Gene-drive systems developed in several organisms result in super-Mendelian inheritance of transgenic insertions. Here, we generalize this “active genetic” approach to preferentially transmit allelic variants (allelic-drive) resulting from only a single or a few nucleotide alterations. We test two configurations for allelic-drive: one, copy-cutting, in which a non-preferred allele is selectively targeted for Cas9/guide RNA (gRNA) cleavage, and a more general approach, copy-grafting, that permits selective inheritance of a desired allele located in close proximity to the gRNA cut site. We also characterize a phenomenon we refer to as lethal-mosaicism that dominantly eliminates NHEJ-induced mutations and favors inheritance of functional cleavage-resistant alleles. These two efficient allelic-drive methods, enhanced by lethal mosaicism and a trans-generational drive process we refer to as “shadow-drive”, have broad practical applications in improving health and agriculture and greatly extend the active genetics toolbox.
Efficient super-Mendelian inheritance of transgenic insertional elements has been demonstrated in flies1, mosquitoes2,3, yeast4, and mice5. While numerous potentially impactful applications of such so-called gene-drive systems have been proposed6,7, they are currently limited to copying relatively large DNA cargo sequences (~1–10 Kb). Many desired genetic traits (e.g., drought tolerance in plants, crop yield, pest-resistance, or insecticide sensitivity), however, result from allelic variants altering only one or a few base pairs. An efficient system for super-Mendelian inheritance of such subtle genetic variants would accelerate a wide array of efforts to disseminate favorable traits throughout populations or to assemble complex genotypes consisting of point-mutant alleles in combination with insertional transgenes for a multitude of research and applied purposes.
Widely used CRISPR-Cas9-based gene editing approaches8 involve enzymatic cleavage of a sensitive allele and repair by copying information from an exogenously provided cut-resistant oligonucleotide or double-stranded DNA template9,10. With regard to germline editing, however, we reasoned that, in heterozygous individuals carrying two different alleles of a gene, it might be possible to repair a cleavage-sensitive allele with sequences provided by a cut-resistant allele present on the companion chromosome. This type of allelic-drive could supplement a gene-drive system that copies itself in one genomic location by adding a second guide RNA (gRNA) to the gene-drive cassette that directs selective cleavage of a non-preferred allele at a separate genomic site. Such a dual gRNA drive system (e.g., Fig. 1a, b) should result in efficient super-Mendelian inheritance of both the gene-drive element and the beneficial allelic variant via germline transmission when carrier individuals mate with recipient individuals bearing the undesired cleavage-sensitive allele.
Here we present experimental evidence for two forms of allelic-drive. The first, copy-cutting involves a Cas9-gRNA complex selectively cutting one allelic variant, followed by homology-directed repair (HDR)-mediated repair and replacement with a non-cleavable allele of the same gene provided in-trans. The second, and more generally applicable form of allelic-drive, which we refer to as copy-grafting, involves copying a short genomic interval that encompasses a favored allele in proximity to a gRNA cut site. In the case of copy-grafting, the favored allele is associated with neighboring sequences resistant to gRNA cleavage.
Allele-specific Cas9-dependent cleavage
The X-linked Drosophila Notch (N) locus is particularly well suited for testing the concept of allelic-drive since both loss- and gain-of-function dominant alleles of this locus have been characterized. Loss-of-function N− mutations, which are non-viable when homozygous in females (or hemizygous in males), produce dominant wing margin notching and thickened veins phenotypes in heterozygous females (Fig. 1c, black arrows), while homozygous viable dominant gain-of-function alleles, designated as Abruptex (NAx, denoted as N* in the figures) generate a contrasting vein-loss phenotype (Fig. 1c, light blue arrows). We noticed that one previously identified NAx allele (Ax16) eliminates a PAM site present on the wild-type allele (Fig. 1b, pink box) resulting in a Gly → Arg amino acid substitution11 (Supplementary Fig. 6). We designed a gRNA (gRNA-N+) anchored by this PAM site to direct cleavage of the wild-type N+ allele, but not the NAx16 allele (Fig. 1a, b). The gRNA-N+ was incorporated into a DsRed-marked gRNA-only “CopyCat” element (ccN) designed to insert into, and copy itself, at the closely linked yellow locus, which is located 2 centiMorgans distal to Notch relative to the centromere (Fig. 1a, Supplementary Fig. 4b). Since genomic insertion of the ccN CopyCat element disrupts the function of the yellow locus we denote this allele as y<ccN> (see Methods for full allele nomenclature). We hypothesized that, in the presence of an unlinked source of Cas9, this DsRed marked y<ccN> CopyCat element would copy itself at the yellow locus and might also result in super-Mendelian inheritance of the gRNA-insensitive NAx16 allele via copy-cutting.
