Chromatin Enrichment for Proteomics in Plants (ChEP-P) Implicates the Histone Reader ALFIN-LIKE 6 in Jasmonate Signalling

doi:10.21203/rs.3.rs-669473/v1

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Research Article

Chromatin Enrichment for Proteomics in Plants (ChEP-P) Implicates the Histone Reader ALFIN-LIKE 6 in Jasmonate Signalling

https://doi.org/10.21203/rs.3.rs-669473/v1

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published 22 Nov, 2021

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Background

Covalent modifications of core histonesgoverndownstream DNA-templated processes such as transcription by altering chromatin structure and function. Previously, we reported that the plant homeodomain protein ALFIN-LIKE6 (AL6), a bona fide histone reader that preferentially binds trimethylated lysin 4 on histone 3 (H3K4me3), is critical for recalibration of cellular phosphate (Pi) homeostasis and root hair elongation under Pi-deficient conditions.

Results

Here, we demonstrate that AL6 is also involved in the response of Arabidopsis seedlings to jasmonic acid (JA) during skotomorphogenesis, possibly by modulating chromatin dynamics that affect the transcriptional regulation of JA-responsivegenes. Dark-grown al6 seedlings showed a compromised reduction in hypocotyl elongation upon exogenously supplied JA, a response that was calibrated by the availability of Pi in the growth medium. A comparison of protein profiles between wild-type and al6 mutant seedlings using a quantitative Chromatin Enrichment for Proteomics (ChEP) approach,that we modified for plant tissue and designated ChEP-P (ChEP in Plants), yielded a comprehensive suite of chromatin-associated proteins and candidates that may be causative for the mutant phenotype.

Conclusions

Altered abundance of proteins involved in chromatin organization in al6 seedlings suggests a role of AL6 in coordinating the deposition of histone variants upon perception of internal or environmental stimuli. Our study shows that ChEP-P is well suited to gain holistic insights into chromatin-related processes in plants. Data are available via ProteomeXchange with identifier PXD026541.

Molecular Genetics

Biotechnology and Bioengineering

Medical Genetics

Molecular Biology

Chromatin

histone reader

jasmonate

jasmonate signalling

proteomics

skotomorphogenesis

The dynamic interplay between the incorporation of histone variants into chromatin and posttranslational modifications (PTMs) of canonical histones govern the accessibility of eukaryotic genomes by facilitating chromatin compaction or decompaction, which in turn steers downstream processes such as transcription and repair [31, 48]. Alone or in combination, histone PTMs such as acetylation, methylation, ubiquitilation or phosphorylation, coordinate a plethora of chromatin-associated events either by altering the physical environment of chromatin or by selective recruitment of effector molecules. The observation that histone PTMs can be associated with different chromatin functions led to the supposition that histone PTMs function as a language or code to govern DNA-templated processes [44], resulting in infinitive combinations that orchestrate the responses to a myriad of internal and external signals. While histone writers (e.g., acetyltransferases, methyltransferases, ubiquitilases, and kinases) add such modifications to histones, proteins that binds to histone PTMs (i.e., ‘histone readers’) harbour specialized domains that recognize those modifications and direct specific downstream events. In Arabidopsis, a suite of 204 putative reader domains have been identified [44], in which members of the Royal family of domains, a structurally related group of protein folds that bind to methylated protein substrates, and PHD (plant homeodomain) fingers were shown to recognize histone lysine methylation [58]. ALFIN-LIKE (AL) is a small, plant-specific gene family of histone readers that preferentially bind to di- or trimethylated lysin 3 of histone H3 (H3K4me3) through a conserved C-terminal PHD zinc finger [1, 24]. The name-giving protein, Alfin 1, has been first identified as a salt stress-inducible protein in alfalfa roots [4], and subsequently in other species including Arabidopsis, which contains seven AL genes [29]. In a previous study, we identified ALFIN-LIKE6 (AL6) in a genetic screen aimed at identifying mutants that are impaired in the elongation of root hairs in response to phosphate (Pi) starvation [8]. Homozygous al6 mutants are undistinguishable from the wild type under control conditions, but display a pleiotropic phenotype when grown under on Pi-deplete media, suggesting a role of AL6 (and possibly other AL proteins) in the interpretation of environmental signals. The molecular basis for the al6 phenotype remains elusive.

Jasmonic acid and its derivates, collectively called jasmonates (JAs), are lipid-derived phytohormones that regulate a plethora of responses to developmental and environmental stimuli, including pathogen defence, root development, leaf senescence, stamen development, and hypocotyl elongation [15]. Hypocotyl elongation is a critical process during skotomorphogenesis (i.e., etiolation), that, together with closed apical hooks and folded cotyledons, aids in penetrating soil layers that covers the seed after germination before exposure to light mediates the transition to photomorphogenesis and initiates autotrophy.

Photomorphogenesis triggers de-etiolation during which hypocotyl cell elongation is repressed, and induces the expression of light-dependent genes and the biosynthesis of mature chloroplasts through the action of photoreceptors. Jasmonates interrupt skotomorphogenesis by repressing the E3 ligase CONSTITUTIVE PHOTOMORPHOGENIC 1 (COP1), which is critical for its maintenance [59]. Jasmonates are perceived by the nuclear localized F-box protein CORONATINE INSENSITIVE 1 (COI1) [18], a component of a functional Skp-Cullin-F-box E3 ubiquitin ligase (SCF^COI1) complex, and activate its E3-ligase activity. In the absence of JA, JASMONATE ZIM-DOMAIN PROTEINs (JAZs), the co-repressor TOPLESS (TPL), and the adaptor protein NINJA form a complex that represses the induction of JA-responsive genes [10, 38]. Activation of SCFCoI1 results in the degradation of JAZ proteins, that activate the transcription factor MYC2 and induce the transcription of JA-responsive genes. Interestingly, MYC2 was identified as a potential target of the AL6 ortholog AL5 in a ChIP-seq approach [15], suggesting a link between the AL family and JA signalling.

