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完整後設資料紀錄
DC 欄位值語言
dc.contributor.advisor金洛仁(Laurent Zimmerli)
dc.contributor.authorYi-Chun Huangen
dc.contributor.author黃義竣zh_TW
dc.date.accessioned2021-06-08T02:56:31Z-
dc.date.copyright2017-08-04
dc.date.issued2017
dc.date.submitted2017-08-02
dc.identifier.citationAcharya, B.R., Raina, S., Maqbool, S.B., Jagadeeswaran, G., Mosher, S.L., Appel, H.M., Schultz, J.C., Klessig, D.F., and Raina, R. (2007). Overexpression of CRK13, an Arabidopsis cysteine-rich receptor-like kinase, results in enhanced resistance to Pseudomonas syringae. Plant J. 50, 488–499.
Adrian, J., Chang, J., Ballenger, C.E., Bargmann, B.O.R., Alassimone, J., Davies, K.A., Lau, O.S., Matos, J.L., Hachez, C., Lanctot, A., et al. (2015). Transcriptome dynamics of the stomatal lineage: birth, amplification, and termination of a self-renewing population. Dev. Cell 33, 107–118.
Albrecht, C., Boutrot, F., Segonzac, C., Schwessinger, B., Gimenez-Ibanez, S., Chinchilla, D., Rathjen, J.P., Vries, S.C. de, and Zipfel, C. (2012). Brassinosteroids inhibit pathogen-associated molecular pattern–triggered immune signaling independent of the receptor kinase BAK1. Proc. Natl. Acad. Sci. USA 109, 303–308.
Bancos, S., Szatmári, A.-M., Castle, J., Kozma-Bognár, L., Shibata, K., Yokota, T., Bishop, G.J., Nagy, F., and Szekeres, M. (2006). Diurnal regulation of the Brassinosteroid-biosynthetic CPD gene in Arabidopsis. Plant Physiol. 141, 299–309.
Belkhadir, Y., Jaillais, Y., Epple, P., Balsemão-Pires, E., Dangl, J.L., and Chory, J. (2012). Brassinosteroids modulate the efficiency of plant immune responses to microbe-associated molecular patterns. Proc. Natl. Acad. Sci. USA 109, 297–302.
Bergmann, D.C., and Sack, F.D. (2007). Stomatal development. Annu. Rev. Plant Biol. 58, 163–181.
Bourdais, G., Burdiak, P., Gauthier, A., Nitsch, L., Salojärvi, J., Rayapuram, C., Idänheimo, N., Hunter, K., Kimura, S., Merilo, E., et al. (2015). Large-scale phenomics identifies primary and fine-tuning roles for CRKs in responses related to oxidative stress. PLOS Genet. 11, e1005373.
Chaiwanon, J., Wang, W., Zhu, J.-Y., Oh, E., and Wang, Z.-Y. (2016). Information integration and communication in plant growth regulation. Cell 164, 1257–1268.
Chen, K., Du, L., and Chen, Z. (2003). Sensitization of defense responses and activation of programmed cell death by a pathogen-induced receptor-like protein kinase in Arabidopsis. Plant Mol. Biol. 53, 61–74.
Chen, K., Fan, B., Du, L., and Chen, Z. (2004). Activation of hypersensitive cell death by pathogen-induced receptor-like protein kinases from Arabidopsis. Plant Mol. Biol. 56, 271–283.
Chinchilla, D., Bauer, Z., Regenass, M., Boller, T., and Felix, G. (2006). The Arabidopsis receptor kinase FLS2 binds flg22 and determines the specificity of flagellin perception. Plant Cell 18, 465–476.
Czyzewicz, N., Yue, K., Beeckman, T., and De Smet, I. (2013). Message in a bottle: small signalling peptide outputs during growth and development. J. Exp. Bot. 64, 5281–5296.
Domínguez-Ferreras, A., Kiss-Papp, M., Jehle, A.K., Felix, G., and Chinchilla, D. (2015). An overdose of the Arabidopsis coreceptor BRASSINOSTEROID INSENSITIVE1-ASSOCIATED RECEPTOR KINASE1 or its ectodomain causes autoimmunity in a SUPPRESSOR OF BIR1-1-Dependent manner. Plant Physiol. 168, 1106–1121.
