Eukaryotic Structure 5 Flashcards

(9 cards)

1
Q

Describe microtubules structure

A

They are hollow tubes.
They are made of 13 protofilaments arranged side by side to form a hollow cylinder.
Made of alpha and beta Tubulin which form heterodimers.
There is a plus and minus end: Beta tubulin is exposed at the plus end, and alpha tubulin at the minus end

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2
Q

What is microtubule dynamic ?

A

The rapid and reversible switching between growth and shrinkage at the plus ends of microtubules

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3
Q

What is MT nucleation ? Describe the process

A

The initiation of a MT.
Microtubule-organising centres (MTOCs), like the centromere in animal cells, are the primary sites of MT nucleation.
1. Y-tubulin binds to the MTOC
2. Y-tubulin ring complex promotes nucleation
3. The plus end of the MT continues to grow

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4
Q

What is MT polymerisation ?

A

The growth of MT that already exist.

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5
Q

Why does MT shrinkage occur ?

A
  1. GTP hydrolysis is faster than addition of new GTP-tubulin dimers so the GTP cap is lost.
  2. Protofilaments containing GDP-tubulin peel away from the microtubule wall
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6
Q

What drugs can affect MT stability ?

A
  1. Taxol- stabilises tubulin in MT lattice so there is no shrinkage. It is a very potent anti-cancer drug.
  2. Colchicine- binds free tubulin dimers, no MT polymerisation
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7
Q

Describe the functions of MT

A
  1. Structural support and cell shape- they provide rigidity
  2. Intracellular transport- help move vesicles throughout the cell eg. Motor protons (kinesin and dynein) bind to MT
  3. Mitotic spindle- formed by MT and attached to kinetichore. Pulls chromatids to opposite ends of the cell.
  4. Motility- MT are the main structural component of cilia and flagella. Organised in a 9+2 arrangement- 9 outer MT pairs and 2 central MT pairs, connected by nexin on the outer pairs
    Dynein movement results in MT of doublets, creating beating motions.
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8
Q

What is the physiological importance of cilia and flagella?

A

Cilia present on cell surface- sense and respond to exterior environment

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9
Q

What are ciliopathies ?

A

Disorders associated with defects in cilia and basal body structure and intraflagellar transport
Eg. Primary ciliary dyskinesia- defects in cilia lining

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