Lecture 1 - Segmentation in flies Flashcards

Provide an understanding of how the anteroposterior axis of drosophila is patterened through the interpretation of morphogen gradients, hierarchy of regulatory genes, establishment of boundaries

1
Q

Why are developmental experiments often done on flies?

A
  • many of the genes that control fly development are the same types of genes that control development of vertebraes
  • sophisticated genetics
  • already have a detailed understanding
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2
Q

What is the structure of the anteropostior segmentation of the adult drosophila?

A
  • at the anterior there are 3 head segments, 3 thoracic segments
  • 8 abdominal segments at posterior
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3
Q

What are the different life stages of Drosophila?

A

Hatches from egg as a lava

lava grows and later metamorphoses to form an adult fly

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4
Q

What are the features of the drosophila larvae denticle belts?

A
  • denticle belt of each segment has a specific pattern of bristles
  • denticle belt sticks out the ventricle side
  • noted by dissolution of larval cuticles by Nusslein-Volhard
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5
Q

What was the process of genetic screen used by Nusslein-Volhard to look for developmental mutants?

A

Forward genetic screen (1980)

-make mutants and look at the phenotypes

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6
Q

What are the three types segmentation genes in drosophila?

A

Classified by mutant phenotypes
Gap genes: lots of cuticles missing, big continuous gaps
Pair-rule genes: missing alternate segments (odd/even)
Segment polarity genes: segments were mirror image diplications of each other, as if the polarity of each segment was reversed

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7
Q

What was the hierachy of segmentation genes identified by Nusslein-Volhard?

A

Maternal gradient
Gap genes
Pair rule genes
Segment polarity genes

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8
Q

What is a multinucleatied syncital blastoderm and when is it present in Drosophila?

A
  • Early drosophila embryos form a multinucleated syncitial blastoderm, nuclei with shared cytoplasm migrate to the edges and pole cells for at the posterior
  • developmental patterning is set up in a syntium
  • Synctium: when nuclei have a shared cytoplasm
  • repeated rounds of nuclear dividion occur without cell division
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9
Q

What occurs at the syncitial bastoderm stage in drosophila?

A

-when the nuclei in the synctium migrate out to the periphery and pole cells form at the posterior (germline cells)

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10
Q

What occurs at the cellular blastoderm stage and what process follows this?

A

When cells form from the syncitial blastoderm stage

Followed by gastrulation

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11
Q

How does the developmental process of insects differ significantly from other organisms?

A

Developmental pattern is set up in a synctium

  • proteins can diffuse through the whole blastoderm
  • molecules such as transcription factors can act as morphogens
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12
Q

What is the importance of maternal gradients in the development of drosophila?

A

Maternal gradient - Bicoid mRNA

  • when the drosophila egg is released from the ovary it already has bicoid mRNA tightly localised to anterior end, (and Nanos and Claudal at the posterior end)
  • the Bicoid protein the forms a gradient along the AP axis (can do this because of the shared cytoplasm)
  • regulates the expression of gap genes e.g. hunchback
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13
Q

What is Bicoid?

A
  • Bicoid is a homeobox transcription factor

- regulates the expression of gap genes e.g. hunchback

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14
Q

What are the gap genes?

A

Hunchback, Giant, Krupple, Knirps

-code for transcription factors

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15
Q

What experimental technique can be used to look for mRNA localisation?

A

In situ hybridisation

-label synthetic probe with complementary mRNA/DNA

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16
Q

What experimental technique can be used to look for protein localisation?

A

Immunostaining using an antibody raised against different proteins
Or conjugate to a label (LacZ/GFP)

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17
Q

Why is bicoid a morphogen?

A

Bicoid manipulates the hunchback gap gene

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18
Q

How does bicod pattern hunchback expression?

A
  • hunchback expression is an interpretation of the bicoid gradient
  • expression is only activated above a certain threshold of bcd
19
Q

How can it be experimentally proven that bicoid patterns hunchback expression over a particular threshold?

A

Put in extra bicoid raising the concentration across the embryo

  • as the protein diffuses further and stays above threshold much further along the AP axis
  • results in an increase in the level of hunchback
20
Q

What is the activity of hunchback?

A
  • transcription factor

- forms a gradient to which other gap genes respond

21
Q

How is krupple activated?

A
  • gap gene
  • activated by low levels of hb protein but repressed by high levels - expressed in a band in the centre of the embryo
  • other gaps genes e.g. giant and knirps also repress krupple (much auto and cross regulation among gap genes)
22
Q

What are the main features of the gap genes?

A
  • respond to maternal gradients and to each other
  • mutations result in large continuous deletons of reions of the embryo
  • expression spans large regions of the embryo
  • edges of the regions of expression are graded and overalpping
23
Q

What do mutations in the gap genes result in?

A

-mutations result in large continuous deletons of reions of the embryo

24
Q

What are the pair rule genes?

A

-ftz and eve
code for transcription factors
-interpret the gap genes

25
Q

What do mutations in pair rule genes result in?

A

-affect homologous parts of alternate segments resulting in double segment periodicity defects

26
Q

What is the expression pattern of pair rule genes?

A
  • initial expression is broad
  • then stripes are formed by both accumulation of gene product in the stripes (continued and increasing expression) and a loss of gene expression in the intervening stripes (transcriptional repression and turnover)
27
Q

Where do the pair rule genes fall in the hierachy of genes involved in drosophila segmentation?

A
  • intermediates between the non-periodic expression of gap genes
  • and the repeated expression pattens of the segment polarity genes
28
Q

What is primary pair rule gene expression determined by? And what is secondary pair-rule gene expression regulated by?

A
  • primary pair rule gene expression is determined by the gap genes alone
  • secondary pair rule gene expression is regulated by other pair-rule genes
29
Q

What is the process by which stripes of pair-rule genes are formed?

A

Gap genes bind to one of the regulatory regions in the promoter of pair-rule genes e.g. even-skipped

  • promoter has activation and repressor binding sites (these overlap)
  • for even-skipped, Bicoid and hunchback are activators, Giant and Kruppel are repressors
  • whether even skipped is expressed depends on whether more of the activators or repressors bind t that particular location in the embryo
30
Q

How can you experimentaly show the expression of gap genes due to the regulatory region?

A
  • create a transgenic fly with a specific enhancer (e.g. a gap gene) driven lacZ
  • when given substrate B galactoside, section that turn blue are controlled by that regulatory region
31
Q

What do high levels of ftz and eve control

A

the expression of segment polarity gene, engrail

32
Q

What are the features of the segment polarity genes?

A

-expressed when the embryo has become cellularised (no longer a synctium)
-not all segment polarity genes code for transcription factors (unline the gap and pair-rule genes)
-diverse group of gene, many coding for elements of signal transduction pathways
-

33
Q

What are teh features of the engrailed class of segment polarity genes?

A
  • 14 stripes in a cellularised embryo
  • expressed in each parasegment
  • acts by fixing the positions of parasegment boundaires
  • this establishes the ginal segment boundaries of the larval epidermis
34
Q

What results from segment polarity mutations?

A
  • disrupt the normal A/P polarity

- phenotypes produced are mirror images or tandem duplications of segments

35
Q

What is the experimental evidence for the order in which Ftz and Engrailed act?

A

Fts and eve followed by engrailed
-used Ftz and eve mutants and molecular immunostaining to identify their localisations

SHOWED:

  • Wt: 7 Ftz stipes and 14 engrailed striped
  • Ftz mutant: lose Ftz stripes, only get alternate engrailed stripes
  • En mutant: 7 stripes of Ftz, lose all engrail stripes
  • Ftz is required for engrailed expression
  • Ftz acts first
36
Q

What are the developmetnally important structures in the drosophila embro and how are these patterned?

A

Parasegments

  • patterned by pair rule genes, gap gene and segment polarity genes
  • offset slightly from segemtns
37
Q

How does wingless and engrailed pattern the segments?

A
  • no ftz, no eve = wingless expression
  • high ftz, high eve = engrailed expressed
  • wingless expressed in the posterior most cell of the parasegment
  • engrailed expressed in the anterior most cell of the parasegment
  • anterior most cell of the parasegment develops in to the most posterior cell in the segments
38
Q

What is the interaction between wingless and engrailed?

A

Expressed in two cells that line up along the parasegment boundary

  • most posterior cell of the first parasegment expressed wingless
  • wingless protein is secreted from this cell and is the ligand for frizzled
  • activation of the frizzled receptor begins a signalling cascade
  • frizzled activated Dsh which surpresses the activity of Zw3
  • this leads to higher levels of armadillo
  • armadillo results in the transcription of engrailed, resultin in the activation of the expression of hedhog by the most anterior cell of the second parasegment
  • hedgehod is secreted from this cell, and is the ligand for the patched receptors
  • activation of patched results results in the transcription of wingless, through the smoothened protein and cubitus interruptus
39
Q

What is the purpose of the interaction between wingless and engrailed (and hedgehod)?

A

To maintain the parasegment boundary

40
Q

How do wingless and hedgehog result in morphogen gradients?

A
  • increased levels of Hh converts more cells to more anterior cell types
  • different cell fates depend on how much signal is recieved:
  • increase in Hh signalling then 4* cells adopt a more anterior (2* or 3*) cell fate
  • Hh initially acts to maintain Wg expression
  • later it acts to pattern the parasegmnent in a concentraion dependent manner
41
Q

How does the feedback between the en expressing cell and the adjacent wg expressing cell maintain the compartment (parasegment) boundary?

A
  • segment polarity genes wingless and hedgehog are signalling molecules
  • wg maintains the expression of en in cells posterior to wg expressing cells
  • en expressing cells activate the expression of Hh which signals to the adjacent cell and maintains the expression of wingless
  • in the absence of wg, expression of hh and en is lose
  • loss of segment polarity
42
Q

What does a loss of wg result in?

A
  • loss of expression of both hh and en

- loss of segment polarity

43
Q

What is a morphogen?

A

A substance governing the pattern of tissue development in the process of morphogenesis
-produces specific cellular responsees depending on it local concentration

44
Q

Where are fts and eve expressed?

A

In the most anterior cell of alternate para segments

-form a gradient