With TPL-like co-repressor proteins in vivo. Even so, we did not recognize
With TPL-like co-repressor proteins in vivo. However, we did not identify CO in these pull-down experiments, which is most likely a result with the low abundance in the CO protein. Alternatively, miP1a/b may well form diverse kinds of repressor complexes that also involve other CO-like proteins. In order to locate added proteins interacting with either TPL or JMJ14, which may shed light on the formation of a potential higher-order repressor complicated, we also generated plants overexpressing FLAG-TPL and FLAGJMJ14 to co-purify extra interacting proteins (Supplementary Information Set four). Similar to miP1a/b, we also performed parallel IPs with Col-0 and transgenic plants expressing FLAG-GFP, but this time performed an more active coal purification step prior to injection in to the mass spectrometer. Comparative analysis of those four 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 data set integrated a Free Fatty Acid Receptor Activator review protein group of NAC transcription aspects NAC50 and NAC52 that had previously been located to interact with JMJ14 (Ning et al., 2015). TPL co-precipitated all other TPLrelated (TPR) proteins, supporting the recent acquiring that TPL/TPR proteins include a tetramerization interface (Martin-Arevalillo et al., 2017). These examples confirm that our mass spectrometry mmunoprecipitation (MS P) approach identified bona fide JMJ14- and TPL-interacting proteins. We note that we could not detect previously identified TPL/ TPR-interacting repression-domain containing transcription factors (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 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 five 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 5.7 11.6 four.1 114.1 15.three 4.1 eight.8 four.six 11.1 7.6 five.six 12.five 51.7 20.two 4.5 218.7 6.0 five.5 21.6 4.1 19.7 six.9 FDR 1.02E-13 1.67E-33 five.86E-04 2.55E-15 9.67E-04 1.31E-08 four.70E-06 1.94E-28 1.10E-05 5.89E-05 4.24E-06 five.70E-58 6.44E-06 7.30E-04 4.23E-20 two.40E-50 4.28E-12 4.10E-04 three.50E-06 1.44E-12 six.03E-56 2.82E-15 four.55E-18 4.66E-22 1.52E-31 1.18E-79 4.89E-13 1.78E-08 eight.35E-15 1.85E-07 5.57E-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 repeat family protein AT2G35380 Peroxidase superfamily protein AT1G62510 ATGL manufacturer 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 loved ones protein AT3G22231 PCC1 j PATHOGEN AND CIRCADIAN CONTROLLED 1 AT2G25130 ARM repeat superfamily protein AT1G12940 ATNRT2.5, NRT2.5 j nitrate transporter2.five 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 family members protein AT4G21830 ATMSRB7, MSRB7, methi.
