DNA?

A

Mutations are changes to the DNA base sequence, altering the genetic code.
• Types include point mutations (change in one base) and frameshift mutations (insertion or deletion, altering reading frame).
• Mutations can occur naturally during DNA replication or from external factors (e.g., radiation, chemicals).

21
Q

What types of mutations can occur, and how do they affect genetic information?

A

Point Mutation: A single base change that may alter one amino acid in the protein.
• Frameshift Mutation: Insertions or deletions shift the reading frame, often changing multiple amino acids and resulting in a dysfunctional protein.
• Silent Mutation: A mutation that does not affect the protein’s amino acid sequence due to redundancy in the genetic code.

22
Q

How can mutations be classified based on their effects on the organism?

A

Mutations can be neutral, beneficial, or harmful.
• Neutral: Have no effect on protein function or organism fitness.
• Beneficial: Improve the organism’s ability to survive or reproduce.
• Harmful: Lead to malfunctions in proteins, potentially causing diseases or developmental issues.

23
Q

What is a neutral mutation, and why doesn’t it impact an organism’s phenotype?

A

Neutral Mutation: A change in DNA that doesn’t alter the protein or affect its function.
• Often occurs in non-coding regions of DNA or involves synonymous codons that produce the same amino acid.
• Neutral mutations do not impact the organism’s traits or fitness, so they are usually silent in the phenotype.

24
Q

Provide an example of a beneficial mutation and how it aids survival.

A

An example is the sickle cell mutation, which provides resistance to malaria in carriers (heterozygous individuals).
• This mutation affects hemoglobin shape in red blood cells, creating an advantage in malaria-endemic areas.
• Beneficial mutations like this one can be naturally selected for, as they increase the organism’s chances of survival in specific environments.

25
Q

What are harmful mutations and how can they lead to disease?

A

Harmful mutations result in dysfunctional proteins, potentially disrupting biological processes.
• Example: Cystic fibrosis caused by mutations in the CFTR gene, leading to defective chloride channels and mucus buildup.
• Such mutations can impair health, lead to genetic diseases, or disrupt normal development.

26
Q

How can mutations influence gene expression and lead to developmental abnormalities?

A

Mutations can impact regulatory regions, affecting when, where, or how much a gene is expressed.
• Misregulation of body plan genes (e.g., homeobox genes) due to mutations can cause malformations or abnormal development patterns.
• For instance, incorrect activation of genes controlling limb formation may lead to duplicated or missing limbs.