Cellular Biology II Flashcards

1
Q

What causes wrinkles of aging?

A

Reduced production of collagen and elastin (p.79)

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2
Q

Cellular Biochemistry Questions

A

Answers + First Aid Page Number

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3
Q

What regulates checkpoints between phases of the cell cycle?

A

Cyclins, CDKs, tumor suppressors (p.74)

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4
Q

What is the shortest phase of the cell cycle and what phases are of variable duration?

A

Mitosis is shortest; G0 and G1 are of variable duration (p.74)

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5
Q

What is the order of subphases in Mitosis?

A

Prophase, Metaphase, Anaphase, Telophase (p.74)

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6
Q

What phases of the cell cycle compose Interphase?

A

G1, S, G2 (p.74)

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7
Q

Compare CDKs to Cyclins.

A

CDKs (cyclin dependent kinases) are constitutive and inactive; Cyclins are regulatory proteins that control cell cycle events, are phase specific and activate CDKs; In Cyclin-CDK complexes, both must be either active or inactivated for the cell cycle to progress (p.74)

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8
Q

Name 2 Tumor Suppressors.

A

1.) p53; 2.) hypophosphorylated Rb. Both normally inhibit progression from G1 –> S (p.74)

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9
Q

What is the function of the Rough Endoplasmic Reticulum?

A

Site of synthesis of secretory (exported) proteins and of N-linked oligosaccharide addition to many proteins. Contains free ribosomes where synthesis of cytosolic and organellar proteins occurs (p.74)

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10
Q

What is Rough ER in neurons called and what is its function?

A

Nissl bodies- synthesize enzymes ChAT, Ach, and peptide NTs (p.74)

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11
Q

Name two cell types that are rich in Rough ER.

A

1.) Mucus secreting goblet cells of the small intestine; 2.) Antibody secreting plasma cells (p.74)

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12
Q

What is the function of the Smooth Endoplasmic Reticulum?

A

Site of steroid synthesis and detoxification of drugs and poisons (p.74)

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13
Q

Name two cell types that are rich in smooth ER.

A

1.) Liver hepatocytes; 2.) Steroid hormone producing cells of the adrenal cortex (p.74)

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14
Q

Where does cell trafficking occur?

A

Golgi apparatus is the distribution center for proteins and lipids from the ER to the vesicles and plasma membrane (p.75)

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15
Q

What modification are made in the Golgi apparatus for cell trafficking?

A

1.) Modification of N-oligosaccharides on asparagine; 2.) Addition of O- oligosaccharides on serine and threonine; 3.) Addition of Mannose 6- phosphate to proteins for trafficking to lysosomes (p.75)

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16
Q

What is the function of endosomes in cell trafficking?

A

Sorting centres for material from outside the cell or from the Golgi; sends material to lysosomes for destruction or back to the golgi/ membrane for further use (p.75)

17
Q

What is the pathology of I-Cell Disease?

A

Inherited lysosomal storage disorder. Failure of addition of mannose-6-phosphate to lysosome proteins causes enzymes to be secreted outside the cell instead of targeted to the lysosome (p.75)

18
Q

What is the clinical Presentation of I-Cell Disease?

A

Coarse facial features, clouded corneas, restricted joint movement, high plasma levels of lysosomal enzymes; often fatal in childhood (p.75)

19
Q

Name the three vesicular trafficking proteins and their direction of trafficking.

A

1.) COPI: Golgi –> Golgi (retrograde) OR Golgi –> Endoplasmic Reticulum; 2.) COPII: Golgi –> Golgi (anterograde) OR ER –> Golgi; 3.) Clathrin: trans-Golgi –> lysosomes OR plasma membrane –> endosomes (receptor mediated endocytosis) (p.75)

20
Q

What is a peroxisome?

A

A membrane enclosed organelle involved in catabolism of very long fatty acids and amino acids (p.75)

21
Q

What is a proteosome?

A

A barrel shaped complex that degrades damaged or unnecessary proteins tagged for destruction with ubiquitin (p.75)

22
Q

Describe the structure of a microtubule?

A

Cylindrical structures composed of a helical array of polymerized dimers of a and b-tubulin. Each dimer has 2 GTP bound. Microtubules grow slowly and collapse quickly (p.76)

23
Q

What structures/ functions involve microtubules?

A

They are incorporated into flagella, cilia, mitotic spindles, and are also involved in slow axoplasmic transport in neurons (p.76)

24
Q

Name 2 molecular motor proteins and their direction of transport.

A

1.) Dynein –> retrograde to microtubule (+ –> -); 2.) Kinesin –> anterograde to microtubule (- –> +) (p.76)

25
Q

What is the function of molecular motor proteins?

A

To transport cellular cargo towards opposite ends of microtubule tracks (p.76)