Fig. S1a: Conserved motif analysis of Solanaceae DMTases. The motifs (1–10) identified using MEME search tool with default parameters have been marked on.

Slides:



Advertisements
Similar presentations
Phylogenetic Tree A Phylogeny (Phylogenetic tree) or Evolutionary tree represents the evolutionary relationships among a set of organisms or groups of.
Advertisements

Genes Involved in Plant Stress Response and Evolution of their Responsiveness Cheng Zou 11/09/2007.
Suppl. Fig. S1 Suppl. Fig. S1 The nucleotide sequence and its deduced amino acid sequences of CaSAMDC. The full-length of CaSAMDC (GenBank Accession No.
Figure S1. Genomic PCR of in vitro potato plants transformed with StPTB1 prom (top) and StPTB6 prom (bottom) constructs using nptII-specific primers. Thirty.
Ca 2+ signaling in plant Light Cold stress Heat shock Mechanical stresses (Touch, wind & Wounding) Pathogen invading Phytohormones (Auxin, ABA, GA) Gravity.
Figure S1_Yao Qin et al. Figure S1 Occurrence and distribution of trihelix family in different plant species. Red branches in the cladogram indicate that.
Supplementary Fig. S1: Hierarchical clustering of AUX/IAA genes, showing significant differential expression under at least one abiotic stress condition.
Cluster I. Cluster II Cluster III (contiued) Cluster IV.
Gene expression (signal intensity) Control Osmotic Salt Drought Root Control Gene expression (signal intensity) Treatment.
Fig. S1. Amino acid sequence alignment of MYBS3 proteins. MYBS3 protein sequences of Arabidopsis thaliana (MYBH; NP_199550); (At3g16350; NP_188256), Glycine.
Supplementary Fig. 1. (A) PCR amplification of wheat TaHSP26 genomic, cDNA and ORF clones. (B) ORF and protein sequence of TaHSP26. An arrowhead indicates.
HKT1 form Arabidopsis relative extremophile Thellungiella work as Na/K co-transporter.
Supplemental Fig. S1 A B AtMYBS aa AtMYBS
Julián Mateus1 • Stef de Haan2 Carlos Chuquillanqui2
WRKY transcription factors in potato genome factors in potato genome
Julián Mateus1 • Stef de Haan2 Carlos Chuquillanqui2
SI-II A SI-II. Expression analysis of bladder cancer functionally active genes and significantly mutated genes. Comprehensive transcriptome profiling of.
Warm Up Who was Charles Darwin?
Carlos Chuquillanqui1 • Ian Barker1
AtIAA18 AtIAA6 AtIAA19 VvIAA19 AtIAA10 AtIAA20 AtIAA7 AtIAA30 AtIAA11
Volume 9, Issue 10, Pages (October 2016)
Carlos Chuquillanqui1 • Ian Barker1
Zhu Hui-Fen , Fitzsimmons Karen , Khandelwal Abha , Kranz Robert G.  
Julián Mateus1 • Stef de Haan2 Carlos Chuquillanqui2
Julián Mateus1 • Stef de Haan2 Carlos Chuquillanqui2
WRKY transcription factors in potato genome factors in potato genome
Volume 4, Issue 1, Pages (January 2011)
Phylogeny and the Tree of Life
