Lecture 6- Neurogenesis and determination of cell fate I (Drosophila) Flashcards

1
Q

What is specification?

A
  • imparting of positional information to cell populations, restriction
  • The process whereby a cell becomes capable of differentiating autonomously into a [cell type] cell in an environment that is neutral with respect to the developmental pathway. Upon specification, the cell fate can be reversed.
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2
Q

What is determination?

A
  • Imparting information that commits a cell to become (differentiate into) a certain cell type
  • expresses a phenotype of a cell
  • state where a cell has irreversibly acquired fate (potency = fate)
  • The process whereby a cell becomes capable of differentiating autonomously into a [cell type] cell regardless of its environment; upon determination, the cell fate cannot be reversed.
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3
Q

What controls specification/differentiation?

A
  • Cell extrinsic- communication with other cells (Fgf, Shh, Delta/Jagged)
  • Cell intrinsic programmes- gene specific transcription factors (Suppressor of Hairless Su(H), achaete scute (asc)).
  • cell intrinsic programmes= commit a cell, gene transcription in the cell
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4
Q

What is the effect of Notch in drosophila?

A

-mutant/Notch has notched wing

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5
Q

What does Notch do?

A
  • inhibits neurogenesis
  • Notch mutant embryos contain too many neurons, therefore Notch is required to restrict the number of neurons

(white dots= neurons)

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6
Q

What is the story with Drosophila bristles?

A
  • each bristle represents a neuron as it is connected to one on 1-1 basis
  • in Notch mutants there are more bristles and are less well ordered
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7
Q

What does neurogenesis require?

A
  • positive and negative signals
  • have pro-bristle genes that promote neurogenesis and bristle genes that are required to inhibit neurons
  • the interaction of positive and negative signals is crucial in successful neurogenesis
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8
Q

What is a Notch mosaic animal?

A

-animal made up of two distinct genetic cell populations

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9
Q

What did the Notch mosaics tell us?

A
  • Nocth acts cell autonomously (intrinsically), acts on its own, doesn’t affect surrounding tissue
  • Delta acts non-cell autonomously (extrinisically), affects cells in the surrounding tissue
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10
Q

What is lateral inhibition?

A
  • discovered thanks to the analysis of Notch mosaics
  • the NB(=neuroblast) tells the cells around it to not become NB as well, that is how you get a distinct number of neuroblasts in the embryo
  • the cell destined to become the NB inhibits other competent cells from adopting that fate
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11
Q

What is Notch?

A
  • transmembrane receptor (protein)
  • extracellular domain consists of multiple epidermal growth factor-like (EGF) repeats, and an intracellular domain consists of multiple, different domain types
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12
Q

What is a neuroblast?

A
  • a dividing cell that will develop into a neuron often after a migration phase
  • the main difference between a neuroblast and a neuron is the ability to divide; neuroblasts can still undergo mitosis, whereas neurons are postmitotic
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13
Q

What is delta?

A

-a ligand that binds to Notch initiating the Notch signalling pathway

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14
Q

What is the structure and cleavage sites of the Notch receptor?

A
  • the extracellular domain (containing the EGF-like repeats) interacts with the ligand Delta
  • when Delta binds, conformational change in the Notch receptor takes place
  • this activates proteases that cleave the Notch receptor, first the ADAM cleaves it at site 2 (mimicked by NotchdeltaE)
  • then gamma secretase cleaves it at site 3 (mimicked by Notch(intra))
  • the intracellular domain of the Notch receptor is now free to go to the nucleus to alter gene transcription
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15
Q

What is the Delta/Notch pathway critical for?

A
  • for signalling out of the neuroblast
  • the Notch signal allows one cell in the proneural cluster to maintain achaete scute levels (so will become neuroblast and later neuron)
  • low Notch receptor activity= cell will adopt neural fate and become neuroblast
  • high Notch receptor activity= epidermal fate
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16
Q

What is the Delta/Notch signalling pathway like?

A
  1. Delta binds to the extracellular domain of the Notch receptor
  2. This activates Notch and causes a cleavage event that releases the Notch intracellular domain into the cytoplasm
  3. The intracellular domain moves into the nucleus (as it has nuclear-localisation signal on it) and there it forms a complex with a protein SuH (Supressor of Hairless)
  4. The complex of SuH, Notch intracellular domain and another protein called Mastermind acts as a transcriptional activator when it binds to the DNA sequence GTGGAA in the cis regulatory regions of genes.
17
Q

What does SuH do?

