Apomixis: genetic basis and controlling genes

Abstract

Apomixis is the phenomenon of clonal reproduction by seed. As apomixis can produce clonal progeny with exactly the same genotype as the maternal plant, it has an important application in genotype fixation and accelerating agricultural breeding strategies. The introduction of apomixis to major crops would bring many benefits to agriculture, including permanent fixation of superior genotypes and simplifying the procedures of hybrid seed production, as well as purification and rejuvenation of crops propagated vegetatively. Although apomixis naturally occurs in more than 400 plant species, it is rare among the major crops. Currently, with better understanding of apomixis, some achievements have been made in synthetic apomixis. However, due to prevailing limitations, there is still a long way to go to achieve large-scale application of apomixis to crop breeding. Here, we compare the developmental features of apomixis and sexual plant reproduction and review the recent identification of apomixis genes, transposons, epigenetic regulation, and genetic events leading to apomixis. We also summarize the possible strategies and potential genes for engineering apomixis into crop plants.

Introduction

Generally, angiosperms go through sporophytic and gametophytic generations alternately, and produce future generations by sexual reproduction. However, some plants can also reproduce asexually by apomixis. Apomixis is an asexual reproduction process that produces seeds in the absence of meiosis and fertilization [1, 2]. As apomictic plants can produce clonal offspring that fully retain the genotype of their mother plant through seeds, apomixis can provide many agronomic advantages for crop production: the stable fixation of heterosis through seed; the rapid generation of new superior germplasms; the simplification of hybrid seed production procedures; and the purification and rejuvenation of some vegetatively propagated varieties, such as perennial woody fruit trees [3]. Applying apomixis to the seed production of crops will drive a new green revolution in agricultural science [4].

Apomixis was initially discovered in Alchornea ilicifolia [5], and subsequently had been described in more than 400 flower plant species [6]. Many important genera in Asteraceae and Poaceae are reported as typical apomictic plants, such as Hieracium, Taraxacum, and Pennisetum. Some species in these genera are widely studied to dissect the genetic control of apomixis [7–12]. Apomixis also occurs widely in horticultural crops, including citrus [13], crabapple [14], walnut [15], mango [16], pepper [17], and Chinese chive [18]. However, apomixis is relatively infrequent in major crop species [6]. Understanding the mechanism and control of apomixis in existing apomictic plants is the prerequisite for applying apomixis in agriculture.

In this review, the developmental features of apomixis and sexual plant reproduction are described. We summarize the recent understanding of the factors influencing apomixis, including genetic control, transposons, epigenetic regulation, polyploidization, and hybridization. We also propose possible strategies and potential genes to create gametophytic or sporophytic apomixis for application in agriculture.

Developmental features of apomixis and sexual reproduction

During normal sexual reproduction, the megaspore mother cell (MMC) divides into four reduced megaspores through meiosis. Three of these megaspores undergo apoptosis and the remaining functional megaspore develops into a seven-celled, eight-nucleate embryo sac, consisting of one egg cell, one central cell, two synergid cells, and three antipodal cells. When the pollen tube penetrates into the embryo sac, double fertilization occurs [19]. One sperm cell fuses with the egg cell to form a zygote, while the other sperm cell fuses with the central cell and then develops into endosperm, which provides nutrients for embryo development (Fig. 1). In the process of sexual reproduction, meiosis ensures the formation of a reduced embryo sac. Double fertilization not only produces the zygote and triploid nucleus, but also activates the initial development of the zygote by complicated signals from both egg cell and sperm cells [20, 21].

Figure 1.

Schematic representation of sexual and apomictic embryo formation. In the process of amphimixis, the megaspore mother cell (MMC) undergoes mitosis and meiosis and develops into a seven-celled, eight-nucleate embryo sac, and then produces a zygotic embryo after double fertilization. For diplospory, the MMC undergoes ameiotic division and divides into two non-reduced megaspores. One of the non-reduced megaspores develops into an unreduced embryo sac. Then the diploid egg cell can directly develop into a parthenogenetic embryo. For apospory, the aposporous initial cell from the nucellus forms an unreduced embryo sac and eventually develops into an asexual embryo. For sporophyte apomixis, at the same time as normal amphimixis, the nucellus-derived nucellar embryo initiation cells divide rapidly and enter the embryo sac, forming one or more nucellar embryos, which can coexist with the zygotic embryo.