We first tested whether the y<ccN> allele would efficiently copy itself, as well as the neighboring uncleavable NAx16 allele, onto a wild-type (y+ N+) X chromosome (Fig. 1a) when combined with an autosomal source of Cas9-provided in-trans (Fig. 1d). F0 females (♀) bearing the y<ccN> and NAx16 alleles were crossed to wild-type males (♂) homozygous for a Cas9 source on the third chromosome to generate F1 y<ccN> NAx16/++; Cas9/+ ♀ progeny, which we hereafter refer to as “master females” (abbreviated MF in figures). In parallel, F0 ♀ were crossed to w– ♂ (lacking Cas9), to generate control F1 females (y<ccN> NAx16/++; +/+ ♀), which we used to assess baseline Mendelian inheritance in the absence of Cas9-mediated drive. F1 master females (and control females) were crossed to wild-type (y+ N+) ♂ carrying a normal X chromosome (or the multiply inverted FM7 balancer chromosome, which suppresses recombination, Fig. 1d). The resulting F2 progeny were then scored both for transmission of the DsRed-marked y<ccN> element and the NAx16 allele.
Transmission percentages for the y<ccN> (DsRed+) and dominant NAx16 alleles in F2 ♂ revealed highly biased inheritance of both alleles wherein 85.3% of these progeny were DsRed+ and yet a higher percentage (93.6%) were NAx16 (Fig. 1e). Since loss-of-function null N− alleles are non-viable in males, which carry only a single X chromosome, F2 ♂ were either NAx16 or N+. Evidence that such lethal N− alleles were indeed being generated as a result of imprecise DNA repair mediated by the non-homologous end joining (NHEJ) pathway is provided below. Additionally, consistent with the observation that nearly all F2 ♂ displayed a yellow− mutant phenotype, sequence analysis of individuals from non-DsRed lines revealed that they all carried NHEJ-induced loss-of function mutations (Fig. 1d, Supplementary Fig. 2).
We also observed super-Mendelian inheritance of the DsRed-marked y<ccN> element in F2 ♀ progeny (72.4%) but were unable to score Notch-related phenotypes with certainty due to a high degree of mosaicism in which wings often displayed a mixture of wild-type, gain-, and loss-of-function phenotypes (Supplementary Fig. 3). Such somatic mosaicism most likely results from the maternal perdurance of Cas9–gRNA complexes deposited into the egg, even in animals that did not inherit the Cas9-GFP transgene3,5,12,13. In order to circumvent this difficulty in scoring Notch phenotypes in F2 ♀, we established 104 individual lines derived from single F2 females (selected for absence of the Cas9-GFP transgene), thus permitting unambiguous scoring of N phenotypes in subsequent generations (Fig. 1d). DNA was prepared from each isogenic line and PCR products from the Notch locus were sequenced to determine what alterations, if any, were present at the Notch-gRNA cleavage site (Supplementary Tables 2 and 3). In this latter analysis, we also identified DNA sequence polymorphisms located in an intron adjacent to the NAx16 mutation (6.5 Kb upstream of the NAx16 mutation) that unambiguously distinguished the donor y<ccN> NAx16 bearing chromosome from the recipient chromosome (Supplementary Fig. 4a). Results of the phenotypic and molecular analysis of the individual F2 ♀ lines are summarized in Fig. 1d (see Supplementary Table 2 and 3 for extensive analysis and sequence data). Overall, the findings parallel those for F2 ♂ as we observed super-Mendelian transmission of the DsRed-marked y<ccN> element (75%) and yet greater inheritance of the NAx16 allele (87.5%) among the female founder lines (Fig. 1d). Also, no N− alleles were recovered, which in this case was surprising as such loss-of-function alleles generated by NHEJ would be expected to be viable in a heterozygous condition (see explanation below).
