mea seeds can be paternally rescued

When mea ovules are pollinated with wild-type pollen from the Landsberg erecta accession (hereafter referred to as Ler), seeds undergo excessive cell proliferation and abort before completing embryogenesis [21]. However, mea ovules pollinated with pollen from other Arabidopsis accessions (such as Cvi-0 or C24) can give rise to viable plump mea seeds (Fig 1A and S1 Fig). To dissect the relative paternal and maternal contributions to mea seed rescue, we introgressed mea-2 (originally in the Ler background) into Cvi-0 and C24. After six generations of backcrossing, we crossed three independent Cvi-0^mea/MEA and C24^mea/MEA lines with pollen from Ler, C24, and Cvi-0: all the pollinations made with Ler pollen resulted in high rates of seed abortion, whereas the pollinations made with Cvi-0 or C24 resulted in mostly viable plump seeds, independently of the genotype of the maternal plant used (Fig 1B). The magnitude of the Cvi-0 and C24 paternal rescue was modulated by the maternal genotype (e.g. in a Cvi-0^mea/MEA maternal background the paternal effect of Cvi-0 was stronger and the effect of C24 was very weak). This suggests that the rescue of mea seeds is primarily a paternal-specific effect that can be partially modulated by the maternal genotype, indicating the existence of strong reciprocal interactions between the two parental genomes.

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Fig 1. mea seed abortion can be paternally suppressed.

(A) Mature F1 seeds derived from crosses between Ler or homozygous mea-1/mea-1 and pollen from Ler, C24, and Cvi-0. The scale bar represents 500μm. (B) Percentage of viable plump seeds derived from crosses between heterozygous mea-2/MEA introgressed into C24 and Cvi-0 backgrounds and pollen from Ler, Cvi-0, and C24. Three independent backcross lineages were generated for each accession, and one maternal individual per lineage was assayed. (C) Percentage of viable plump seeds derived from crosses between heterozygous mea-2/MEA, fis2/FIS2 and fie/FIE and pollen from Ler, Cvi-0, and C24. The numbers in the bars indicate the number of seeds sampled; the error bars denote 95% binomial confidence intervals.

https://doi.org/10.1371/journal.pgen.1005806.g001

Since MEA is an imprinted gene (only its maternal allele is expressed) a potential explanation for mea seed rescue could be an activation of the paternal wild-type MEA allele. However, this hypothesis cannot easily be tested using allele-specific expression assays, because maternal mea mutations already induce low levels of paternal MEA expression [20,31–33]. To determine genetically if the paternal MEA allele is required for mea seed rescue, we examined the F2 progeny of crosses between mea-2 and different Arabidopsis accessions. If a paternal MEA allele was required for the rescue, we would not expect to recover viable homozygous mea/mea seeds. However, we recovered 9–20% of viable mea/mea plants in the F2 progeny of crosses with the accessions C24, Hs-0, and Lomm1-1 (S1 Table). This result clearly indicates that a paternal MEA allele is not required for mea seed rescue in these crosses. In the crosses with Cvi-0 we only recovered 3% of homozygous mea/mea seeds; when these different F2 homozygous Cvi-0^mea/mea individuals were self-fertilized, however, we observed a range of 1–60% plump F3 seeds in their progeny (S2 Fig). This finding suggests that in mea crosses with Cvi-0, the paternal MEA allele (or a closely linked locus) can enhance but is not required for the rescue of mea seeds.

MEA encodes a subunit of the FIS-PRC2 complex, which also contains the zinc finger protein FERTILIZATION-INDEPENDENT SEED2 (FIS2) and the WD40 domain protein FERTILIZATION-INDEPENDENT ENDOSPERM (FIE) [22]. To test whether Cvi-0 and C24 can also rescue seed abortion caused by mutations in these genes, we crossed heterozygous fis2/FIS2 and fie/FIE plants with pollen from Ler, Cvi-0, and C24 (Fig 1C). While Cvi-0 could rescue fis2 seeds, there was no significant seed rescue using C24 pollen. fie seeds could not be rescued by pollen of either Cvi-0 or C24. These results indicate that the mea seed paternal rescue does not simply occur at the FIS-PRC2 level; rather it supports the hypotheses that the different FIS-PRC2 subunits play distinct roles [34] and that MEA participates in multiple protein complexes during seed development [32].

