Materials and Reagents

1. Consumables
   
   1. Small sieve for washing embryos (Nylon mesh 150, pore size about 100 microns) 
   2. Artist’s brush (0 number painting brush)
   3. Double sided tape
   4. Slides and coverslips
   
   
2. Plasmids
   pFlip-flop-P0 for phase 0
   pFlip-flop-P1 for phase 1
   pFlip-flop-P2 for phase 2
   p3xP3-EGFP.vas-int.NLS
   PhiC31 integrase expressing vector
   Note: All the constructs can be obtained from the Drosophila Genomics Resource Center (DGRC).
   
   
3. Fly stocks
   Gene specific MiMIC insertion (Nagarkar-Jaiswal et al., 2015)
   
   1. Stock number: 53104 Genotype: y¹w^*;Mi{MIC}SNF4Aγ^MI09417/TM3,Sb¹Ser¹ (Gene: SNF4Agamma)
   2. Stock number: 58593 Gentotype: y¹w^*;Mi{MIC}Trim9^MI12525 (Gene: Trim9)
   
   Additional stocks for genetic manipulation and evaluation
   
   1. y¹w^67c23;In(2LR)Gla, wg^Gla−1/SM6a
   2. y¹w^67c23;D/TM6b, Hu, Tb
   3. w[*];L[2] Pin[1]/CyO,P{w[+mC]=GAL4-Kr.C}DC3,P{w[+mC]=UAS-GFP.S65T}DC7
   4. y[1]w[*];D*gl[3]/TM3,P{w[+mC]=GAL4-Kr.C}DC2,P{w[+mC]=UAS-GFP.S65T}DC10, Sb[1]
   5. P{ry[+t7.2]=hsFLP}12,y[1]w[*];sna[Sco]/CyO 
   6. P{ry[+t7.2]=hsFLP}12,y[1]w[*];Dr e/TM3,Sb
   7. y[d2]w[1118] P{ry[+t7.2]=ey-FLP.N}2
   8. P{w[+mC]=tubP-GAL80[ts]},w[*]/FM7a;P{w[+mC]=UAS-FLP.D}JD2
   9. y[1]w[*];P{w[+mC]=UAS-FLP.D}JD1
   10. y[1]w[1118];P{y[+t7.7] w[+mC]=nSyb-GAL4.P}attP2
   
   
4. PCR Primers
   Tag-specific primers:
   (1) EGFP-TAG-Rev: GAGTACAACTTCAACAGCCAC
   (2) mCherry-TAG-Fwd: GGCCACCCTTGGTCACCT
   MiMIC specific primers:
   (1) MiL-F: GCGTAAGCTACCTTAATCTCAAGAAGAG
   (2) MiL-R: CGCGGCGTAATGTGATTTACTATCATAC
   
   
5. Reagents
   
   1. Yeast paste
   2. Bleach (50% Clorox; final concentration: 2.5% hypochlorite), freshly prepared
   3. Halocarbon oil 700 (Sigma, catalog number: H8898)
   4. PureLink^TM Genomic DNA Mini Kit (Invitrogen, catalog number: K182001)
   5. GoTaq^® Green Master Mix (Promega, catalog number: M712)
   6. Formaldehyde (37% w/v, Sigma-Aldrich, catalog number: 252549)
   7. Normal goat serum (Jackson ImmunoResearch Labs, catalog number: 005-000-001)
   8. PBS with 0.2% (v/v) Triton X-100
   9. Anti-GFP antibody (Abcam, catalog number: ab13970)
   10. Anti-mCherry antibody (Clontech, catalog number: 632496)
   11. Secondary antibodies (Anti-Chicken Alexa 488, Jackson ImmunoResearch Labs, catalog number: 703-545-155; Anti-Rabbit Cy3, Jackson ImmunoResearch Labs, catalog number: 111-585-003)
   12. Agar
       
   13. Sugar
   14. Welch's grape juice concentrate
   15. Ethanol
   16. Glacial acetic acid
   17. Sucrose
   18. Grape juice agar plates (see Recipes)
   19. 10% sucrose agar plates (see Recipes)

Equipment

1. Fly cages
2. FemtoJet 4x (Eppendorf, catalog number: 5253000017)
3. Femtotips (Eppendorf, catalog number: E5242952008)
4. Incubator for culturing flies
5. Circulating water bath (Thomas Scientific Julabo, catalog number:1181j40) 
6. Dissecting microscope (Stemi 305 Microscope) (Zeiss, catalog number: 435063-9010-100) 
7. Fine dissection tools:
   Scissors (Fine Science Tools, catalog number: 16143-12)
   Forceps (Fine Science Tools, catalog number: 11413-12)
8. Microwave (LG, catalog number: MS3042GM)
   