Julián Mateus1 • Stef de Haan2 Carlos Chuquillanqui2
Volume 5, Issue 2, Pages (March 2012)
Reading Phylogenetic Trees
Volume 6, Issue 3, Pages (May 2013)
Volume 64, Issue 3, Pages (November 2016)
Volume 6, Issue 5, Pages (September 2013)
Mechanism of Triton binding to ShHTL7
Volume 2, Issue 4, Pages (July 2009)
Volume 11, Issue 1, Pages (January 2018)
Evolution of Eukaryotic DNA Methylation and the Pursuit of Safer Sex
Matthew W Jones-Rhoades, David P Bartel  Molecular Cell 
Volume 1, Issue 5, Pages (September 2008)
Volume 11, Issue 1, Pages (January 2018)
Volume 6, Issue 6, Pages (November 2013)
Julián Mateus1 • Stef de Haan2 Carlos Chuquillanqui2
Volume 9, Issue 7, Pages (July 2016)
Volume 132, Issue 6, Pages (March 2008)
CARPEL FACTORY, a Dicer Homolog, and HEN1, a Novel Protein, Act in microRNA Metabolism in Arabidopsis thaliana  Wonkeun Park, Junjie Li, Rentao Song,
Volume 7, Issue 8, Pages (August 2014)
Phylogenetic Trees Jasmin sutkovic.
Posttranscriptional Gene Silencing Is Not Compromised in the Arabidopsis CARPEL FACTORY (DICER-LIKE1) Mutant, a Homolog of Dicer-1 from Drosophila  E.Jean.
Insights into Subunit Interactions in the Heterotetrameric Structure of Potato ADP- Glucose Pyrophosphorylase  Aytug Tuncel, Ibrahim Halil Kavakli, Ozlem.
Volume 3, Issue 6, Pages (June 1999)
Volume 4, Issue 6, Pages (November 2011)
Expression of the AREB1 Gene and Subcellular Localization of the AREB1 Protein.(A) Structure of AREB1 family proteins. Expression of the AREB1 Gene and.
Julián Mateus1 • Stef de Haan2 Carlos Chuquillanqui2
Volume 2, Issue 4, Pages (April 2002)
Volume 24, Issue 7, Pages (July 2016)
Volume 94, Issue 2, Pages (July 1998)
PtrHB7, a class III HD-Zip Gene, Plays a Critical Role in Regulation of Vascular Cambium Differentiation in Populus  Yingying Zhu, Dongliang Song, Jiayan.
LIR motif consensus and structural determinants of LIR–ATG8 interactions. LIR motif consensus and structural determinants of LIR–ATG8 interactions. (A)
Overview of HEAT-motif-containing proteins.
Volume 2, Issue 2, Pages (March 2009)
Jia-Wei Wu, Amy E. Cocina, Jijie Chai, Bruce A. Hay, Yigong Shi 
Fig. 2. —Phylogenetic relationships and motif compositions of some representative MORC genes in plants and animals. ... Fig. 2. —Phylogenetic relationships.
Volume 6, Issue 2, Pages (March 2013)
Volume 12, Issue 3, Pages (March 2019)
Volume 12, Issue 12, Pages R412-R414 (June 2002)
Volume 3, Issue 2, Pages (March 2010)
Volume 97, Issue 6, Pages (June 1999)
DNA Damage-Induced Transcription of Transposable Elements and Long Non-coding RNAs in Arabidopsis Is Rare and ATM-Dependent  Zhenxing Wang, Rainer Schwacke,
Volume 1, Issue 5, Pages (September 2008)
Presentation transcript:

Fig. S1a: Conserved motif analysis of Solanaceae DMTases. The motifs (1–10) identified using MEME search tool with default parameters have been marked on protein sequences. The length and order of the boxes represents the actual length and position of the conserved domain in the protein sequence. The bottom panel represents the consensus sequence of the predicted motifs SlMET1 2.SlCMT2 3.SlCMT4 4.SlCMT3 5.SlDRM5 6.SlDRM7 7.SlDRM6 8.SlDNMT2 9.SlDRM8 10.SpeCMT4 11.SpeCMT3 12.SpeCMT2 13.SpeMET1 14.SpeDRM5 15.SpeDRM7 16.SpeDRM6 17.SpeDRM8 18.SmeMET1 19.SmeDRM5 20.SmeDRM7 21.SmeDNMT2 22.CaDRM6 23.CaMET1a 24.CaCMT3 25.CaCMT4 26.CaDRM5a 27.CaCMT3b 28.CaDRM8a 29.CaDRM5b 30.CaDNMT2b 31.CaDRM8b 32.CaMET1b 33.CaCMT2 34.StDRM7 35.StCMT2 36.StDRM6 37.StDRM5 38.StCMT4 39.StMET1

Fig. S1b: Conserved domain analysis of Solanaceae DMTases. The domains (1–10) were identified using MEME search tool with default parameters in methyltransferase domains of DMTases. The upper panel shows the arrangement of these domains whereas the lower panel represents the consensus sequence of the predicted domains. StCMT2 SlCMT2 SlCMT4 CaCMT4 SlCMT3 StCMT4 CaCMT3a SlMET1 StMET1 CaMET1b CaMET1a SlDRM5 StDRM5 CaCMT3b CaDRM5b CaDRM5a StDRM7 SlDRM7 SlDRM6 StDRM6 CaDRM6 SlDRM8 CaDRM8b CaDRM8a SlDNMT2 CaDNMT2b CaCMT2

Fig. S2: Phylogenetic relationship among various DMTases. Full length protein sequences of DMTase proteins from Chlamydomonas reinhardtii (Cr), Selaginella moellendorffii (Sm), Arabidopsis (At), rice (Os), Vitis vinifera (Vv), populus (Pt), human (Hs), Drosophila (Dm), yeast (Sp) and Solanaceae members, including tomato (Sl), S. pennellii (Spe), potato (St), eggplant (Sme), pepper (Ca) and N. benthamiana (Nb) were included in the construction of an unrooted tree using JTT-matrix based method in MEGA 6. This analysis classified DMTases into four different classes, namely MET, DRM, CMT and DNMT2. Though DNMT2 homologs had a DNA_methylase domain, emerging evidence suggest that these proteins act as RNA methyltransferases. Relatively higher phylogenetic relatedness was observed among DMTase homologs within Solanum taxon and name of these proteins are presented in ‘bold’ in each clade. Similarly, name of the rice DMTase homologs are presented in ‘italics’. The bootstrap values are based on 1000 iterations and the support values are represented at each node.

Fig. S3: Expression profiles of DMTases in S. pimpinellifolium. Publically available RNA-seq datasets were retrieved to analyze expression patterns. Heatmaps were generated using ‘gplots’ in ‘R” package. Color scale represents log 2 RPKM values. IG, immature green; B, breaker; B+5, 5 days after breaker.

Fig. S4: Expression levels of S. pennellii (a) and S. tuberosum (b) DMTase genes are perturbed by both biotic and abiotic stresses. Publically available RNA-seq datasets on stresses for S. pennellii and potato were retrieved to analyze expression patterns [33, 43]. Heat maps were generated using ‘ gplots ’ in ‘ R ’ package. Color scale represents log 2 RPKM and FPKM values, respectively. Five-week-old hydroponically grown S. pennellii seedlings were used for stress treatments [33]. In S. pennellii: C.1, control for biotic stress; C.2, control for cold and drought stress on small leaves; C.3, control for cold and drought stress on mature leaves and root; C.4 and C.5, control for low- and hi-salt stress on stem; C.6 and C.7, control for low- and hi-salt stress on roots. In potato, control represents control for salt and mannitol stresses whereas control.1 serves control for heat stress. For potato, the details of plant growth conditions and stress treatments have been described previously and can be accessed at the weblink ( [43] http://

SlMET1SpeMET1 StMET1 CaMET1 Fig. S5: The intermolecular interactions between the BAH domain of Solanaceae MET syntelogs with the bound H3(1–32)K9me2 peptide state. Green dashed line depicts hydrogen bonding and red half sun like points represent hydrophobic interactions.

Fig. S6: The intermolecular interactions between chromo and BAH domains of Solanaceae CMT2 syntelogs with the bound H3(1–32)K9Me2 peptide state. Green dashed line depicts hydrogen bonding and red half sun like points represent hydrophobic interactions. ChromoBAH SlCMT2 ChromoBAH SpeCMT2 ChromoBAH CaCMT2 ChromoBAH StCMT2