In the present study, we explore a putative involvement of AL6 in the JA-mediated repression of skotomorphogenesis through a proteomics approach aimed at identifying proteins that may interact with AL6 in the nucleus. Since AL6 acts at the chromatin level, we adopted a Chromatin Enrichment for Proteomics (ChEP) [22] protocol that we optimized for plant tissue and designated as ChEP-P (ChEP in Plants). ChEP has been successfully employed to survey nuclear proteins in various organisms such as human cells [22, 20], mouse [49], dinoflagellates [6], and the human malaria parasite [5], but has not been applied to plants so far. In this approach, chromatin-associated proteins are in vivo cross-linked to DNA with formaldehyde, and non-covalently bound proteins are removed by washing with highly denaturing extraction buffers followed by digestion and LC-MS-MS analysis. Here, we use ChEP-P to catalogue and quantify chromatin-associated proteins of etiolated seedlings that have been exposed to media supplemented with JA. Since AL6 has been previously associated with the response to Pi deficiency [8], and Pi deficiency alters JA levels in Arabidopsis [19], we also exposed the seedlings to low Pi media and a combination of both treatments. Our ChEP-P survey revealed a suite of differentially accumulating proteins that may play important roles in JA-mediated modulation of hypocotyl elongation. We also show that AL6 is critical for JA-induced inhibition of hypocotyl elongation in etiolated Arabidopsis seedlings, possibly by compromising the transition of H3K4me3 to H3K27me3 and the deposition of the histone variant H2A.Z. We further demonstrate that this response is modulated by the availability of Pi in the growth media, which act antagonistically to JA on hypocotyl elongation.

AL6 is critical for the response of etiolated Seedlings to JA

We have previously shown that mutants defective in the expression of AL6 display a pleiotropic phenotype when grown on Pi-deplete media, suggesting a role of AL6 in the interpretation of environmental cues [8]. Based on its function as a bona fine histone methylation reader, it can be assumed that AL6 has additional functions, possibly in the response to environmental or developmental conditions that alter the methylation state of lysine residues in histone H3. In the present study, we observed that etiolated al6 seedling produced hypocotyls that were significantly longer than those of the wild type and displayed a severely compromised response to exogenously applied JA. In the wild type, application of 50 µM JA reduced hypocotyl length by 52.8%, an effect which was markedly reduced in al6 mutant plants (Fig. 1A, B). Application of JA to low Pi-grown (low Pi + JA) plants dampened the JA-induced growth inhibition to 37.7 and 21% in wild-type and mutant plants, respectively, indicative of altered JA signalling in Pi-deficient seedlings (Fig. 1A, B). Determination of longitudinal hypocotyl cell lengths revealed a trend towards longer cells in al6 mutants under all conditions, and a marked reduction in both wild-type and mutant plants after application of JA (Fig. 1C-E). Analysis of JA concentrations showed that, except for the anticipated increase of JA levels in JA-treated plants, no differences in internal JA levels were apparent between the genotypes, suggesting that the observed alterations in the JA response between wild-type and al6 mutant plants and among the growth types were not caused by compromised JA biosynthesis (Fig. 1F). Together, these data show that exogenously supplied JA represses skotomorphogenesis of etiolated seedlings, a response that is modulated by the Pi status of the plants. It further appears that functional AL6 is critical for a proper response of dark-grown seedlings to JA.

Chep-p Identified A Comprehensive Subset Of Chromatin-associated Proteins

A ChEP-P approach was used to survey proteins that support, repress, or mediate the interplay of AL6 with chromatin. Essentially, we adopted a protocol described for mammalian cells with various alterations, which proved to be critical to make this method suitable for identifying chromatin-associated proteins in plants (Fig. 2). In particular, formaldehyde crosslinking appears to require special emphasis in the protocol for plants, necessitating a procedure which is similar to that applied for chromatin immunoprecipitation (ChIP) to avoid the dissociation of lowly abundant proteins such as transcription factors. The workflow of ChEP-P, highlighting steps that need adaptation to make this technique applicable to plants, is outlined in Fig. 2.

In total, our ChEP-P survey captured 5,174 unique proteins that were identified by at least two distinct peptides with an FDR < 0.05 when both genotypes and all growth types were considered (Supplementary Dataset S1). Under control conditions, subsets of 3,343 and 2,546 proteins were identified in wild-type and al6 mutant plants, respectively (Fig. 3A). Considering only proteins that were detected in two or more replicates resulted in subsets of 1,425 and 1,608 proteins for the genotypes under study. These numbers remained largely unchanged among the various treatments and genotypes, with large overlaps among the treatments (Fig. 3B). Only samples from al6 plants grown on low Pi media deviated from this pattern. ChEP-P of low Pi-treated al6 seedlings yielded a by 51% higher number of total proteins when compared with plants grown on Pi-replete media, and an 31% increase for low Pi + JA vs + JA-treated al6 plants (Fig. 3A), suggesting a more elaborated response to Pi deficiency in the mutant relative to wild-type plants.

Gene ontology (GO) analysis of the proteins identified in two or more replicates revealed overrepresentation of the molecular process category ‘jasmonic acid biosynthesis’ in both genotypes treated with JA. Also, JA treatment decreased the abundance of proteins involved in translation and, albeit less pronounced, protein folding. Proteins in the category ‘response to oxidative stress’ were more abundant in JA-treated plants. Unexpectedly, this analysis further revealed reduced abundance of proteins related to mRNA binding and rRNA binding in JA-treated plants, the latter trend being more pronounced in wild-type plants (Fig. 3C). A more detailed analysis of the biological process revealed overrepresentation of the categories ‘response to symbiotic fungus’, response to wounding’, ‘oxylipin biosynthesis’ and ‘root development in JA-treated plants, proteins involved in mRNA processing were less prominent in this group of plants (Supplementary Fig. S1). Robust differences between the genotypes were not evident from this analysis.

Chep-p Complements Other Proteomic Approaches

Our ChEP-P dataset is largely complementary to two different proteomic studies using the same material; a suite of proteins defined as the ‘RNA-binding proteome’ [42], and an approach aimed at identifying ubiquitilated proteins [2]. Only a relatively small subset of 71 proteins was identified in all three approaches and can thus be classified as core proteins of etiolated Arabidopsis seedlings (Fig. 4A). Curating proteins derived from the ChEP-P dataset for nuclear localization yielded a suite of 194 chromatin-associated proteins (Table 1). Of those, DNA- and RNA-binding proteins, and proteins involved in histone modifications constitute the largest fractions (Fig. 4C). Moreover, chromatin-binding proteins, DNA transcription factors, and proteins involved in DNA metabolism are better represented in the ChEP-P data set when compared to other approaches (Fig. 4B). For example, ChEP-P identified 6-fold more DNA-binding and 10-fold more chromatin-binding proteins than the study targeting RNA-binding proteins [42], suggesting that ChEP-P is suitable to provide a comprehensive catalogue of proteins that are covalently linked or transiently associated with chromatin. Gene ontology of the nuclear-located proteins revealed pronounced overrepresentation of proteins involved in chromosome organization, DNA damage response, nucleocytoplasmic transport, RNA processing, as well as categories related to stimulus response (Fig. 4D).

Table 1

Chromatin-associated proteins identified by ChEP.
Locus/isoform	Name	Function	Unique peptides	Genotype
DNA binding
At4g21710.1	NRPB2	DNA-templated transcription	6	WT; al6
At4g09000.2	GRF1	Regulation of transcription	13	WT; al6
At1g14410.1	WHY1	Regulation of transcription	5	WT; al6
At2g02740.1	WHY3	Regulation of transcription	8	WT; al6
At4g24800.1	MRF3	Regulation of transcription	13	WT; al6
At1g77180.1	SKIP	Regulation of transcription	3	WT; al6
At5g65430.3	GRF8	Regulation of transcription	7	WT; al6
At1g22300.1	GRF10	Regulation of transcription	15	WT; al6
At1g09770.1	CDC5	Regulation of transcription	8	WT; al6
At5g63190.1	MRF1	Regulation of transcription	6	WT; al6
At5g38480.1	GRF3	Regulation of transcription	14	WT; al6
At5g65410.1	ZHD1	Regulation of gene expression	4	WT; al6
At1g15750.1	TPL	Regulation of transcription	7	WT; al6
At5g04430.2	BTR1	Regulation of transcription	16	WT; al6
At2g32080.1	PUR-ALPHA-1	Regulation of transcription	3	WT; al6
At2g45640.1	SAP18	Regulation of transcription	4	WT; al6
At2g42560.1	LEA25	Unknown function	7	al6
AT3G58680.1	MBF1b	Transcriptional coactivator	4	al6
At3g05060.1	SAR DNA-binding protein	Box C/D RNP complex	12	WT; al6
At1g76010.1	ALBA1	Chromatin structure	9	WT; al6
At1g20220.1	ALBA2	Chromatin structure	5	WT; al6
At2g32080.1	PUR ALPHA-1	DNA replication	3	WT; al6
At1g48610.1	AT-hook motif	DNA binding	11	WT; al6
At3g42170.1	DAYSLEEPER	Transposase-like	8	WT; al6
At3g10690.1	GYRA	DNA topological change	12	WT; al6
At5g04130.1	GYRB2	DNA topological change	7	WT
At4g25210.1	DNA-binding storekeeper protein-related	Mediator complex	2	WT; al6
At4g39680.1	SAP domain-containing protein	Nucleic acid binding (nucleus)	18	WT; al6
At4g36020.1	CSP1	DNA duplex unwinding	7	WT; al6
At4g26110.1	NAP1;1	DNA repair	8	WT; al6
At5g10010.1	HIT4	Negative regulation of gene silencing	7	WT; al6
RNA binding
At3g49601.1	pre-mRNA-splicing factor	mRNA splicing	5	WT; al6
At2g18510.1	JANUS	mRNA splicing	3	WT
At2g37340.1	RSZ33	mRNA splicing	4	WT
At3g55460.1	SCL30	mRNA splicing	6	WT; al6
At3g55220.1	SAP130B	mRNA splicing	9	WT; al6
At1g09760.1	U2A’	mRNA splicing	4	WT; al6
At3g61240.1	RH12	mRNA binding (nucleus)	2	WT; al6
At2g14880.1	SWIB2	Regulation of transcription by RNA polymerase II	5	WT; al6
At4g17520.1	HLN	mRNA binding (nucleus)	12	WT; al6
At5g39570.1	PLDRP1	mRNA binding (nucleus)	11	WT; al6
At4g34110.1	PAB2	mRNA binding (nucleus)	15	WT; al6
At2g23350.1	PAB4	mRNA binding (nucleus)	17	WT; al6
At5g47210.1	Hyaluronan	mRNA binding (nucleus)	18	WT; al6
At1g51510.1	Y14	mRNA binding (nucleus)	3	WT; al6
At5g42820.2	U2AF35B	mRNA splicing	3	WT; al6
At1g02140.1	HAP1	mRNA splicing	3	WT; al6
At3g49430.1	SRP34A	mRNA splicing	6	WT; al6
At1g49760.1	PAB8	mRNA binding (nucleus)	13	WT; al6
At1g04080.3	PRP39	mRNA splicing	10	WT; al6
At5g04280.1	RZ1C	mRNA splicing	7	WT; al6
At3g13570.1	SLC30A	mRNA splicing	4	WT; al6
At3g26560.1	ATP-dependent RNA helicase	mRNA splicing	2	WT
At2g33340.1	MAC3B	mRNA splicing	12	WT; al6
At1g80070.1	SUS2	mRNA splicing	22	WT; al6
At4g31580.1	RSZ22	mRNA splicing	7	WT; al6
At4g39260.1	CCR1	mRNA splicing	11	WT; al6
At2g24590.1	RSZ22A	mRNA splicing	3	al6
At1g16610.3	SR45	mRNA splicing	3	WT; al6
At1g14650.1	SWAP	mRNA splicing	4	WT; al6
At2g13540.1	ABH1	mRNA splicing	4	WT; al6
At5g64270.1	Splicing factor	mRNA splicing	11	WT; al6
At2g38770.1	MAC7	mRNA splicing	7	WT; al6
At1g20960.1	BRR2	mRNA splicing	34	WT; al6
At5g41770.1	Crooked neck protein	mRNA splicing	3	WT; al6
At5g52040.2	RS41	mRNA splicing	6	WT; al6
At5g54900.1	RBP45A	mRNA binding (nucleus)	8	WT; al6
At1g11650.2	RBP45B	mRNA binding (nucleus)	5	WT
At2g42520.1	RH37	mRNA binding (nucleus)	6	WT; al6
At3g58510.1	RH11	mRNA binding (nucleus)	9	WT; al6
At1g29250.1	ALBA1	mRNA-binding (nucleus)	5	WT; al6
At2g33410.1	RBGD2	mRNA-binding (nucleus)	4	WT; al6
At4g00830.1	LIF2	mRNA-binding (nucleus)	5	WT; al6
At5g07350.2	TSN1	mRNA binding (nucleus)	25	WT; al6
At1g13190.1	RNA-binding (RRM/RBD/RNP motifs) family protein	mRNA binding (nucleus)	2	WT; al6
At5g61780.1	TSN2	mRNA binding (nucleus)	22	WT; al6
At3g04610.1	FLK	mRNA binding, regulation of gene expression	4	WT; al6
At1g48920.1	PARL1	rRNA processing	24	WT; al6
At5g52470.1	FIB1	RNA methylation	10	WT; al6
At2g21660.1	CCR2	mRNA export from the nucleus	10	WT; al6
At3g10650.1	NUP1	mRNA export from the nucleus	6	WT; al6
At2g05120.1	NUP133	mRNA export from the nucleus	4	WT; al6
At1g14850.1	NUP155	Nucleoporin	12	WT; al6
At1g69250.1	NTF2	mRNA export from the nucleus	4	al6
At2g16950.1	TRN1	Nuclear import	4	al6
At3g06720.1	IMPA-1	Nuclear import	3	WT; al6
At4g16143.1	IMPA-2	Nuclear import	9	WT; al6
At1g09270.1	IMPA-4	Nuclear import	5	WT; al6
At1g75660.1	XRN3	miRNA catabolic process	4	WT; al6
At1g26110.1	DCP5	mRNA decapping	3	al6
AT5G25757.1	RNA polymerase I-associated factor PAF67	RNA polymerase I-associated	9	WT; al6
At2g06990.1	HEN2	mRNA processing	3	WT; al6
At3g03920.1	H/ACA ribonucleoprotein complex	snoRNA guided rRNA pseudouridine synthesis	4	al6
At3g57150.1	NAP57	mRNA pseudouridine synthesis	12	WT; al6
DNA repair
At3g02540.1	RAD23C	DNA repair	3	al6
At5g38470.1	RAD23D	DNA repair	3	WT; al6
At4g31880.1	PDS5C	DNA repair	15	WT; al6
At5g55660.1	DEK domain-containing chromatin associated protein	DNA repair	10	WT; al6
At2g36060.2	MMZ3	DNA repair	4	WT; al6
