Eukaryotes Flashcards

(47 cards)

1
Q

Why is cell size limited in eukaryotes

A

SA/vol ratio
Diffusion rates of molecules (partly determined by particle size)
The need for high concentrations of compounds and enzymes for reactions

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2
Q

What is the use of compartmentalisation of eukaryotic cells

A

Compartmentalisation = processes localised and concentrated
Subdivide into membrane bound compartments (organelles)
Need for active and organised transport system (cell signalling, cytoskeleton etc)

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3
Q

Use of differentiated eukaryotic cells

A

Compartmentalisation = specialisation of specific tasks
Important for multicellular organisms
May have random mutation during development

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4
Q

stem cells in eukaryotes

A

Can become anything
Regulated by intra/extracellular signals (biotic and abiotic)
In both plants and animals

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5
Q

What are the 3 ways to study organelles

A
  • drawings
  • fluorescence microscopy (tag organelle with fluorescent protein)
  • electron microscopy (fix cell and cut slices then stain with OsO4
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6
Q

Describe transport/secretory vesicles

A

Membrane bound
Contains proteins for transport/export
Only secretory if actually being secreted
Trafficked along cytoskeleton

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7
Q

Describe lysosomes

A

Storage for enzymes that break up cellular components
Contain at least 50 hydrologic enzymes
Can break down almost any biological molecule so must remain separated
Degradation of organelles via autophagy = organelles delivered to lysosomes for degradation
A lot of diseases related to misfunction of lysosomes

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8
Q

Describe peroxisomes

A

Assist lysosomes in cell clean up
Generate and degrade hydrogen peroxide
Breakdown fatty acids/lipid components of membranes
Detoxify harmful compounds

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9
Q

Describe centrosome

A

Very different between plants and animals
Important in cell division
Taxol (form of trees) important in cancer treatment: Causes binding of centrosomes and microtubules

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10
Q

Describe cytoskeleton

A
Frame work: shape and structure 
Forms basis of internal transport 
Cellular movement 
Contraction of skeletal muscle 
Made of microtubules, microfilaments, intermediate filaments and Actin
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11
Q

Describe microtubules

A

Monomers that polymerise
Very hard to see in electron microscope - if used fluorescence whole cell glows
Organised in bundles
Constantly built (polymerisation end) and broken down (depolymerisation end)

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12
Q

Describe actin

A

Influence locomotion and movement

Major cytoskeleton component of muscle cells

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13
Q

Describe nuclear pores

A

30 different proteins used to make a pore
- proteins made in cytosol
Outer diameter 120nm
Fusion of inner and outer membrane
Small particles injected into the cell can directly enter the nucleus: channels freely permeable to ions and small molecules

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14
Q

Describe proteins used for nucleus pores

A

Made in the cytosol
Contains NLS: nuclear localisation signal (specific amino acids sequence)
NLS recognised by receptor protein called importin they bind and regulate transport through pore
She’s ATP delivered by RAN-GTPase

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15
Q

Describe how RNA leaves the nucleus

A

Transported through a nuclear pore into cytosol
Binds to protein containing nuclear export signal (NES)
NES recognised by exportin receptor protein
Exportin transports them through the pore

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16
Q

Describe the nuclear matrix

A

Genetic information located there
Each chromosome has its own discrete location
Maintains shape of nucleus: made of insoluble network fibrous proteins Called Latins
- line the inner membrane
-provides mechanical strength
Newly synthesised nucleic acids associate with the matrix

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17
Q

Describe the nucleolus

A

Dedicated for ribosome production
1+ spherical structures, several micrometers in diameter
Number and size corresponds to level of protein synthesis

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18
Q

What are the functions of the smooth endoplasmic reticulum

A
Drug detoxification 
Carbohydrate metabolism 
-hepatocytes break down stored glycogen
Calcium storage 
- sarcoplasmic reticulum in muscle cells 
-released in response to extracellular signalling fr muscle contraction 
Steroid biosynthesis 
- adrenal glands, testes, ovaries 
- cholesterol and steroid based hormones
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19
Q

What are the 3 types of endoplasmic reticulum

A

Rough
Smooth
Transitional (exit site of proteins leaving rough ER)

20
Q

How do vesicles move along the cytoskeleton

A

Via active transport
Microtubules = long range transport
Actin = short range
Adaptor (attachment) and motor (walking) proteins use them to move along.