Compared with sexual reproduction, apomixis alters several steps during the initiation and formation of the female germline and produces an asexual embryo with a genotype identical to that of the mother plant (Fig. 1). Based on the origin of the embryo, apomixis can be divided into two types, gametophytic apomixis and sporophytic apomixis (adventitious embryo) [1]. Gametophytic apomixis refers to the asexual embryos derived from the unreduced embryo sac, which can be further divided into diplospory and apospory according to the origin of the cell that initiates unreduced embryo sac formation [22, 23]. In diplospory, the MMC undergoes a modified meiosis and divides into two non-reduced megaspores. One of the unreduced megaspores develops into a diploid embryo sac, in which the diploid egg cell can directly develop into a parthenogenetic embryo without double fertilization [24]. In apospory, a nucellar (somatic) cell near the MMC acquires a gametophytic fate and directly gives rise to the gametophytic lineage without meiosis. The apomictic germline lineage can repress the development of the sexual gametophyte and form an unreduced embryo sac, in which a parthenogenetic embryo is directly developed from the diploid egg cell without fertilization. In some cases, many aposporous initial cells occur in a single ovule and develop into more than one aposporous embryo sac [25, 26]. Gametophytic apomixis completely replaces amphimixis, and is regarded as obligate apomixis [23], while in most apomictic plants both sexual and asexual reproduction processes occur simultaneously in the same ovule, which is termed facultative apomixis [27]. In both diplosporous and aposporous ovules, the endosperm can develop spontaneously without fertilization or through pseudofertilization, providing nutrients for the development of the embryo [19].

For sporophytic apomixis, adventitious embryos are developed from nucellar or integument cells and coexist with the zygotic embryo, leading to the development of a polyembryonic ovule [28]. Generally, the adventitious embryo initial cells appear to be morphologically distinguishable after the formation of the sexual embryo sac. Then they enter the sexual embryo sac and compete with the sexual embryo for nutrients. The survival of the adventitious embryo depends on the fertilization of the sexual embryo sac, which can offer important nutrient and growth signals from the fertilized endosperm [29]. Multiple adventitious embryos can initiate in an individual ovule (Fig. 1).

Apomixis-controlling loci and related genes

From an evolutionary perspective, apomixis may have evolved from the same molecular framework as that which supports sexual reproduction. When sexual reproduction is aborted as a result of the mutation of corresponding genes, apomixis occurs to overcome infertility. In Arabidopsis, a set of mutants have been reported to display phenotypes resembling apomixis (Table 1), such as ago9 [30] and swi1 [31], which participate in chromatin remodeling; spo11-1/2 [32, 33], mtopVIB [34], dfo [35], prd1 [36], and rad50 [37, 38], which are involved in double-strand break formation; dmc1 [39], msh4 [40], and asy1 [41], which are essential for chromosome synapsis; rec8 [42], scc3 [43], and ahp2 [44], which are involved in the first meiotic division; osd1 [45] and tam [46, 47], which are related to the meiosis I–meiosis II transition; tdm1 [48], which controls meiotic termination after meiosis II; msi1 [49], which is able to initiate parthenogenetic development; cenh3 [50], which can induce haploid formation; and fie [51] and fis [52], which can induce endosperm development without fertilization. Most apomictic plants are facultative, which offers the possibility of genetic analyses of apomixis. In all species studied so far apomixis has been proved to be heritable. In citrus and mango, inheritance of sporophytic apomixis as single dominant locus has been proposed [16, 53], while in some diplosporous apomicts genetic loci controlling the key steps of apomixis (apomeiosis, parthenogenesis, and automatic endosperm development) are independent of each other. For example, two separate loci that control diplospory and parthenogenesis have been identified in Erigeron and Taraxacum species [54, 55]. Apospory and parthenogenesis are determined by two different loci in Hypericum [56], Poa [57], and Cenchrus [58] species. In Hieracium, three independent loci, LOA, LOP, and AutE, have been discovered to control apospory, parthenogenesis, and autonomous endosperm development, respectively [59, 60].