Procedure

1. Choosing the MiMIC and determining the appropriate phase of the MiMIC lines
   
   1. Publicly available MiMIC lines are listed in Bloomington Drosophila Stock Center (BDSC) database and can be accessed from FlyBase (http://Flybase.org) or at the stock center website (https://bdsc.indiana.edu).
   2. Choose a MiMIC insertion that tags your gene of interest, preferably one that tags all of the transcriptional isoforms of the gene (called “gold” MiMICs in Nagarkar-Jaiswal et al., 2015). As an example, in this protocol, we are using MiMIC lines that tag the genes SNF4Agamma and Trim9.
   3. Using RMCE resources page (http://flypush.imgen.bcm.tmc.edu/pscreen/rmce/) from the Bellen lab at Baylor College of Medicine, determine the phase for the chosen MiMIC line. The proper functioning of the Flip-flop cassette is dependent on the in-frame translation of the Flip-flop cassette with the preceding exon. The in-frame translation is determined by the last codon of the preceding exon (preceding codon) and can result in one of the three phases of translation for Flip-flop: Phase 0 or Phase 1 or Phase 2. Choose the corresponding plasmid donor for the Flip-flop as dictated by the MiMIC insertion. Also, determine the relative orientation of the MiMIC element with that of the recipient gene. This information is necessary for the molecular validation of Flip-flop cassette insertion using PCR.
      
      
2. Generation of Flip-flop fly lines
   In this section, we describe the generation of the Flip-flop alleles by co-injecting the Flip-flop cassettes with the PhiC31 integrase plasmid into embryos carrying the MiMIC insertion. 
   
   1. Using a stock of flies carrying gene specific MiMIC (yellow⁺) inserted in a coding intron [F0], set up a small fly cage (~150-300 adult flies, about 50-100 males and 100-200 females that are less than 15 days old) and collect 0.5-1 h old embryos of on grape juice plates supplemented with yeast paste. 
   2. Prepare embryos [F1] for microinjection as described in Kiehart et al. (2007). Briefly, collect the embryos from the grape juice plate and wash with water. Resuspend them in 50% bleach and stir continuously for about 2 min. Wash off the bleach and align the embryos in a line on a small piece of grape juice agar. Stick the embryos on a coverslip with double-sided tape by gently lowering the coverslip onto the embryos. Cover them with Halocarbon oil 700. 
   3. Co-inject the phase-specific Flip-flop plasmid (concentration 400 ng/µl) and PhiC31 integrase expressing vector (concentration 300 ng/µl) along with the food color into embryos using the Femtotips and FemtoJet 4x as described in Kiehart et al., 2000. 
   4. Let the embryos develop at 18 °C.
   5. Collect individual male/female adults from F1, and cross them to appropriate balancer stock depending on the chromosomal location of the MiMIC insertion. From these crosses, screen for flies that have lost the MiMIC-yellow marker (yellow^-) indicating successful RMCE event [F2]. Self-cross transgenic F2 flies and establish Flip-flop stocks. 
   
   
3. Confirmation of orientation of the Flip-flop cassette
   The Flip-flop cassette is flanked by two inverted attB that allow replacement of the MiMIC core located between two inverted attP sites (Figure 2). Since recombination can occur between any of two attP and attB sites, the Flip-flop cassette can be inserted in either a PT or a GT orientation (Figure 2). In this section, we will determine the orientation of the Flip-flop transgenic line.
   
   1. From the stock of Flip-flop flies that was established in the previous section, extract genomic DNA from 8-10 flies using the PureLink^TM Genomic DNA Mini Kit (Invitrogen).
   2. Perform four PCR reactions for each Flip-flop line to confirm the orientation of the Flip-flop cassette (protein trap versus gene trap): (1) First PCR reaction with MiL-F and EGFP-TAG-Rev primers (2) second reaction with Mil-F and mCherry-TAG-Fwd primers, (3) third reaction with MiL-R with EGFP-TAG-Rev primers and (4) the fourth reaction with MiL-R and mCherry-TAG-Fwd primers. 
   