There is extensive variation in the penetrance of mea in different Arabidopsis accessions

To determine the extent of species-wide variation on MEA-dependent parental interactions, we pollinated 164 Arabidopsis accessions with mea-2 to generate F1s that were allowed to self-fertilize to examine seed viability rates in the F2 generation. Each of the F2 populations segregates (1) MEA and mea, and (2) chromosomes from Ler and the respective parental accessions: therefore, we expected to obtain 50% viable seeds from accessions that do not modify the penetrance of mea (such as Ler), and up to 75% viable seeds from accessions with a strong paternal rescue effect (assuming no epistatic effects). Accordingly, we observed 52% plump seeds in the control Ler crosses, while in the Cvi-0 and C24 crosses there were 65% and 68% plump seeds, respectively (Fig 2A–2C). Roughly half of the accessions tested showed between 55% and 70% plump seeds, suggesting that alleles that modify the penetrance of mea seed abortion are widespread among natural Arabidopsis accessions.

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Fig 2. Cryptic genetic variation for parent-of-origin effects during Arabidopsis seed development.

(A-C) Percentage of viable plump seeds in the F2 progeny of mea-2 with 164 Arabidopsis accessions. See also S2 Table. Error bars indicate 95% binomial confidence intervals. (D) Manhattan plots indicating the significance of associations between variation at SNPs across the genome and mea rescue. The black triangles indicate the position of the peaks from the Bulk-Seq analysis. The dashed line indicates the 5% significance threshold with Bonferroni correction.

https://doi.org/10.1371/journal.pgen.1005806.g002

Half of the strongest mea rescuers originate from latitudes more southern than 45° (Fig 2A), but we found no significant linear correlation between the geographical origin of the accessions and their effect on the penetrance of mea. We compared the mea rescue effect of these accessions with over 100 phenotypes reported for a large set of A. thaliana accessions [35]. The only statistically significant traits correlated with the rescue of mea were in planta magnesium and calcium concentrations (Pearson correlation, 5% false discovery rate) (S3 Fig). We also found evidence for an association between flowering time and mea rescue, as half of the strongest mea rescuers included very early flowering accessions under field or short day conditions (Cvi-0, C24, Se-0, Ts-1 and Co) (S3 Fig). We did not find a correlation between mea rescue and the size of self-fertilized or outcrossed Arabidopsis seeds [30,36].

We performed a genome-wide association study (GWAS) to identify regions in the genome whose species-level variation is linked to mea rescue. However, we were unable to detect clear statistically significant associations (Fig 2D), likely due to the weak power of GWAS to detect polygenic traits with low effect sizes [37]. Nevertheless, some of the most highly associated SNPs were in the vicinity of the regions identified with the Bulk-Seq analysis (see below).

QTL analyses identify six loci that contribute to the rescue of mea seeds

We crossed homozygous mea/mea plants (generated using an inducible MEA-glucocorticoid receptor system) with pollen from 80 Cvi-0/Ler recombinant inbred lines (RILs) for which a detailed genetic map is available [38]. The percentage of plump seeds that originated from these crosses followed a continuous distribution (Fig 3A), indicating that the rescue of mea seeds is a polygenic trait. The broad-sense heritability H² (the percentage of total phenotypic variance that can be explained by genetic factors) is 85%, indicating that mea seed rescue is under strong genetic control. We used maximum likelihood standard interval mapping to identify regions that are significantly associated with mea seed rescue. As expected from the continuous phenotype distribution, we identified multiple QTL peaks on several chromosomes (Fig 3B). Using a multiple-QTL approach [39], we narrowed down these regions to six QTLs, located on chromosome 1 (64.3cM and 101cM), chromosome 2 (65cM), chromosome 3 (77cM) and chromosome 5 (21 and 63.5cM) (Fig 3C). The six QTLs contribute independently to seed rescue (i.e. there was no evidence for epistatic interaction between QTLs) and together explain 73.1% of the phenotypic variance. Each QTL has a relatively small effect and explains a small proportion (5–11%) of the overall phenotypic variation (Fig 3D and Table 1). Nevertheless, the effect of multiple QTLs increases exponentially: every additional Cvi-0 QTL increases the rescued seed rate by roughly 50% (e.g. pollen donors with two, three or four Cvi-0 QTLs generate on average 18%, 28% or 42% plump seeds, respectively) (Fig 3E).

