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Notes de cours

LT1-2 Concept of Organelles

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Publié le
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Écrit en
2014/2015

First 2 introduction lectures to the course - what is an organelle, definition of an organelle, information on the nucleus, endoplasmic reticulum, chloroplast, peroxisomes, lysosomes, some non-organelles and a brief note on the evolutionary origin of organelles

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Publié le
6 avril 2016
Fichier mis à jour le
6 avril 2016
Nombre de pages
11
Écrit en
2014/2015
Type
Notes de cours
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Inconnu
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Lecture 1-2: Structural and Functional Compartmentalisation

Definiton of a cell: a long lived structure with an overall function typically
bounded by membrane(s) or phase separated from the surrounding medium in
order to include some specific function and/or exclude other functions

Why compartmentalise?

1) Capacity for complexity
Eukaryotes: Clearly compartmentalised
Prokaryotes: Compartments are less obvious though still present
2) Include/Exclude specific functions

What is an organelle?

 A long-lived sub-cellular structure with an overall function typically
bounded by membrane(s) or phase separated from surrounding cell
 To divide a cell into organelles allows a cell to physically segregate
activities/ environments
 As a concept, it enables biologists to link location to function – allows
simplification (create a model for hypothesis testing and experimentation)


Major Nucleus, secretory pathway
(ER/Golgi/endosomes/lysosomes), mitochondria,
peroxisomes, lipid droplets
Sub-divisions ER, SER, RER, Sarcoplasmic Reticulum
Mitochondria: several sub-compartments, cristae
Lysosomes: lysosome related organelles, melanosomes, lytic
granules, α- granules
Protein Assemblies with Nucleolus, P-body, aggresome, Sec body
contents but without
limiting membranes
Cell-type specific Melanosome, rod outer-segment, elliposime, acrosome
NOT organelles Cytoskeletal elements, ribosome, proteasome (complexes),
argosome, (chromosome)

,  Controls cell activity – contains more than 99.5% of
genetic material (DNA)
 Has many subdomains not separated by membranes
– only the nucleolus can be clearly seen using light
microscopy – others are visualised by
immunofluorescence microscopy
 Nucleus allows protection of DNA and complex gene
regulation
 Nuclei range from 1 -10 micrometres – vary in size and shape

Nuclear Envelope

 Is a double membrane
 Outer membrane is continuous with Rough
ER, conspicuously perforated with nuclear
pores (3000-4000)
 Nuclear pore complexes (NPCs) serve as
channels for the exchange of
macromolecules between the nucleus and
the cytoplasm

Nucleolus (outside of this is the nucleoplasm)

 Manufactures ribosomes using the information in its own DNA
 Area rich in ribosomal RNA, ribosomal proteins (imported from cytoplasm)
 Usually 1-2 in a nucleus
 Shapes and presence are different
depending on organism/condition –
yeast cells can destroy its nucleolus
in adverse conditions
 Nucleolus only present if ribosomal
units are being produced – disappears
if rRNA transcription is inhibited
 tRNA genes (clustered around nucleoli) also transcribed here, as well as
processing

,Chromatin

 Coils of DNA bound to proteins – they occupy specifc domains
 Cell division: chromatin aggregates to form chromosomes
 Heterochromatin (found near periphery) and euchromatin – chromsomes
within the nucleus are arranged spatially and do not intertwine
 Telomeres are anchored to the nuclear envelope – likely to avoid
entanglement
 Areas chromatin-free are interchromosomal domains
 Genes adjacent to interchromosomal domains vary depending on cell type
– in situ hybridisation and other techniques allow the location of
transcripts to be identified in the nucleus – facilitates the diffusion of
abundant mRNAs to NPCs
 Genes abundantly transcribed placed close to NPCs

*Diffusion in the cytoplasm is a slow process (slower than water) – around 1s

Nuclear Bodies

 Other smaller subcompartments of the nucleus, believed to increase
biological efficiency of certain processes by concentrating
macromolecules
 RNA splicing factors: arranged spatially in speckles – concentration of
splicing factors
 Cajal/colied body: contain protein coilin , small nucleolar RNAs (snoRNA),
small nuclear RNAs (snRNA) – thought to be sites of post-transcriptional
RNA modification
 Gemini Body (GEM): not found in all cells but share some components of
Cajal bodies
 PML bodies: function unknown – has proteins that recruit other proteins

, Structure and Function
 Embedded into cytoplasm
 Wall: two thin membranes – finger like
cristae that project into the matrix
 Site of cellular (aerobic) respiration
- Cristae : LARGE S/A – more work done,
more energy released, more efficient
- Stalked particles – ATP made
- Enzymes in matrix: final stages of
respiration = glucose to CO2 and H2O
- Ribosomes and loops of DNA allow the
mitochondria to replicate themselves when the cell divides, so daughter
cells will have enough

Cristae

 Cristae form a complex three
dimensional network – attempts
to map out cristae in 3D
achieved through tomography
of mitochondria in chick
cerebellum
 The mitochondrial site is
complex – there are new views of how the network/mitochondrial
architecture is exactly arranged
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