In most plants, the female germline starts with the differentiation of one megaspore mother cell (MMC) in each ovule that produces four megaspores through meiosis, one of which survives to become the functional megaspore (FM). The FM further develops into an embryo sac. Little is known regarding the control of MMC formation to one per ovule and the selective survival of the FM. The ICK/KRPs (interactor/inhibitor of cyclin-dependent kinase (CDK)/Kip-related proteins) are plant CDK inhibitors and cell cycle regulators. Here we report that in the ovules of Arabidopsis mutant with all seven ICK/KRP genes inactivated, supernumerary MMCs, FMs and embryo sacs were formed and the two embryo sacs could be fertilized to form two embryos with separate endosperm compartments. Twin seedlings were observed in about 2% seeds. Further, in the mutant ovules the number and position of surviving megaspores from one MMC were variable, indicating that the positional signal for determining the survival of megaspore was affected. Strikingly, ICK4 fusion protein with yellow fluorescence protein was strongly present in the degenerative megaspores but absent in the FM, suggesting an important role of ICKs in the degeneration of non-functional megaspores. The absence of or much weaker phenotypes in lower orders of mutants and complementation of the septuple mutant by ICK4 or ICK7 indicate that multiple ICK/KRPs function redundantly in restricting the formation of more than one MMC and in the selective survival of FM, which are critical to ensure the development of one embryo sac and one embryo per ovule.
Research Article; Biology and life sciences; Plant science; Plant anatomy; Fruit and seed anatomy; Ovules; Cell biology; Cell processes; Cell cycle and cell division; Meiosis; Chromosome biology; Plant embryo anatomy; Embryo sac; Developmental biology; Embryogenesis; Plant embryogenesis; Plant growth and development; Plant development; Embryology; Embryos; Seeds; Endosperm; Research and analysis methods; Experimental organism systems; Model organisms; Arabidopsis thaliana; Organisms; Eukaryota; Plants; Brassica; Plant and algal models
In most plants, the female germline starts with the differentiation of one megaspore mother cell (MMC) in each ovule that produces multiple megaspores through meiosis. One of the megaspores in a fixed position survives to become the functional megaspore (FM) while the other megaspores undergo degeneration. The FM further develops into an embryo sac. We have been working on the functions and regulation of a family of plant cyclin-dependent kinase inhibitors called ICKs or KRPs. We observed that in the ovules of Arabidopsis mutant with all seven ICK/KRP genes inactivated, multiple MMCs, FMs and embryo sacs were formed, and the embryo sacs could be fertilized to produce two embryos with separate endosperm compartments. Further, in mutant ovules the number and position of surviving megaspores from one MMC were variable and ICK4-YFP (yellow fluorescence protein) fusion protein was strongly expressed in the degenerative megaspores but absent in the FM. Those findings together with other results in our study indicate that multiple ICK/KRPs function redundantly in controlling the formation of one MMC per ovule and also in the degeneration of non-functional megaspores, which are critical for the subsequent development of one embryo sac per ovule and one embryo per seed.
The cyclin-dependent kinase (CDK) inhibitors are proteins of usually small molecular masses able to inhibit CDKs through direct binding. Since CDKs are central to cell cycle regulation in eukaryotes, CDK inhibitors are important cell cycle regulators. The ICK/KRP family of plant CDK inhibitors was initially discovered in Arabidopsis and share limited similarity in the C-terminal region with the mammalian Kip/Cip family of CDK inhibitors [[
The CDK inhibitory function of the ICK/KRP CDK inhibitors has been demonstrated both in vitro [[
A number of studies have shown that constitutive overexpression of an ICK/KRP gene can have dramatic effects on plant growth and morphology, including reduced cell numbers, smaller plant sizes and serrated leaves in Arabidopsis [[
Knockout or down-regulation could provide more insightful information on the functions of different ICK/KRPs. However, partly due to a possible overlap in functions among ICK/KRPs only a few studies were reported. Knockout of ICK2/KRP2 was found to promote formation of lateral roots in Arabidopsis [[
The phenotypic changes from ICK/KRP down-regulation observed in the previous studies were relatively mild and often appear beneficial in terms of plant growth, raising a question regarding why seven ICK/KRP genes are needed in plants. The fact that all ICK/KRP genes have been retained during evolution and expressed in Arabidopsis suggests that each of the seven ICK/KRP genes is required in normal plants and there is a positive selection pressure for maintaining them. We hypothesize that additional important functions for the ICK/KRP genes remain to be discovered. To that end, we created the septuple mutant in which all seven ICK/KRP genes were inactivated and in this unique background uncovered surprising functions of ICK/KRPs in controlling the number of megaspore mother cell and also the survival of megaspores during the female gametophyte development.