An important feature of the analysis of gRNA-induced events in the individual F2 ♀ lines was our ability to assign specific copying or non-copying outcomes at the Notch locus to donor vs. receiver chromosomes. In order to achieve the same end while analyzing larger numbers of progeny, we marked the donor chromosome with the tightly linked white-apricot (wa) allele (0.5 centiMorgans from Notch, Supplementary Fig. 4b), which causes an orange eye phenotype (i.e., y<ccN> wa NAx16). F1 master females (y<ccN> wa NAx16/y+ w– N+; Cas9/+) were crossed to w– males (Supplementary Fig. 4), and the resulting F2 individuals could be scored with ~ 99.5% precision for inheritance of donor (wa) vs. receiver (w−) chromosomes. Compiled results from ~20 such crosses conducted in parallel (Fig. 1f) reveal the same overall trend regarding the conversion frequencies observed in the F2 ♀ lines (Fig. 1d), with allelic conversion rates of N+ to NAx16 averaging to 79.5%, a rate approximately a third higher than for copying of the y<ccN> CopyCat element (~60%). This is particularly notable given that gRNA-induced cleavage events at the yellow locus (100% in our study—Supplementary Fig. 2) were consistently greater than at the Notch site, where 8–10% of progeny typically retained an unaltered wild-type target sequence (Fig. 1d, Supplementary Table 2, and Supplementary Fig. 5b).
We also examined the relative proportions of receiver vs. donor chromosomes in F2 progeny of F1 master females and observed a ~2-fold overabundance of donor chromosomes in males and a more modest, but highly statistically significant (p < 0.0001 in unpaired parametric t test analysis), parallel bias in females (Fig. 2a, blue circles). In contrast, among control crosses (for which no source of Cas9 was introduced), a greater proportion of male progeny inherited the wild-type (receiver) chromosome than the NAx16 donor chromosome, presumably reflecting a fitness cost associated with the NAx16 allele (Fig. 2a, gray circles). One potential explanation for the pronounced Cas9-induced reciprocal inheritance bias of the NAx16 donor allele is that a fraction of gRNA-N+-induced cleavage events at the Notch locus on the receiver chromosome may result in NHEJ-induced N− loss-of-function alleles. In males, such alleles would be hemizygous lethal resulting in strong embryonic neurogenic phenotypes causing much of the ventral epidermis to differentiate inappropriately as nervous system14. To test this hypothesis, we collected embryos from F1 master females (y<ccN> NAx16/++; Cas9/+ ♀) crossed to wild-type ♂ and observed an abundant class of mutants (~20%) with strong neurogenic phenotypes (Fig. 2b, c). As expected, neurogenic mutant embryos were absent from control crosses (i.e., from F1 y<ccN> NAx16/++ ♀, Fig. 2c).
Dominant elimination of lethal NHEJ alleles
While the above results provide strong evidence for Cas9-dependent generation of N− alleles in the progeny of F1 master females, they do not readily account for the failure to recover any heterozygous N− alleles among the isogenic F2 ♀ lines. One possibility is that, if F2 ♀ progeny derived from F1 master females inherit a N− allele from their mothers, the “wild-type” paternal allele might be acted on in a mosaic fashion by maternally perduring Cas9-gRNA complexes3,5,12,13. Such a maternal effect could result in a large enough proportion of somatic cells having two mutant copies of the Notch gene to preclude viability in heterozygotes. This hypothetical mechanism, which we refer to as lethal mosaicism, is consistent with the high frequency of mosaic wing phenotypes in F2 ♀ females we observed (Supplementary Fig. 3). One prediction of the lethal mosaic hypothesis is that, if F1 master females were crossed to males carrying the non-cleavable NAx16 allele instead of wild-type males, the observed fraction of N− F2 embryos should decrease significantly as a result of rescued lethality in females, and this was indeed the case (Fig. 2c).
Another avenue for testing the lethal mosaicism hypothesis was provided by sequencing our single F2 ♀ lines that inherited phenotypically wild-type N+ alleles (Supplementary Figs. 5b and 6). This analysis revealed that, while most of these “wild-type” N+ alleles matched the original native allele, one had point mutations in the gRNA core sequence (i.e., between 1 and 4 nucleotides from the PAM site). Such mutations would be predicted to result in cleavage-resistant or “insensitive” (N+IS) alleles (see Fig. 2d for sequence of specific N+IS allele used below). As in the case of crossing master F1 females to NAx16 ♂, we expected that crossing them to N+IS ♂ (Fig. 2d) would also protect heterozygous female F2 progeny from lethal mosaicism since such individuals would carry one cleavage resistant functional N+ allele. The advantage of using N+IS over NAx16 fathers for such experiments is that N−/N+IS ♀ heterozygotes are fully viable, whereas N−/NAx16 ♀ exhibit significantly reduced viability. As predicted by the lethal mosaic hypothesis, a significant percentage (average = 22%; p < 0.0001 in unpaired parametric t test analysis) of F2 females derived from crosses of F1 master females to N+IS ♂ displayed a typical heterozygous N−/+ wing phenotype in a Cas9-dependent fashion (Fig. 2d). Sequencing of several of such N− alleles from individual F2 females revealed an array of DNA alterations centered at the cut site consisting of frameshifts, amino acid substitutions, and deletions (Supplementary Figs. 5a and 6). In addition, consistent with the embryo studies described above, from which we inferred that F2 females could be rescued from mosaic lethality by carrying a cleavage-insensitive Notch allele (Fig. 2c), we observed a 20% excess of females to males (p < 0.0001 in unpaired parametric t test analysis) among adult F2 progeny derived from crosses of master females to N+IS ♂, which was not evident in parallel crosses to wild-type ♂ bearing the sensitive N+ allele (Supplementary Fig. 7).