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Fig 3. QTL analysis demonstrates that six loci contribute independently to mea seed rescue.

(A) Percentage of viable plump seeds derived from crosses between homozygous mea-1/mea-1 and pollen from a Ler/Cvi RIL population. Error bars indicate 95% binomial confidence intervals. The inset is a histogram representation of the same data. (B) Standard QTL interval mapping. The dotted line represents the 1% significance LOD threshold. (C) Bayesian estimates for the localization of each of the six QTLs from a multiple QTL model. The values above the peaks represent the best estimate for the localization of the QTL. (D) Effect of individual QTLs. In each subpanel the percentage of plump seeds of all the 80 RILs as in panel A are shown, but sorted according to the genotype (Cvi-0 or Ler) at the respective QTL. The black horizontal line and error bars represent the mean and standard errors. (E) Cumulative effects of Cvi-0 QTLs. The percentage of plump seeds of all the 80 RILs is shown, but sorted according to the total number of Cvi-0 alleles in the six QTLs. The red horizontal lines represent the mean and standard errors. See also Table 1.

https://doi.org/10.1371/journal.pgen.1005806.g003

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Table 1. Location of the Cvi-0 QTLs identified using the RIL population.

https://doi.org/10.1371/journal.pgen.1005806.t001

We then crossed mea/mea homozygous plants with pollen from a population of Cvi-0/Ler near-isogenic lines (NILs) [40]. Unlike RILs, which have mosaic genomes with a similar proportion of Ler and Cvi-0 genetic backgrounds, these NILs contain only one or a few small introgressions of Cvi-0 in an otherwise homogenous Ler genetic background. We used 33 NILs that together cover 93–98% of the genome with isogenic Cvi-0 fragments. While Cvi-0 pollen gave rise to 85% mea plump seeds, almost all the NILs showed no significant differences from Ler (3% viable seeds) (Fig 4A). The three NILs that clearly showed an effect (13–23% viable seeds) actually contain multiple Cvi-0 fragments that overlap two or three of the identified QTLs (Fig 4B). Together, the RIL and NIL analyses suggest the existence of at least six loci in Cvi-0 that contribute to the rescue of mea seeds.

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Fig 4. A Cvi/Ler NIL population confirms the polygenic architecture of mea rescue.

(A) Percentage of viable plump seeds in crosses between homozygous mea-1/mea-1 and pollen from 33 Cvi/Ler NILs. The numbers under the bars represent the number of seeds sampled. Error bars denote 95% binomial confidence intervals. The asterisks indicate that the proportions are significantly different from the crosses with Ler pollen (Bonferroni-corrected one-sided binomial tests, * p < 0.01, ** p < 0.001). (B) Genetic map of the Cvi-0 introgressions in each of the 33 NILs [40]. The solid boxes correspond to the Cvi-0 segments. The thin grey lines indicate the position of Ler segments. The colour scale represents the percentage of viable plump seeds as in panel A. The blue lines indicate the position of the six QTLs identified using the RIL population.

https://doi.org/10.1371/journal.pgen.1005806.g004

We also scored seed abortion in the F2 progeny of a cross between mea-2 and C24 (genotyped at 14 markers throughout the genome). Despite the low statistical power caused by the segregation of MEA in this population, we found evidence for one QTL at the bottom of chromosome 1 that could explain 15% of the observed phenotypic variation (S4 Table). Thus, even this analysis with limited power identified one of the loci on chromosome 1 that was mapped using RILs and NILs.