We reported phenotypic changes from down-regulating five ICK/KRP genes in the ick1 ick2, ick5 ick6 ick7 mutant [[
Compared with the wild type (WT) and quintuple ick12567 mutant [[
To understand the reason for the ovule abortion phenotype in the septuple mutant, we examined embryo sac development. In the mature WT Arabidopsis mature embryo sac (FG7), the egg, central and two synergid cells, which could be easily recognized by their perspective nuclei, were arranged in a particular configuration (Fig 2A). Surprisingly, 47% of the septuple mutant embryo sacs (n = 186) did not have any recognizable egg, central cell (secondary) and synergid nuclei as observed in a mature WT embryo sac. On the other hand, about 46% of the ovules (93 out of 204 ovules surveyed), which contained gamete nuclei, had extra nuclei. In those ovules, the nuclei could usually be recognized as two, three or four sets of egg, secondary and synergid nuclei (Fig 2B to 2I and S2 Table). The egg and secondary nuclei of the same set were usually close to each other (e.g. Fig 2D). Within each set there was only one central and egg cell. Often clear boundaries between different sets of cells could be seen and distinguished (Fig 2B). These observations suggest the formation of multiple embryo sacs in the ovules of the septuple mutant, with each sac containing a set of egg and central cells. To further identify the gametes, we used a pEC1.1: :GUS marker for egg cells [[
To further confirm that the phenotypes are due to inactivation of ICKs, we performed complementation experiments. Re-introducing either an ICK4 (S6 and S7 Figs) or ICK7 genomic fragment (S8 and S9 Figs) was sufficient to rescue the septuple mutant. These results show that the observed phenotypes were due to specific inactivation of all ICKs, instead of a non-target gene(s). Since the difference between ick123567 and the septuple mutant was the addition of the ick4 mutant, we further investigated whether the phenotypes in the septuple mutant were due to any non-specific effect conferred by the ick4 mutant. Thus, we obtained and analyzed the triple ick467 and hextuple ick123467 mutants along with WT, ick4 single mutant and septuple mutant for ick gene expression, silique length, number of seeds and aborted ovules (S10 Fig). There seemed to be a trend of mild and gradual reductions in the silique length and number from the single to ick123467 mutant (S11 Fig), similar to what was observed for ick123567 mutant (Fig 1). However, the most dramatic changes were observed in the septuple mutant compared to the hextuple and lower order of mutants, indicating that the observed seed setting and ovule abortion phenotypes in the septuple mutant were specifically due to the inactivation of all seven ICK genes.
The multiple embryo sacs observed in the septuple mutant could be due to multiple megaspore mother cells (MMCs) or multiple functional megaspores (FMs). To determine whether multiple MMCs were formed in the mutant, developing ovules at stage 2-II (when the inner integument is being initiated according to [[
To determine whether the multiple MMCs in the ick septuple mutant ovule are capable of entering meiosis, we performed immunostaining using antibodies against DMC1 and ASY1 proteins which have been shown to be specifically expressed during meiosis [[
During meiosis, callose is usually deposited at the newly synthesized cell plate following the first and second divisions, and can be detected by aniline blue staining. In the WT ovule, before meiosis, weak and punctate callose deposition was visible in the cell wall surrounding MMC (Fig 5A). Following the first division, a strong callose disk or band was present in the newly formed cell plate as well as strong callose deposition pointed at the micropylar end of the nucellus (Fig 5B). Following the second division, a new callose band below the first callose band was observed as a result of division by the daughter nucleus on the chalazal side. However little or no callose was observed for the expected cell plate from the division by the daughter nucleus close to the micropylar end (between the first callose band and the pointed callose deposition at micropylar end). As a result, the WT ovule at this stage had a typical callose pattern consisted of a middle band (usually strong) from the first meiotic division, a second callose band on the chalazal side and pointed callose deposition at the micropylar end, as shown in Fig 5C. If callose was present, the MMC in the WT ovule at different stages (before meiosis, after the first division and after the second division) could thus be distinguished by the callose deposition pattern. Based on the callose patterns, we therefore estimated the number of MMCs that have completed meiosis (Fig 5E to 5H; S12C Fig). In the septuple mutant, about 17% of ovules had one such typical callose deposition pattern from one MMC (Fig 5E), while about 61% ovules had two such callose patterns, and 22% of ovules had three or more such callose patterns (Fig 5F to 5H). These data clearly demonstrate that the multiple MMCs in the septuple mutant could complete meiosis.
In Arabidopsis as in most other plants, the MMC undergoes meiosis and produces four megaspores and only one megaspore close to the chalazal end becomes the FM while the other three degenerate [[
The occurrence of multiple MMCs in the mutant ovules raises a question regarding whether each of the multiple FMs was derived from one MMC as in the WT. It was difficult to determine the origin of each FM under the DIC microscope since the boundaries among the FMs from multiple MMCs were often not clear. However, sometimes the multiple FMs in an ovule were arranged in a way indicating that they were likely derived from one MMC. For instance, in Fig 6C, four megaspores were likely produced by the same MMC, with the two pairs of megaspores produced through the two second meiotic divisions. The two megaspores at the micropylar end seemed degenerating based on the much smaller size while the two megaspores close to the chalazal end appeared surviving. Similarly, in Fig 6D, three megaspores that appeared to be from one MMC resembled the functional megaspore in the WT.