Table 1.

Information on candidate genes related to apomixis

Component of apomixis	Gene	Description	Genus	References
Apomeiosis	APOLLO	APOLLO is associated with egg cell formation in apomicts. It is highly expressed in apomictic ovules.	Boechera	64, 65
	UPGRADE2	UPGRADE2 represents a long non-coding RNA and its expression is related to the formation of unreduced pollen.	Boechera	66
	AGO104	AGO104 is involved in chromatin condensation during meiosis. Mutation of AGO104 can produce an apomixis-like phenotype, producing functional unreduced female gametes.	Tripsacum	67
	PAIR1	PAIR1 protein is essential for homologous chromosome pairing in early meiotic prophase in rice.	Oryza	68
	ago9	AGO9-dependent sRNA silencing is important for specification of cell fate and initiation of gametogenesis in the Arabidopsis ovule.	Arabidopsis	30
	swi1	SWI1 encodes an unknown protein that is important for sister chromatid cohesion in the meiosis process.	Arabidopsis	31
	spo11-1/2	SPO11-1 and SPO11-2 encode Topo VIA proteins, which can induce meiotic double-strand break (DSB), which is required for meiotic recombination.	Arabidopsis	32,33
	mtopVIB	MTOPVIB encodes Topo VIB protein, which can interact with Topo VIA proteins to promote meiotic DSB formation.	Arabidopsis	34
	dfo	DFO is involved in DSB formation. Mutation of DFO severely affected homolog synapsis and recombination during meiosis.	Arabidopsis	35
	prd1	PRD1 participates in meiotic recombination and is required for meiotic DSB formation.	Arabidopsis	36
	rad50	Rad50 protein is required for telomere maintenance. Mutation of Rad50 will stimulate chromosomal recombination.	Arabidopsis	37,38
	dmc1	DMC1 is involved in meiotic recombination. Mutants of DMC1 exhibit defects in meiotic DSB formation.	Arabidopsis	39
	msh4	MSH4 is involved in crossover formation at the early step of recombination.	Arabidopsis	40
	asy1	ASY1 plays an essential role in homologous chromosome synapsis.	Arabidopsis	41
	rec8	Cohesin Rec8 plays an important role in reductional chromosome segregation.	Arabidopsis	42
	scc3	SCC3 protein is essential for the maintenance of centromere cohesion.	Arabidopsis	43
	ahp2	AHP2 is involved in bivalent formation and homologous chromosome segregation.	Arabidopsis	44
	osd1	OSD1 mutants cannot go into the second meiotic division.	Arabidopsis	45
	tam	TAM encodes an A-type cyclin that is involved in both meiosis I and meiosis II.	Arabidopsis	46,47
	tdm1	TDM1 is essential for meiotic termination after meiosis II.	Arabidopsis	48
Apospory	QGJ	QGJ is involved in the development of non-reduced embryo sacs in apomictic plants.	Paspalum	69
	GID1	Ectopic expression of GID1 leads to the occurrence of MMC-like cells in the nucellus that do not have MMC identity.	Brachiaria	70
	DEFICIENSH	DEFICIENSH may be related to cellular differentiation of the MMC and megagametogenesis.	Hieracium	71
	PnTgs1-like	PnTgs1-like probably determines the fate of nucellar cells, as its reduced expression is associated with initiation of the apomictic pathway.	Paspalum	72
	SERK	Activation of SERK in nucellar cells can induce formation of the aposporous initial cell and development of the asexual embryo sac.	Poa	73
Endosperm development	ORC3	Defective ORC3 mutants exhibit a normal female gametophyte but development of the embryo and endosperm is abolished.	Paspalum	74
	FIE	Expression of FIE is negatively correlated with parthenogenesis capacity. Mutant FIE allows endosperm development without fertilization.	Malus, Arabidopsis	51,75,76
	fis	FIS controls seed development after double fertilization. In fis mutants, partial development of seeds can occur without pollination.	Arabidopsis	52
Parthenogenesis	ASGR-BBML	ASGR-BBML is expressed in unfertilized egg cells of apomictic Pennisetum squamulatum and activation of its expression in sexual pearl millet can also trigger parthenogenesis.	Pennisetum, Cenchrus	12,77
	PAR	The dominant PAR allele of dandelion is specifically expressed in egg cells and can trigger embryogenesis without fertilization.	Taraxacum	78
	MTL1	MTL1 encodes a pollen-specific phospholipase that is involved in fertilization. Mutation of the MTL1 gene can induce haploid formation in maize.	Zea	79
	msi1	The MSI1 gene functions in chromatin assembly. Mutants of MSI1 can produce parthenogenetic embryos.	Arabidopsis	49
	cenh3	Alteration of centromere-specific histone CENH3 can induce genome elimination and haploid formation.	Arabidopsis	50
Adventitious embryogenesis	RWP	The CitRWP gene co-segregates with the citrus nucellar embryo and is preferentially expressed in nucellar embryo initiation cells. Loss of CitRWP function can abolish nucellar embryogenesis in citrus.	Citrus	80,81
	AGL11	AGL11 is a MADS-box transcription factor and is preferentially expressed at the apomictic nucellar embryo stage in Zanthoxylum bungeanum. Ectopic expression of ZbAGL11 can lead to abnormal flower development and induce apomixis-like phenotypes in Arabidopsis.	Zanthoxylum	82

