Unit 4 objectives Flashcards

(30 cards)

1
Q

o Draw and explain GPCRs, including how they function and what they do

A

Steps:
1. Ligand binds to receptor, conformational change
2. G alpha subunit replaces GDP with GTP
3. G alpha moves from G beta/gamma to effector, activating it.
4. Activated effector makes cAMP
5. GTPase hydrolyzes GTP, deactivating G alpha
6. G Alpha associates with G beta gamma, deactivating effector.
7. Receptor phosphorylated with G protein
8. Receptor bound to arrestin, deactivates receptor and marks it to be destroyed

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2
Q

o Draw and explain RTKs, including how they function and what they do

A

translate the presence of extracellular messenger molecules into changes inside the cell by receptor dimerization followed by activation of the receptor’s protein-kinase domain. phosphorylate specific tyrosine residues of cytoplasmic substrate proteins, turning them on/off

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3
Q

o How does signal transmission happen in cells?

A

Cells use extracellular messaging molecules, which signal to nearby cells. Autocrine cells make molecules for themselves to respond to. Paracrine molecules travel short distances. Endocrine molecules travel through the bloodstream

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4
Q

o What is the purpose of adenylate cyclase? What second messenger is made and why is
it significant?

A

Signal amplifier, cAMP. Interacts with the proteins adenylate cyclase tries to amplify and regulates their activity

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5
Q

o What is the purpose of phospholipase C? What second messenger is made and why is it
significant?
* Link the previous material into signal transduction/mitosis.

A

Receptor and secretor- cAMP, regulates activity of phospholipase C. (ADD MORE DETAIL)

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6
Q

o Apoptosis signaling? Extrinsic vs. intrinsic?

A

Programmed cell death. Extrinsic- tumor necrosis factor sends external signal
Intrinsic-Bax/Bak are released into cell, destroying it

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7
Q

o Explain how piwi-RNAs differ from other RNAs

A

Move transposons

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8
Q

o How does the proteasome fit into controlling the cell cycle?

A

Degrades proteins that control cell divisions

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9
Q

o How does chromosome condensation happen?

A

Interphase chromatin turns into thread like structures as DNA wraps around histones. Condensins come in and promote supercoiling. H3 histone marks for condensation.

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10
Q

▪ Draw out/Explain the structure of condensin, including their
functionalities

A

Condensin pulls DNA into loops, causing positive supercoiling and condensing it. Structure with smc4/2, 2 dimers wrapped around each other

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11
Q

▪ Describe and explain the difference between glucagon and insulin pathways

A

Both + regulated. Insulin acts theough receptor protein tyrosine kinase. Ligand binding pocket for both receptors is different. **

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12
Q

▪ Explain the Ras-MAP kinase cascade. What is the purpose of GEFs?

A

Controls cell proliferation and differentiation. Growth factor binds to EC domain of RTK. End path turns on GEF, which activates small GTPases

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13
Q
  • Explain the difference between first and second messengers in signaling pathways.
A

A substance that is formed in the cell as the result of the binding of a first messenger—a hormone or other ligand—to a receptor at the outer surface of the cell

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14
Q

▪ Draw out/Explain the structure of cohesin, including their
functionalities

A

Hold sister chromatids together through G2. Cleavage causes separation of sister chromatids and starts anaphase. SMC 1/3 holdsit together, 2 dimers wrapped around each other

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15
Q

S phase

A

DNA replication and chromosome duplication

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16
Q

G1

A

Normal metabolism, organelle duplication

17
Q

G2

A

Cell grows and prepares for mitosis

18
Q

Prophase

A

the duplicated chromosomes are prepared for segregation and the mitotic machinery is assembled.

19
Q

Metaphase

A

chromosomes have become aligned at the spindle equator, with one chromatid of each chromosome connected to one pole and its sister chromatid connected to the opposite pole

20
Q

Anaphase

A

sister chromatids separate from one another

21
Q

Prometaphase

A

mitotic spindle is formed and the chromosomes are moved into position at the center of the cell

22
Q

Telophase

A

daughter cells return to the interphase condition: the mitotic spindle disassembles, the nuclear envelope reforms, and the chromosomes become more and more dispersed until they disappear from view under the microscope

23
Q

Cytokinesis

A

physical division of the cell into two daughter cells occurs

24
Q

o RB –

A

regulates cell cycle, G1 to S checkpoint

24
o p53 –
transcription factor, can halt cell cycle and initiate apoptosis. Involved with many other proteins
25
* Explain and describe the two main categories of genes that are commonly mutated in cancers: o Proto-oncogenes
Genes that could become cancerous- involve normal cell processes
26
o Tumor-suppressor genes
Genes that regulate cell growth and division
27
* Describe or draw the nuclear pore complex
Donut shaped structure with nucleoporins that allow stuff in and out. Central scaffold allows stuff in, FG domain in channel. Nuclear ring and basket allow stuff in nucloplasm
28
o What determines which RNAs and proteins can move through the NPC?
Whether or not they have a nuclear localization sequence
29
o What determines the directionality of movement?
Whether importins or exportins interact with them