To further address this issue, we obtained the callose and DIC images of the same ovules. Since a recognizable callose pattern was left by one MMC following meiosis (Fig 5C), when both callose deposition and FMs could be observed, we could determine whether the multiple FMs were originated from one or different MMCs. The callose staining in Fig 6G indicates the completion of meiosis by one MMC and overlaying of the callose image with the DIC image revealed that the two megaspores close to the chalazal end were surviving (Fig 6H). In the WT, cell plate from the division by the dyad cell at the micropylar side was usually not observed (Fig 5C). In contrast, this callose band was often clearly observed in septuple mutant ovules resulting in a callose pattern consisted of three callose bands plus the pointed callose deposition at the micropylar end (Fig 6I). In this ovule, the first and third megaspores from the chalazal end were surviving (Fig 6J). The callose pattern in Fig 6K indicates clearly that two MMCs had completed meiosis. While four megaspores derived from the MMC at one side were all surviving, no megaspore from the other MMC appeared to be surviving (Fig 6L). These results indicate that megaspores from different MMCs could have very different fates and multiple megaspores derived from one MMC could survive in the septuple mutant.
To exclude the possibility that the presence of multiple MMCs might have affected the selection and polarity of surviving megaspores, we examined megaspore survival when there was only one MMC in the mutant ovule. Ovules with one MMC could be determined based on the callose staining pattern as well as DIC image since following meiosis ovules with multiple MMCs had more complex callose patterns and cellular arrangements than ovules with one MMC (Fig 5E to 5H). Our analysis showed that in the WT, only the megaspore closest to the chalazal end survives without an exception (n = 120 ovules), while for the mutant ovules with one MMC, both the number and position of surviving megaspores varied (S14 Fig). The frequencies for 0, 1, 2, 3 and 4 surviving megaspores were 13%, 42%, 37%, 4% and 4% respectively (
null: Frequency of surviving megaspores at each of the four positions in ick septuple mutant ovules with one MMC.
Line Position of surviving megaspore Frequency WT 1st 120 (100%) Septuple 1st 24 (30%) 2nd 17 (21%) 3rd 13 (16%) 4th 20 (25%) none survived 7 (9%)
1 The mutant ovules with one MMC were identified after meiosis based on callose staining with aniline blue and DIC microscopy. In the WT, only the megaspore closest to the chalazal end survives. The surviving megaspores in the mutant are grouped based on their positions. The position numbers indicate the 1st to 4th positions from the chalazal to micropylar end.
These results clearly suggest a critical role of ICKs in restricting the number of MMCs and also in the selective degeneration of megaspores. To gain an understanding on ICK expression during ovule development, we fused ICK4 with YFP (yellow fluorescence protein). We used an ICK4 lacking the C-terminal 29 amino acids so that it should not have the CDK inhibitory activity [[
Further at FG2 stage during female gametogenesis, the WT embryo sac had one typical pair of nuclei (S15A Fig) while the mutant ovules showed two to four pairs often with clear boundaries between them (S15B to S15D Fig), indicating that multiple FMs could develop further in gametogenesis in the same ovule.
We further investigated the embryo development. Three days after flowering, the WT ovules had one embryo with the endosperm nuclei of uniform morphology distributed throughout the embryo sac (Fig 8A), whereas in the mutant ovules different types of nuclei and interestingly two embryos were observed (Fig 8B to 8F). In the mutant ovules with one embryo, additional nuclei, distinct from the endosperm nuclei, resembling and presumably derived from the unfertilized secondary nuclei, were found in different locations (Fig 8B and 8C). Often, in addition to one endosperm, a separate sac with a secondary nucleus was observed at the chalazal end, indicating that an unfertilized embryo sac with the membrane still intact had been pushed to the chalaza by the fertilized and expanding embryo sac (Fig 8B and 8C). Some ovules had one embryo but two separate endosperm compartments (Fig 8D), suggesting the possible development of one endosperm compartment without an embryo. About 2.6% mutant ovules had two embryos and typically two separate endosperms with a clear boundary (Fig 8E), and in rare cases three separate endosperm compartments were observed (Fig 8F). An analysis was performed to determine the frequency of ovules with more than one endosperm compartment as well as extra nuclei resembling the secondary nucleus (S4 Table). All WT ovules (n = 168) had one embryo and one endosperm compartment with uniform nuclei without any secondary nucleus, while about 26% mutant ovules had two endosperm compartments (S4 Table). In addition, extra secondary nuclei were found in one location (about 15%) or two locations (about 3.2%) in the mutant ovules. GUS staining of ovules after fertilization revealed the expression of pEC1.1: :GUS marker in developing embryo (Fig 8G), and also confirmed the presence of egg nucleus in the embryo sac at the chalaza (Fig 8H) or in the developing endosperm (Fig 8I). Consistent with the development of double embryos, twin seedlings (Fig 9) were observed in about 2.1% mutant seeds (58 out of 2760 seeds), while none was observed in the WT seeds (S5 Table).
In plants, the germline cells are not set aside early during embryogenesis as in animals, but differentiate much later in the life cycle from somatic cells. The female gametophyte development is consisted of two phases: megasporogenesis and megagametogenesis. In megasporogenesis, one somatic cell in the nucellus of a young ovule enlarges, changes in morphology and further differentiates into a megaspore mother cell (MMC), which is defined by its ability and commitment to undergo meiosis [[
Several studies have suggested a role in restricting the differentiation of multiple MMCs by a type of receptor-like kinases and a small interacting protein. In rice, MULTIPLE SPOROCYTE (MSP1) encodes a leucine-rich repeat receptor-like kinase and the msp1 mutant had excess megasporocytes and microsporocytes [[
The multiple MMCs in the ick septuple mutant could be differentiated from multiple nucellar cells. In such a case, ICK/KRPs in the WT plants would function to restrict the additional nucellar cells from developing into MMCs. Alternatively, the multiple MMCs in the septuple mutant might be due to extra rounds of mitotic divisions by a single MMC after its differentiation. While our manuscript was under preparation, a study was published and showed that triple ICK/KRP mutants as well as rbr1 mutant also display multiple MMC and embryo sac phenotypes [[
Although the multiple MMC phenotype was similarly observed in our study and by Zhao et al. [[
Although the basic molecular functions of the major cell cycle regulators have been relatively well established, how these cell cycle regulators are specifically wired into various developmental processes is not clearly understood. Previously, some cell cycle regulators have been found to be important for certain aspects of germline cell specification and gametogenesis. In the Arabidopsis CDKA;1 mutant, the second mitosis in pollen is inhibited resulting in one-sperm pollen [[
Since multiple MMCs in the septuple mutant could complete meiosis, an interesting question is whether each MMC in the mutant produces one FM as in the WT ovule. We observed that in some mutant ovules, two or more megaspores from the same MMC could survive, while in others all megaspores seemed to undergo degeneration. In this regard, it has been shown that overexpression of an Arabidopsis cell wall protein AGP18 resulted in the survival of multiple megaspores acquiring an FM identity, but those megaspores failed to develop further [[
Our results point to dual functions for ICK/KRPs in restricting the number of MMC and in the degeneration of megaspores. The MMC differentiation and degeneration of non-functional megaspores are closely connected events, both spatially and temporarily. The process of non-functional megaspore degeneration likely has initiated before the completion of meiosis, since frequently after the first meiotic division the cell close to the micropylar end degenerates without completing the second meiotic division [[
In angiosperms, only one embryo is formed in each ovule following double fertilization, in which the egg and central cells are fertilized by two sperm nuclei of a single pollen grain. The synergids play the role of pollen guidance and sperm release. During double fertilization, usually only one pollen tube reaches the embryo sac and releases the two sperm nuclei with the receptive synergid degenerating at the same time [[
We observed a trend of mild and gradual decreases in silique length and seed number from lower to hextuple mutants indicating some dosage effect (Fig 1 and S11 Fig). However, the dramatic phenotypes in ovule abortion and seed setting were only observed in the septuple mutant indicating that the strong phenotypic effects in the septuple mutants require inactivation of most or all seven ICK/KRPs. The fact that in vast majority of flowering plants only one MMC is formed per ovule and only one megaspore is selected to become FM implies a positive selection pressure during evolution for these developmental features to ensure that only one embryo would develop per seed. There is some evidence to suggest that seedlings from double embryos may be less fit than seedlings from single embryos [[
Arabidopsis thaliana ecotype ‘‘Columbia” and its mutant lines were grown in a growth room or chamber (20 °C constant, 16/8 h day/night photoperiod with a fluence rate of 90 ± 10 μmoles/m
Arabidopsis genomic DNA was extracted for genotyping analysis by PCR. Genotyping of the T-DNA insertion lines was performed as described[[
For seedling biomass analysis, seeds of WT, ick12567 and septuple mutants were planted in soil in the plant growth room. For each line, three pots each having five plants were used in the analysis. At 21 days after planting, seedlings were collected from each pot and weighed immediately for the fresh weight. Experiments were repeated at four different locations in the growth room. The relative fresh weight for each mutant (fresh weight of mutant/fresh weight of WT) was obtained.
For morphological phenotyping, the 1
A 3786-bp ICK4 genomic region (consisted of 2040 bp before ATG, the coding region and 717 bp of the region after the STOP codon) was amplified from Arabidopsis genomic DNA with Pfu DNA polymerase as a fragment containing BamHI and SacI sites with the primers HW1001 (5’-gactggatcccttgacatagagttttctaca) and HW1002 (5’-gactgagctcattactactccgcataggc). An ICK7 genomic region (consisted of 1335 bp before ATG, the coding region and 838 bp of the region after the STOP) was similarly amplified with the primers HW1003 (5’-cagtggatccggtctctttacgaatatctta) and HW1004 (5’-cagtgagctcgatatgtagtgagtgggtac). The fragments were cut with BamHI and SacI enzymes, and cloned into pCambia1300 that has the hygromycin resistant marker for plant selection (
For observation of female gametophyte development, emasculated flowers or developing buds at specific stages were used. Sample preparations and DIC (differential interference contrast) microscopic observations were performed as described [[
Aniline blue staining was based on a procedure described [[
Immunolocalization of DMC1 and ASY1 proteins in young ovules was performed as described [[
For preparing GUS report constructs, first a HindIII-EcoRI fragment containing a promoter: :GUS reporter was cut from a pBI121-based construct previously prepared in our lab and cloned into pCamiba1300 (resulting in S113-D2). The 1819-bp FIS2 [[
To determine ICK4 protein expression, an ICK4 genomic fragment, spanning the 4100-bp sequence upstream of ATG and 167 amino acid region downstream of ATG, was amplified with the primers: 5’-cagtctgcagaattagttgtccatagttgtg and 5’-cagtgtcgactcttgactctctagctccg. After the restriction digest, the genomic fragment was cloned into a YFP vector and translationally fused to the N-terminus of YFP. The construct was used to transform Arabidopsis WT plants. ICK4-YFP expression was analyzed in the initial transformants and progeny plants.