Ederli, L., Madeo, L., Calderini, O., Gehring, C., Moretti, C., Buonaurio, R., Paolocci, F., and Pasqualini, S. (2011). The Arabidopsis thaliana cysteine-rich receptor-like kinase CRK20 modulates host responses to Pseudomonas syringae pv. tomato DC3000 infection. J. Plant Physiol. 168, 1784–1794.
Fletcher, J.C., Brand, U., Running, M.P., Simon, R., and Meyerowitz, E.M. (1999). Signaling of cell fate decisions by CLAVATA3 in Arabidopsis shoot meristems. Science 283, 1911–1914.
Geisler, M., Nadeau, J., and Sack, F.D. (2000). Oriented asymmetric divisions that generate the stomatal spacing pattern in arabidopsis are disrupted by the too many mouths mutation. Plant Cell 12, 2075–2086.
Goda, H., Shimada, Y., Asami, T., Fujioka, S., and Yoshida, S. (2002). Microarray analysis of brassinosteroid-regulated genes in Arabidopsis. Plant Physiol. 130, 1319–1334.
Guo, Y., Han, L., Hymes, M., Denver, R., and Clark, S.E. (2010). CLAVATA2 forms a distinct CLE-binding receptor complex regulating Arabidopsis stem cell specification. Plant J. Cell Mol. Biol. 63, 889–900.
Hara, K., Kajita, R., Torii, K.U., Bergmann, D.C., and Kakimoto, T. (2007). The secretory peptide gene EPF1 enforces the stomatal one-cell-spacing rule. Genes Dev. 21, 1720–1725.
Hara, K., Yokoo, T., Kajita, R., Onishi, T., Yahata, S., Peterson, K.M., Torii, K.U., and Kakimoto, T. (2009). Epidermal cell density is autoregulated via a secretory peptide, EPIDERMAL PATTERNING FACTOR 2 in Arabidopsis leaves. Plant Cell Physiol. 50, 1019–1031.
He, J.-X., Gendron, J.M., Sun, Y., Gampala, S.S.L., Gendron, N., Sun, C.Q., and Wang, Z.-Y. (2005). BZR1 is a transcriptional repressor with dual roles in brassinosteroid homeostasis and growth responses. Science 307, 1634–1638.
Hunt, L., and Gray, J.E. (2009). The signaling peptide EPF2 controls asymmetric cell divisions during stomatal development. Curr. Biol. CB 19, 864–869.
Huot, B., Yao, J., Montgomery, B.L., and He, S.Y. (2014). Growth–Defense Tradeoffs in Plants: A Balancing Act to Optimize Fitness. Mol. Plant 7, 1267–1287.
Ito, Y., Nakanomyo, I., Motose, H., Iwamoto, K., Sawa, S., Dohmae, N., and Fukuda, H. (2006). Dodeca-CLE peptides as suppressors of plant stem cell differentiation. Science 313, 842–845.
Jiménez-Góngora, T., Kim, S.-K., Lozano-Durán, R., and Zipfel, C. (2015). Flg22-triggered immunity negatively regulates key BR biosynthetic genes. Front. Plant Sci. 6.
Jones, J.D.G., and Dangl, J.L. (2006). The plant immune system. Nature 444, 323–329.
Jun, J., Fiume, E., Roeder, A.H.K., Meng, L., Sharma, V.K., Osmont, K.S., Baker, C., Ha, C.M., Meyerowitz, E.M., Feldman, L.J., et al. (2010). Comprehensive analysis of CLE polypeptide signaling gene expression and overexpression activity in Arabidopsis. Plant Physiol. 154, 1721–1736.
Kang, S., Yang, F., Li, L., Chen, H., Chen, S., and Zhang, J. (2015). The Arabidopsis transcription factor BRASSINOSTEROID INSENSITIVE1-ETHYL METHANESULFONATE-SUPPRESSOR1 is a direct substrate of MITOGEN-ACTIVATED PROTEIN KINASE6 and regulates immunity. Plant Physiol. 167, 1076–1086.
Kondo, T., Kajita, R., Miyazaki, A., Hokoyama, M., Nakamura-Miura, T., Mizuno, S., Masuda, Y., Irie, K., Tanaka, Y., Takada, S., et al. (2010). Stomatal density is controlled by a mesophyll-derived signaling molecule. Plant Cell Physiol. 51, 1–8.