   
   Figure 2. RMCE event screening. By knowing of the orientation of the MiMIC insertion with respect to the gene using Step A3, the PCR products as shown in (A), (B), (C) and (D) can be used to determine the orientation of the Flip-flop cassette with respect to the gene: when the MiMIC cassette is inserted in the same orientation as the gene (A) and (B), and when MiMIC is inserted in the opposite orientation of the gene (C) and (D). Gel images on the left hand side show amplification in different PCR reactions that distinguish between integration of Flip-flop in PT or GT orientations: (1) First PCR reaction with MiL-F and EGFP-TAG-Rev primers (2) second reaction with Mil-F and mCherry-TAG-Fwd primers, (3) third reaction with MiL-R with EGFP-TAG-Rev primers and (4) the fourth reaction with MiL-R and mCherry-TAG-Fwd primers. When the MiMIC insertion is in the same orientation as the gene (SNF4Aγ), a positive amplification in reactions 1 and 4 will confirm the PT orientation (A), while positive bands in 2 and 3 will confirm the GT orientation (B). If the MiMIC insertion and the gene are in the opposite orientation (Trim9), positive reactions in 2 and 3 will confirm the PT insertion (C) and 1 and 4 will confirm the GT insertion (D).
   
   
4. Induction of Flip-flop cassette inversion to facilitate conditional knock-down
   In this section, we provide generic schemes for generating experimental animals that can be used for Flip-flop mediated mosaic analysis in different tissues using different sources of FLPs (Figure 3). We refer to the gene of interest as “gene” in these schemes. Consequently, gene^null is used to refer to a strong loss of function allele that is derived from a different source other than the Flip-flop stock. Flip-flop stocks are indicated with gene^{EGFP-T2A-mCherry}- indicating that they are in the PT orientation. We also provide selected examples of results of mosaic tissue generated using Flip-flop in mitotic as well as post-mitotic cells from our previous study. We track the formation of mosaics using genetically encoded fluorescent markers that are expressed from the genomic location of the corresponding genes.
     For mosaic analysis using Flip-flop, we recommend using a combination of Flip-flop and a strong loss of function allele (gene^null) in order to prevent the confounding effects of secondary mutations that may be present in the Flip-flop line. This is standard practice in Drosophila genetics, as an independently derived allele of the gene, it is unlikely to also have the same secondary mutations as Flip-flop. We also recommend the use of fluorescent balancers, such as TM3,Kr-GAL4 UAS-GFP or TM3,P{w[+mC]=sChFP}3,Sb[1] which permit easy identification of non-balancer-carrying animals (inferred as gene^{EGFP-T2A-mCherry}/gene^null larvae) through the absence of GFP or mCherry signal.
   
   Conditional gene inactivation in mitotic cells
   In this section, we describe Flip-flop mediated gene inactivation in mitotically active cells in a tissue-specific manner as well as in random mosaics. We used a Flip-flop insertion in a gene encoding AMP kinase gamma subunit, SNF4Aγ, as an example. To reverse the Flip-flop insertion in SNF4Aγ in a tissue-specific fashion we used eyeless promoter driven FLP (ey-FLP). This promoter drives the expression of FLP in the presumptive eye-antenna imaginal disc as well as part of the optic lobe of the larval brain. For random mosaics generation throughout the animal’s body, we used heat-shock inducible FLP (hs-FLP) expression. The expression of FLP from this source is stochastic and induced upon a heat shock to the larvae at 37 °C.
   
   
   1. Flip-Flop cassette inversion in eye antenna disc
      
      1. Using standard genetic crosses create appropriate fly stocks carrying a transgenic source of eyeless FLP and a severe loss of function allele and null mutants of the gene (ey-FLP/Y;gene^null/CyO,Kr-GAL4 UAS-GFP or TM3,Kr-GAL4 UAS-GFP) and cross them with gene^{EGFP-T2A-mCherry}/gene^{EGFP-T2A-mCherry} carrying flies. A schematic of cross strategy is shown in Figure 3A. Raise these crosses at 25 °C.
      2. Collect larvae 48 h post-egg-laying and select non-GFP third instar larvae. Dissect the eye-antenna disc under the dissecting microscope and stain with anti-GFP and anti-mCherry antibodies as described in Nagarkar-Jaiswal et al., 2017. Briefly, fix the dissected larvae with 4% formaldehyde for 30 min, wash three times with PBS-0.2% Triton X-100 and block with 10% Normal Goat Serum for 1 h at room temperature. Incubate samples with anti-GFP and anti-mCherry at 4°C overnight. Wash samples three times with PBS-0.2% Triton X-100 and incubate with Secondary antibodies for 2 h at room temperature. Mount the sample in mounting media.
      
      
   2. Mosaic generation in the adult gut
      
      1. Create fly stocks hs-FLP/Y;gene^null/CyO,Kr-GAL4 UAS-GFP or TM3,Kr-GAL4 UAS-GFP using conventional genetic approach and then cross them with y¹w^*;gene^{EGFP-T2A-mCherry}/gene^{EGFP-T2A-mCherry} Flip-flop flies and keep at 18 °C. A schematic of cross strategy is shown in Figure 4A. Collect appropriate progeny carrying the Flip-flop allele and the null allele (hs-FLP/y¹w^*;gene^null/gene^{EGFP-T2A-mCherry}) and maintain them at 18 °C for 3 days. 
      2. Heat shock adult females on Day 3 for 2 h at 37 °C and keep them at 25 °C.
      3. Optional: Starvation assay or drug feeding assay could be performed to compare the effect of starvation or drug on the mutant gut cells.
      4. Dissect guts and stain with anti-GFP and anti-mCherry antibodies as described in Nagarkar-Jaiswal et al., 2017.
   
   Conditional gene inactivation in mitotically inactive cells
   Neurons are mitotically inactive cells. This precludes the use of traditional mosaic analysis techniques such as MARCM, which depend on mitotic separation of mutant and heterozygous cells. Application of Flip-flop, however, does not require mitotic separation of the mutant cells and therefore can be used to conditionally inactivate genes in adult neurons. To demonstrate the applicability of Flip-flop to non-mitotic cells such as neurons, we describe conditional inactivation of Trim9 in adult neurons by using neuronal driver nSyb-GAL4 and UAS-FLP (Figures 5A and 5B). We chose nSyb-GAL4 as it is a well-characterized driver of GAL4 expression in mature neurons. However, it is constitutively expressed in neurons. To achieve conditional inactivation in adult neurons and not in larval neurons, we limited the activity of nSyb-GAL4 during development using a temperature sensitive GAL80 (GAL80^ts). GAL80 is a well-known inhibitor of GAL4 and can be used to suppress the expression of GAL4/UAS-driven FLP during development. Maintaining the suppressed FLP (GAL4/UAS-FLP, GAL80^ts) carrying stocks at low temperature and then switching to a higher temperature in adults will restrict FLP expression at low temperature and drive the expression of FLP at high temperature. Hence, a temperature shift post-development will lead to Flip-flop cassette inversion predominantly in the adults. This approach can be used for the identification of adult neuronal functions of genes which are essential for proper development. Below, we describe a generic scheme wherein any neuronal GAL4 can be used to generate stocks that permit conditional gene inactivation in neurons during development as well as in adult brain using Flip-flop (Figure 5A).
   
   Gene inactivation in neurons
   
   1. Create fly stocks tubP-GAL80^ts;gene^null/CyO,Kr-GAL4 UAS-GFP or TM3,Kr-GAL4 UAS-GFP;UAS-FLP/UAS-FLP and cross them to gene^{EGFP-T2A-mCherry}/gene^{EGFP-T2A-mCherry};Neuronal-GAL4/Neuronal-GAL4 using conventional genetic approach. Maintain the crosses at 18 °C until eclosion.
   2. Shift the adults to 29 °C on Day 4 after eclosion. Dissect the brains on Day 4 after shifting to 29 °C and stain as described in Nagarkar-Jaiswal et al., 2017.
   Note: The same strategy can be used to study the developmental role of the genes in larval neurons. In such a case, above-mentioned crosses can be kept either at 29 °C throughout or animals can be shifted from 18 °C to 29 °C at a specific time point during development. A description of such an analysis of the larval brain is also provided in Nagarkar-Jaiswal et al., 2017.
   

Data analysis

Flip-flop mediated mosaic generation in the eye-antennal imaginal discs and the adult gut allows to evaluate the requirement of SNF4Aγ in eye development and in the induction of autophagy in adult guts. We also used Flip-flop to generate mutant mosaics in the adult brain. In this section, we describe the functional insights into the role of SNF4Aγ, obtained through the use of Flip-flop using methods described in Procedures A, B, and D.

1. Generation of SNF4Aγ and Trim9 Flip-flop lines:
   We generated SNF4Aγ and Trim9 Flip-flop lines by co-injecting Flip-flop constructs and PhiC31 integrase plasmids as described in Procedure A. We further confirmed the orientation of Flip-flop cassette by PCR assay described in Procedure C. We established biologically functional protein trapped lines for both the genes (Figure 2A and 2B), which were further used for Flip-flop assays.
   
