Temperature-dependent jumonji demethylase modulates flowering time by targeting H3K36me2/3 in Brassica rapa.

Brassica rapa / genetics Flowers / genetics Gene Expression Regulation, Plant Histones / metabolism Quantitative Trait Loci Jumonji Domain-Containing Histone Demethylases / metabolism Plant Proteins / genetics Temperature Thermotolerance / genetics Methylation Plants, Genetically Modified Chlorophyll / metabolism

Journal

Nature communications
ISSN: 2041-1723
Titre abrégé: Nat Commun
Pays: England
ID NLM: 101528555

Informations de publication

Date de publication:
28 Jun 2024
Historique:
received: 02 01 2023
accepted: 12 06 2024
medline: 28 6 2024
pubmed: 28 6 2024
entrez: 27 6 2024
Statut: epublish

Résumé

Global warming has a severe impact on the flowering time and yield of crops. Histone modifications have been well-documented for their roles in enabling plant plasticity in ambient temperature. However, the factor modulating histone modifications and their involvement in habitat adaptation have remained elusive. In this study, through genome-wide pattern analysis and quantitative-trait-locus (QTL) mapping, we reveal that BrJMJ18 is a candidate gene for a QTL regulating thermotolerance in thermotolerant B. rapa subsp. chinensis var. parachinensis (or Caixin, abbreviated to Par). BrJMJ18 encodes an H3K36me2/3 Jumonji demethylase that remodels H3K36 methylation across the genome. We demonstrate that the BrJMJ18 allele from Par (BrJMJ18

Identifiants

DOI: 10.1038/s41467-024-49721-z PMID: 38937441
pubmed: 38937441
doi: 10.1038/s41467-024-49721-z
pii: 10.1038/s41467-024-49721-z
doi:

Substances chimiques

Histones 0
Jumonji Domain-Containing Histone Demethylases EC 1.14.11.-
Plant Proteins 0
Chlorophyll 1406-65-1

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

5470

Informations de copyright

© 2024. The Author(s).