Kondo, Y., Hirakawa, Y., Kieber, J.J., and Fukuda, H. (2011). CLE peptides can negatively regulate protoxylem vessel formation via cytokinin signaling. Plant Cell Physiol. 52, 37–48.
Kondo, Y., Nurani, A.M., Saito, C., Ichihashi, Y., Saito, M., Yamazaki, K., Mitsuda, N., Ohme-Takagi, M., and Fukuda, H. (2016). Vascular cell induction culture system using Arabidopsis leaves (VISUAL) reveals the sequential differentiation of sieve element-like cells. Plant Cell 28, 1250–1262.
Kurihara, D., Mizuta, Y., Sato, Y., and Higashiyama, T. (2015). ClearSee: a rapid optical clearing reagent for whole-plant fluorescence imaging. Dev. Camb. Engl. 142, 4168–4179.
Lau, O.S., Davies, K.A., Chang, J., Adrian, J., Rowe, M.H., Ballenger, C.E., and Bergmann, D.C. (2014). Direct roles of SPEECHLESS in the specification of stomatal self-renewing cells. Science 345, 1605–1609.
Lee, H.-J., Park, Y.-J., Seo, P.J., Kim, J.-H., Sim, H.-J., Kim, S.-G., and Park, C.-M. (2015). Systemic immunity requires SnRK2.8-mediated nuclear import of NPR1 in Arabidopsis. Plant Cell tpc.15.00371.
Li, J., Wen, J., Lease, K.A., Doke, J.T., Tax, F.E., and Walker, J.C. (2002). BAK1, an Arabidopsis LRR receptor-like protein kinase, interacts with BRI1 and modulates brassinosteroid signaling. Cell 110, 213–222.
Lin, W., Lu, D., Gao, X., Jiang, S., Ma, X., Wang, Z., Mengiste, T., He, P., and Shan, L. (2013). Inverse modulation of plant immune and brassinosteroid signaling pathways by the receptor-like cytoplasmic kinase BIK1. Proc. Natl. Acad. Sci. USA 110, 12114–12119.
Liu, Y., and Zhang, S. (2004). Phosphorylation of 1-aminocyclopropane-1-carboxylic acid synthase by MPK6, a stress-responsive mitogen-activated protein kinase, induces ethylene biosynthesis in Arabidopsis. Plant Cell 16, 3386–3399.
Lozano-Durán, R., and Zipfel, C. (2015). Trade-off between growth and immunity: role of brassinosteroids. Trends Plant Sci. 20, 12–19.
Lu, D., Wu, S., Gao, X., Zhang, Y., Shan, L., and He, P. (2010). A receptor-like cytoplasmic kinase, BIK1, associates with a flagellin receptor complex to initiate plant innate immunity. Proc. Natl. Acad. Sci. U. S. A. 107, 496–501.
Ma, X., Xu, G., He, P., and Shan, L. (2016). SERKing coreceptors for receptors. Trends Plant Sci. 21, 1017–1033.
Macho, A.P., and Zipfel, C. (2014). Plant PRRs and the activation of innate immune signaling. Mol. Cell 54, 263–272.
Matsubayashi, Y. (2014). Posttranslationally modified small-peptide signals in plants. Annu. Rev. Plant Biol. 65, 385–413.
Monaghan, J., and Zipfel, C. (2012). Plant pattern recognition receptor complexes at the plasma membrane. Curr. Opin. Plant Biol. 15, 349–357.
Nakagami, H., Pitzschke, A., and Hirt, H. (2005). Emerging MAP kinase pathways in plant stress signalling. Trends Plant Sci. 10, 339–346.
Nakamura, A., Shimada, Y., Goda, H., Fujiwara, M.T., Asami, T., and Yoshida, S. (2003). AXR1 is involved in BR-mediated elongation and SAUR-AC1 gene expression in Arabidopsis. FEBS Lett. 553, 28–32.
Nam, K.H., and Li, J. (2002). BRI1/BAK1, a receptor kinase pair mediating Brassinosteroid signaling. Cell 110, 203–212.