null. Genotyping and RT-PCR of ick3 and ick4 T-DNA insertion mutants.(A) Genotyping of ick3 (SALK_053533) and ick4 (Sail_548_B03) single mutants with WT as a control. For both genes, a pair of gene-specific primers was used for amplifying the full-length WT coding sequence of ICK3 or ICK4 while a T-DNA left border primer and a gene specific primer were used to amplify a fragment of the T-DNA insert allele. (B) Analysis of ICK3 transcript in WT (left lane) and ick3 single mutant (right lane) by RT-PCR. cDNA synthesized from total RNA and gene-specific primers were used for amplifying the full-length ICK3 coding sequence (upper row), and the reference actin sequence (lower row). (C) Analysis of ICK4 transcript in WT (left lane) and ick4 single mutant (right lane) by RT-PCR. cDNA synthesized from total RNA and gene-specific primers were used for amplifying the full-length ICK4 coding sequence (upper row), and the reference actin sequence (lower row).(PDF)
null. Crosses used to produce various ick mutants from ICK single mutants and ick12567 mutant.(PDF)
null. Genotyping and RT-PCR of ick septuple mutant.(A) Gene-specific primers for ICK1, ICK2, ICK3, ICK4, ICK5, ICK6 and ICK7 were used to confirm the genotype of ICK septuple mutant with WT genomic DNA as a control. (B) Analysis of ICK transcripts in the WT (first lane) and septuple mutant (second lane), with WT genomic DNA as a control (third lane). Gene-specific primers were used for amplifying the full-length sequences of ICK1 to ICK7. Actin was used as a control (the last row).(PDF)
null. Phenotyping of WT, ick12567 and septuple mutant plants.(A) Seedlings of WT, ick12567 and septuple mutants at 26 days after planting in soil. (B) Fresh seedling weight of 21-day-old WT, ick12567 and septuple mutants. For each line, 3 pots each with 5 plants were used in the analysis. The averages and standard deviations are shown. (C—E) Leaf area (C), blade length (D) and leaf length/width ratio (E) of 21-day-old WT, ick12567 and septuple mutant plants (6 plants from each line were used). The 1
null. Reciprocal crosses to determine the transmission of the short silique phenotype through the parents.Reciprocal crosses (indicated as female X male) were made between the WT and septuple mutant. The length of fully-elongated siliques was measured. In each treatment, four plants with 4 siliques for each plant were used. The averages and standard deviations are showed. Data were analyzed using one-way ANOVA and post-hoc Tukey test, and significant differences are indicated by different letters (upper case) at p<0.01 level.(PDF)
null. Genotyping of WT, septuple mutant and complementation lines with a genomic ICK4 fragment.An ICK4 genomic fragment (including 2040 bp before ATG, 1028 bp of the coding region and 717 bp of the region after the STOP codon) was introduced into the septuple mutant. Multiple independent lines were identified that showed complementation of the silique length phenotypes. Two independent T2 lines are presented here. PCR was used to determine the genotypes of the WT, septuple mutant and complementation lines. For each gene, duplex PCR was performed to detect the WT allele (with gene-specific primers for the full-length coding region) and the T-DNA allele using (with a gene-specific primer and a left border primer of T-DNA). The complementation lines are the same as the septuple mutant except for the presence of the WT ICK4 band.(PDF)
null. RT-PCR and phenotyping of WT, septuple mutant and complementation lines with a genomic ICK4 fragment.(A) ICK4 transcript analysis. cDNAs synthesized from total RNAs were used to detect the ICK4 transcripts in WT, septuple mutant and two complementation lines (T2 generation). Actin (ACT8) was amplified was a control. (B) Silique length of WT, septuple mutant and the two complementation lines. Four plants and in each plant the 6
null. Genotyping of WT, septuple mutant and complementation lines with a genomic ICK7 fragment.An ICK7 genomic fragment was introduced into the septuple mutant. Many transformants (6/40) with normal silique length were observed and the analysis of two independent transformants (1243–4 and 1243–23) is shown here. PCR was used to determine the genotypes of the WT, septuple mutant and transformants with ICK7 genomic fragment. For each gene, duplex PCR was performed to detect the WT allele (with gene-specific primers for the full-length coding region) and the T-DNA allele using (a gene-specific primer and a left border primer of T-DNA). The transformants are the same as the septuple mutant except for the presence of the WT ICK7 band.(PDF)
null. RT-PCR and phenotyping of WT, septuple mutant and transformants with ICK7.(A) ICK7 transcript analysis. cDNAs synthesized from total RNAs were used to detect the ICK7 transcripts in WT, septuple mutant and two transformants with ICK7 genomic fragment. Actin (ACT8) was amplified was a control. (B) Silique length of WT, septuple mutant and the two transformants. Ten siliques (6
null. Genotyping of WT, ick4, ick467, ick123467 and septuple mutants.Gene-specific primers for ICK1, ICK2, ICK3, ICK4, ICK5, ICK6 and ICK7 genes, and a T-DNA left border primer were used to confirm the genotypes of WT, ick4, ick467, ick123467 and septuple mutants.(PDF)
