Lecture 3: Basic Molecular Cell Biology 1 Flashcards

1
Q

a stem cell is a (relatively) primitive cell that is capable of:

A
  • Self-renewal: making a copy of oneself
  • Make a range of cell types (potency)
  • convert to a range of different cell types (differentiation)
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2
Q

The features of stem cells allow them to:

A
  • build embryos, and tissues (development )

- Repair tissues (regeneration)

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3
Q

All the processes of stem cells require cells to

A

receive and process information

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4
Q

growth factors:

A

stimulate growth (increased cell size) by promoting synthesis and inhibiting degradation of macromolecules.

This requires signals - i.e. a method to get information into the cells and process it

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5
Q

death factors:

A

promote apoptosis

–may be an active process

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6
Q

Survival factors:

A

suppress apoptosis

–may be an active process

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7
Q

animal cells require ______ to divide, grow & survive

A

extracellular signals

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8
Q

information flow in cells:

A

-DNA (replication)
-RNA
-Protein (links back to all previous)
signals ions
Environment

Stem cells process this information to either, Self renew, Differentiate or Die by changing gene expression

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9
Q

stem cells express genes that define it’s …

A

‘state’

These states are actively maintained by receiving external signals.

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10
Q

external signals to stem cells can be:

A
  • soluble ligands for receptors

- internally generated signals

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11
Q

what components are needed to process signals?

A

Signalling:

  • Signals
  • Membrane
  • Intracellular effectors

Gene expression:

  • transcription factors
  • -leads to state change (gene expression change)
  • Histones Chromatin remodelling factors
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12
Q

gene expression (stem cell to diff cell or another stem cell)

A
  • to differentiate i.e. change cellular state
  • you have to turn genes on & off AND lock those changes in
  • i.e. chromatin has to be altered to allow or close down TRANSCRIPTION
  • POST-TRANSCRIPTION the amount of a protein that is made can be controlled at many levels
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13
Q

chromatic structure

A
  • short region of DNA double helix
  • “beads-on-a-string” form of chromatin
  • 30-nm chromatin finer of packed nucleosomes
  • interphase: extended scaffold-associated chromatin
  • condensed scaffold-associated chromatin
  • metaphase chromosome
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14
Q

the building blocks of chromatin are

A

nucleosomes.

-nucleosomes can be covalently modified - these structural changes to chromatin affect gene expression.

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15
Q

how do covalent modifications to nucleosomes affect gene expression

A

the chromatin becomes more or less condensed. This changes the accessibility to transcription factors

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16
Q

which specific part of nucleosome are covalently modified

A

N-terminal lysine-rich tails of core histones project radially from the nucleosomal core

17
Q

heterochromatin means

A

‘closed’

18
Q

euchromatin =

A

‘open’

19
Q

methylation of DNA can block transcription by two distinct pathways

A

1) direct blocking of TFIID binding (TATA binding protein)

2) Recruitment of histone deacteylases

20
Q

Whats the TATA box?

A

the TATA box is a DNA sequence found in the promoter region of genes

21
Q

TFIID is a transcription factor which binds to

A

TATA box

22
Q

TATA box is the binding site of

A

1) general transcription factors (TFIID)
2) histones
binding of a transcription factor blocks the binding of a histone and vice versa

23
Q

control of transcription:by expressing specific proteins such as transcription factors in different cells types

A

-only a certain repertoire of genes are switched on

24
Q

control of transcription: chromatin condensed

A

Gene ‘off’

unravelled = gene ‘on’

25
Q

tissue-specific enhancers job

A

drive expression differently in different cell types and times

26
Q

Alternative RNA splicing

A

removal of introns but also potentially some of the axons. –> single gene codes for multiple proteins

27
Q

degradation of mRNA:

A

is a control of transcription.
siRNA (small interfering RNA) is the most commonly used RNA interference. siRNA is a synthetic RNA duplex designed to specifically target a particular mRNA for degradation.

28
Q

blockage of translation is

A

another way of controlling transcription

29
Q

miRNA

A

A microRNA (abbreviated miRNA) is a small non-coding RNA molecule that functions in RNA silencing and post-transcriptional regulation of gene expression.

30
Q

post-translation controls of gene expression

A
  • Protein processing, transport.

- Proteasomes degrade ubiquitin-tagged proteins.

31
Q

degradation of a protein by a proteasome

A

Ubiquitin protein tags other proteins for destruction by proteasome.

1) protein to be degraded
2) Ubiquitin binds to protein = ubiquitinated protein
3) proteasome recognises & protein enters proteasome
4) proteasome and ubiquitin released to be recycled
5) final product = degraded protein (peptides)

32
Q

the choice cells make are governed at

A

lots of levels

33
Q

transcription and translation can be controlled by:

A
  • Chromatin modifications (DNA methylation, Histone acetylation),
  • cell specific TF’s,
  • alternative splicing,
  • degradation of mRNA, -blockage of translation,
  • protein processing,
  • transport,
  • proteasome degradation

All converge to result in a particular expression level of proteins which define a cells state