Ogawa, M., Shinohara, H., Sakagami, Y., and Matsubayashi, Y. (2008). Arabidopsis CLV3 peptide directly binds CLV1 ectodomain. Science 319, 294–294.
Ohyama, K., Shinohara, H., Ogawa-Ohnishi, M., and Matsubayashi, Y. (2009). A glycopeptide regulating stem cell fate in Arabidopsis thaliana. Nat. Chem. Biol. 5, 578–580.
Okamoto, S., Shinohara, H., Mori, T., Matsubayashi, Y., and Kawaguchi, M. (2013). Root-derived CLE glycopeptides control nodulation by direct binding to HAR1 receptor kinase. Nat. Commun. 4, 2191.
Pillitteri, L.J., and Torii, K.U. (2012). Mechanisms of stomatal development. Annu. Rev. Plant Biol. 63, 591–614.
Pillitteri, L.J., Peterson, K.M., Horst, R.J., and Torii, K.U. (2011). Molecular profiling of stomatal meristemoids reveals new component of asymmetric cell division and commonalities among stem cell populations in Arabidopsis. Plant Cell 23, 3260–3275.
Robert-Seilaniantz, A., Grant, M., and Jones, J.D.G. (2011). Hormone crosstalk in plant disease and defense: More Than Just JASMONATE-SALICYLATE Antagonism.
Sanabria, N.M., Huang, J.-C., and Dubery, I.A. (2010). Self/nonself perception in plants in innate immunity and defense. Self/Nonself 1, 40–54.
Santiago, J., Brandt, B., Wildhagen, M., Hohmann, U., Hothorn, L.A., Butenko, M.A., and Hothorn, M. (2016). Mechanistic insight into a peptide hormone signaling complex mediating floral organ abscission. eLife 5.
Shimizu, N., Ishida, T., Yamada, M., Shigenobu, S., Tabata, R., Kinoshita, A., Yamaguchi, K., Hasebe, M., Mitsumasu, K., and Sawa, S. (2015). BAM 1 and RECEPTOR-LIKE PROTEIN KINASE 2 constitute a signaling pathway and modulate CLE peptide-triggered growth inhibition in Arabidopsis root. New Phytol. 208, 1104–1113.
Shinohara, H., Moriyama, Y., Ohyama, K., and Matsubayashi, Y. (2012).

Biochemical mapping of a ligand-binding domain within Arabidopsis BAM1 reveals diversified ligand recognition mechanisms of plant LRR-RKs. Plant J. Cell Mol. Biol. 70, 845–854.
Shiu, S.H., and Bleecker, A.B. (2001). Receptor-like kinases from Arabidopsis form a monophyletic gene family related to animal receptor kinases. Proc. Natl. Acad. Sci. U. S. A. 98, 10763–10768.
Singh, P., Kuo, Y.-C., Mishra, S., Tsai, C.-H., Chien, C.-C., Chen, C.-W., Desclos-Theveniau, M., Chu, P.-W., Schulze, B., Chinchilla, D., et al. (2012). The lectin receptor kinase-VI.2 is required for priming and positively regulates Arabidopsis pattern-triggered immunity. Plant Cell 24, 1256–1270.
Smedegaard-Petersen, V., and Tolstrup, K. (1985). The limiting effect of disease resistance on yield. Annu. Rev. Phytopathol. 23, 475–490.
Song, W., Han, Z., Wang, J., Lin, G., and Chai, J. (2017). Structural insights into ligand recognition and activation of plant receptor kinases. Curr. Opin. Struct. Biol. 43, 18–27.
Strange, R.N., and Scott, P.R. (2005). Plant Disease: A Threat to Global Food Security. Annu. Rev. Phytopathol. 43, 83–116.
Sugano, S.S., Shimada, T., Imai, Y., Okawa, K., Tamai, A., Mori, M., and Hara-Nishimura, I. (2010). Stomagen positively regulates stomatal density in Arabidopsis. Nature 463, 241–244.
Sun, Y., Fan, X.-Y., Cao, D.-M., Tang, W., He, K., Zhu, J.-Y., He, J.-X., Bai, M.-Y., Zhu, S., Oh, E., et al. (2010). Integration of brassinosteroid signal transduction with the transcription network for plant growth regulation in Arabidopsis. Dev. Cell 19, 765–777.
Takáč, T., