Transcriptomic evidence for distinct mechanisms underlying abscission deficiency in the Arabidopsis mutants haesa/haesa-like 2 and nevershed

Objective In Arabidopsis, the abscission of floral organs is regulated by two related receptor-like protein kinases, HAESA and HAESA–like 2 (HAE/HSL2). Signaling by HAE/HSL2 leads to expression of genes encoding secreted cell wall remodeling and hydrolase enzymes. hae hsl2 mutants fail to induce expression of these genes and retain floral organs indefinitely. Mutants in the gene NEVERSHED (NEV) also fail to abscise floral organs and phenotypically resemble hae hsl2. NEV encodes an ADP-ribosylation factor GTPase-activating protein that localizes to the trans-Golgi network and early endosome. nev displays altered Golgi morphology and aberrations in vesicular trafficking. The mechanism by which nev fails to abscise is presently unknown. It has been hypothesized that nev fails to activate HAE/HSL2 signaling. In this study we use RNA-Sequencing to test this hypothesis. Results We show that the transcriptional alterations in hae hsl2 and nev are highly divergent. hae hsl2 displays a clear reduction in expression of genes associated with cell wall remodeling and pectin degradation, while nev displays vast transcriptional changes associated with response to pathogens. These results suggest that the mechanism of the defect between hae hsl2 and nev are distinct. Electronic supplementary material The online version of this article (10.1186/s13104-018-3864-x) contains supplementary material, which is available to authorized users.


Introduction
In plants, abscission is the programmed shedding of entire organs resulting from environmental stimuli or an endogenous developmental program. Post-pollination abscission of sepals, petals, and stamen in Arabidopsis has emerged as an important model developmental signaling system. Floral abscission is regulated by the redundant receptor protein kinases HAESA and HAESA-LIKE 2 [1,2]. Double hae/hsl2 mutants fail to activate an intracellular signaling pathway controlling abscission and their floral organs fail to abscise [1,3].
In addition to plants defective in the HAE/HSL2 signaling pathway, mutants in the ADP-ribosylation factor GTPase-activating Protein (Arf-GAP) encoding NEVER-SHED display a strong abscission defect [4]. Analysis of floral abscission zone cells shows that these nev mutants display aberrant Golgi morphology and over-accumulation of paramural vesicles, suggesting disruption of the secretory system [4]. The exact molecular defect causing abscission deficiency in the nev mutant is not known. It has been hypothesized that nev may fail to activate intracellular signaling mediated by HAE/HSL2 [5]. In this study, we utilized RNA-sequencing to compare the transcriptome of a hae hsl2 mutant and a nev mutant in order to test this hypothesis.

Lines used in this study
The nev-3 mutant, isolated in Ler and outcrossed to Col-0, and the nev-3 serk1-5 suppressor in the outcrossed

BMC Research Notes
*Correspondence: walkerj@missouri.edu 1 Division of Biological Sciences, University of Missouri, Columbia, MO 65211, USA Full list of author information is available at the end of the article nev-3 background were kindly provided by Dr. Sarah Liljegren [4,6]. hae-3 hsl2-3 has been previously described, and is deposited at ABRC.

Plant growth conditions
Plant were grown in a 16 h light cycle, ~ 700 lx, at 22 °C, ~ 65% relative humidity, and fertilized once at 3 weeks post-germination with 1 × strength Miracle-Gro (Scotts Miracle-Gro Company).

RNA-sequencing analysis
A minimum of 8 and maximum of 15 mid-stage 15 floral receptacles were isolated and pooled per biological replicate. Three biological replicates per genotype were prepared in each experiment. RNA was isolated using the Trizol reagent (Life Technologies). Each receptacle was dissected by taking a 1 mm section of floral tissue comprised of 1/3 mm stem and 2/3 mm receptacle. Libraries were created using the TruSeq mRNA Library Prep Kit (Illumina). Libraries from each experiment were individually barcoded, pooled, and run on a single lane of Illumina Sequencing using the NextSeq 500 instrument.
Reads were mapped to The Arabidopsis Information Resource (TAIR) 10 gene sequences and quantified using TopHat (v. 2.9) and Cufflinks (v2.1.1) [7]. We utilized default settings for alignments, and performed differential expression analyses using cuffdiff with default settings. Data were analyzed and visualized in R using CummeRbund and ggplot2 [7]. GO analysis was performed utilizing AgriGo [8]. Differential expression was chosen to denote an FDR < .05 from cufflinks output.

RNA-sequencing of abscission deficient mutants hae-3 hsl2-3 and nev-3
nev mutants are abscission deficient and resemble hae hsl2 where floral organs remain strongly attached to the developing fruit [4] (Fig. 1a). To investigate the potential mechanistic relationship between these two mutants, we performed RNA-Sequencing comparing wildtype Col-0 and the two previously described abscission deficient mutants hae-3 hsl2-3 and nev-3 [4,9]. In this study, we sampled RNA derived from mid-stage 15 floral receptacles. Stage 15 is the floral developmental stage where pollination has occurred and abscission signaling has been initiated, but floral abscission has not been completed [3] (Additional file 1: Figure S1).
After RNA-Sequencing, we assessed transcript abundance measurements for genes known to be regulated by HAE/HSL2 [output of differential expression analysis for RNA-Sequencing experiments included in Additional file 2: Dataset 1. Previous studies have identified two genes encoding secreted polygalacturonases QRT2 and PGAZAT with a partially abscission defective double mutant phenotype and whose expression is regulated Asterisks below represent statistical significance at FDR < .05. c Heatmap of differentially expressed genes between Col-0, hae-3 hsl2-3, and nev-3 by HAE/HSL2 [3,10]. These genes are hypothesized to contribute to the loosening of the cell wall at the site of abscission [11]. While these genes are a non-exhaustive sample of those likely regulated by HAE/HSL2, they serve as a reliable indicator or pathway activity. Their transcript abundance measurements are plotted in Fig. 1b.
The results confirm a significant reduction in hae-3 hsl2-3 in comparison to Col-0 for both QRT2 and PGAZAT (Fig. 1b). In contrast, nev-3 showed a transcript abundance level statistically similar to wildtype for QRT2, but a dramatic > 8 fold increase in PGAZAT transcript abundance. These data suggest that, unlike hae-3 hsl2-3, nev-3 does not exhibit generally reduced abscission signaling, but surprisingly exhibits strong and apparently dysregulated expression of key HAE/HSL2 regulated genes.
Global differential expression and gene ontology (GO) analysis demonstrated statistically significant differences of 1055 and 326 genes in the Col-high/hae-3 hsl2-3-low and Col-low/hae-3 hsl2-3-high comparisons, respectively. GO analysis identified moderate enrichment in terms such as response to stimulus, response to stress, cell wall, and other terms similar to those previously associated with gene expression changes in the hae hsl2 mutant [full results for all GO analyses included in Additional file 3: Dataset 2. In contrast, nev-3 shows evidence of dramatic transcriptional reprogramming, with 4627 and 4753 statistically significantly different genes in the Colhigh/nev-3-low and Col-low/nev-3-high comparisons, and 4861 and 5079 statistically significantly different genes in the hae-3 hsl2-3-high/nev-3-low and hae-3 hsl2-3-low/nev-3-high comparisons. A heat map displaying relative levels of all differentially expressed genes between the three genotypes is displayed in Fig. 1c. GO analysis of genes with higher expression in nev identified extremely significant enrichment of terms such response to stress, response to biotic stimulus, kinase activity, cell death, and other terms associated with response to biotic stress. There is less of a clear pattern to the terms enriched in genes in the Col-high/nev-3 low comparison. Potentially informative terms include lipid metabolic process and endomembrane system.
Overall, these results are surprising in that the pattern of abscission associated polygalacturonase gene expression in nev-3 bears little resemblance to that of hae-3 hsl2-3. There also appears to be general transcriptional reprogramming in the nev mutant and over-activation of pathogen response signaling. These results suggest the mechanism of abscission defect in nev is dissimilar to that of hae hsl2.

RNA-sequencing of nev-3 and nev-3 serk1-5
Results of a nev suppressor screen have shown that loss of function mutations of SERK1 are capable of suppressing the abscission defect and subcellular Golgi defects of nev [6] (Fig. 2a). SERK1, along with the related SERK2, SERK3/BAK1, and SERK4, have been shown to positively regulated abscission by encoding HAE/HSL2 coreceptors [12,13]. It has not been clear how mutating a Considering the results of the nev RNA-Seq experiment above, we hypothesized there may be a SERK1 regulated signaling pathway over-activated in nev that leads to transcriptional reprogramming and that interferes with abscission by an unknown mechanism. We further hypothesized that mutating SERK1 may lead to suppression of the abscission defect of nev by reducing signal strength of this pathway. To test this hypothesis, we performed RNA-Sequencing to compare nev-3 to the previously described double loss of function suppressor mutant nev-3 serk1-5 [6].
We first examined expression of QRT2 and PGAZAT. nev-3 serk1-5 displays a slightly lower level of transcript abundance for QRT2, and a > 5 fold reduction in transcript abundance of PGAZAT (Fig. 2b). These data are consistent with a model whereby mutation in SERK1 suppresses the dysregulated expression in nev-3.
We further performed global gene expression analysis and GO term enrichment in a similar manner as above. We observed 4756 genes with a statistically significantly higher transcript abundance in nev-3 compared to nev-3 serk1-5, and 4848 genes with a lower transcript abundance in nev-3 compared to nev-3 serk1-5. GO term analysis of genes with higher levels in nev-3 compared to nev-3 serk1-5 shows that the top terms in the Biological Process category include response to stimulus, response to stress, multi-organism process, cell death, and other terms associated with biotic stress response (Additional file 2: Dataset 2). 8 of the top 10 terms in this comparison are identical to those in the top 10 Biological Process terms associated with genes higher in nev-3 compared to Col-0. These data suggest that in nev-3 serk1-5, there is a reduction in an intracellular signaling pathway and are consistent with a model where the defect of nev is caused by over-activation of SERK1 signaling.
Finally, to test the hypothesis that mutation of SERK1 can reverse gene expression changes in nev, we performed linear regression on the log(fold change) values from the Col-0/nev-3 comparison versus those from the nev-3/nev-3 serk1-5 comparison. We hypothesized that we would observe an inverse relationship between these log(fold change) measurements. Consistent with this expectation, we observe a highly statistically significant negative relationship, indicating that gene expression changes in nev-3 compared to wildtype tend to be offset in nev-3 serk1-5 (Fig. 2c). This result is further consistent with the hypothesis that mutation of SERK1 reduces the signal strength of the over-active signaling process in nev.

Conclusion
Overall, these data suggest that in nev-3 there is overactivation of SERK1 mediated signaling that leads to widespread transcriptional reprogramming and consequent cellular dysfunction in the abscission zone, leading to an abscission defect. Mutation of SERK1 likely reduces the strength of this over-activated signal and allows abscission to occur. Determination of what effect this mis-regulated signaling has on abscission zone function is a direction for future research. One possibility was illuminated by a recent report demonstrating that floral abscission zone cells exhibit a regulated lignification pattern, and that the nev mutant exhibits disorganized and ectopic lignification [14]. It is possible this ectopic lignification underlies the phenotype of nev, perhaps by interfering with the normal cell separation processes that occur as a result of the modification of abscission zone cell walls and dissolution of the middle lamella. In this scenario, the nev phenotype and associated transcriptomic changes could occur by activation of SERK1 signaling that aberrantly feeds into a lignification pathway, as well as pathways regulating abscission related hydrolases such as PGAZAT and pathogen response genes. This model presumes the inhibitory effect on abscission of ectopic lignification overrides the effect of strong abscission hydrolase expression. This model will require substantial additional detailed genetic and physiological investigation. However, its strength is that it offers an explanation for two counterintuitive properties of the nev mutant: that nev exhibits high levels of expression of hydrolase genes such as PGAZAT and QRT2, and that the nev phenotype can be suppressed by mutation of SERK1, a positive regulator of abscission signaling [4,6].

Limitations
In this paper we show that the nev mutant exhibits widespread transcriptional reprogramming, including a stark increase in pathogen response gene expression, and that reducing this transcriptional response by mutating SERK1 suppresses the abscission defect of nev. However, this work does not provide a fundamental physiological explanation for why nev does not abscise, nor does it point to a mechanism by which SERK1 signaling is activated in the nev mutant. It only presents evidence at the transcriptional level that the mechanism of abscission deficiency between hae hsl2 and nev appears to be quite distinct. Further work on the nev mutant and its suppressors will be required to more fully understand this phenomenon.