   
2. SNF4Aγ is essential for proper pattern formation during eye development:
   We used a severe loss of function allele SNF4Aγ^Df along with the Flip-flop insertion in PT orientation derived from the y¹w^*;Mi{MIC}SNF4Aγ^MI09417/TM3,Sb¹Ser¹. We crossed ey-FLP; SNF4Aγ^Df/TM6b, Hu, Tb flies with y¹w^*;SNF4Aγ^{MI09417-GFP-T2A-mCherry}/SNF4Aγ^{MI09417-GFP-T2A-mCherry} and collected ey-FLP/y¹w^*;SNF4Aγ^Df/SNF4Aγ^{MI09417-GFP-T2A-mCherry} progeny. We dissected the eye-antennal discs from these animals and stained for EGFP and mCherry expression. We found the robust inversion of Flip-flop cassette in these eye discs, marked by the switch from EGFP expression in control animals to mCherry expressing mosaics in ey-FLP carrying flies (Figure 3B). Following up on the developmental inversion of Flip-flop, We also found a marked change in the arrangement of eye ommatidia and an electrical response to stimulation with light (Electroretinogram, ERG) in the adult eyes in SNF4Aγ mutant mosaics (described in Nagarkar-Jaiswal et al., 2017).
   
   
3. SNF4Aγ is required for autophagy induction in adult gut following starvation
   We used a severe loss of function allele SNF4Aγ^MI09417 along with the Flip-flop PT insertion derived from the same MiMIC insertion, SNF4Aγ^{MI09417-FF-EGFP-mCherry}. We crossed hs-FLP/Y;SNF4Aγ^MI09417/TM6b, Hu, Tb flies with y¹w^*;SNF4Aγ^{MI09417-GFP-T2A-mCherry}/SNF4Aγ^{MI09417-GFP-T2A-mCherry} and collected hs-FLP/y¹w^*;SNF4Aγ^MI09417/SNF4Aγ^{MI09417-GFP-T2A-mCherry} progeny flies. We gave heat shocks to the collected flies on Days 4 and 5 at 37 °C in an air-incubator for 2 h and starved by keeping them in vials containing 10% sucrose agar for 24 h (Figure 4B). Following starvation, we analyzed adult guts for Flip-flop inversion and induction of autophagy (Figure 4C). We found that the SNF4Aγ mutant flies fail to induce autophagy (Nagarkar-Jaiswal et al., 2017).
   
   
   Figure 3. ey-FLP mediated conditional gene inactivation. A. Schematic showing cross strategy for Flip-flop cassette inversion in the eye-antennal disc. B. Eye-antennal discs from ey-FLP/y¹w^*;SNF4Aγ^Df/SNF4Aγ^{MI09417-GFP-T2A-mCherry} larvae showing loss of EGFP signal (green) and mCherry (red) following tissue-specific switch of the Flip-flop cassette with ey-FLP. Scale bars = 50 µm. (Adapted from Nagarkar-Jaiswal et al., 2017)
   
   
4. Flip-flop mediated loss of Trim9 in adult neurons
   We used a deficiency spanning Trim9 (Trim9^Df) as a loss of function allele in examining the PT insertion in Trim9. We used tubP-GAL80^ts to suppress FLP-expression during development and raised Trim9^{MI12525EGFP-T2A-mCherry}/Trim9^Df;UAS-FLP/nSyb-GAL4 animals at 18 °C until four days after eclosion. Following four days of adulthood at 18 °C, the animals were shifted to 29 °C to induce FLP-expression. As expected, immunostaining the brain of these animals shows mCherry-expressing neuronal cells in which the cassette inversion has occurred.
   