An additional prediction of the lethal-mosaic hypothesis is that progeny inheriting the ccN drive element and any NHEJ-induced N− allele from their mothers should be inviable if they also carried a zygotic source of Cas9. We tested this prediction by establishing three different lines in which NHEJ-induced N− alleles (N−17, N−20, and N−21—Supplementary Fig. 5) were associated with the ccN element. When such F0 females (y<ccN> N−/Balancer) were crossed to homozygous vasaCas9 males (Fig. 2e), the only viable female F1 adult progeny recovered carried the N+ balancer (BAL) chromosome (Fig. 2e). The absence of emerging N− F1 females in the Cas9 crosses contrasts with the expected 50% Mendelian transmission rate observed in non-Cas9 control crosses. These experiments demonstrate that NHEJ-induced N− alleles, such as those created in the germline of master females, cannot be transmitted to the next generation in the presence of Cas9 since they produce fully penetrant dominant lethality in heterozygous animals carrying the ccN element.
As a yet more stringent test of the lethal mosaic hypothesis, we separately crossed both males and females carrying the ccN element combined with a wild-type cleavage sensitive N+ allele (N+S) to flies carrying the vasaCas9 transgene. Again, no surviving F1 progeny inherited the y<ccN> allele (Supplementary Fig. 8). We conclude that lethal mosaicism is a highly potent process that eliminates all progeny carrying the y<ccN> allele, a hemizygous or homozygous cleavage-sensitive Notch allele, and a Cas9 source (either maternally or paternally provided). A corollary conclusion is that only progeny maintaining an association between the y<ccN> and NAx alleles (or the very rarely generated N+IS cleavage-insensitive alleles) can survive in the presence of Cas9.
The observation of pervasive somatic and lethal mosaicism in crosses of F1 master females to wild-type males raised the possibility that maternally inherited Cas9–gRNA complexes in F2 ♀ might also persist and act in the germline to generate some degree of gene-drive or allelic-drive in the F3 generation, even in animals that did not inherit the Cas9 transgene. We tested this possibility by crossing F2 y<ccN> NAx16/++;+/+ (non-Cas9) ♀ to N+IS ♂ (Fig. 3a). F3 progeny from this cross did indeed manifest a substantial degree of perduring germline Cas9/gRNA activity as indicated by several measures (Fig. 3b), including: (1) copying of the DsRed-labeled y<ccN> element onto the y+N+ receiver chromosome (29.3% and 31.8% conversion of the receiver chromosome in males and females, respectively), (2) copying of the NAx16 allele (27% conversion of the receiver chromosome in males), (3) recovery of N−/N+ ♀ (12%), and (4) Cas9-dependent depletion of receiver chromosomes in males (40.8% compared to 51.1% in control animals). Each of these measures of residual drive observed in the F3 generation (Fig. 3b), which we refer to as shadow-drive, was considerable, amounting to roughly half of that observed in the prior F2 generation.
