Cell Bio Flashcards

1
Q

Components of intercellular signaling systems

A

Ligands
Receptors
Secondary Messengers
Signal Transduction
Inactivation methods
Coupling

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2
Q

4 major classes of signal transduction networks

A
  1. cascade of protein phosphorylation reactions
  2. G-protein coupled reactions
  3. Facilitated transport w/ Ach receptors
  4. Diffusing across membrane by lipid derivatives
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3
Q

Explain Signal transduction involveing a cascade of protein phosphorylation reactions

A

Protein kinase enzymes can be activated here by phosphorylation

Then later activate downstream kinases

Amplification pathways

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4
Q

Explain g-protein coupled reactions

A

Odorant ligands connecting to G Protein Coupled receptor (GPCR) - which connects to a G protein which connects to an enzyme that turns ATP to cAMP (a second messenger) that causes a Na/Ca and Cl gradient channels to open to depolarize the membrane to relay message to the brain

Ligand -> receptor -> protein -> another protein (enzyme) -> channels opening and message being relayed

Hydrolysis of cAMP inactivated pathway

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5
Q

Explain facilitated transport w/ Ach receptors for signal transduction

A

Muscle contraction - receptors also acting as channels - responding to Ach in the environment

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6
Q

explain signal transduction of lipid derivatives

A

Estrogen can get into the cell AND into the nucleus no help needed where it bonds to a receptor on the DNA

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7
Q

Shared features of sensing/signaling pathways

A

• selective recognition of the arriving signal
– formation of a Receptor/Signal complex
• signal amplification
– Production of soluble, intracellular “second messengers”
– Reversible protein phosphorylation as a means of signal transduction
• Appropriate nature and duration of response
– Does the biochemical response fit the biological one?
– Similarities and differences short- vs. long-term responses
• Graded nature of response
– Greater amount/duration of stimulus -» greater magnitude of response
• Mechanisms of control
– Feedback (+/-)
– Desensitization, re-sensitization

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8
Q

classic second messenger

A

cAMP

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9
Q

Recognize the central role of protein phosphorylation in signal transduction

A

Phosphorylation is the addition of a phosphoryl (PO3) group to a molecule. In biological systems, this reaction is vital for the cellular storage and transfer of free energy using energy carrier molecules.

Protein phosphorylation is when a channel protein on the membrane of the cell gets a phosphate group from ATP (turning it into ADP)

After the land connects with the receptor it alerts the second messengers which are protein kinases who talk to other protein kinases

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10
Q

Explain the types of feedback and control mechanisms operative in representative signaling systems

A

Most common is negative feedback

Interconversion of metabolites in a series of enzymatic reactions

Returning the cell back to normal by hydrolysis is a negative feedback mechanism

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11
Q

Plasma membrane refresher

A

Forms a solubility/permeability barrier

• Opportunity for establishment of concentration gradients
(source of potential energy)

• Site of sensors (receptor proteins) to monitor extracellular environment

• Provides mechanism for selective entry

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12
Q

What is the central dogma of molecular biology

A

DNA -> RNA -> protein

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13
Q

DNA to RNA is called

A

transcription (nucleotide base-pairing)

-uses RNA polymerase

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14
Q

RNA to protein is called

A

translation (3 nucleotide units code for amino acids)

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15
Q

Describe the mechanisms by which information encoded in DNA can be replicated during cell division or accessed during regulated gene expression. (3)

A

Gene expression can be regulated by transcription factors
-Proteins that bind to DNA promoter regions to prevent/ allow transcription to occur

RNA polymerase - creating RNA polymer from DNA strand during transcription

Through the cell cycle and mitosis

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16
Q

cell cycle steps

A

Mitosis -> interphase repeat

interphase = G1 (gap 1) -> S phase (DNA Synthesis) -> G2 (gap 2)

G0 can split from g1 where cells stop dividing

17
Q

Gap 1 of mitosis

A

growing in size and accumulation of ATP

18
Q

S phase of mitosis

A

chromosomes are replicated and transcription ceases

19
Q

Gap 2 of mitosis

A

ATP restored to prepare for distribution of chromosomes and organelles

Regulation of interphase is important
Things can go wrong and mechanisms are in place to stop it

20
Q

Identify the cell death pathways that prevent propagation of damaged chromosomes

A

Cell death is essential

Response to UV radiation, chemical agents, etc

Orderly dismantling of critical cell survival components
-Seperate from necrosis
-Cell death from disordered lysis- happens during inflammatory responses

21
Q

Describe the function of cell cycle checkpoints

A

Mechanism to maintain genomic integrity
Monitor/surveil for damage and to attempt repair if possible
M-phase checkpoints

22
Q

Describe the requirements for effective repair of errors and the consequences of ineffective repair

A

DNA damage is detected by sensors (pathways in the nucleus)

Transducer cells communicate with effectors that lead to
-DNA repair
-Cell cycle arrest
-Transcription of damage-responsive genes
-Apoptosis (regulated cell death)
If these mechanisms fail it can lead to persistence of mutations
-Genomic instability
-Birth defects, genetic diseases, notably cancer

23
Q

Recognize the types of mechanisms that control progression through the Cell Cycle

A

Landmark phases of the cell cycle are controlled by protein complexes
-Cyclins
-Cyclin-dependent protein kinases (Cdk)
= Both are regulated by phosphorylation interaction
Fidelity and timing of the process are closely monitored

24
Q

transcription can be activated by …

A

signal transduction pathways involving ligands and receptors at the surface

25
Q

Steps of mitosis

A

prophase -> metaphase -> anaphase -> telophase

26
Q

Regulation of gene expression and mitosis (including entry into or progression through the cell cycle) occur by

A

mechanisms similar to those in other signaling pathways

Amplification cascades involving reversible protein phosphorylation, formation of multi-subunit complexes, negative feedback

27
Q

Transcriptional errors

A

during transcription gene expression can be altered by timing, magnitude of transcription rate, and the fidelity of base pairing

RNA Polymerase can detect and repair mismatches , but consequences can range if they are not fixed

28
Q

M-phase checkpoints

A

certain mutations in proteins controlling m-phase of mitosis can allow it to fail a checkpoint
(causes +/- chromosomes or cancer)

spindle checkpoints
-detect failure of spindle fibers attachment in metaphase
-will trigger apoptosis is damage is not fixed