   
   Figure 4. Random mosaic generation in adult gut. A. Schematic showing cross strategy for a random mosaic generation in adult gut. B. Experimental plan for starvation in adult flies. The image displaying the adult midgut from amino acid starved hsFLP;SNF4Aγ^{MI09417EGFP-T2A-mCherry}/SNF4Aγ^MI09417 animals, stained for GFP (a, d), mCherry (b, d), p62 (c, d) and DAPI (white) (d). Red arrows indicate control cells expressing SNF4Aγ-EGFP-SNF4Aγ, revealing higher levels of p62. In contrast, mutant cells are mCherry positive and have reduced p62 levels, indicating a defect in autophagy induction, scale bar = 5 µm. (Adapted from Nagarkar-Jaiswal et al., 2017)
   
   
   Figure 5. Gene inactivation in adult neurons. A. Crossing scheme for conditional gene inactivation in adult neurons combining the Flip-flop cassette with FLP expressed using the GAL4/GAL80/UAS binary system. B. Adult brain of tubP-GAL80^ts;Trim9^{MI12525EGFP-T2A-mCherry}/Trim9^Df;UAS-FLP/nSyb-GAL4 animals stained for EGFP (green), mCherry (red) and Elav (blue). The temperature sensitive GAL80 (GAL80^ts), expressed under a tubulin promoter (tubP) was used to prevent nSyb-GAL4 from driving expression of UAS-FLP during development. (a-d) Adult brains of tubP-GAL80^ts;Trim9^{MI12525EGFP-T2A-mCherry}/Trim9^Df;UAS-FLP/nSyb-GAL4 control animals, raised at 18 °C display Trim9-EGFP-Trim9 (green, a and d) and do not show any mCherry expression (red, b and d). (a’-d’) Adult brains of tubP-GAL80^ts;Trim9^{MI12525EGFP-T2A-mCherry}/Trim9^Df; UAS-FLP/nSyb-GAL4 animals, raised at 18 °C until four days after eclosion, and then shifted to 29 °C to induce FLP-expression, show mCherry-expressing neuronal cells in which the cassette inversion has taken place (red, b’ and d’), scale bars = 50 µm. (Adapted from Nagarkar-Jaiswal et al., 2017)
   

Recipes

1. Grape juice plates
   300 ml double distilled H₂O
   12 g agar
   22 g sugar
   100 ml Welch's grape juice concentrate
   10 ml ethanol
   5 ml glacial acetic acid
   
   1. Add agar and sugar to cold ddH₂O
   2. Microwave until dissolved (max. 12 min), stirring occasionally
   3. Add grape juice concentrate
   4. Cool to 65 °C and add Ethanol and acetic acid
2. 10% sucrose agar plates
   10 g sucrose
   2 g agar
   Make up the volume with water to 100 ml and microwave until dissolved, stirring occasionally
   

Acknowledgments

We thank Hugo J. Bellen for comments on the manuscript. SNJ and PP are supported by the Department of Science & Technology, Ramanujan Fellowship (SB/S2/RJN-157/2017). SNM is supported by NIH T32 (5T32HL098039-08).

Competing interests

The authors declare no competing interests.

References

1. Kiehart, D. P., Crawford, J. M. and Montague, R. A. (2007). Collection, dechorionation, and preparation of Drosophila embryos for quantitative microinjection. CSH Protoc 2007: pdb prot4717.
2. Kiehart, D. P., Crawford, J. M. and Montague, R. A. (2000). Quantitative microinjection of Drosophila embryos: general strategy. CSH Protoc 2000: pdb top5.
3. Nagarkar-Jaiswal, S., Lee, P. T., Campbell, M. E., Chen, K., Anguiano-Zarate, S., Gutierrez, M. C., Busby, T., Lin, W. W., He, Y., Schulze, K. L., Booth, B. W., Evans-Holm, M., Venken, K. J., Levis, R. W., Spradling, A. C., Hoskins, R. A. and Bellen, H. J. (2015a). A library of MiMICs allows tagging of genes and reversible, spatial and temporal knockdown of proteins in Drosophila. Elife 4: e05338.
4. Nagarkar-Jaiswal, S., DeLuca, S. Z., Lee, P. T., Lin, W. W., Pan, H., Zuo, Z., Lv, J., Spradling, A. C. and Bellen, H. J. (2015b). A genetic toolkit for tagging intronic MiMIC containing genes. Elife 4: e08469.
5. Nagarkar-Jaiswal, S., Manivannan, S. N., Zuo, Z. and Bellen, H. J. (2017). A cell cycle-independent, conditional gene inactivation strategy for differentially tagging wild-type and mutant cells. Elife 6: e26420.
6. Venken, K. J., Schulze, K. L., Haelterman, N. A., Pan, H., He, Y., Evans-Holm, M., Carlson, J. W., Levis, R. W., Spradling, A. C., Hoskins, R. A. and Bellen, H. J. (2011). MiMIC: a highly versatile transposon insertion resource for engineering Drosophila melanogaster genes. Nat Methods 8(9): 737-743.