Références

Elvis, K., Quezada, D., Ihien, E., Vasquez-Teuber, P. & Mason, A. Interspecific hybridization for Brassica crop improvement. Crop Breed. Genet. Genom. https://doi.org/10.20900/cbgg20190007 (2020).
Qi, X. et al. Genomic inferences of domestication events are corroborated by written records in Brassica rapa. Mol. Ecol. 26, 3373–3388 (2017).
pubmed: 28371014 doi: 10.1111/mec.14131
Prakash, S., Wu, X.i. & Bhat, S. R. History, Evolution, and Domestication of Brassica Crops, Plant Breed. Rev. 35, 19–84 (2011).
Purugganan, M., Boyles, A. L. & Suddith, J. I. Variation and selection at the CAULIFLOWER floral homeotic gene accompanying the evolution of domesticated Brassica oleracea. Genetics 155, 855–862 (2000).
pubmed: 10835404 pmcid: 1461124 doi: 10.1093/genetics/155.2.855
McClung, C. R., Lou, P., Hermand, V. & Kim, J. A. The importance of ambient temperature to growth and the induction of flowering. Front. plant sci. 7, 1266 (2016).
pubmed: 27602044 pmcid: 4993786 doi: 10.3389/fpls.2016.01266
Del Olmo, I., Poza-Viejo, L., Piñeiro, M., Jarillo, J. A. & Crevillén, P. High ambient temperature leads to reduced FT expression and delayed flowering in Brassica rapa via a mechanism associated with H2A.Z dynamics. Plant j. 100, 343–356 (2019).
pubmed: 31257648 doi: 10.1111/tpj.14446
Yui, S. & Yoshikawa, H. Breeding of bolting resistance in Chinese cabbage. critical day length for flower induction of late bolting material with no chilling requirement. Engei Gakkai Zasshi 61, 565–568 (1992).
doi: 10.2503/jjshs.61.565
Wei, Q., et al. The New Variation in the Promoter Region of FLOWERING LOCUS T Is Involved in Flowering in Brassica rapa. Genes 13, 1162 (2022)
Lu Y. Evaluation of heat tolerance and analysis of allele variation of heat tolerance candidate gene in flowering Chinese cabbage. Doctoral dissertation, Guangzhou University, (2020).
Rameeh, V. Correlation analysis in different planting dates of rapeseed varieties. J. Agric. Sci. 7, 76–84 (2012)
Morrison, M. J. & Stewart, D. W. Heat stress during flowering in summer Brassica. Crop Sci. 42, 797–803 (2002).
doi: 10.2135/cropsci2002.7970
Cheng, F. et al. Subgenome parallel selection is associated with morphotype diversification and convergent crop domestication in Brassica rapa and Brassica oleracea. Nat. Genet. 48, 1218–1224 (2016).
pubmed: 27526322 doi: 10.1038/ng.3634
Goto, S. et al. Organizing and computing metabolic pathway data in terms of binary relations. Pac. Symp. Biocomput. 1997, 175–186 (1997).
Yang, H. et al. A companion cell-dominant and developmentally regulated H3K4 demethylase controls flowering time in Arabidopsis via the repression of FLC expression. PLoS Genet. 8, e1002664 (2012).
pubmed: 22536163 pmcid: 3334889 doi: 10.1371/journal.pgen.1002664
Poza-Viejo, L. et al. Conserved and distinct roles of H3K27me3 demethylases regulating flowering time in Brassica rapa. Plant Cell Environ. 45, 1428–1441 (2022).
pubmed: 35037269 doi: 10.1111/pce.14258
Mehraj, H. et al. Characterization of histone H3 Lysine 4 and 36 Tri-methylation in Brassica rapa L. Front. Plant Sci. 12, 659634 (2021).
pubmed: 34163501 pmcid: 8215614 doi: 10.3389/fpls.2021.659634
Yue, L. et al. Gene co-expression network analysis of the heat-responsive core transcriptome identifies hub genes in Brassica rapa. Planta 253, 111 (2021).
pubmed: 33905008 doi: 10.1007/s00425-021-03630-3