At2g29570.1	PCNA2	DNA repair	2	WT; al6
At5g47690.1	PDS5A	DNA repair	11	WT; al6
At3g04880.1	DRT102	DNA repair	5	WT; al6
Nucleus organization, transport, and chromatin remodeling
At1g74560.3	NRP1	Nucleosome assembly	1	WT; al6
At3g18035.1	HON4	Nucleosome assembly	9	WT;al6
At2g19480.1	NAP1;2	Nucleosome assembly	11	WT; al6
At5g56950.1	NAP1;3	Nucleosome assembly	3	WT; al6
At1g20693.1	HMGB2	Chromatin assembly/disassembly	2	WT; al6
At1g48620.1	HON5	Nucleosome assembly	7	WT; al6
At5g58230.1	MSI1	Chromatin assembly	3	WT; al6
At1g27970.2	NTF2B	Nucleocytoplasmatic transport	5	WT; al6
At1g65440.1	GTB1	Regulation of transcription; chromatin assembly	5	WT; al6
At4g26630.1	DEK3	Chromatin remodeling	10	WT; al6
At3g06400.3	CHR11	Chromatin remodeling	2	WT; al6
At5g67630.1	ISE4	Chromatin remodeling	9	WT; al6
At1g67230.1	LINC1	Nuclear structure	18	WT; al6
At4g31430.2	KAKU4	Nuclear membrane organization	5	WT; al6
At5g55190.1	RAN3	Nuclear transport of proteins	8	WT; al6
At2g47970.1	NPL4	Nuclear pore localization protein	5	WT; al6
At4g15900.1	PRL1	Protein binding (nucleus)	6	al6
At5g17020.1	XPO1	Nuclear export	7	WT; al6
At3g44110.1	ATJ	DNA replication	4	WT; al6
At2g46520.1	XPO2	Protein export from nucleus	5	WT; al6
At1g79280.2	NUA	Nuclear transport of proteins	22	WT; al6
At5g43960.1	Nuclear transport factor 2 (NTF2) family protein	Nuclear transport of proteins	6	WT; al6
At1g56110.1	NOP56	snoRNA binding	11	WT; al6
At1g14900.1	HMGA	Chromosome condensation	3	WT; al6
At5g20200.1	Nucleoporin-like protein	Nuclear membrane organization, DNA replication	6	WT; al6
At5g60980.2	NTF2	Nuclear transport	4	WT; al6
At3g51050.1	NERD1	Unidimensional cell growth	2	WT; al6
At1g19880.1	RCC1	Chromosome condensation	3	WT; al6
At5g11170.1	UAP56A	RNA-directed DNA methylation	19	WT; al6
At3g15670.1	LEA76	Nuclear protein	9	WT; al6
At1g15340.1	MBD10	Methyl-CpG-binding domain	7	WT; al6
At1g61000.1	NUF2	Kinetochore organization	1	WT; al6
At5g63860.1	UVR8	Chromatin binding	7	al6
At1g47200.1	WPP2	Mitosis	6	WT; al6
Histone modification
At5g03740.1	HDT3	Histone deacetylation	7	WT; al6
At2g19520.1	NFC4	Histone modification	8	WT; al6
At5g22650.1	HAD4	Histone deacetylation	5	WT; al6
At5g08450.1	HDC1	Histone deacetylation	4	WT; al6
At4g38130.1	HD1	Histone deacetylation	2	al6
At5g45690.1	Histone acetyltransferase	Histone acetylation	13	WT; al6
Chromatin constituents
At1g08880.1	HTA5	Histone superfamily protein	1	WT; al6
At5g65360.1	HRT1	Histone superfamily protein	4	WT; al6
At2g30620.1	H1.2	Histone superfamily protein	8	WT; al6
At3g46030.1	HTB11	Histone superfamily protein	1	WT; al6
At1g01370.1	HTR12	Histone superfamily protein	2	al6
At5g59970.1	Histone superfamily protein	Histone superfamily protein	14	WT; al6
Low Pi only
At1g61730.1	DNA-binding storekeeper protein-related transcriptional regulator	Regulation of transcription	6	al6
At3g01540.2	RH14¹	rRNA processing	9	al6
At5g02530.1	ALY2	mRNA binding (nucleus)	3	al6
At2g20490.1	EDA27	rRNA pseudouridine synthesis	3	WT
At1g80930.1	MIF4G domain-containing protein / MA3 domain-containing protein	mRNA splicing	1	al6
At4g35800.1	NRBP1¹	RNA polymerase II	8	WT; al6
At3g62310.1	DEAH RNA helicase homolog PRP43	mRNA binding (nucleus)	2	al6
At3g50670.1	U1SNRNP¹	mRNA splicing	3	WT; al6
At1g65090.2	Nucleolin²	Nucleolar protein	3	al6
At1g06760.1	HON1¹	Nucleosome positioning	3	WT; al6
At3g11200.1	AL2¹	Histone binding	2	WT
At1g14510.1	AL7¹	Histone binding	1	WT; al6
At3g18165.1	MOS4²	Protein binding (nucleus)	5	WT; al6
At4g05420.1	DDB1A	Regulation of transcription	2	WT; al6
At5g27670.1	HTA7²	Histone H2A.5 protein	2	WT; al6
+JA only
At3g44600.1	CYP71	Chromatin binding	5	WT
At3g50670.1	U1SNRNP¹	mRNA splicing	3	WT; al6
At4g32720.1	LA1	rRNA processing	2	al6
At4g35800.1	NRBP1¹	RNA polymerase II	7	al6
At3g01540.2	RH14¹	rRNA processing	4	WT
At5g53620.1	MNC6.16	RNA polymerase II degradation	2	al6
At4g24270.2	EMB140	RNA processing	3	al6
At1g33240.1	GTL1	Negative regulation of transcription	3	al6
At5g28040.1	VFP4	Regulation of transcription	1	al6
At3g50370.1	Hypothetical protein	mRNA binding (nucleus)
At2g27100.1	SE³	mRNA splicing	8	WT; al6
At1g06760.1	HON1¹	Nucleosome positioning	3	al6
At3g11200.1	AL2¹	Histone binding	3	WT; al6
At3g42790.1	AL3	Histone binding	2	al6
At1g14510.1	AL7¹	Histone binding	1	WT; al6
At4g27000.1	RBP45C	mRNA binding (nucleus)	4	WT
At1g23860.1	RSZ21	mRNA splicing	1	al6
At1g65010.1	Microtubule-associated protein	Reciprocal meiotic recombination	10	al6
At5g37720.1	ALY4	mRNA export from the nucleus	5	al6
At2g15430.1	NRPB3	RNA polymerase II, IV and V	2	al6
At4g36690.1	U2AF65A	mRNA splicing	5	al6
Low Pi + JA only
At2g27100.1	SE³	mRNA splicing	8	al6
At5g27670.1	HTA7²	Histone H2A protein	2	al6
At1g65090.2	Nucleolin²	Nucleolar protein	3	al6
At2g02470.1	AL6	Histone binding	1	al6
At2g41620.1	Nucleoporin interacting component	mRNA export from the nucleus	2	al6
At3g18165.1	MOS4²	Protein binding (nucleus)	5	al6
At3g11450.1	ZRF1A	Chromatin silencing	3	al6
At1g18800.1	NRP2	Chromatin assembly	1	al6
At5g22880.1	HTB2	Histone family protein	1	WT;al6
Proteins identified by ChEP-P in at least two replicates with predominant nuclear localization were considered. ¹in low Pi + JA; ²in low Pi and low Pi + JA; ³in +JA and low Pi + JA; WT, wild type.