null. RT-PCR and phenotyping of WT, ick4, ick467, ick123467 and septuple mutants.(A) Analysis of ICK transcripts in the WT (the first lane), ick4 (the second lane), ick467 (the third lane), ick123467 (the fourth lane) and septuple mutant (the fifth lane), with WT genomic DNA as a control (the last lane). Gene-specific primers were used for amplifying the full-length sequences of ICK1 to ICK7. Actin was used as a control (last row). (B) Silique length. The average and standard deviation are shown for the length of fully extended siliques (4 plants per line with 8 siliques from each plant measured). (C) Opened siliques showing silique length and aborted ovules of WT, ick4, ick467, ick123467 and septuple mutants. (D) Number of seeds per silique (4 plants per line with 6 siliques from each plant). The averages and standard deviations are shown. (E) Number of aborted ovules per silique. Fully extended siliques were opened and aborted ovules counted under a dissecting microscope (4 plants per line with 6 siliques from each plant). The averages and standard deviations are shown. Data in (B, D, E) were analyzed using one-way ANOVA and post-hoc Tukey test, and significant differences are indicated by different letters (upper case) at p<0.01 level.(PDF)
null. Number of megaspore mother cells determined by DIC, DMC1 immunostaining and callose deposition patterns.(A) WT and septuple ovules at stage 2-II were surveyed under a DIC microscope and determined for the number of enlarged MMC-like cells prior to meiosis. Number of ovules counted: WT = 129 and mutant = 149. (B) Number of MMCs undergoing meiosis as revealed by immunostaining with an antibody against DMC1, a protein specifically expressed during meiosis, but not at MMC and FG1 stages (for images see Fig 4). Number of ovules counted: WT = 59 and mutant = 60. (C) Number of MMCs estimated based on the callose deposition following meiosis. The callose deposition could be attributed to one, two, three or more MMCs since a typical pattern is produced as the result of meiosis from one MMC. Number of ovules counted: WT = 127 and mutant = 227.(PDF)
null. Identification of megaspore mother cells (MMCs) in meiosis by ASY1 immunostaining.Developing ovules were prepared and immunostained with an antibody against ASY1, which is specifically expressed during meiosis. (A—C) WT ovules at MMC (A), meiosis (B) and FG1 (C) stages. (D—I) Mutant ovules at MMC (D), meiosis (E—H) and FG1 (I) stages. One to four cells in the mutant ovules could be stained with DMC1 (E—H). Scale bars equal 5 μm.(PDF)
null. Analysis of surviving megaspores in WT and septuple mutant ovules with one MMC.Ovules with a single MMC were identified based on callose staining with aniline blue and DIC microscopy. For each ovule, the callose fluorescence image is shown at the top and the DIC image at the bottom. The numbers in the images indicate the 1
null. Early megagametogenesis in WT and ick septuple mutant.WT (A) and septuple (B—D) ovules at FG2 stage. The WT ovule had one pair of nuclei. The mutant ovules had two (B), three (C) and four (D) pairs of nuclei, with each pair likely derived from a functional megaspore. The two nuclei in each pair are close to each other and have similar appearance. The boundary between different pairs is often visible (B, D). Different numbers in (B—D) indicate different pairs of nuclei. Scale bar in (A) is for all images equals 10 μm.(PDF)
null. Analysis of mature pollen grains in WT and ick septuple mutant.Mature pollen grains from ten nascent flowers each line were collected and stained with DAPI. Vegetative and sperm cell nuclei were observed and counted under a fluorescence microscope (Leica DM2500) with a 63× (NA = 1.40) oil lens.(PDF)
null. Observation of female gametes in mature embryo sacs in the WT and ick septuple mutant.The flower buds just before opening were emasculated and left for 1 day. Ovules (from about 15 gynoecia for each line) were prepared and observed under a microscope with DIC optics. If one central cell (secondary) nucleus and one egg nucleus, usually close to each other, could be identified, they were considered as one set. The synergid nuclei were not always recognizable when there were three or four sets of gametes. For the mutant, a large portion (about 47% by a separate analysis) of embryo sac did not contain any observable secondary and egg nuclei, and were not included in this survey.(PDF)
null. Development of functional megaspore (FM) in ovules of the WT and ick septuple mutant.The ovules were checked and those at functional megaspore stage were included in the analysis. They were observed under a microscope with DIC optics. The presence and number of functional megaspores in ovules (from about 15 gynoecia) were counted.(PDF)
null. Analysis of endosperm development and presence of extra central cells after fertilization in the WT and ick septuple mutant.Three days after flowers opened, ovules were collected and prepared for DIC observation. Only the ovules containing at least one developing embryo were included (about 20 gynoecia from each line used). All the WT ovules had one endosperm compartment with uniform endosperm nuclei, while some mutant ovules had two endosperm compartments. Nuclei resembling the secondary nucleus were also present in the endosperm of the mutant. The secondary nucleus might have divided into several nuclei, which were recognizable against the background of endosperm nuclei (See Fig 8C). The nuclei that were close to each other physically and looked similar morphologically were considered to be derived from one original secondary nucleus. “+1CC”, “+2CC” and “+3CC” indicate the number of central cells that are inferred to based on the extra secondary nuclei present.(PDF)
null. Frequency of twin seedlings in the WT and ick septuple mutant.WT and septuple mutant seeds were plated on ½ MS plates. Four days after plating, seedlings were screened under a dissecting microscope for the occurrence of twin seedlings.(PDF)
We thank the Arabidopsis Biological Resource Center and Nottingham Arabidopsis Stock Centre for the T-DNA insertion mutants, Dr. YX Wang at Fudan University for sharing the ASY1 antibody, and Drs. Guosheng Liu and Jiangying Tu for technical assistance with the use of a confocal microscope.