Bulk segregant sequencing (Bulk-Seq) analysis confirm the location of the Cvi-0 QTLs

To independently validate the results of the QTL analyses, we developed a novel method for mapping parent-of-origin effects using whole-genome sequencing. The strategy is to create an F2 population that contains one set of chromosomes from one parent but inherits two segregating sets from the other parent. These two sets should have opposing effects in pre- or post-fertilisation fitness or viability, so that they will not be equally transmitted. DNA is then extracted from pools of viable F2 seedlings, and whole-genome sequencing is used to identify genomic regions that exhibit biased transmission of the two segregating paternal (or maternal) genotypes.

In this case, we took advantage of the differential survival of mea seeds depending on the inheritance of Cvi-0 against Ler paternal alleles. First, we generated F1 hybrid plants by reciprocally crossing Ler and Cvi-0 plants (Fig 5A). The Ler/Cvi-0 hybrids were then used to pollinate (1) Ler plants and (2) homozygous mea/mea plants (Ler background). The resulting F2 progenies will therefore exclusively inherit Ler chromosomes from the mother (with and without mea) but different combinations of Ler and Cvi-0 alleles from the father (due to recombination and segregation of chromosomes during male gametogenesis in the F1 plant). Only mea F2 seeds that inherit Cvi-0 alleles that rescue mea are able to generate viable seedlings: therefore, genomic regions that are linked to these Cvi-0 alleles will be predominantly transmitted to viable F2 plants. We can identify these by sequencing pools of viable plants and quantifying the relative proportion of Cvi-0 and Ler SNPs throughout the genome. To account for biases in the paternal transmission of Cvi-0 and Ler SNPs that occur independently of mea, we determined the transmission of Cvi-0 SNPs in a control cross using wild-type Ler instead of mea plants. In this wild-type (WT) control ('WT pool'), we expect the percentage of Cvi-0 reads throughout the genome to be close to 25%; in the 'mea pool', regions that are associated with mea rescue will be enriched in Cvi-0 reads (up to 50%).

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Fig 5. Bulk-Seq analysis to map parent-of-origin effects.

(A) Schematic representation of the procedure for Bulk-Seq. (B) Relative proportion of Cvi-0 reads in the mea (red) and WT (blue) pools. The dashed line represents the expected 25% average proportion of Cvi-0 reads in the WT pool in the absence of segregation distortion. (C) Enrichment of Cvi-0 reads in the mea pool relative to the WT pool. The dotted lines indicate the position of the main peaks; see also Table 2. See S4 Fig for plots of the three independent replicates.

https://doi.org/10.1371/journal.pgen.1005806.g005

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Table 2. Peaks of Cvi-0 enrichment in the Bulk-Seq analysis.

https://doi.org/10.1371/journal.pgen.1005806.t002

We pooled genomic DNA from a total of 2400 viable mea seedlings and 1400 WT seedlings in three biological replicates. We then used a dataset of known Ler and Cvi-0 polymorphisms [41,42] to estimate the proportion of Cvi-0 reads throughout the genome (Fig 5B and S4 Fig). In the WT pool, there is clear evidence for segregation distortion in several genomic regions, including a low proportion of Cvi-0 reads at the top of chromosome 3 and the middle of chromosome 1, and a high proportion at the bottom of chromosome 1 and the top of chromosomes 2 and 4. Most of these regions were previously shown to exhibit segregation distortion in crosses between Ler and Cvi-0 [38]. To identify the regions that are associated with mea seed rescue, we calculated the difference in the proportion of Cvi-0 reads between the mea and WT pools (Fig 5C). There was an overall increase in Cvi-0 reads throughout the genome in the mea pool, likely reflecting the highly polygenic nature of mea seed rescue; but the enrichment in Cvi-0 reads was particularly pronounced in the middle and bottom of chromosome 1, the bottom of chromosomes 2 and 3, and in the top and middle of chromosome 5: in these regions there was an increase of 15–30% in the proportion of Cvi-0 alleles relative to the WT pool (Fig 5C, Table 2). These peaks were reproducible between the three biological replicates (S4 Fig). Each of the peaks identified by Bulk-Seq is located in the vicinity of the QTLs identified by the RIL-QTL analysis (Table 1); some of the peaks (particularly b, d, and g) are also close to SNPs that were identified by the GWAS analysis as associated (although non-significantly) with mea rescue (Fig 2D). Taken together, the Bulk-Seq analysis provides strong support to the existence and predicted location of the multiple Cvi-0 alleles that underlie the rescue of mea seeds.

Plant material and growth conditions

The mea-1 and mea-2 [21], fis2-1 [76] and fie (SALK_042962) [77,78] mutants, as well as the RIL and NIL Ler/Cvi populations [38,40] were previously described. The Landsberg erecta (Ler-1), Cape Verde Islands (Cvi-0), and C24 accessions used in this study are derived from lines N22618, N22614, and N22620, respectively, and were a gift of Ortrun Mittelsten Scheid (GMI Vienna). All plants were grown on standard soil (ED73, Einheitserde, Germany) in a greenhouse chamber with 16h light at 20°C and 8h dark at 18°C with an average of 60% humidity.

Seed and embryo analyses

For seed viability assays, individually crossed siliques were harvested 1–2 days before dehiscence; seeds were then examined under a stereomicroscope and categorised as plump or aborted based on shape, size, and colour. For embryo quantification, seeds at different stages of development were fixed overnight at -20°C with 90% acetone, cleared with chloral hydrate/water/glycerol (8:2:1 w/v/v), and analysed under a Leica DMR microscope.

Introgression of mea into Cvi-0 and C24

For the generation of Cvi-0^mea/MEA and C24^mea/MEA lines, mea-2/MEA plants (Ler background) were used to pollinate Cvi-0 and C24. The F1 progeny was selected in Murashige and Skoog (MS) medium supplemented with 50μg/ml kanamycin (mea-2 is marked by a kanamycin resistance gene) and backcrossed to Cvi-0 and C24, respectively. Individual backcrossed (BC1) kanamycin-resistant plants were used to pollinate Cvi-0 or C24 and generate independent BC2 lines. Backcrossing was performed for another four generations; BC6 plants were genotyped with a sequence length polymorphism marker linked to the MEA locus (3.286 Mbp distance) using primers 5'-AATTGAAGCTTTTCTGC-3' and 5'-AGAAAATGAAAAACTTATGG-3' to select plants with homozygous Cvi-0 introgressions close to mea. Seed abortion was scored in the progeny of a single BC6 individual from each of three independently generated Cvi-0^mea/MEA and C24^mea/MEA lines.

Segregation analyses

Cvi-0, Hs-0, C24, and Lom-1 were crossed with pollen from mea-2, the F1 populations were allowed to self-fertilize, and DNA was extracted from viable seedlings. mea-2 plants were genotyped using primers 5'-CCAATGCACAAATCGACAATG-3' and 5'-CACCAAGAGTGCCATCTCCA-3' (WT genomic DNA), and 5'-CGATTACCGTATTTATCCCGTTCG-3' (Ds insertion tightly linked to the mea-2 allele [21]).

Generation of homozygous mea/mea seeds

To obtain pMEA::MEA-GR, an 8.6 kb genomic fragment (4.4kb upstream region + 4.2 kb MEA ORF) was amplified from the previously generated plasmid pCambia 1381Z [20] using primers proMEA-BPfor (AAAAAGCAGGCTCACTAAGATATGTTGGGTC) and MEA-BP-GRrev (AGAAAGCTGGGTCTGCTCGACCTGCCCGA), and recombined into pDONR207 using Gateway cloning (Invitrogen). The resulting entry vector was subsequently recombined into pDEST-GR (pARC146 without 35S promoter) [79], and the fusion between MEA and the GR domain sequence was confirmed by sequencing. The construct was introduced into the Agrobacterium strain GV3101::pMP90, and transformed into Ler plants using floral dip [80]. Lines expressing the construct were crossed with mea-1, and the offspring was continuously watered with 10 μM dexamethasone (DEX) (Sigma cat. D1756) to identify reduced seed abortion and thus rescue by the construct. Several lines were identified that complemented the mea-1 seed abortion phenotype to a large extent only in the presence of 10 μM DEX. The best complementing line (line 18) was used to raise the homozygous mea-1/mea-1 plants used in this study.

RIL QTL analyses

A total of 47,619 seeds derived from crosses between homozygous mea-1/mea-1 plants and 80 Ler/Cvi RILs were scored. The genotype map for these lines included 144 markers [38,81] and was kindly provided by Joost Keurentjes (Wageningen University and Research Centre). Broad-sense heritability was estimated with an analysis of variance of a linear mixed-effects model, using the lmer function of the 'lme4' R package [82]. Means and confidence intervals for each RIL were estimated using a binomial regression, and normalised using a cubic root transformation. QTL analyses were performed using the 'R/qtl' R package [39]. Genotype data across the genome was estimated using multiple imputation at a 1cM density, and interval mapping was calculated using standard maximum likelihood estimation; the LOD (logarithm of odds) threshold at 1% was calculated using a permutation test with 5000 replicates. Multiple-QTL models were selected using a combination of automated stepwise model selection and iterative individual QTL location refinement as implemented in 'R/qtl'; the penalized LOD scores used to guide model selection were derived using a permutation test with 1000 replicates of a two-dimensional, two-QTL genome scan. The best fit-model we identified had six loci and no epistatic interactions between the QTLs. Finer localizations of each of the QTLs of the best-fit model along the chromosomes were estimated using a Bayesian approach, as implemented in the bayesint function of 'R/qtl'. The effect of individual QTLs was estimated as the proportion of phenotypic variance they explain. The approximate physical location was estimated using the physical location of genetic markers [38,81].

For the mea-2 x C24 QTL analysis, an F2 population of 247 individuals was generated and genotyped using 14 sequence length polymorphism markers. An ANOVA regression was calculated for each marker: the values on S4 Table are the p-values for a regression made using a subset of 35 homozygous mea/mea plants.

Preparation of DNA pools for Bulk-Seq

Ler and Cvi-0 were reciprocally crossed to generate Ler/Cvi-0 hybrids. These were then used to pollinate homozygous mea/mea or Ler plants. Three independent replicates were generated, each using different parental individuals and at different days. In total, around 10,000 and 4,000 F2 seeds were generated from mea/mea and Ler mothers, respectively. Seeds were surface sterilised for 10 minutes using 1% sodium hypochlorite, washed extensively with water, and sown in MS medium. After 10–14 days of growth at 22°C, leaves from viable seedlings were collected (825, 800, and 775 seedlings for each of the WT pool replicates; 600, 400, and 400 individuals for each of the mea pool replicates). DNA was extracted in groups of 50 leaves using the DNeasy Plant Mini Kit (Qiagen cat. 69104), and quantified using the Qubit dsDNA HS Assay kit (Life Technologies cat. Q32854). DNA from the different extractions was pooled in equi-amounts, precipitated using sodium acetate and isopropanol, and resuspended in 25 μl TE buffer for each replicate at a final concentration of 100–150 ng/μl.

Library preparation and sequencing

The TruSeq DNA Sample Prep Kit v2 (Illumina) was used in the succeeding steps. DNA samples (1 μg) were sonicated and the fragmented DNA samples end-repaired and polyadenylated. TruSeq adapters containing the index for multiplexing were ligated to the fragmented DNA samples. The ligated samples were run on a 2% agarose gel and the desired fragment length was excised (50bp +/- the target fragment length). DNA from the gel was purified with MinElute Gel Extraction Kit (Qiagen). Fragments containing TruSeq adapters on both ends were selectively enriched with PCR. The quality and quantity of the enriched libraries were validated using Qubit (1.0) Fluorometer and the Caliper GX LabChip GX (Caliper Life Sciences). The product is a smear with an average fragment size of approximately 260 bp. The libraries were normalized to 10nM in Tris-Cl 10 mM, pH8.5 with 0.1% Tween 20. The TruSeq SR Cluster Kit (Illumina) was used for cluster generation using 5 pM of pooled normalized libraries on the cBOT. Sequencing of single reads was performed on one lane of the Illumina HiSeq 2000 using the TruSeq SBS Kit v3-HS (Illumina Inc, USA).

Read mapping and SNP segregation analyses

Reads were quality-checked using FastQC (http://www.bioinformatics.babraham.ac.uk/projects/fastqc) and trimmed with the FASTX-Toolkit (http://hannonlab.cshl.edu/fastx_toolkit/). Processed reads were aligned to the TAIR10 version of the Arabidopsis genome (Col-0 accession) using Bowtie2 [83] and the SAMtools package [84]. SNPs were called using the mpileup command from SAMtools. Known SNPs from Ler-1 and Cvi-0 [41,42] were retrieved from http://1001genomes.org/data/MPI/MPISchneeberger2011/releases/current//Ler-1/Marker/Ler-1.SNPs.TAIR9.txt (461,070 Ler-1/Col-0 SNPs) and from http://signal.salk.edu/atg1001/data/Salk/quality_variant_filtered_Cvi_0.txt (657027 Cvi-0/Col-0 SNPs). After removing common Ler/Cvi-0 SNPs, we obtained a list with 765,643 SNPs. This list was combined with the SNP calls from the bulk sequencing dataset; for each of the datasets (three replicates of each pool), we then removed positions that were (1) ambiguous in the reference sequence; (2) did not match between the Bulk-Seq samples and the published SNPs; and (3) had very high coverage (above the 99% percentile of a Poisson distribution with λ = median coverage of the sample). These quality-filtering steps resulted in an average of 390,000 SNPs for each of the six datasets. The three replicates were combined by summing up the number of reads at each SNP position. SNP positions that had no Ler or no Cvi-0 reads in the combined dataset were discarded, as were the top and low 1% quantiles of coverage. This resulted in a final combined dataset of 352,491 SNPs with an average read coverage of 16 Ler and 6 Cvi-0 reads, respectively (S3 Table). The same quality filtering steps were performed in each of the three replicates. To calculate the relative proportion of Cvi-0 and Ler reads across the genome, we first summed the read counts of groups of 50 neighbouring SNPs across the genome using a rolling window. We then calculated the proportion of Cvi-0 and Ler reads, and the relative enrichment of Cvi-0 reads in the mea pool relative to the WT pool:

Finally, we smoothed Cvi enrichment across neighbouring positions by computing the median of Cvi-0 enrichment with a rolling window of 100 SNPs.

Genome-wide association mapping

We used mea-2 to pollinate 167 Arabidopsis accessions obtained from the Nottingham Arabidopsis Stock Centre (NASC) or as a kind gift from Ortrun Mittelsten Scheid (Gregor Mendel Institute) and Takashi Tsuchimatsu (University of Zurich). Accessions are detailed in S1 Table. The F1 progeny was selected in MS medium supplemented with 50μg/ml kanamycin and allowed to self-fertilize. We collected individual fruits 1–2 days before dehiscence and visually scored seed phenotypes; some fruits had a high proportion of autonomous seeds (mea autonomous endosperm development depends on the genetic background [85]); to avoid a bias in the aborted/plump seed ratio calculations, we did not use fruits that had more than 8% autonomous seeds (225 out of 2046 fruits; there was no correlation between mea rescue and autonomous seed development). We discarded three outliers (accessions with a low number of scored seeds or relatively high percentage of autonomous seed development) and obtained a final dataset consisting of 93,884 seeds from 164 accessions. Genotypic information (250k snp data v3.06) was downloaded from https://cynin.gmi.oeaw.ac.at/home/. For correlation analysis with the dataset of 107 phenotypes [35], we calculated Pearson correlations and corrected p-values for multiple testing using the Benjamini-Hochberg false discovery rate procedure.

Genome-wide association mapping was performed with compressed mixed linear models [86] implemented in the 'GAPIT' R package [87] and in the web-based GWAPP portal [88] using the proportion of plump seeds as a phenotype (cubic root normalised). Plots were generated using the 'ggplot2' R package [89].