21
Q

What are the 3 regions if the golgi

A

Cis

  • contains golgi network and cis cisternae
  • receives proteins from ER and acts as sorting station

Medial
-cisternae

Trans
- golgi network and trans cisternae

22
Q

What are the 2 methods of how the Golgi body turn vesicles into secretory vesicles

A

Vesicular transport theory

Cisternal maturation theory

23
Q

Describe vesicular transport theory

A

Vesicles enter from bottom to top (cis to trans)
Resident enzymes stay in cisternae
Proteins are moved between the cisternae

24
Q

Describe cisternal maturation theory

A

Currently favoured theory
- cis cisternae mature into trans cisternae and new cis created from fusion of vesicles at cis face
Enzymes move from trans down to cis

25
How do golgi differ in plants from animals
``` Animals = few large Golgi localised around nucleus Plants = loads of small golgi ```
26
What is anterograde transport of vesicles
Forward pathway of vesicles for secretion
27
What is retrograde transport
Vesicles released in opposite direction | Vesicles fo back to endoplasmic reticulum and eventually the cytosol
28
Why do mitochondria have such elaborate structures?
- is the site of aerobic respiration Glucose + oxygen = carbon dioxide and water (ATP synthesised) Needed for the oxidation of glucose = proton gradient, pumps protons into intercellular space and drives ATP synthesis
29
Describe mitochondrial matrix
Contains enzymes, DNA and ribosomes and other enzymes encoded in the nucleus and imported
30
What does mitochondrial DNA code for
RRNA TRNA Inner membrane proteins
31
Describe mitochondrial Cristae
Used to increase SA (inner 5 : outer 1) Can accommodate large number of protein complexes Number of mitochondria and number of Cristae ~ activity of cells
32
Describe mitochondria inner membrane
Permeability barrier to most solutes | Partitions the mitochondria into 2 components: creates inter membrane space
33
Describe mitochondrial outermembrane
No significant permeability barrier | Contains trans membrane channel proteins called porins
34
Describe endocytosis
Imports extracellular material Uses cell/tissue specific receptors localised in plasma membrane (isn’t passive) Protein will be complementary = bind and form complex which creates coat proteins that make coat complex on inside of the cell When complex made membrane will invaginate and create vesicle: inside is coated pit
35
Describe endosomes
Endocytic vesicles fuse to create early endosome then fuse again to create late endosome During process PH decreases: due to degrading enzymes from golgi Endosomes create lysosomes and vesicles produced by golgi contains lysosomal proteins then leave the cell via exocytosis Transport material to golgi, lysosome or vacuole (plants)
36
Describe exosomes
Extracellular vesicles Formed from cell membrane Components enter from cytoplasm and binds back with membrane then releases components out of cell Play large role in cell-cell signalling
37
What are the roles of microtubules
1. Organisation of cell shape and polarity 2. Intracellular transport of vesicles and organelles 3. Chromosome movements
38
What are the microtubules subunits and how do they form microtubules
Alpha - tubulin Beta - tubular Together they form tubulin dimer Tubulin dimers form Oligomers and then protofilaments - sheet of protofilaments form a microtubule
39
How do microtubules grow
They exam and from the plus end and also break down from the plus end
40
Describe motor proteins
Kinesin = moves towards plus end Dynein = moves towards the negative end Energy dependent process
41
What are the subunits of microfilaments
Subunits = g-actin monomer
42
What are the functions of microfilaments
``` Cell locomotion Cytokinesis Muscle contraction Maintenance of cell shape Intracellular transport ```
43
Describe polymerisation of microfilaments
G actin builds up and creates filamentous actin (f actin) | Can become many different types of proteins
44
Describe depolymerisation of microfilaments
``` Depolymerises from the pointed end of the actin filaments Capping proteins bind to actin filaments = barbed end and prevents filament assembly Protrusion filpodium (protrusions created by actin bundles) prevented ```
45
Describe the movement of actin
Extension at the front Adhesion Translocation via contraction at the back De-adhesion of back section
46
What are functions of intermediate filaments and its subunits
``` Subunit: dimers Functions: -structural support -maintenance of cell shape - nuclear lamina ```
47
How does the intermediate filament subunits build up
Becomes tetramer then protofilaments then filament