A Ppi Network Links Al Proteins To Plant Immunity

As expected from their similar subcellular distribution, most proteins of this core set of nucleus-localized proteins have multiple predicted or validated protein-protein interactions (PPIs), including AL2, AL3, AL6, and AL7 (Fig. 5). A PPI network considering the closest partners of the AL proteins revealed a central position of CELL DEVISION CYCLE 5 (CDC5), a MYB3R- and R2R3-type transcription factor that was shown to control growth and miRNA biogenesis [37, 56]. Together with MODIFIER OF SNC1,4 (MOS4) and the nuclear WD40 protein PLEIOTROPIC REGULATORY LOCUS 1 (PRL1), CDC5 forms the MOS4-Associated Complex (MAC) that confers innate immunity [26, 35, 55]. LHP1-INTERACTING FACTOR 2 (LIF2), another MOS4-interacting protein, also functions in plant innate immunity [23]. Notably, LIF2 was shown to be recruited to chromatin upon JA treatment to regulate the transcription of JA-responsive genes [33]. Moreover, the transcriptome of lif2 mutants is enriched in the category ‘JA-mediated signaling pathway’ [23], underscoring the association of this protein to the response to JA. Conspicuously, LIF2 was found to more abundant in regions enriched in H3K4me3 [33]. Another LHP1-interacting factor, CYCLOPHILIN 71 (CYP71), is involved in chromatin assembly and histone modifications [25]. Further, several proteins involved in nucleosome assembly and organization (NRP2, MSI1, NAP1.2, NAP1.2, NAP1.3, NFA6, and CHR11), histone acetylation (FVE, HDC1, HD1, HD2B, and HD2C), and components of the transcriptional machinery (NRPB1, NRPB2 and NRPB3) are part of this core network. ALFIN-LIKE proteins also have predicted interactions with TPL, a component of the JA repressor complex.

Label-free quantification reveals differences in chromatin dynamics between al6 and the wild type

Label-free quantification was employed to identify proteins that differentially accumulate among the treatments or between the genotypes under study. Only a relatively small subset of chromatin-associated proteins was responsive to JA (Supplementary Dataset S2). Of note, in both genotypes the histone variant HTA5 was upregulated in response to JA, but downregulated in low Pi and low Pi + JA. In wild-type plants, the abundance of RNA-BINDING PROTEIN 45A decreased under all experimental conditions, but the protein was not differentially expressed in al6 seedlings.

In wild-type plants, a subset of 89 proteins was responsive to low Pi and accumulated differentially between treated and control plants (Supplementary Dataset S2). Mutant plants responded to low Pi treatment with the differential expression of a markedly larger subset (140 proteins) of differentially expressed proteins (DEPs); only 35 DEPs were common in the data sets of both genotypes, including HTA5, HTA3, and AL7. The more pronounced Pi deficiency response of al6 mutant plants was also reflected by a more complex pattern of overrepresented GO categories (Fig. 6).

When plants were grown on low Pi + JA media, in both genotypes the histones HTB2 and HTA3 showed increased abundance whereas HTB11 and HTA5 decreased in response to this treatment, pointing to alterations in chromatin organization under these conditions. In wild-type seedlings, low Pi + JA treatment resulted in additive enrichment of GO categories observed upon either growth condition, a pattern which was not observed in mutant plants, in which the response to the combined treatment was rather similar to what was observed with JA alone.

Among the chromatin-associated proteins that were differentially expressed between the two genotypes, the expression of NAP1-RELATED PROTEIN 1 (NRP1) and the related NAP1;2 was highly upregulated in al6 relative to wild-type plants (Supplementary Dataset S3). NAP1 was shown to repress the SRW1 chromatin-remodeling complex [50]. In agreement with such a role of NAP1, the SWR1 component CHROMATIN-REMODELING PROTEIN 11 (CHR11) showed a markedly decreased abundance in al6 mutant plants [30]. Noteworthily, several chromatin-related proteins were either not differentially expressed in response to the experimental treatments, anti-directionally regulated in al6 mutants relative to wild-type plants (e.g., HTA5, HTB11, H1.2, RBP45A), were solely regulated in al6 plants (e.g., CHR11, H2B, and HIGH MOBILITY GROUP), or were anti-directionally regulated in both genotypes (HTB11). Moreover, a suite of genes involved in the biosynthesis of or response to JA (CORI7, GSH1) and auxin biosynthesis (SUR1) were only differentially expressed in wild-type plants (Fig. 7).

ChEP-P detects a comprehensive suite of chromatin-associated proteins

The identification of chromatin-associated proteins and changes in their relative abundance upon perception of internal or external cues allows insights into the complex interplay between DNA and regulatory proteins that orchestrate gene activity. Detection of lowly abundant proteins is, however, notoriously difficult which renders approaches aimed at providing a comprehensive inventory of chromatin-associated proteins difficult. Antibody-based methods such as ChIP or tandem affinity purification have been widely employed for mapping the interaction of trans-acting factors with regulatory DNA sequences. However, the requirement for protein-specific antibodies or tagged proteins limits this method to one or a few proteins that can be studied at the same time, restricting the utility of this approach when a more holistic view is desired. Chromatin enrichment coupled with tandem MS-based proteomics profiling allows for unbiased protein identification and is better suited than whole cell proteomics to detect lowly abundant chromatin-associated proteins. Moreover, due to the stringent washing buffer of formaldehyde-crosslinked DNA and the use of RNase A, ChEP provides a significant discrimination against highly abundant ribosomal and cytoplasmic proteins. Despite these obvious advantages, so far ChEP has not been successfully employed to study chromatin-associated proteins in plants. While it remains obscure why this is the case, it should be stated that modifications of each step of the ChEP procedure are required to adopt the method for plant materials (Fig. 2) which may have rendered approaches using a protocol developed for non-plant tissues inefficient.

While ChEP is based on a fast and economic protocol and does not require sophisticated instrumental setups other that MS, the charged nature of chromatin may cause a significant dilution of ChEP-derived protein profiles by proteins from other cell compartments [21]. This was also the case in the present study where contaminants also derived from chloroplasts. However, proteins of origins other than the nucleus may also transport biologically meaningful information, as they may not occur entirely at random [21], or may represent proteins that are transiently bound to chromatin. Moreover, enrichment for chromatin-associated proteins appears to depend on the material under study and the conditions of the experiment, yielding a different degree of enrichment [22].

Altered chromatin dynamics could be causative for the low Pi and JA signalling phenotypes of al6

The present study associates the histone reader AL6 with the response of etiolated seedlings to JA, resulting in the repression of skotomorphogenesis by inhibiting hypocotyl cell elongation. The exact molecular mechanism underlying the role of AL6 in the response to JA is presently unclear. Previously published results links AL to Polycomb Group (PcG) protein-mediated gene silencing. More specifically, it was demonstrated that AL6 and AL7 interact with the C-terminus of core components of PcG-Repressive Complex 1 (PRC1), triggering a switch from the active H3K4me3 mark to the repressive H3K27me3 via recruitment of PRC2 [32]. It was further demonstrated that the H3K27me3 reader protein LIKE-HETEROCHROMATIN PROTEIN 1 (LHP1), a component of PRC1, regulates the transcription of stress-responsive genes in concert with the heterogeneous nuclear ribonucleoprotein Q protein LIF2 [33]. Application of methyl jasmonate (MeJA) was found to recruit LIF2 to chromatin [33], suggesting a mechanistic link between PcG proteins and JA signalling. More recently, LHP1 was shown to interact with JAZ proteins to repress the transcription of JA-responsive genes by introducing repressive chromatin modifications [27], indicating a dynamic interplay of histone methylation and JA signalling. Conspicuously, LIF2 is closely co-expressed with AL6 (atted.jp and Supplementary Fig. S2), further supporting this scenario. Beside AL3 and CDC5 which are also in the PPI network, another protein involved in miRNA biogenesis, MOS2 [53], is part of the AL6 co-expression network, indicating a possible involvement of miRNAs in AL-mediated processes. Interestingly, MOS2 was associated with innate immunity in a forward genetic screen [57].

In the present study, an involvement of AL6 in dynamic changes at the chromatin level can be inferred from label-free quantification of proteins that accumulate differentially between the two genotypes. For example, the histone chaperons NUCLEOSOME ASSEMBLY PROTEIN 1;2 (NAP1;2) and NAP1-RELATED PROTEIN 1 (NRP1) were highly upregulated in al6 seedlings. NRP1 negatively regulates the deposition of the histone H2A variant H2A.Z in chromatin by repressing the SWR1 chromatin-remodelling complex [50]. Notably, NAP1;2 was shown to be critical for the recalibration of Pi homeostasis in Arabidopsis, possibly by modulating H2A.Z deposition at the transcriptional start sites of Pi-responsive genes [16, 43]. The SWR1 component CHR11 was downregulated in al6 mutant plants. Thus, it may be speculated that H2A.Z deposition of a subset of genes may be compromised in al6 mutants, leading to a more pronounced response to Pi starvation as it was observed in mutants harbouring defects in the SWR1 subunit ACTIN-RELATED PROTEIN 6 (APR6), in which H2A.Z deposition is repressed [11, 43]. In fact, we previously found that, similar to al6, arp6 mutants form very short root hairs upon Pi starvation, suggesting that compromised H2A.Z deposition is causative for the deregulated Pi starvation response in both mutants [45]. H2A.Z is colocalized with H3K4me3 and promotes formation of H3K27me3 [7], matching the pattern of the putative distribution and function of AL6.

Al6 May Participate In The Repression Of Ja Signalling

Taken together, our data support a model in which AL6, and possibly other AL proteins, act as a component of the repressor complex in JA signalling, supporting the deposition of repressive histone modifications by recruiting PcG proteins (Fig. 8). This supposition is supported by the validated binding of AL6 to PRC1 components [32] and predicted interactions of AL proteins with JA signalling inhibitors such as TPL. The JA-insensitive phenotype of the al6 mutant appears, at first sight, counterintuitive if a role of AL6 in repressing JA responses is supposed. However, the available data suggest a more complex picture for the interplay of histone modifications and JA signalling. Loss of AL6 function appears to be associated with reduced H2A.Z deposition, an assumption that is inferred from the differential accumulation of NAP1 and CHR11, the aggravated response of al6 Pi deficiency and the short root hair phenotype of al6 mutants under such conditions, which resemble mutants defective in H2A.Z deposition [8, 45, 43] Regions targeted by LIF2 and the PcG protein LHF1 were found to be enriched in H2A.Z [33], a condition which is not met in the absence of AL6 and may lead to a delayed or compromised response to JA. Strikingly, we found that reduced HDA19 transcript levels led to a phenotype that is similar to al6 under the present conditions and treatments (Supplementary Fig. S3), supporting this conclusion. Similar to what is assumed for AL6, HDA19 and HDA6 were shown repress the transcription of JA-responsive genes as part of a co-repressor complex and required for the repression of photomorphogenesis [60, 52]. Noteworthily, H3K4 trimethylation of a subset of stress-responsive genes was impaired in the HDA6 mutant axe1-5, suggesting that histone acetylation is linked to H3K4 methylation [54]. Similar to al6, mutants harbouring defects in HDA6 and HDA19 form short root hairs under low Pi conditions and show a compromised Pi starvation response [9], suggesting that histone acetylation is critical for both the adaptation to low Pi availability and proper JA signalling. Interestingly, Pi deficiency was shown to trigger JA biosynthesis and signalling [19], linking the two responses at a biochemical level. However, in contrast to what has observed for roots, in etiolated seedlings low Pi availability does not induce JA biosynthesis and rather repress the response to JA

In conclusion, we show here that the histone reader AL6 is involved in the response to JA during skotomorphogenesis, possibly mediated by a PRC1/2-mediated switch in H3K4me3 to H3K27me3 and altered deposition of the histone variant H2A.Z. The pleiotropic phenotype of al6 mutants supports a critical role of AL6 in the interpretation of environmental information and highlights its at least partly non-redundant role within members of the enigmatic AL protein family. We further show that processes as diverse as root responses to Pi starvation and hypocotyl elongation of etiolated seedlings converge at critical nodes at the chromatin level that modulate the phenotypic readout in a vast array of environmental and developmental responses. While the exact molecular mechanism by which AL6 mediates the response to JA requires further experimentation, it can be stated that ChEP-P is a suitable approach to allow for holistic insights into chromatin-associated changes between genotypes and treatments and to provide a suite of candidates that directs follow-up research.

Plant materials and growth conditions

Arabidopsis thaliana Col-0 was used as wild type in this study. Seeds of the accession Col-0 and the T-DNA insertion mutant al6 (SALK_040877C) were purchased from ABRC (Ohio State University, Columbus, OH, USA). The al6 mutant was described previously [8]. Arabidopsis seeds were surface sterilized with 35% bleach for 5 min and washed five times with sterile water (5 min each). Sterile seeds were placed on a growth medium described by Estelle and Somerville [13] composed of 5 mM KNO₃, 2 mM MgSO₄, 2 mM Ca(NO₃)₂, 2.5 mM KH₂PO₄, 70 µM H₃BO₃, 14 µM MnCl₂, 1 µM ZnSO₄, 0.5 µM CuSO₄, 0.01 µM CoCl₂, 0.2 µM Na₂MoO₄, and 40 µM Fe-EDTA, and solidified with 0.4% Gelrite Pure. MES (1 g/L) and 1.5% (w/v) sucrose were included, and the pH was adjusted to 5.5 with KOH (ES medium). Seeds were stratified on plates for 2 d at 4°C in the dark, transferred to a growth chamber and grown at 22°C in the dark with 70% relative humidity. For low Pi-treated plants, media were supplemented with 2.5 µM KH₂PO₄ and 2.5 mM KCl. For jasmonate (JA) elicitation, seedlings were grown for 5 days on ES or low Pi medium containing 50 µM JA. An equal amount of DMSO was added as a control in ES and low Pi plates.

Plant Imaging And Hypocotyl Measurement

Images of 5-d-old seedlings were taken with a digital camera (Canon EOS 90D). The images included a ruler placed on top of the plate for further analysis. Hypocotyl lengths were measured with the ImageJ software (http://rsb.info.nih.gov/ij) from a suite of 60 JPG images per replicate and treatment (three independent replicates) from seedlings grown on mock or low Pi media and media supplemented with 50 µM JA. Graphs, calculations, and statistical analyses were performed using the GraphPad Prism software version 8.0 for Mac.

Confocal laser and cryogenic scanning (cryo-SEM) microscopy and cell size measurements

Etiolated hypocotyls were dipped in 10 µg/mL propidium iodide (PI) in H₂O for 20 min in the dark, rinsed twice with H₂O for 1 min, and the PI fluorescence was visualized using a 20x objective on a Zeiss LSM880 confocal laser scanning microscope. For cryo-SEM, hypocotyls were frozen in liquid nitrogen before imaging. Images were obtained using a FEI Quanta 200 scanning electron microscope with cryo system (Quorum PP2000TR FEI) operating at an acceleration voltage of 3kV. For cell size measurement, 30 cells of at least 10 etiolated hypocotyls for each treatment were used and processed using the ImageJ software. Statistical analysis was performed using the GraphPad Prism software version 8.0 for Mac.

Jasmonate Quantification

For extraction of JA, etiolated hypocotyls (∼200 mg fresh weight) were collected and frozen with liquid nitrogen. The ground tissue was dissolved in 550 µL of working solution (50 µL MeOH, 10 ng d5-JA, 2-propanol/H₂O/concentrated HCl, 2:1:0.002) and shaken at 100 rpm for 30 min at 4°C. One ml of dichloromethane was added and shaken for 30 min at 4°C. The samples were centrifuged at 13,000g for 5 min at 4°C, and 900 µL of the lower phase was transferred to a fresh Eppendorf tube, desiccated for 40 min using nitrogen evaporate, and dissolved in MeOH for further analysis by liquid chromatography-tandem mass spectrometry. Graphs, calculations, and statistical analyses were performed using the GraphPad Prism software version 8.0 for Mac.

Gene Ontology

Gene ontology (GO) enrichment analysis of DEPs was performed using the Singular Enrichment Analysis (SEA) available on the ArgiGO v2.0 toolkit web-server [47]. The analysis was performed using the following parameters: selected species: Arabidopsis thaliana;

Reference: TAIR genome locus (TAIR10_2017); Statistical test method: Fisher; Multi-test adjustment method: Yekutieli (FDR under dependency); Significance level: 0.05; Minimum number of mapping entries: 5; Gene ontology type: Complete GO. Significantly enriched GO terms were summarized and visualized using REVIGO [46] with a similarity setting of 0.7 and SimRel as the semantic similarity measure. Final figures were plotted in R (version 3.6.2). Scatterplots show clusters that are representative of the distribution of GO terms represented as bubbles. Semantically similar GO terms will be closer together, the sizes of the bubbles indicate the frequency of GO term they represent. The gradient colour denotes the significance obtained from the enrichment analysis (log 10 P value). Gene ontology enrichment for all proteins identified by ChEP-P in wild-type and al6 mutant plants in at least in two biological repeats per treatment depicted as heatmaps was computed by TopGO using the elim method [3] by implementation of GOBU (https://gobu.sourceforge.io/). Heatmaps were generated with the pheatmap package in R.

Chromatin enrichment for proteomics in plants (ChEP-P)

Chromatin samples were isolated from shoots of 5-day-old etiolated seedlings using a protocol adapted from Kustatscher et al. [22]. Briefly, 200 mg of tissue were cross-linked with 10 mL buffer A (0.4 M sucrose, 10 mM Tris pH 8, 1 mM EDTA, 1 mM PMSF, 1% formaldehyde) under vacuum for 20 min at room temperature. Cross-linking was quenched by adding 0.1 M glycine for 10 min at room temperature [36]. The tissue was then washed trice with distilled water, incubated in 1 mL lysis buffer (25 mM Tris pH 7.4, 0.1% (v/v) Triton X-100, 85 mM KCl and 2X Roche protease inhibitor tablets) for 15 min on ice, and centrifuged at 16,100g for 35 min at 4°C. The nuclear pellet was resuspended in 500 µL lysis buffer containing 200 µg/mL RNase A and incubated for 15 min at 37°C. The pooled nuclei suspension was centrifuged at 16,100g for 35 min at 4°C. The nuclei pellet was resuspended in 500 µL 4 % SDS buffer (50 mM Tris pH 7.4, 10 mM EDTA, 4% (w/v) SDS, 1 mM PMSF, and 2X Roche protease inhibitor tablets), and incubated for 10 min at room temperature. A 1.5 mL aliquot of freshly prepared 8 M urea buffer (10 mM Tris pH 7.4, 1 mM EDTA and 8 M urea) were added to the sample, mixed by inverting the tube several times, and centrifuged at 16,100g for 30 min at 25°C. The supernatant was discarded, and the transparent pellet was washed twice with 500 µL of 4% SDS buffer and centrifuged at 16,100g for 25 min at 25°C. Subsequently, the pellet was resuspended in 0.2 mL storage buffer (10 mM Tris pH 7.4, 1 mM EDTA, 25 mM NaCl, 10% (v/v) glycerol, 1 mM PMSF, and 2X Roche protease inhibitor tablets). The sample was sonicated trice for 5 min on ice with an amplitude of 10% in alternating ‘on’ and ‘off’ intervals (30 s each), centrifuged at 16,100g for 30 min at 4°C, and the supernatant containing the cross-linked chromatin was transfer to a new tube.

On-bead trypsin digestion, quantitative label-free LC-MS/MS analysis, and protein identification

Ten µg chromatin samples were digested with 12.5 µg of modified trypsin (Promega) at 37°C overnight, and acidified with trifluoroacetic acid to a final concentration of 0.1%. Samples containing the peptides were redissolved in solvent containing 0.1% formic acid and 3 % acetonitrile in water (J.T. Baker), and 3 µg protein sample were injected for nano-HPLC-MS/MS analysis with an LC retention time alignment of 210 min per sample. For peptide quantification, three biological replicates were run trice, and label-free quantification was performed using the Proteome Discoverer™ Software 2.2 (Thermo Fisher) using the Sequest search algorism. All peptide spectrum matches were filtered with a q-value threshold of 0.05 (5% RDR), proteins were filtered with medium confidence threshold (0.05 q-value, 5% FDR).

Due to the limited sensitivity of LC-MS/MS analysis, reads for the intensity of low abundant peptides may be zero [14]. Zero values from label-free mass spectrometry were analysed and normalized according to the maximum likelihood theory selection and exclusion of peptides and proteins as described by Karpievitch et al. [17]. For statistical analysis, the method described by Cox and Mann [12] was used. Log2 ratios were calculated for at least two biological repeats of the quantified proteins and analysed for normal distribution. For the mean and SD, 95% confidence (Z score = 1.96) was used to select proteins with a distribution far from the main distribution. Downregulated and upregulated proteins were calculated using a confidence interval of mean ratio − 1.96 x SD and + 1.96 x SD, respectively.

The mass spectrometry proteomics data are available in the ProteomeXchange Consortium via the PRIDE [39] partner repository with the dataset identifier PXD026541 (http://www.ebi.ac.uk/pride/archive/projects/PXD026541).

ChEP-P: Chromatin enrichment for Proteomics in Plants

DEP:Differentially expressed proteins

PTM:Posttranslational modifications

PHD:plant homeodomain

SCF^CoI1:Skp-Cullin-F-box E3 ubiquitin ligase

PcG:Polycomb Group

PRC:PcG-Repressive Complex

Cryo-SEM: Cryogenic scanning microscopy

SEA:Singular Enrichment Analysis

Ethics approval and consent to participate

Permissions for using the materials and to perform the experiments was obtained from Academia Sinica and complies with relevant institutional, national, and international guidelines and legislation.

Consent for publication

Not applicable.

Availability of data and materials

The mass spectrometry proteomics data are available in the ProteomeXchange Consortium via the PRIDE [39] partner repository with the dataset identifier PXD026541(http://www.ebi.ac.uk/pride/archive/projects/PXD026541).

Competing interests

The authors declare that they have no competing interests.

Funding

Work in the Schmidt laboratory is funded by Academia Sinica and the Ministry of Science and Technology

Authors’ Contributions

I.C.V-B. performed the experiments; I.C.V-B. and W.S. conceived the project, analysed the data, and wrote the manuscript.All authors read and approved the final manuscript.

Acknowledgements

We thank Mei-Jane Fang and Dr.Wann-Neng Jane from the IPMB Live Cell Imaging Core Laboratory for their help with confocal and cryo-SEM imaging, Drs. Tuan-Nan Wen and Chuan-Chih Hsu from the IPMB Proteomics Core Laboratory for their help with proteomic data analysis and Dr.Wendar Lin from the Bioinformatic Core Laboratory for help with GO enrichment analysis. Proteomic mass spectrometry analyses, in-gel digestion, and label-free quantification were performed by the Proteomics Core Laboratory sponsored by the Institute of Plant and Microbial Biology and the Agricultural Biotechnology Research Center, Academia Sinica. We also acknowledge the Metabolomics Core Laboratory at ABRC, Academia Sinica, for providing help with JA analysis. I.C.V-B was supported by fellowships provided by the Ministry of Science and Technology (MOST) and Academia Sinica. Work in the Schmidt laboratory is supported by Academia Sinica and MOST.

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Chromatin Enrichment for Proteomics in Plants (ChEP-P) Implicates the Histone Reader ALFIN-LIKE 6 in Jasmonate Signalling

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Journal Publication

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Abstract

Figures

Background

Results

AL6 is critical for the response of etiolated Seedlings to JA

Chep-p Identified A Comprehensive Subset Of Chromatin-associated Proteins

Chep-p Complements Other Proteomic Approaches

A Ppi Network Links Al Proteins To Plant Immunity

Discussion

ChEP-P detects a comprehensive suite of chromatin-associated proteins

Al6 May Participate In The Repression Of Ja Signalling

Conclusions

Methods

Plant materials and growth conditions

Plant Imaging And Hypocotyl Measurement

Jasmonate Quantification

Gene Ontology

Abbreviations

Declarations

Ethics approval and consent to participate

Consent for publication

Competing interests

Authors’ Contributions

References

Additional Declarations

Supplementary Files

Status:

Journal Publication

Version 1