Co-transmission of a protected allele and drive element
One surprise emerging from analysis of the copying efficiency of the y<ccN> CopyCat element vs. the NAx16 allele, which was also a striking trend in the 104 single female lines (Fig. 1d), was an unexpected high positive correlation between these two conversion events. In nearly all cases where the CopyCat element was copied to a receiver chromosome, so too was the NAx16 allele. This co-drive phenomenon can be most readily appreciated by considering the fraction of NAx16 conversion events among DsRed+ (y<ccN>) receiver chromosomes (92.2%), which is nearly double that of NAx16 conversion among receiving chromosomes that failed to copy the y<ccN> element (51.6%) (Fig. 3c). Similarly, among the single F2 female lines, 96% of the receiver chromosomes carrying the DsRed+ y<ccN> element also copied the NAx16 allele, in contrast to only 38% of progeny having copied the NAx16 allele to a receiver chromosomes in the absence of y<ccN> copying (Fig. 1d). We examined whether this co-drive phenomenon depended on chromosome pairing by placing the y<ccN> NAx16 chromosome in-trans to a multiply inverted balancer X chromosome (Basc). This chromosomal arrangement resulted in a loss of co-drive as well as a marked reduction in the frequency of NAx16 copying (Fig. 3d). It is notable that the frequency of DsRed copying in these crosses was only slightly reduced relative to that observed with a wild-type receiver chromosome, consistent with the tip of the Basc chromosome, which includes the yellow locus, being co-linear with wild-type chromosomes (note: the Basc 1B3 inversion breakpoint is located between y and N). We also tested whether co-drive of the NAx16 allele depended on active copying at the yellow locus by placing the y<ccN> NAx16 chromosome in-trans to a receiver chromosome carrying an NHEJ-induced point mutation at the y-gRNA cleavage site. In this “single cut” configuration, we observed reduced transmission of the NAx16 allele relative to that in control crosses using a wild-type (y+N+) receiver chromosome (Supplementary Fig. 9). This latter experiment indicates that copying the y<ccN> element increases allelic-drive at the N locus. Finally, we examined the impact of cis- vs. trans- configurations for the y<ccN> and NAx16 alleles by generating master females of the genotype y<ccN> N+S/y+ NAx16; Cas9/+ (Supplementary Fig. 10) and observed efficient drive of both the DsRed-marked y<ccN> element (76% conversion) and the NAx16 allele (93% conversion) indicating that both cis- and trans- configurations of the two elements sustain potent drive.
While copying of the Ax16 allele from the donor to the receiver chromosome was the overwhelmingly prevalent event in the above allelic-drive experiments, we also identified rare in-frame NHEJ-induced indels induced at the gRNA-N+ cut site that generated de novo Abruptex alleles (Supplementary Figs. 5c and 6). We tested whether it was possible to produce allelic-drive with one such de novo allele (Ax103) by recombining NAx103 with the y<ccN> element. We found that it performed equivalently to the NAx16 allele in driving conversion of a wild-type N+ allele to an Abruptex phenotype (Supplementary Fig. 11). This finding demonstrates that allelic variants with mutations at the Cas9 cleavage site are equally well suited as those disrupting a PAM site for sustaining efficient allelic-drive.
Copy-grafting is a broadly applicable allelic-drive strategy
The experiments described above demonstrate highly efficient allelic-drive of NAx alleles via copy-cutting mechanism, exceeding by nearly a third that observed for the y<ccN> gene-drive CopyCat element. While these results are encouraging, the obvious limitation of such a strategy lies in the requirement for a gRNA to selectively cut the targeted undesired allele. This constraint requires that the preferred allele either lacks a PAM site or differs from the targeted allele in core gRNA sequences (~1–5 nucleotides from the PAM site), which would occur in only a fraction of cases (~60% of single-nucleotide polymorphisms if GG di-nucleotides occur at a frequency of 1/16 and are randomly distributed). We speculated that it might be possible to develop a more general allelic-drive method by making use of the fact that HDR is often accompanied by local gene conversion events spanning as much as several hundred nucleotides from the double-stranded cleavage site15. This local repair phenomenon has been well documented in Drosophila16,17,18 and may reflect the range of 3′ resection during the DNA repair process16.
With the above motivating concept in mind and the rich array of genetic variants available in Drosophila, as well as those we generated in this study, we conceived of a reverse-drive scenario wherein the wild-type N+IS allele should be preferentially inherited over a different cleavage-sensitive, Abruptex allele (AxE2). The NAxE2 allele results from a C → T substitution located 21 bp upstream of the cleavage-resistant NAx16 G → A alteration (Fig. 4a). The NAxE2 allele, however, should be sensitive to cleavage by the gRNA-N+ carried on the y<ccN> CopyCat element since it lies at a sufficient distance from the gRNA cut site (17 bp, Fig. 4a, NAxE2 indicated as N*S in Fig. 4b). We reasoned that, if the y<ccN> CopyCat element were recombined with the wild-type N+IS cleavage-insensitive allele, which carries a single-nucleotide change (C → A) at the −4 position (Fig. 4a), it might be possible to drive that wild-type N allele onto a receiving chromosome carrying the NAxE2 allele. This inverse-drive scheme depicted in Fig. 4b is referred to as copy-grafting.
