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LT14 Drosophila Mosaic Analysis

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Drosophila Mosaic Analysis - eye mutants

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Drosophila: Mosaic Analysis and Modifier mutations

Characteristics

 Life cycle: 10 days
 Hardy and prolific
 4 chromosome pairs – chr 2 and 3 very big, 4 very small,
X chromosome
 Polyteny in larval tissues – easy to do physical maps,
much finer banding structure
 Special chromosomes – balancer chromosomes (read) –
multiple inversions, recombination impossible
 P-elements
 Genome size: 1.7x108bp




Classical genetics Forward genetic screens, linkage analysis, mosaic analysis,
modifier screens
Molecular Genetics Transgenesis, binary misexpression, site specific recombination
Genomics Genome, Transcriptome, Proteome, Epigenome, mutant and
transgenic insertion collections
 Powerful genetics + model dementia (brain lesions and degenerating cellular
structures), cancer, effects of alcohol (attraction to alcohol in response to
depletion in neuropeptide F – can see if it is conserved in humans)
- Powerful behavioural, disease model

Drosophila eye structure and development

 Each eye composed of 600-700 simple units
(ommatidia)
- Ommatidia form a highly regular array
- Core of 8 photoreceptors (R1-R8)
- Surrounded by 4 cone cells (lens) then by pigment
- Each photoreceptor cell has a unique identity
 Adult Drosophila epidermis derived from imaginal discs
- Cells proliferate in larva
- Evert and replace larval epidermal cells during
metamorphosis
 Eye forms from eye-antennal disc

, - Disc itself arises from 20 cells of the optic primordiu in the
embryonic blastoderm to produce a flattened sac of
epithelium
- By 3rd instar larva – 2000 cells
- During the middle of 3rd intar, dorsal ventral furrow forms,
differentiation from posterior to anterior – furrow progression requires
hedgehog (site where commitment to photoreceptor fate is initiated – hh
activates dpp
- Morphogenetic furrow marks boundary between differentiating and
undifferentiated ommatidia
- Photoreceptors differentiate in a fixed order ending with R7
- Anterior to furrow cells divide asynchronously in furrow division stops
- Cells go through 2 further synchronous cell divisions
 Mutations affect many different aspects of eye development and function
- Eg. white (no pigment), rough (losing one ommatidia, they will not arrange is a
regular array), bar (eyes reduced to a slit), sine oculis
 Mutations affecting the R7 photoreceptor can be isolated by behavioural screens
for UV insensitivity
- Could get some lazy fly phenotypes, but the target phenotypes have been
enriched
- UV insensitive mutants include 2 in which R7 cell completely fails to develop

Modifier Loci

 Effects of double mutants are additive: eg. w/w (white) + Bar/+ (small slit eyes) =
w/w ; Bar/+ (white and small)
BUT not if the mutations act in the same pathway (eg. C. elegans – lin3/lin3 +
let23/+ = lin3/lin3 ; let23/+ (multivulvae)
 Sometimes mutations in the same (or parallel)
pathways act synergistically eg. So1/+ (normal) +
ey/ey (small) = so1/+ ; ey/ey (no eye) – sine oculis is
a dominant modifier of eyeless
 Modifiers can enhance or suppress a phenotype
- Roughest acts upstream of Drosophila cell
death genes

Screens for dominant modifiers of eyeless (ey)

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