Zhang, L. et al. Heat stress response in Chinese cabbage (Brassica rapa L.) revealed by transcriptome and physiological analysis. PeerJ 10, e13427 (2022).
pubmed: 35637719 pmcid: 9147330 doi: 10.7717/peerj.13427
Balciunas, D. & Ronne, H. Evidence of domain swapping within the jumonji family of transcription factors. Trends Biochem. Sci. 25, 274–276 (2000).
pubmed: 10838566 doi: 10.1016/S0968-0004(00)01593-0
Clissold, P. M. & Ponting, C. P. JmjC: cupin metalloenzyme-like domains in jumonji, hairless and phospholipase A2beta. Trends Biochem. Sci. 26, 7–9 (2001).
pubmed: 11165500 doi: 10.1016/S0968-0004(00)01700-X
McAlvay, A. C. et al. Brassica rapa domestication: untangling wild and feral forms and convergence of crop morphotypes. Mol. biol. Evol. 38, 3358–3372 (2021).
pubmed: 33930151 pmcid: 8321528 doi: 10.1093/molbev/msab108
Luo, G. A analysis of historical materials about the time and place of the origin of the peking cabbage. Stud. Hist. Nat. Sci. 2, 171–176 (1992).
Ainsworth, E. A. & Ort, D. R. How do we improve crop production in a warming world? Plant Physiol. 154, 526–530 (2010).
pubmed: 20921178 pmcid: 2949002 doi: 10.1104/pp.110.161349
As, W., Galani, S., Ashraf, M. & Foolad, M. Heat tolerance in plants: An overview. Environ. Exp. Bot. 61, 199–223 (2007).
doi: 10.1016/j.envexpbot.2007.05.011
Collins, N. C., Tardieu, F. & Tuberosa, R. Quantitative trait loci and crop performance under abiotic stress: where do we stand? Plant Physiol. 147, 469–486 (2008).
pubmed: 18524878 pmcid: 2409033 doi: 10.1104/pp.108.118117
Jha, U. & Singh, N. Heat stress in crop plants: Its nature, impacts and integrated breeding strategies to improve heat tolerance. Plant Breed. 133, 679–701 (2014).
Li, X. M. et al. Natural alleles of a proteasome α2 subunit gene contribute to thermotolerance and adaptation of African rice. Nat. Genet. 47, 827–833 (2015).
pubmed: 25985140 doi: 10.1038/ng.3305
Cappetta, E. et al. Tomato genomic prediction for good performance under high-temperature and identification of loci involved in thermotolerance response. Hortic. Res. 8, 212 (2021).
pubmed: 34593775 pmcid: 8484564 doi: 10.1038/s41438-021-00647-3
Li, M. et al. Overcoming reproductive compromise under heat stress in wheat: physiological and genetic regulation, and breeding strategy. Front. plant sci. 13, 881813 (2022).
pubmed: 35646015 pmcid: 9137415 doi: 10.3389/fpls.2022.881813
Le Martelot, G. et al. Genome-wide RNA polymerase II profiles and RNA accumulation reveal kinetics of transcription and associated epigenetic changes during diurnal cycles. PLoS Biol. 10, e1001442 (2012).
pubmed: 23209382 pmcid: 3507959 doi: 10.1371/journal.pbio.1001442
Pokholok, D. K. et al. Genome-wide map of nucleosome acetylation and methylation in yeast. Cell 122, 517–527 (2005).
pubmed: 16122420 doi: 10.1016/j.cell.2005.06.026
Smolle, M. et al. Chromatin remodelers Isw1 and Chd1 maintain chromatin structure during transcription by preventing histone exchange. Nat. Struct. Mol. Biol. 19, 884–892 (2012).
pubmed: 22922743 pmcid: 3560298 doi: 10.1038/nsmb.2312
Vakoc, C. R., Sachdeva, M. M., Wang, H. & Blobel, G. A. Profile of histone lysine methylation across transcribed mammalian chromatin. Mol. Cell Biol. 26, 9185–9195 (2006).
pubmed: 17030614 pmcid: 1698537 doi: 10.1128/MCB.01529-06