Despite the discovery of multiple apomixis-linked loci in various species, it is still difficult to identify the specific genes controlling apomixis, as the apomixis-linked loci are usually recombination-inhibited and located in repetitive regions [61–63]. So far, a few genes have been identified that are involved in different components of apomixis (Table 1). For apomeiosis, two different candidate genes, APOLLO (apomixis-linked locus) and UPGRADE2 (unreduced pollen grain development), have been identified in Boechera. The expression of APOLLO and UPGRADE2 is strongly correlated with the formation of apomeiotic eggs and pollen, respectively [64–66]. In Tripsacum, AGO104, which is involved in DNA methylation, is proposed to be required for proper chromatin condensation during meiosis [67]. In Oryza sativa, the PAIR1 gene was identified to play an essential role in chromosome synapsis in early meiotic prophase [68]. For apospory, a MAP3K-coding QUI-GONJINN (QGJ) gene in Paspalum notatum is suggested to be essential for aposporous embryo sac formation [69]. In Brachiaria brizantha, the specific expression pattern of GIBBERELLIN-INSENSITIVE DWARF1 (GID1) suggests its function in aposporous initial cell differentiation to form the aposporic embryo sac [70]. In apomictic Hieracium, transient downregulation of a floral organ-identity gene (DEFICIENS) in the chalazal region is associated with aposporous initial cell formation [71]. Similarly, in P. notatum, PnTgs1-like was proposed to play an important role in nucellar cell fate, as its reduced expression is associated with the initiation of the aposporous pathway [72]. In Poa pratensis, PpSERK is proposed to be responsible for the formation of the aposporous initial cell and the development of the asexual embryo sac [73]. For autonomous endosperm formation, ORC3 and FIE were proved to be vital candidate genes. The accurate expression of ORC3 in germ cell lineages determines the development of the endosperm in apomictic Paspalum simplex [74]. In Malus hupehensis, FIE is involved in the regulation of asexual seed formation [75]. Ectopic expression of MhFIE in tomato produces parthenocarpic fruit [76]. For parthenogenesis, ASGR-BBML has been proved to be the most promising candidate. ASGR-BBML is expressed in unfertilized egg cells of apomictic Pennisetum squamulatum and transformation of sexual pearl millet with the ASGR-BBML gene can trigger parthenogenesis [12, 77]. Recently, a PARTHENOGENESIS (PAR) gene was isolated from apomictic common dandelion, which can induce embryo-like structures without fertilization in lettuce [78]. In addition, mutation of a pollen-specific phospholipase, MTL1, can induce paternal genome elimination and haploid formation in maize and rice [79]. For adventitious embryogenesis, several candidate genes have also been reported. In citrus, the CitRWP gene was identified by genetic analysis of segregating populations and proved to be associated with nucellar embryo formation [80, 81]. In another typical sporophytic apomictic plant, Zanthoxylum bungeanum, the expression of AGL11 shows correlation with nucellar embryo development and its ectopic expression can lead to abnormal flower development and simulate apomixis phenotypes in Arabidopsis [82].