A

-directly regulates the transcription of enhancer split complex E(spl)

18
Q

What does E(spl) do?

A
  • the E(spl) genes code for proteins that are similar to those coded for by acaete scute (ASC) but instead of being transcription activators they are strong transcription supressors
  • supress ASC transcription (so this cell will not become a neuron)
  • expressed in cells surrounding the developing neuroblast and repress neural fate
19
Q

How does the Delta/Notch pathway mediate lateral inhibition in the cells of the proneural cluster?

A
  • initially all the cells are equivalent
  • if the central cell in the proneural cluster expresses achaete scute (ASC) than the others, the ASC directly activates the Delta promoter, then this cell will also express higher levels of Delta than the other cells of the cluster
  • the high level of Delta in this cell activates Notch on the neighbouring cells causing more Notch-ICD (intracellular domain) translocation to the nucleus
  • the Notch-ICD complexes with SuH protein, resulting in the expression of E(spl) in these cells
  • the E(spl) bind to an N-box in the ASC gene promoter and repress its transcription
  • this downregulates Delta expression and prevents them from becoming neuroblasts
20
Q

What does Notch signalling require?

A

-endocytosis (not phosphorylation)

21
Q

What is the initial setup of two cells in the proneural cluster in the Drosophila?

A

-ectodermal cells are initially equivalent

  • in the embryonic epiderm none are commited to become neurons
  • two cells, both experessing delta and notch receptors
  • delta expression is upregulated in one cell via ASC
22
Q

What happens when Delta expression is increased in 1 cell?

A
  • Delta binds ti Notch on adjacent cell
  • once it has more delta then it binds to the notch receptor of the receiving/adjacent cell
23
Q

What does Notch activation release?

A
  • releases SuH which induces E(spl) expression
  • notch intracellular domain is associated with SuH after cleavage events and then translocated to the nucleus
  • enhancer of supressor hair gene interact with proteins of the ASC proteins
  • ASC is downregulated in one cell and active in the other
  • the ASC are the ones responsible for neuorgenesis
  • the one with no ASC will not be neuron
  • the one with more delta and active ASC will be neuron
24
Q

What does E(spl) do after Notch activation?

A

-blocks ASC therefore Delta and Neural gene expression

25
Q

What does decrease in Delta in the inhibited cell mean for the developing neuroblast?

A

-leads to more Delta and Neural gene expression in putative neuroblast

26
Q

What happens at the end of the Notch interaction between the two cells?

A

-one cell now neuroblast (neuronal progenitor) and one epidermal

27
Q

How is the Notch/ Delta intraction between adjacent cells a feedback mechanism?

A
  • as some express ASC= upregulate delta
  • which in turn downregulates it in the neighbouring cells, the more delta in the neuroblast the less in the surrounding cells (lateral inhibition)
28
Q

How are proneural genes initially expressed?

A

-in patches but become successively restricted to single cells as the feedback mechanism of Delta/Notch pathway takes place

29
Q

What do drosophila embryos with:

a) normal neural cell determination/differentiation
b) overexpression of Notch
c) lack of Notch

look like?

A

a) normal, SuH and ASC balanced
b) all ectoderm/epiblast (Su(H)on)
c) all neuroblasts when lack of Notch (ASC on)

30
Q

What types of Notch modifiers are components of the Notch signalling pathway?

A
  1. Pro-neural genes: loss-of-function mutations lead to loss of neurons (promote neural cell fate)
    - achaete-scute (asc)
    - lethal-of-scute
    - atonal (ato)
  2. Neurogenic genes: loss-of-function mutations lead to gain of neuron/loss of epidermis (supress neurons, promote epidermal cell fate)
    - Notch
    - Delta
    - Supressor of Hairless Su(H)
31
Q

What does the Notch signalling do?

A

-specifies which cell will differentiate into a neuron

(REMEMBER: all of this is about Drosophila Notch signalling)

32
Q

Is Notch signalling a conserved mechanism?

A
  • yes, the signalling pathway components are conserved in mammals
  • the components are just named differently
  • ASC= Mash (Mammalian achaete scute homologue)
  • E(spl)= Hes (Hairy Enhancer of split)
  • SuH= RBP-Jk
  • Delta= Delta1, 3
  • Notch= Notch 1,2,3
  • BUT the biology is different. In mammals “proneural genes” act in the cells already specified to become neurons (the neuroepithelium)