Results in Fig. 4c reveal that the efficiency of inverse allelic-drive via copy-grafting (78.2% conversion of receiver chromosomes in males) was comparable to that observed by copy-cutting (79.5% conversion—Fig. 1f). Also, as we observed for copy-cutting, copy-grafting resulted in a dearth of receiver chromosomes in F2 ♂ progeny, in the generation of N− alleles (~16%; when F1 master females were crossed to N+IS ♂ to protect the paternal chromosome from lethal mosaicism), and in strongly correlated co-drive between the y<ccN> and NAxE2 alleles (Supplementary Fig. 12).
In this study, we have demonstrated the feasibility of two forms of allelic-drive: copy-cutting, which applies to cases in which a gRNA can be designed to selectively target a non-preferred allele; and copy-grafting, a more general strategy in which one associates a cleavage-resistant site in proximity to a favored allelic variant (Fig. 4d). Both allelic-drive systems were significantly more efficient than a gene-drive CopyCat element inserted into the yellow locus. An important mechanism contributing to the efficient allelic-drive we observed, which is of potential relevance to field applications, is the phenomena of lethal mosaicism, which dominantly eliminates all NHEJ-induced drive-resistant non-functional loss-of-function alleles of an essential gene such as Notch. Shadow-drive, in which perduring Cas9–gRNA complexes transmitted maternally for one generation in the absence of the Cas9 or gRNA transgenes, should also act as a genetic slingshot to extend gene- or allelic-drive for one additional generation should they become separated from a Cas9 source. Interestingly, we observed a strong correlation between copying events resulting in preferential transmission of both the gene-drive cassette and the preferred non-cleavable allele. This co-drive phenomenon depends on chromosome pairing, as it is not observed when the receiver chromosome carries an inversion affecting the targeted gene. We note that similar correlated genome editing events have been reported recently in other systems including in the germline19 and in somatic cells20. With regard to copy-cutting, the recent development of Cas9 variants with broadened PAM specificity21,22 may substantially increase the fraction of alleles that can potentially be driven by this method. Development of such systems should function with various sources Cas9, as we have also observed allelic-drive with a nanosCas9 transgene as efficiently as with vasaCas9 (Supplementary Fig. 13). Altogether, our study suggests that allelic-drive strategies are likely to be broadly applicable to various gene targets in diverse experimental and agricultural contexts.
One important category of potential applications active genertics is the aggregation of multiple favored naturally occurring allelic variants in plants or animals. In plants, allelic-drive schemes could facilitate combining favorable traits to improve crop yields and resistance to environmental stresses, particularly in polyploid species (e.g., wheat or rye). Similarly, in animal models, allelic-drives could accelerate the construction of complex genotypes for biomedical and basic research. For example, one could envision crossing individual plants or animals bearing a favored allele to a strain carrying a Mendelian cassette with Cas9 and a gRNA that target the corresponding non-preferred alleles. The Cas9-bearing progeny also inheriting the first favored allele could then be crossed to a strain carrying the second favored allele and a gRNA targeting the second unwanted allele and so on until all favored alleles are gathered into a single strain. Finally, one could perform a final cross to segregate out the Cas9-gRNA cassettes. In polyploid crops, such a strategy should permit assembly of several preferred alleles providing drought resistance23, higher yields24, optimal architectures25, or more rapid growth26 that would be long, difficult, or impossible to assemble into a single strain by standard genetic crossing schemes.
Another potentially important class of allelic-drive applications would be to reverse pesticide resistance in pest species. Use of insecticides has repeatedly led to the emergence of specific insecticide-resistant alleles in insect disease vectors and crop pests. Many pesticides target essential components of the nervous system such as the Na+ channel or glutamate receptor27. In principle, allelic-drive systems could help revert these populations back to their wild-type-sensitive state, which would be aided by the reduced fitness of certain prominent insecticide-resistant alleles in the absence of pesticide use28,29,30. It is worth noting that even modest reductions in the incidence of resistant alleles (e.g., to prevalence of <50%) can have major positive impacts on disease-reduction strategies31,32. Similarly, allelic-drives could be used to favor genetic variants that prevent host species from serving as disease vectors or pests.