DIAGRAM: Fig 1: Silique and seed development in WT, ick12567 , ick123567 and septuple mutants. (A) Silique length. The average and standard deviation are shown for the length of fully extended siliques (4 plants per line with 10 siliques from each plant measured). (B) Number of aborted ovules per silique. Fully extended siliques were opened and aborted ovules counted under a dissecting microscope (4 plants with 6 siliques from each plant counted). The averages and standard deviations are shown. (C) Opened siliques showing silique length and aborted ovules of the septuple mutant. (D) Number of seeds per silique (4 plants per line with 6 siliques from each plant). The averages and standard deviations are shown. (E) Seed weight. Three different seed lots were used. For each lot, seeds were harvested from four plants in one pot and one thousand seeds were counted. The averages and standard deviations are shown. Data in (A, B, D, E) were analyzed using one-way ANOVA and post-hoc Tukey test, and significant differences are indicated by different letters (upper case) at p<0.01 level.
DIAGRAM: Fig 2: Embryo sac development in WT and ick septuple mutant. (A#x2014;I) DIC observation of embryo sac. Ovules from flowers just before opening were prepared and observed under a microscope with DIC optics. (A) A typical WT embryo sac showing secondary (central, C), egg (E) and synergid (S) nuclei. (B—C) Two optical sections of a septuple mutant ovule showing the embryo sac area with two sets of secondary (C), egg (E) and synergid (S) nuclei. The gamete and synergid nuclei are arranged in a configuration similar to that in the WT and the boundary between the two sets of gametes is clearly visible (arrow in B), indicating the presence of two embryo sacs in the ovule. (D—E) Three optical sections of a mutant ovule with three sets of secondary (C), egg (E) and synergid (S) nuclei. (F—I) Four optical sections of a mutant ovule with four set of secondary (C), egg (E) and synergid (S) nuclei. The synergids for the 3rd and 4th sets could not be easily observed. Different sets of gametes in the mutant are indicated by numbers “1”, “2”, “3” and “4”, respectively. The two syngergid nuclei of the same pair are differentiated with or without an “′”, e.g. “S1, S1′, S2, and S2′” referring to two pairs of synergid nuclei. (J—M) Ovules from the septuple mutant carrying a pEC1.1: :GUS marker for the egg cell were stained for GUS. The GUS staining shows the presence of one to four egg cells in these ovules. (N—P) Ovules from the septuple mutant carrying a pFIS2: :GUS marker for the central cell were stained for GUS. The GUS staining shows the presence of one to three central cells in these ovules. Scale bars in (A), (J), and (N) are for (A—I), (J—M), and (N—P) respectively, and all equal 10 μm.
DIAGRAM: Fig 3: Development of megaspore mother cell and expression of the pKNU-GUS reporter in WT and septuple ovules. Developing ovules at stage 2-II were observed with DIC microscopy for development of megaspore mother cell (A—H) and ovules at around stage 2-III were analyzed for the expression of the pKNU-nlsGUS reporter, which is strongly expressed in MMC (I—L). (A—B) WT ovules. Most of WT ovules had one enlarged cell (A) and about 5% of ovules had two enlarged cells (B). (C—H) Septuple mutant ovules with one (C), two (D), three (E), four (F) and five (G, H) enlarged cells (G and H show two focal planes of the same ovule). (I–J) Strong pKNU-nlsGUS reporter expression relative to the surrounding cells indicates the presence of one (I), two (J), three (K) and four (L) MMCs in the mutant ovules. Scale bar in (A) is for all images and equals 10 μm.
DIAGRAM: Fig 4: Identification of megaspore mother cells (MMCs) in meiosis by DMC1 immunostaining. Developing ovules were prepared and immunostained with an antibody against DMC1, which is specifically expressed during meiosis. (A—C) WT ovules at MMC (A), meiosis (B) and FG1 (C) stages. (D—I) Mutant ovules at MMC (D), meiosis (E—H) and FG1 (I) stages. One to four cells in the mutant ovules could be stained with DMC1 (E—H). Scale bars equal 5 μm.
DIAGRAM: Fig 5: Analysis of callose deposition patterns in WT and septuple mutant ovules. Ovules were stained for callose with aniline blue. For each ovule, the callose fluorescence image is shown at the top and the DIC image at the bottom. (A—D) WT ovules at different stages. (A) Before meiosis, there was weak and punctate callose deposition surrounding the MMC. (B) Callose deposition after the first division of meiosis showing a bright callose band (disc) at the place of newly formed cell plate. (C) Typical callose deposition pattern at the end of meiosis usually with two prominent calluse bands (discs) and also focused accumulation of callose at the micropylar end. One of the callose bands came from the first division and one from the second of the division by the nucleus close to the chalazal end. This pattern indicates the result of meiosis by one MMC. (D) At functional megaspore stage, the callose deposition was much reduced. (E—H) Septuple mutant ovules showing callose deposition from one (E), two (F), three (G) and likely four (H) MMCs. Scale bar in (A) is for all images and equals 10 μm.
DIAGRAM: Fig 6: Functional megaspore (FM) development in WT and ick septuple mutant. (A—F) Ovules at functional megaspore stage and observed under a DIC microscope. (A) WT ovule with a typical FM. (B–E) ick septuple ovules with 1–4 FMs. A typical FM was present in (B). In (C), two pairs of nuclei appear to be derived from the second meiotic divisions. The two megaspores at the micropylar end are degenerating while the two close to the chalazal end were surviving. In (D), three megaspores of similar size and morphology were surviving, while in (E), four megaspores with different sizes and appearances were surviving. (F) No typical FM was observed in the ovule. (G—L) Callose staining and DIC images were obtained for the same mutant ovules at functional megaspore stage to determine which megaspore survived. The positions of megaspores from each MMC are indicated with a number, with position 1 indicating the megaspore closest to the chalazal end. (G, I, K) show callose staining while (H, J, M) show the corresponding DIC images with superimposed callose staining. (G, H) show that one MMC finished meiosis and two megaspores were surviving. (I, J) also show the result from one MMC, but megaspores at positions 1 and 3 (counting from the chalazal end) were surviving. Note that there are three callose bands plus the pointed callus deposition at the micropylar end. (K, L) indicate that two MMCs completed meiosis (K). While four megaspores derived from the MMC at one side were all surviving, no megaspore from the other MMC appeared to be surviving. Arrows in (C–E) indicate FMs, numbers in (G–L) indicate the megaspore positions counted from the chalazal end, and scale bars equal 10 μm.
DIAGRAM: Fig 7: ICK4-YFP expression during megasporogenesis. Developing ovules of ICK4-YFP transgenic line (WT background) were observed under a confocal microscopy. (A, D, G, J, M) show confocal images, (B, E, H, K, N) show bright field images, and (C, F, I, L, O) show the overlays of the confocal and bright field images. (A—C) A stage 2-I ovule. (D—F) A stage 2-II ovule. (G—I) A stage 2-III ovule. (J—L) A stage 2-IV ovule at the end of meiosis I. (M—O) A stage 3-I ovule after meiosis. The numbers in (N, O) indicate the positions of megaspores counting from the chalazal to micropylar end. The arrow in (N, O) points to the nucleus of functional megaspore. The scale bars in (A), (D), (G), (J) and (M) are for (A—C), (D—F), (G—I), (J—L) and (M—O) respectively.
DIAGRAM: Fig 8: Embryo and endosperm development in WT and ick septuple mutant. Three days after flowers opened, the young developing seeds were prepared for DIC observations or stained for GUS first and then prepared for observations. (A) A typical WT embryo sac with a globular embryo and endosperm nuclei of uniform morphology distributed throughout the embryo sac. (B—F) Embryo and endosperm development in mutant ovules. (B) In addition to the typical embryo and endosperm, a separate compartment is seen to contain a secondary nucleus. (C) In the chalazal area, there are also a few nuclei like the secondary nucleus (yellow star signs) in the endosperm as well as a secondary nucleus in a separate embryo sac (red star signs). (D) There is one embryo, and two separate compartments of endosperm. (E) There are two embryos, and two separate compartments of endosperm. (F) There are two embryos, and three separate compartments of endosperm. (G—I) Embryo and egg cells identified by pEC1.1: :GUS expression in the septuple mutant. (G) A young embryo showing GUS staining. (H) In addition to the developing embryo, strong GUS staining is seen at the chalazal end of the embryo sac where a separate sac is often present. (I) In addition to the developing embryo, GUS staining is present at two other loci indicating the presence of extra egg cells. White arrows indicate embryos and black arrows indicate the boundaries between two separate compartments of endosperm. Stars indicate extra egg cells or secondary nuclei. Scale bar in (A) is for (A—I) and equals 10 μm.
DIAGRAM: Fig 9: Occurrence of twin seedlings in the ick septuple mutant. A typical 4-day Arabidopsis seedling (left) and twin mutant seedlings (right). Scale bar equals to 1 mm.
By Ling Cao, Writing – review & editing; Sheng Wang, Writing – review & editing; Prakash Venglat, Visualization; Lihua Zhao, Methodology; Yan Cheng, Resources; Shengjian Ye, Methodology; Yuan Qin, Writing – review & editing; Raju Datla, Writing – review & editing; Yongming Zhou, Writing – review & editing and Hong Wang, Writing – review & editing