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Lecture 7 Development of a body plan

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Total cards: 19•Content version: v4•Public deck•Updated: 8/1/2026

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#1
Front (Question)

Segmentation is an … and…. way of building bodies

Back (Answer)

ancient conserved

#2
Front (Question)

Define saturation mutagenesis

Back (Answer)

‘induction + recovery of large no. of mutations in 1 area of the genome or in 1 biological function to identify all the genes in that area or affecting that function’. You statistically hit the genes many times so you can be statistically confident that there are no more genes – as these would have also been hit

#3
Front (Question)

What was identified in saturation mutagenesis x5

Back (Answer)

• 26,978 lines (with mutations in them) • 18,136 lethal mutations • 4,332 mutations causing embryonic lethality • 580 mutations caused embryonic phenotypes • 139 complementation groups (genes) were identified

#4
Front (Question)

Why were most mutation not embryonic lethal

Back (Answer)

Most are lethal later as they are able to survive off maternal contributions e.g. RNA in the first few hours

#5
Front (Question)

Define a complementation group

Back (Answer)

• A complementation group is a collection of mutant alleles that fail to complement and restore the WT when tested in all pair-wise combinations. The mutation will be in the same gene. Crossing 2 species will form a heterozygous mutant that will show the phenotype

#6
Front (Question)

What occurs if the mutation is in different genes

Back (Answer)

Complement No phenotype

#7
Front (Question)

What occurs if mutation is in the same genes

Back (Answer)

No complementation Phenotype

#8
Front (Question)

How is bicoid loaded

Back (Answer)

Maternally loaded into the developing oocyte

#9
Front (Question)

Name 3 maternal genes and their location

Back (Answer)

Bicoid - anterior Torso - middle Nanos - posterior

#10
Front (Question)

When there are 0 copies of the bicoid gene what occurs to the segmentation pattern

Back (Answer)

• 5 stripes instead of 7 which have been pushed forwards - This corresponds with the loss of A head structures as the 1st 2 stripes have gone

#11
Front (Question)

Explain what happens if bicoid is overexpressed

Back (Answer)

• Overexpressing bicoid • 7 stripes still form but pushed more posterior i.e. there is a large gap between A tip and 1st pair rule gene • Because bicoid is now too high at the extreme anterior to aloe for dev of head structures (jack Q wrong here)

#12
Front (Question)

What are gap genes

Back (Answer)

Gap genes read the maternal gene gradients to define broad ‘blocks’ or domains of gene expression

#13
Front (Question)

How is the expression of pair rule genes controlled

Back (Answer)

stripe by stripe

#14
Front (Question)

What are HOX genes controlled by

Back (Answer)

A combination of gap and pair-rule genes

#15
Front (Question)

Mutation in antennapedia complex

Back (Answer)

mutation leads to legs instead of antenna (segment is the same but the combination of selector genes is wrong)

#16
Front (Question)

Describe long germ band insects

Back (Answer)

• Drosophila is a ‘long germ band’ insect i.e. all 14 segments are defined at once • Quick- embryogenesis complete in just 24 hours • Complicated- maternal, gap, pair rule genes interact for every segment

#17
Front (Question)

Describe short and intermediate germ band insects

Back (Answer)

• Start with head and thoracic segments - probably via an ancestral version of the system drosophila now uses • Add abdominal segments sequentially - posterior disc (proctodeum) appears to bud off segments as it gets smaller • Moderate complexity and not too slow • Likely to represent the original ‘ancestral’ segmentation mechanism

#18
Front (Question)

Describe how delta signals via Notch

Back (Answer)

Delta ligand activates the notch receptor Short range signal Immediately adjacent See rings of delta and notch activation and a series of zones of notch activation

#19
Front (Question)

Describe feedback loop segmentation clock

Back (Answer)

Notch activation causes down regulation of notch ligand. This is because Notch activation switches on the expression of Her/Hes (inhibitor) which binds to the promotor of the delta gene to switch it off and so downregulate delta ligand. This means that this cell stops making signal for neighbour so stops seeing activation and so stops making the repressor and so delta comes back on again and Notch is turned back on. This cycle repeats