Miniature inverted-repeat transposable element transposons mediate activation of apomixis-controlling genes

Transposon insertions can affect the expression and function of adjacent genes and can cause phenotypic changes in plants [83–85]. With the development of research on apomixis, some evidence suggests that transposons may be involved in apomixis. In both aposporous Cenchrus ciliaris and P. squamulatum, the apospory-specific genomic region (ASGR) is located on a single chromosome that contains transposons and repeated sequences [9, 86, 87]. The hemizygous chromosomal region containing the LOSS OF APOMEIOSIS (LOA) locus in Hieracium also has abundant complex repeats and transposon sequences [88]. These structural features of the apomixis loci suggest that transposons might take part the induction or maintenance of apospory in these plants. Notably, our previous genetic analysis identified a miniature inverted-repeat transposable element (MITE) transposon insertion in the promoter region of the candidate gene (CitRWP) controlling sporophytic apomixis in Citrus [80]. This MITE transposon showed complete co-segregation with the polyembryony trait of Citrus in both natural and segregating populations. In polyembryonic citrus varieties, the CitRWP gene with a MITE transposon insertion is highly expressed. While in monoembryonic varieties, no MITE transposon insertion was found in the promoter region of the CitRWP gene and its expression was barely detectable. All these results suggest that the MITE transposon insertion in the promoter region of the CitRWP gene is required to enable sporophytic apomixis in citrus (Fig. 2A). Similarly, in apomictic dandelion (Taraxacum officinale) and hawkweed (Hieracium piloselloides) MITE transposons also exist in the upstream region of the parthenogenesis gene (PAR) [78]. The MITE-containing promoter from dandelion can activate the PAR-homologous gene from sexual lettuce to reproduce the dandelion parthenogenetic phenotype, suggesting the decisive effect of the MITE transposon on parthenogenesis (Fig. 2B).

Figure 2.

Typical cases of apomixis induced by MITE transposons. (A) A MITE transposon inserted in the CitRWP promoter activates gene expression, leading to multiple nucellar embryos in one seed of the polyembryonic citrus. In monoembryonic citrus there are no MITE transposon inserts in the CitRWP promoter and the gene is weakly expressed. (B) In sexual dandelions the PAR allele from the female parent with no MITE transposon insertion is not expressed in the egg cell, and the sexual diploid embryo comes from double fertilization. In polyploid apomicts the PAR allele with a MITE transposon insertion in its promoter is activated in the egg cell. Then the egg cell can directly develop into a haploid embryo without fertilization; this is parthenogenesis.

In both Citrus and dandelion, the MITE transposons inserted in the promoter region may be associated with upregulation of the adjacent genes, thereby controlling apomixis. It is likely that MITE insertions in the promoter of CitRWP or PAR genes lead to a transition from sexual reproduction to adventitious or parthenogenetic embryo development. Generally, MITE insertion in the promoter may impact gene expression through two different mechanisms: (i) by introducing a spatiotemporally specific activating element within the MITE; and (ii) by disrupting a repressive regulatory element that normally represses adjacent gene expression. Another mechanism influencing alteration of DNA methylation patterns should also be considered. Recently, a DNA methylome analysis revealed hypermethylation in the promoter of CitRWP in polyembryonic citrus, which contains a MITE insertion, while hypomethylation was detected in the promoter of CitRWP in monoembryonic citrus without a MITE insertion [89]. This result suggests that the MITE insertion may be related to the hypermethylation of CitRWP, which might activate gene transcription and further enable cells in the ovules of polyembryonic citrus to switch to an apomictic pathway.

