Reverse Genetics in Drosophila

I. P elements in reverse geneticsA. P element insertional mutagenesis projectsB. Using P elements to make mutations

II. RNA interferenceA. Basics of RNAiB. RNAi methods in flies

III. Targeted gene replacement

target geneenhancer

lacZ white

enhancer trap: expresses Gal in same pattern as target gene

P element constructs

UASwhite

controlled misexpression: expresses target gene in Gal4-dependent manner

P element constructs

GAL4 white

GAL4 enhancer trap: expresses Gal4p in same pattern as target gene

yellowwhite

insulators: block enhancers and position effects on expression

P element constructs

P{PZ} enhancer trap 523

P{lacW} enhancer trap 1176

P{Gal4} Gal4 expression 141

P{EP} UAS-controlled expression

P{SUPor-P} insulator

263

2076

P{GT1} gene trap 511

Mapped P element Insertion Lines(Bloomington Stock Center, as of 11/12/02)

4690

w P{w+}P element onX chromosome

Sb 2-3+

P transposase(chromosome 3)

dominantmarker

Transposition of P Elements

w+

;Y

P{w+}

new insertion on autosome

w P{w+} Sb 2-3+

;Y

wscreen forred-eyed sons

Spradling et al. (1995)

P elements rarely insert into coding sequences

w ; P{w+} Sb 2-3+

P element onchromosome 3

P transposase(chromosome 3)

dominantmarker

w

Excision of P Elements

Sb 2-3P{w+}w

Y;

w+

;Y

P{w+}**

screen for loss of w+, indicating excision

white

P transposase

...ATGCCAAACATGATGAAATAACATAAGGTGGTCCCGTCG...

...TACGGTTTGTACTACTTTATTGTATTCCACCAGGGCAGC...

31-bp P inverted repeat8-bp target site

P transposase

...ATGCCAAACATGATGAAATAACATA

...TACGGTTT17-nt 3’ overhang

different products, depending on: template for repair

extent of repairgap widening before repair

non-homologousend-joining homologous

recombination

(double-strand break)

whi

internal deletion of P element (w-)sometimes alters expression of target gene

A. Repair using sister chromatid as a template

white

restoration of P element (w+)

B. Repair using homologous chromosome as a template

precise excisionuseful for proving that phenotypes are due to P element insertion

C. “Imprecise excision”

exonuclease

repair

deletion of flanking DNA

RNA Interference

dsRNA

Dicer endonuclease 21-23 bp (or nt) siRNA

destroy mRNA

find complementary mRNA

(RISC complex)

Functions for RNA InterferenceRepression of repeated genes (e.g., transposable elements)Defense against viruses (plants)Developmental control of gene expression (small temporal

RNAs)X chromosome inactivation (mammals)Silencing of mating type loci and centromeric regions (S. pombe)DNA elimination in macronuclei (Tetrahymena)

Experimental manipulation of gene function.

RNAi Methods in Drosophila1. Addition of dsRNA to cell culture2. Injection of dsRNA into embryos3. Expression of hairpin RNA in vivo.

UAS

Gal4

RNA

dsRNA

Gene Targeting TechnologiesS. cerevisiae

Generate linear targeting DNA by PCRTransform suitable strainPlate on medium for positive selection (10-

8?)M. musculus

Generate targeting DNA by cloning, cuttingTransform ES cellsConduct positive and negative selections (typical =

10-7)

Gene Targeting in DrosophilaProblems

No culture system for germline stem cellsDNA introduced by injection in single embryos

Existence of DNA repair in early development questionable

Solution (Rong and Golic)Generate linear DNA in vivo:

Obtain stable transformants of donor constructUse FLP – FRT system to excise donor DNA from chromosomeUse I-SceI to linearize donor DNAUse visible marker gene to screen for potential

homologous gene replacements

FRT

FLP Recombinase Catalyzes Exchange BetweenTarget Sequences (FRTs)

FLP recombinase

crossover

FRTFRT

Intrachromosomal Recombination Between Tandem FRTsResults in Excision from the Chromosome

extrachromosomal circlewith 1 FRT

chromosome with 1 FRT

5' ATTACCCTGTTATCCCTAAATT 3'3' TAATGGGACAATAGGGATTTAA 5'

5' ATTACCCTGTTAT CCCTAAATT 3'3' TAATGGGAC AATAGGGATTTAA 5'

I-SceI

I-SceI makes a double-strand break at an 18-bptarget sequence

FRTFRT

donor construct (integrated P element)

I-SceI site

FLP recombinase

extrachromosomal circular donor

I-SceI endonuclease

DSB

*

*

integration

tandem duplication

w+ *FLP recombinaseI-SceI endonuclease

*

*w+

integration

*w+

I-CreI endonuclease

*w+

DSB

I-CreI site

*

Repair of a DSB between direct repeats

Tandem Duplications can be Reduced to Single Copy

Reverse Genetics in Drosophila

I. P elements in reverse geneticsA. P element insertional mutagenesis projectsB. Using P elements to make mutations

II. RNA interferenceA. Basics of RNAiB. RNAi methods in flies

III. Targeted gene replacement