With TPL-like co-repressor proteins in vivo. Nonetheless, we did not recognize
With TPL-like co-repressor proteins in vivo. Having said that, we didn’t recognize CO in these pull-down experiments, which is likely a result on the low abundance on the CO protein. Alternatively, miP1a/b may possibly type diverse kinds of repressor complexes that also involve other CO-like proteins. As a way to uncover more proteins interacting with either TPL or JMJ14, which may well shed light on the formation of a prospective higher-order repressor complicated, we also generated plants overexpressing FLAG-TPL and FLAGJMJ14 to co-purify added interacting proteins (Supplementary Data Set four). Comparable to miP1a/b, we also performed parallel IPs with Col-0 and transgenic plants expressing FLAG-GFP, but this time performed an additional active coal purification step prior to injection in to the mass spectrometer. Comparative analysis of those 4 data sets revealed 97 JMJ14-interacting proteins and 96 TPL-interacting proteins (Figure 5B). In total, we identified 24 proteins co-precipitating with JMJ14 and TPL. The JMJ14 information set incorporated a protein group of NAC transcription variables NAC50 and NAC52 that had previously been identified to interact with JMJ14 (Ning et al., 2015). TPL co-precipitated all other TPLrelated (TPR) proteins, supporting the recent locating that TPL/TPR proteins include a tetramerization interface (Martin-Arevalillo et al., 2017). These examples confirm that our mass spectrometry mmunoprecipitation (MS P) strategy identified bona fide JMJ14- and TPL-interacting proteins. We note that we could not detect previously identified TPL/ TPR-interacting repression-domain containing transcription things (Causier et al., 2012). This could indicate that these| PLANT PHYSIOLOGY 2021: 187; 187Rodrigues et al.Table 1 Loci showing differential methylation and differential gene expression in transgenic Dopamine β-hydroxylase Molecular Weight miP1a-OX plants versus WTAGI code Annotation [ ] me WT 67 60 58 56 48 0 0 0 three 20 12 25 39 21 68 60 53 49 46 45 66 57 11 40 0 12 9 25 5 22 38 24 0 0 15 31 [ ] me miP1a-OX 0 0 0 0 0 71 67 42 61 68 57 67 81 63 0 0 0 0 0 0 23 16 52 83 46 59 59 75 56 73 91 80 58 60 77 one hundred [FC] 0.0319 0.1021 0.0090 0.0576 0.1755 0.1062 0.2013 0.2451 0.0060 0.0070 0.1620 0.0004 0.0058 0.1510 five.7 11.six four.1 114.1 15.3 four.1 eight.8 four.6 11.1 7.6 5.6 12.five 51.7 20.two 4.5 218.7 6.0 five.5 21.six 4.1 19.7 six.9 FDR 1.02E-13 1.67E-33 5.86E-04 2.55E-15 9.67E-04 1.31E-08 four.70E-06 1.94E-28 1.10E-05 5.89E-05 four.24E-06 five.70E-58 six.44E-06 7.30E-04 four.23E-20 two.40E-50 four.28E-12 four.10E-04 three.50E-06 1.44E-12 6.03E-56 two.82E-15 4.55E-18 four.66E-22 1.52E-31 1.18E-79 four.89E-13 1.78E-08 eight.35E-15 1.85E-07 five.57E-44 2.64E-18 1.94E-37 three.61E-26 1.45E-11 1.77E-26 A/hypomethylated and downregulated genes in miP1a-OX AT4G29030 Putative membrane lipoprotein AT4G14390 Ankyrin Adrenergic Receptor Agonist review repeat family members protein AT2G35380 Peroxidase superfamily protein AT1G62510 Bifunctional inhibitor/lipid-transfer protein AT3G20865 AGP40 B/hypermethylated and downregulated genes in miP1a-OX AT4G20000 VQ motif-containing protein AT1G66830 Leucine-rich repeat protein kinase family protein AT3G22231 PCC1 j PATHOGEN AND CIRCADIAN CONTROLLED 1 AT2G25130 ARM repeat superfamily protein AT1G12940 ATNRT2.5, NRT2.five j nitrate transporter2.5 AT2G35980 NHL10, ATNHL10, YLS9 AT1G65480 FT AT4G12500 Bifunctional inhibitor/lipid-transfer protein AT5G40010 AATP1, AAA-ATPase 1 C/hypomethylated and upregulated genes in miP1a-OX AT2G37260 ATWRKY44, DSL1, TTG2 AT2G39330 JAL23, jacalin-related lectin 23 AT1G03940 HXXXD-type acyl-transferase household protein AT4G21830 ATMSRB7, MSRB7, methi.