Pajoro, A., Severing, E., Angenent, G. C. & Immink, R. G. H. Histone H3 lysine 36 methylation affects temperature-induced alternative splicing and flowering in plants. Genome Biol. 18, 102 (2017).
pubmed: 28566089 pmcid: 5452352 doi: 10.1186/s13059-017-1235-x
Jones, M. A., Morohashi, K., Grotewold, E. & Harmer, S. L. Arabidopsis JMJD5/JMJ30 acts independently of LUX ARRHYTHMO within the plant circadian clock to enable temperature compensation. Front. Plant Sci. 10, 57 (2019).
pubmed: 30774641 pmcid: 6367231 doi: 10.3389/fpls.2019.00057
Bloomer, R. H. et al. The Arabidopsis epigenetic regulator ICU11 as an accessory protein of polycomb repressive complex 2. Proc. Natl. Acad. Sci. USA 117, 16660–16666 (2020).
pubmed: 32601198 pmcid: 7368280 doi: 10.1073/pnas.1920621117
Gan, E. S. et al. Jumonji demethylases moderate precocious flowering at elevated temperature via regulation of FLC in Arabidopsis. Nat. Commun. 5, 5098 (2014).
pubmed: 25267112 doi: 10.1038/ncomms6098
Whittaker, C. & Dean, C. The FLC Locus: A platform for discoveries in epigenetics and adaptation. Annu. Rev. Cell Dev. Biol. 33, 555–575 (2017).
pubmed: 28693387 doi: 10.1146/annurev-cellbio-100616-060546
Li, B., Carey, M. & Workman, J. L. The role of chromatin during transcription. Cell 128, 707–719 (2007).
pubmed: 17320508 doi: 10.1016/j.cell.2007.01.015
Margueron, R. & Reinberg, D. The polycomb complex PRC2 and its mark in life. Nature 469, 343–349 (2011).
pubmed: 21248841 pmcid: 3760771 doi: 10.1038/nature09784
Young, M. D. et al. ChIP-seq analysis reveals distinct H3K27me3 profiles that correlate with transcriptional activity. Nucleic Acids Res. 39, 7415–7427 (2011).
pubmed: 21652639 pmcid: 3177187 doi: 10.1093/nar/gkr416
Yang, H., Howard, M. & Dean, C. Physical coupling of activation and derepression activities to maintain an active transcriptional state at FLC. Proc. Natl. Acad. Sci. USA 113, 9369–9374 (2016).
pubmed: 27482092 pmcid: 4995980 doi: 10.1073/pnas.1605733113
Crevillén, P. et al. Epigenetic reprogramming that prevents transgenerational inheritance of the vernalized state. Nature 515, 587–590 (2014).
pubmed: 25219852 pmcid: 4247276 doi: 10.1038/nature13722
Liu, J. et al. An H3K27me3 demethylase-HSFA2 regulatory loop orchestrates transgenerational thermomemory in Arabidopsis. Cell Res. 29, 379–390 (2019).
pubmed: 30778176 pmcid: 6796840 doi: 10.1038/s41422-019-0145-8
Yamaguchi, N. et al. H3K27me3 demethylases alter HSP22 and HSP17.6C expression in response to recurring heat in Arabidopsis. Nat. Commun. 12, 3480 (2021).
pubmed: 34108473 pmcid: 8190089 doi: 10.1038/s41467-021-23766-w
Bac-Molenaar, J. A. et al. Genome-wide association mapping of fertility reduction upon heat stress reveals developmental stage-specific QTLs in Arabidopsis thaliana. Plant cell 27, 1857–1874 (2015).
pubmed: 26163573 pmcid: 4531356 doi: 10.1105/tpc.15.00248
Blázquez, M. A., Ahn, J. H. & Weigel, D. A thermosensory pathway controlling flowering time in Arabidopsis thaliana. Nat. Genet. 33, 168–171 (2003).
pubmed: 12548286 doi: 10.1038/ng1085
Mateos, J. L. et al. Combinatorial activities of SHORT VEGETATIVE PHASE and FLOWERING LOCUS C define distinct modes of flowering regulation in Arabidopsis. Genome Biol. 16, 31 (2015).
pubmed: 25853185 pmcid: 4378019 doi: 10.1186/s13059-015-0597-1
Tsuchiya, T. & Eulgem, T. The Arabidopsis defense component EDM2 affects the floral transition in an FLC-dependent manner. Plant J. Cell Mol. Biol. 62, 518–528 (2010).
doi: 10.1111/j.1365-313X.2010.04169.x
Willmann, M. R. & Poethig, R. S. The effect of the floral repressor FLC on the timing and progression of vegetative phase change in Arabidopsis. Development 138, 677–685 (2011).
pubmed: 21228003 pmcid: 3026413 doi: 10.1242/dev.057448
Chen, M. & Penfield, S. Feedback regulation of COOLAIR expression controls seed dormancy and flowering time. Science 360, 1014–1017 (2018).
pubmed: 29853684 doi: 10.1126/science.aar7361
Yuan, W. et al. mapping of germination speed in Arabidopsis thaliana. Mol. Ecol. 25, 4177–4196 (2016).
pubmed: 27454560 doi: 10.1111/mec.13768
Schmalenbach, I., Zhang, L., Reymond, M. & Jiménez-Gómez, J. M. The relationship between flowering time and growth responses to drought in the Arabidopsis Landsberg erecta x Antwerp-1 population. Front. Plant Sci. 5, 609 (2014).
pubmed: 25426126 pmcid: 4227481 doi: 10.3389/fpls.2014.00609
Ågrena, J., Oakley, C. G., McKay, J. K., Lovell, J. T. & Schemske, D. W. Genetic mapping of adaptation reveals fitness tradeoffs in Arabidopsis thaliana. Proc. Natl. Acad. Sci. USA 110, 21077–21082 (2013).
pubmed: 24324156 doi: 10.1073/pnas.1316773110
Wang, X. et al. The genome of the mesopolyploid crop species Brassica rapa. Nat. Genet. 43, 1035–1039 (2011).
pubmed: 21873998 doi: 10.1038/ng.919
Cai, X. et al. Impacts of allopolyploidization and structural variation on intraspecific diversification in Brassica rapa. Genome Biol. 22, 166 (2021).
pubmed: 34059118 pmcid: 8166115 doi: 10.1186/s13059-021-02383-2
Kitamoto, N., Yui, S., Nishikawa, K., Takahata, Y. & Yokoi, S. A naturally occurring long insertion in the first intron in the Brassica rapaFLC2 gene causes delayed bolting. Euphytica 196, 213–223 (2014).
doi: 10.1007/s10681-013-1025-9
Li, X., Zhang, S., Bai, J. & He, Y. Tuning growth cycles of Brassica crops via natural antisense transcripts of BrFLC. Plant Biotechnol. J. 14, 905–914 (2016).
pubmed: 26250982 doi: 10.1111/pbi.12443
Schranz, M. E. et al. Characterization and effects of the replicated flowering time gene FLC in Brassica rapa. Genetics 162, 1457–1468 (2002).
pubmed: 12454088 pmcid: 1462321 doi: 10.1093/genetics/162.3.1457
Lou, P. et al. Quantitative trait loci for flowering time and morphological traits in multiple populations of Brassica rapa. J. Exp. Bot. 58, 4005–4016 (2007).
pubmed: 18048374 doi: 10.1093/jxb/erm255
Dechaine, J. M., Brock, M. T. & Weinig, C. QTL architecture of reproductive fitness characters in Brassica rapa. BMC Plant Biol. 14, 66 (2014).
pubmed: 24641198 pmcid: 4004417 doi: 10.1186/1471-2229-14-66
Xiao, D. et al. Genetic dissection of flowering time in Brassica rapa responses to temperature and photoperiod. Plant Sci. Int. J. Experiment. Plant Biol. 280, 110–119 (2019).
doi: 10.1111/jipb.12768
Kim, S. Y. et al. Delayed flowering time in Arabidopsis and Brassica rapa by the overexpression of FLOWERING LOCUS C (FLC) homologs isolated from Chinese cabbage (Brassica rapa L.: ssp. pekinensis). Plant Cell Rep. 26, 327–336 (2007).
pubmed: 17024448 doi: 10.1007/s00299-006-0243-1
Xiao, D. et al. The Brassica rapa FLC homologue FLC2 is a key regulator of flowering time, identified through transcriptional co-expression networks. J. Experiment. Bot. 64, 4503–4516 (2013).
doi: 10.1093/jxb/ert264
Burggren, W. Epigenetic Inheritance and Its Role in Evolutionary Biology: Re-Evaluation and New Perspectives. Biology 5, 24 (2016)
McCaw, B. A., Stevenson, T. J. & Lancaster, L. T. Epigenetic responses to temperature and climate. Integr. Comp. Biol. 60, 1469–1480 (2020).
pubmed: 32470117 doi: 10.1093/icb/icaa049
Su, T. et al. A genomic variation map provides insights into the genetic basis of spring chinese cabbage (Brassica rapa ssp. pekinensis) selection. Mol. Plant 11, 1360–1376 (2018).
pubmed: 30217779 doi: 10.1016/j.molp.2018.08.006
Gutenkunst, R. N., Hernandez, R. D., Williamson, S. H. & Bustamante, C. D. Inferring the joint demographic history of multiple populations from multidimensional SNP frequency data. PLoS Genet. 5, e1000695 (2009).
pubmed: 19851460 pmcid: 2760211 doi: 10.1371/journal.pgen.1000695
Chen, H., Patterson, N. & Reich, D. Population differentiation as a test for selective sweeps. Genome Res. 20, 393–402 (2010).
pubmed: 20086244 pmcid: 2840981 doi: 10.1101/gr.100545.109
Duan, N. et al. Genome re-sequencing reveals the history of apple and supports a two-stage model for fruit enlargement. Nat. Commun. 8, 249 (2017).
pubmed: 28811498 pmcid: 5557836 doi: 10.1038/s41467-017-00336-7
Wang, X., Teng, D., Tian, F., Guan, Q. & Wang, J. Comparison of three DNA extraction methods for feed products and four amplification methods for the 5’-junction fragment of Roundup Ready soybean. J. Agric. Food Chem. 60, 4586–4595 (2012).
pubmed: 22515503 doi: 10.1021/jf300827q
Abe, A. et al. Genome sequencing reveals agronomically important loci in rice using MutMap. Nat. Biotechnol. 30, 174–178 (2012).
pubmed: 22267009 doi: 10.1038/nbt.2095
Cao, X. et al. Characterization of DUF724 gene family in Arabidopsis thaliana. Plant Mol. Biol. 72, 61–73 (2010).
pubmed: 19795213 doi: 10.1007/s11103-009-9551-5
Xing, H. L. et al. A CRISPR/Cas9 toolkit for multiplex genome editing in plants. BMC Plant Biol. 14, 327 (2014).
pubmed: 25432517 pmcid: 4262988 doi: 10.1186/s12870-014-0327-y
Clough, S. J. & Bent, A. F. Floral dip: a simplified method for Agrobacterium-mediated transformation of Arabidopsis thaliana. Plant J. Cell Mol. Biol. 16, 735–743 (1998).
doi: 10.1046/j.1365-313x.1998.00343.x
Xu, J. et al. Activation of MAPK kinase 9 induces ethylene and camalexin biosynthesis and enhances sensitivity to salt stress in Arabidopsis. J. Biol. Chem. 283, 26996–27006 (2008).
pubmed: 18693252 doi: 10.1074/jbc.M801392200
Yang, W., Jiang, D., Jiang, J. & He, Y. A plant-specific histone H3 lysine 4 demethylase represses the floral transition in Arabidopsis. Plant J. Cell Mol. Biol. 62, 663–673 (2010).
doi: 10.1111/j.1365-313X.2010.04182.x
Landt, S. G. et al. ChIP-seq guidelines and practices of the ENCODE and modENCODE consortia. Genome Res. 22, 1813–1831 (2012).
pubmed: 22955991 pmcid: 3431496 doi: 10.1101/gr.136184.111
Li, H. et al. The Sequence Alignment/Map format and SAMtools. Bioinformatics 25, 2078–2079 (2009).
pubmed: 19505943 pmcid: 2723002 doi: 10.1093/bioinformatics/btp352
Salmon-Divon, M., Dvinge, H., Tammoja, K. & Bertone, P. PeakAnalyzer: genome-wide annotation of chromatin binding and modification loci. BMC Bioinformatics 11, 415 (2010).
pubmed: 20691053 pmcid: 2923140 doi: 10.1186/1471-2105-11-415
Zhou, X. & Su, Z. EasyGO: Gene Ontology-based annotation and functional enrichment analysis tool for agronomical species. BMC Genomics 8, 246 (2007).
pubmed: 17645808 pmcid: 1940007 doi: 10.1186/1471-2164-8-246

Auteurs

Xiaoyun Xin (X)

State Key Laboratory of Vegetable Biobreeding, Beijing Vegetable Research Center, Beijing Academy of Agriculture and Forestry Science, Beijing, China.
National Engineering Research Center for Vegetables, Beijing Vegetable Research Center, Beijing Academy of Agriculture and Forestry Science, Beijing, China.
Beijing Key Laboratory of Vegetable Germplasms Improvement, Beijing, China.
Key Laboratory of Biology and Genetics Improvement of Horticultural Crops (North China), Beijing, China.

Peirong Li (P)

State Key Laboratory of Vegetable Biobreeding, Beijing Vegetable Research Center, Beijing Academy of Agriculture and Forestry Science, Beijing, China.
National Engineering Research Center for Vegetables, Beijing Vegetable Research Center, Beijing Academy of Agriculture and Forestry Science, Beijing, China.
Beijing Key Laboratory of Vegetable Germplasms Improvement, Beijing, China.
Key Laboratory of Biology and Genetics Improvement of Horticultural Crops (North China), Beijing, China.

Xiuyun Zhao (X)

State Key Laboratory of Vegetable Biobreeding, Beijing Vegetable Research Center, Beijing Academy of Agriculture and Forestry Science, Beijing, China.
National Engineering Research Center for Vegetables, Beijing Vegetable Research Center, Beijing Academy of Agriculture and Forestry Science, Beijing, China.
Beijing Key Laboratory of Vegetable Germplasms Improvement, Beijing, China.
Key Laboratory of Biology and Genetics Improvement of Horticultural Crops (North China), Beijing, China.

Yangjun Yu (Y)

State Key Laboratory of Vegetable Biobreeding, Beijing Vegetable Research Center, Beijing Academy of Agriculture and Forestry Science, Beijing, China.
National Engineering Research Center for Vegetables, Beijing Vegetable Research Center, Beijing Academy of Agriculture and Forestry Science, Beijing, China.
Beijing Key Laboratory of Vegetable Germplasms Improvement, Beijing, China.
Key Laboratory of Biology and Genetics Improvement of Horticultural Crops (North China), Beijing, China.

Weihong Wang (W)

State Key Laboratory of Vegetable Biobreeding, Beijing Vegetable Research Center, Beijing Academy of Agriculture and Forestry Science, Beijing, China.
National Engineering Research Center for Vegetables, Beijing Vegetable Research Center, Beijing Academy of Agriculture and Forestry Science, Beijing, China.
Beijing Key Laboratory of Vegetable Germplasms Improvement, Beijing, China.
Key Laboratory of Biology and Genetics Improvement of Horticultural Crops (North China), Beijing, China.

Guihua Jin (G)

State Key Laboratory of Vegetable Biobreeding, Beijing Vegetable Research Center, Beijing Academy of Agriculture and Forestry Science, Beijing, China.
National Engineering Research Center for Vegetables, Beijing Vegetable Research Center, Beijing Academy of Agriculture and Forestry Science, Beijing, China.

Jiao Wang (J)

State Key Laboratory of Vegetable Biobreeding, Beijing Vegetable Research Center, Beijing Academy of Agriculture and Forestry Science, Beijing, China.
National Engineering Research Center for Vegetables, Beijing Vegetable Research Center, Beijing Academy of Agriculture and Forestry Science, Beijing, China.

Liling Sun (L)

State Key Laboratory of Vegetable Biobreeding, Beijing Vegetable Research Center, Beijing Academy of Agriculture and Forestry Science, Beijing, China.
National Engineering Research Center for Vegetables, Beijing Vegetable Research Center, Beijing Academy of Agriculture and Forestry Science, Beijing, China.

Deshuang Zhang (D)

State Key Laboratory of Vegetable Biobreeding, Beijing Vegetable Research Center, Beijing Academy of Agriculture and Forestry Science, Beijing, China.
National Engineering Research Center for Vegetables, Beijing Vegetable Research Center, Beijing Academy of Agriculture and Forestry Science, Beijing, China.
Beijing Key Laboratory of Vegetable Germplasms Improvement, Beijing, China.
Key Laboratory of Biology and Genetics Improvement of Horticultural Crops (North China), Beijing, China.

Fenglan Zhang (F)

State Key Laboratory of Vegetable Biobreeding, Beijing Vegetable Research Center, Beijing Academy of Agriculture and Forestry Science, Beijing, China. zhangfenglan@nercv.org.
National Engineering Research Center for Vegetables, Beijing Vegetable Research Center, Beijing Academy of Agriculture and Forestry Science, Beijing, China. zhangfenglan@nercv.org.
Beijing Key Laboratory of Vegetable Germplasms Improvement, Beijing, China. zhangfenglan@nercv.org.
Key Laboratory of Biology and Genetics Improvement of Horticultural Crops (North China), Beijing, China. zhangfenglan@nercv.org.
ORCID: 0000-0002-7155-0945

Shuancang Yu (S)

State Key Laboratory of Vegetable Biobreeding, Beijing Vegetable Research Center, Beijing Academy of Agriculture and Forestry Science, Beijing, China. yushuancang@nercv.org.
National Engineering Research Center for Vegetables, Beijing Vegetable Research Center, Beijing Academy of Agriculture and Forestry Science, Beijing, China. yushuancang@nercv.org.
Beijing Key Laboratory of Vegetable Germplasms Improvement, Beijing, China. yushuancang@nercv.org.
Key Laboratory of Biology and Genetics Improvement of Horticultural Crops (North China), Beijing, China. yushuancang@nercv.org.
ORCID: 0000-0001-7270-2472

Tongbing Su (T)

State Key Laboratory of Vegetable Biobreeding, Beijing Vegetable Research Center, Beijing Academy of Agriculture and Forestry Science, Beijing, China. sutongbing@nercv.org.
National Engineering Research Center for Vegetables, Beijing Vegetable Research Center, Beijing Academy of Agriculture and Forestry Science, Beijing, China. sutongbing@nercv.org.
Beijing Key Laboratory of Vegetable Germplasms Improvement, Beijing, China. sutongbing@nercv.org.
Key Laboratory of Biology and Genetics Improvement of Horticultural Crops (North China), Beijing, China. sutongbing@nercv.org.
ORCID: 0000-0002-3411-7341

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Classifications MeSH

questionsmedicales.fr › Eucaryotes › Viridiplantae › Streptophyta › Embryophyta › Tracheobionta › Magnoliopsida › Brassicaceae › Brassica › Brassica rapa › Temperature-dependent jumonji demethylase...
questionsmedicales.fr › Structures de plante › Parties aériennes de plante › Sommités fleuries › Fleurs › Temperature-dependent jumonji demethylase...
questionsmedicales.fr › Phénomènes génétiques › Régulation de l'expression des gènes › Régulation de l'expression des gènes végétaux › Temperature-dependent jumonji demethylase...
questionsmedicales.fr › Acides aminés, peptides et protéines › Protéines › Nucléoprotéines › Histone › Temperature-dependent jumonji demethylase...
questionsmedicales.fr › Phénomènes génétiques › Structures génétiques › Génome › Composants de génome › Locus génétiques › Locus de caractère quantitatif › Temperature-dependent jumonji demethylase...
questionsmedicales.fr › Enzymes et coenzymes › Enzymes › Oxidoreductases › Oxygénases › Dioxygenases › Jumonji Domain-Containing Histone Demethylases › Temperature-dependent jumonji demethylase...
questionsmedicales.fr › Acides aminés, peptides et protéines › Protéines › Protéines végétales › Temperature-dependent jumonji demethylase...
questionsmedicales.fr › Environnement et santé publique › Environnement › Concepts météorologiques › Atmosphère › Temps (météorologie) › Température › Temperature-dependent jumonji demethylase...
questionsmedicales.fr › Phénomènes biologiques › Adaptation biologique › Adaptation physiologique › Acclimatation › Thermotolérance › Temperature-dependent jumonji demethylase...
questionsmedicales.fr › Métabolisme › Alkylation › Méthylation › Temperature-dependent jumonji demethylase...
questionsmedicales.fr › Stades d'organismes › Organismes génétiquement modifiés › Végétaux génétiquement modifiés › Temperature-dependent jumonji demethylase...
questionsmedicales.fr › Composés polycycliques › Composés macrocycliques › Tétrapyrroles › Chlorophylle › Temperature-dependent jumonji demethylase...