Epigenetic regulation of apomixis

The initiation of apomixis is believed to be attributable to the downregulation of important genes in sexual reproduction, and epigenetic regulation enables reversible conversion between the two reproductive modes in plants. Transcriptome comparison of apomictic Boechera, Hieracium, and Hypericum with related sexual lines revealed changes in siRNA synthesis and RNA-directed DNA methylation (RdDM)-related gene expression [90–92]. DNA methylation analysis showed that the overall methylation level of gametophyte-apomictic C. ciliaris [93] and sporophyte-apomictic citrus [89] was lower than that of sexually reproducing plants, suggesting that hypomethylation is related to apomictic reproduction, while in the gametophyte-apomictic Paspalum treatment with the DNA methylation inhibitor 5-azacytidine significantly reduced parthenogenesis frequency, suggesting that a high DNA methylation level may maintain apomictic reproduction [94].

The absence of important epigenetic pathway genes in model plants can lead to a phenotype resembling apomixis. Multiple mutants involved in siRNA synthesis and the RdDM pathway can form additional gametophytic cells, similar to what occurs in diplospory, such as ago9, sgs3, rdr2, rdr6, and dcl3 [95]. Recent studies have shown that AGO9 and RDR6 gene mutations lead to ectopic expression of SPL/NZZ, which controls the differentiation of MMC cells, resulting in multiple MMC-like cells in the ovule [96].

Genetic events lead to apomixis: polyploidization and hybridization

Hybridization and polyploidization can widely activate transposable elements that are silenced by epigenetic modifications [83, 97]. Most gametophytic apomicts are polyploid, and a causal relationship has been proposed between apomixis and polyploidization [6]. With respect to the cytological mechanism of apomixis, there is really a link between apomixis and polyploidization, as synthetic induction of polyploidy can induce apomixis from sexual plants [98, 99]. Nevertheless, apomixis can also occur in diploid plants [100, 101], suggesting that polyploidy is not a prerequisite of apomixis. The causal relationship between apomixis and polyploidization remains unclear. The point of view has been put forward that a polyploid genome can promote the optimum expression of apomixis [99], while it is also proposed that polyploidization may be a result of apomixis, which confers genomic stability. During the apomixis process, apomeiosis and parthenogenesis may increase the frequency of polyploidization [102, 103].

Most apomictic polyploids are allopolyploids, formed by hybridization between genetically divergent diploid species [104]. So it is also speculated that hybridization, rather than polyploidy, leads to apomixis [27, 105]. In genome-duplicated hybrids, asynchronous expression of the two sets of genes involved in female reproduction may result in precocious embryo sac initiation and embryogenesis [6]. In Boechera, diploid apomicts show high heterozygosity caused by the conjunction of disparate genomes, which suggests that the genomic consequences of hybridization may be related to gametophytic apomixis in this genus [106]. A hybrid origin of apomixis had also been proposed in the Ranunculus cassubicus complex, and some unique alleles that resulted from genomic reorganization in allopolyploids might trigger apomixis [107]. Additionally, some sporophytic apomictic species, such as Citrus [108], Mangifera [109], and Zanthoxylum [110], all have a high level of heterozygosity.

Perspectives for future study and applications of apomixis in breeding

Apomixis is a fascinating phenomenon with great application potential for agriculture. Although increasing numbers of genes associated with apomixis have been identified, the gene regulatory network and molecular mechanisms of apomixis are not clear. Based on the candidate genes currently identified by genetic analysis, further studies are needed to dissect the upstream and downstream regulators. And a clear regulatory network of each component of apomixis will provide a strong foundation for the engineering of apomixis in crops. As apomixis occurs randomly in some genera of angiosperms and all steps of the apomixis process have evolved several times independently, exploring the origin and evolution of apomixis may provide more clues about the mechanism of apomixis. For example, the CitRWP gene has been proved to control nucellar embryony in Citrus, but not in its related genera in Rutaceae, including Zanthoxylum, Murraya, and Poncirus, although these genera exhibit a form of sporophytic apomixis similar to that of Citrus [111]. It is probable that all the genera in Rutaceae undergo the same apomixis pathway, but the mutations associated with apomixis in different genera may have occurred at different nodes of the pathway. Thus, identification of the different mutations leading to nucellar embryogenesis in each genus may contribute to deeper understanding of the regulatory pathways of sporophytic apomixis in Rutaceae.

Artificial creation of apomixis in crops is an effective way to fix heterosis and the ultimate goal of studying apomictic reproductive traits. Several studies have reported the engineering of gametophytic apomixis. The MiMe (substitute mitosis for meiosis) system was first created in Arabidopsis by simultaneous mutation of three key meiotic genes (SPO11-1, REC8, and OSD1) [112]. Hybridization of a cenh3 null mutant expressing altered CENH3 protein, which can induce centromere-mediated genome elimination, with MiMe plants produced clonal reproduction though seeds [113]. In rice, triple mutations of three key meiotic genes (PAIR1, REC8, and OSD1) can also turn mitosis to meiosis (MiMe) [114]. Multiplex editing of the three key meiotic genes and the MTL gene resulted in plants that can propagate clonally through seeds [115]. Moreover, MiMe combined with the expression of a parthenogenesis gene, BBM1, in the egg cell can also induce clonal progeny of hybrid rice that retain genome-wide parental heterozygosity [116]. However, there are still some limitations in the application of the above synthetic apomixis strategies. The MiMe system combined with CENH3 system depends on hybrid pollination [113], which restricted the commercial production of clonal seeds. In both the MiMe combined with MTL1 system and the MiMe combined with BBM1 system, the clonal seeds exhibited relatively low fertility, possibly due to the low frequency of parthenogenesis [115, 116]. Current apomixis strategies might be improved by increasing parthenogenesis induction efficiency. In addition, the MiMe combined with BBM1 system requires self-pollination to initiate endosperm development and thus sexual seeds are also produced together with the clonal seeds. This system could potentially be improved by integrating genes that can promote autonomous endosperm development, such as ORC [74] and FIE [51].

As the mechanisms of sporophytic apomixis are less studied, application of sporophytic apomixis has been difficult. The CitRWP gene identified in citrus is a potential candidate to create sporophytic apomictic crops [80]. RWP-RK domain-containing (RKD) genes play important roles in the maintenance of egg-cell identity and their ectopic expression can promote somatic embryogenesis in Arabidopsis [117]. The specific expression of CitRWP in citrus ovules may enable the nucellar cells to acquire an embryonic fate. Additionally, a C2H2 zinc-finger domain-containing transcription factor gene (CitZFP), which is homologous to the dandelion parthenogenesis gene (PAR), is specifically expressed in apomictic cells [89]. This gene may be another candidate gene for engineering sporophytic apomixis. Further studies on the function and regulation of CitRWP and CitZFP genes in citrus are necessary for the utilization of sporophytic apomixis in apomixis breeding.

Acknowledgements

We thank Prakash Babu Adhikari for critical reading of the manuscript. This study was financially supported by the National Natural Science Foundation of China (32001997), Major Special Projects and Key R&D Projects in Yunnan Province (202102AE090054), and the National Postdoctoral Program for Innovative Talents (BX20200146).

Author contributions

Q.X. and Y.X. planned the outline of the review. Y.X. completed the first draft of the paper. H.J. and C.T. helped with literature collection and discussion. Q.X., X.W., and X.D. revised the paper. All authors approved the final paper.

Conflict of interest

The authors declare no competing interests.