One potential concern in such allelic-drive scenarios is whether NHEJ-induced cleavage-resistant alleles could also be driven by the gRNA intended to drive the favored allele. This run-away NHEJ problem might arise if the primary drive cassette became separated from the preferred allele and instead became associated with an undesired NHEJ-induced allele. Several lines of evidence presented in the current study suggest that this scenario is unlikely so long as the gRNA sustaining allelic-drive targets a critical region of an essential gene such as Notch (or the Na+ ion channel). First, the strong co-drive we observed greatly limits the number of events separating the favored allele from the drive element (only a few percent in our experiments). Second, lethal mosaicism eliminated 100% of the progeny carrying three different NHEJ-induced N− alleles and also killed all offspring carrying the gene-drive element and unprotected wild-type N+ alleles. Finally, allelic-drives work very effectively in-trans as well as in-cis, indicating that, should an uncoupling event occur, it would be rapidly reversed in most instances. Thus all non-functional NHEJ alleles will be eliminated immediately as they are generated, and drive of the favored allele will persist either in-cis or in-trans. The only remaining concern is whether one might not occasionally create a functional non-cleavable version of the undesired allele that could then also be driven. While this is possible (e.g., we did recover rare N+IS and novel Ax alleles), such events are infrequent and should not drive any more efficiently than the overwhelmingly prevalent preferred allele. It may be possible to further reduce the production of such rare events by using two gRNAs simultaneously, one directing copy-cutting and the other copy-grafting of the same preferred allele. Thus it should be practical to drive preferred alleles of essential genes efficiently into a population so long as they do not impart a significant fitness cost relative to the non-preferred allele.
Lethal mosaicism should also have game-changing implications for developing new efficient gene-drive systems. A drive element targeting a critical site in a gene essential for viability or reproduction could also carry a functional recoded (and non-cleavable) portion of that same gene, thereby protecting progeny inheriting this element from lethal (or sterile) mosaicism. In contrast, non-functional NHEJ-induced mutations rendered dominant by lethal mosaicism should be eliminated immediately, thereby “killing or sterilizing the mistakes” and providing a powerful solution to the frequently highlighted drive-resistance problem. These and other diverse applications of allelic-drive should greatly expand the impact of active genetics, accelerating progress in many areas of synthetic biology.
Construction of ccN CopyCat element
Cloning of the ccN CopyCat plasmid followed the same strategy as described in Xu et al.7 using homology arms to the yellow locus abutting gRNA-y1 cleavage site and carrying gRNA-y1, gRNA-N+, and a 3XP3-DsRed eye marker as depicted in Supplementary Fig. 1 (the full DNA sequence of this plasmid is provided in Supplementary Table 1). Following assembly of its components, the ccN CopyCat plasmid was transformed into One Shot® TOP10 competent cells (Invitrogen #C4040) and purified using the Qiagen Plasmid Midi Kit (#12191). An injection mix containing the ccN plasmid (final concentration: 250 ng/µl) was sent to Best Gene Inc. for injection into embryos collected from a wa NAx16 rb− stock (which is resistant to the otherwise lethal mutagenesis of the Notch locus generated by Cas9/gRNA-N+) with a transient source of pHsp70-Cas9 (Addgene plasmid #45945). The wa NAx16 rb− stock was kindly provided by Jim Posakony (UCSD). Male transformants carrying the ccN element were identified in F1 progeny by virtue of their yellow− and DsRed fluorescent eye-marker phenotypes. This genomic insertional allele is referred to as: y<CC|gRNA-y1, gRNA-N+|3XP3DsRed> in accordance with our previously established nomenclature convention6,7 (see Supplementary Fig. 1 for details of the construct). For shorthand in the text, we refer to this allele as: y<ccN>. The ccN plasmid construct was fully sequenced prior to injection as well as that of the ccN genomic insertion for several individual y<ccN> transformant lines, which included PCR amplification and sequencing of endogenous sequences lying adjacent to those included as homology arm templates in the plasmid construct to verify accurate insertion of the ccN element into the intended site (Supplementary Table 1).
Genomic DNA preparation
Genomic DNA from single adult flies were prepared according to protocols by Gloor et al.33. Single flies were crushed in lysis buffer (10 mM Tris pH8.2, 1 mM EDTA, 25 mM NaCl, with 0.3 mg/ml Proteinase K, added right before incubation), incubated at 37 °C for 30 min, and heated at 95 °C for 2 min. One hundred μl of ddH2O were added to each tube before storage at −20 °C.
Flies carrying the donor y<ccN> wa NAx16 chromosome were identifiable through the visible wa orange eye phenotype. y<ccN> wa NAx16/FM7 females were crossed to vasaCas9 homozygous males (BL# 51324) to generate F1 master females as diagrammed in Fig. 1d. Crosses were performed at 25 °C on standard Drosophila food. The y− w+ NAxE2 line carrying a gRNA-N+-sensitive Abruptex allele was kindly provided by Spyros Artavanis-Tsakonas (Harvard University). A cleavage-insensitive N+ allele recovered among the 104 isogenic lines was recombined with y<ccN> wa to generate the donor chromosome in Fig. 4b. For quantitative analyses of F2 progeny (or F3 progeny for the shadow-drive), 20–37 crosses consisting of 3 females mated to 3 males were analyzed for each experiment, yielding an average of ~150 flies per cross. A total of 29,000 progeny were analyzed for this study.
To sequence mutations in the yellow locus, an ~500-bp fragment was amplified by PCR (Q5 Hot Start High-Fidelity 2× Master Mix) with primers 417 (TTTAGTGCCTCAATAATAGTTTGGCCCTGC) and 356 (GGACATACCAAATATACCCTCC), then sequenced with primer 418 (GGAAGTTAATACCAGCGACATTGAAATCGC) at Genewiz. To identify donor vs. receiver chromosomes, a fragment from Notch intron 5 was amplified with primers NintS3 (CTACGAGTGCAAGTGCCCCAAAG) and NintAS3 (CGCCCGGAACGTTGGAATGGAATG) and sequenced with NintS3bis (CAGTAGGAACCAGATTAATCGAGTT). For sequencing mutations in the NAx region, primers NAxS (CCACGAGCAAAACAACGAGTACAC) and NAxAS2 (TTCGAATCACAATCCTGACCACTCAGC) were used to amplify an ~1-Kb fragment and sequenced using primer NAxS3 (GCATCAATGGCTACAACTGTAGC).
Active genetic safety measures
All crosses using active genetics were performed in accordance to an Institutional Biosafety Committee-approved protocol from UCSD in which full gene-drive experiments are performed in a high-security ACL2 barrier facility and split drive experiments are performed in an ACL1 insectary in plastic vials that are autoclaved prior to being discarded in accord with currently suggested guidelines for laboratory confinement of gene-drive systems34,35.
Wing dissection and mounting
Drosophila wings were dissected in isopropanol and mounted in 100% Canada balsam.
Antibody staining of Drosophila embryos
Fixation and antibody staining of embryos using a rat anti-Elav (DSHB# 7E8A10, antibody dilution = 1/20) was performed according to standard procedures. Samples were mounted in Slowfade diamond anti-fade mountant (Thermo Fisher Scientific #S36963) and imaged on a Leica SP5 confocal microscope. Each data point in Fig. 2c corresponds to the analysis of a group of 30–50 embryos on a slide. Embryos of stages 11–16 were scored for N+/N− phenotypes using a Zeiss AXIO ZOOM V16 fluorescent microscope.
Ethical conduct of research
We have complied with all relevant ethical regulations for animal testing and research and conformed to the UCSD institutionally approved biological use authorization protocol (BUA #311).
Further information on experimental design is available in the Nature Research Reporting Summary linked to this article.
All relevant data are available from the authors.
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We thank Anthony James, Bill McGinnis, Omar Akbari, Helena Araujo, Sara Werner, and members of the Bier laboratory for comments and suggestions on the manuscript. We thank Jim Posakony (UCSD) and Spyros Artavanis-Tsakonas (Harvard) for kindly providing the Ax16 and AxE2 fly stocks, respectively. We also thank the reviewers for constructive comments on the manuscript. These studies were supported by an NIH grant R01 GM117321 and a Paul G. Allen Frontiers Group Distinguished Investigators Award to E.B., an NIH grant DP5OD023098 supported V.M.G, and a gift from the Tata Trusts in India to TIGS-UCSD and TIGS-India. Confocal microscopy was performed at UCSD School of Medicine Microscopy Core, supported by Grant P30 NS047101.
E.B. and V.G. have equity interest in Synbal Inc. and Agragene, Inc., companies that may potentially benefit from the research results and also serves on the company’s Board of Directors and Scientific Advisory Board. The terms of this arrangement have been reviewed and approved by the University of California, San Diego in accordance with its conflict of interest policies. The other authors declare no competing interests.
Journal peer review information: Nature Communications thanks Nikolai Windbichler and the other anonymous reviewer(s) for their contribution to the peer review of this work.
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Guichard, A., Haque, T., Bobik, M. et al. Efficient allelic-drive in Drosophila. Nat Commun 10, 1640 (2019). https://doi.org/10.1038/s41467-019-09694-w
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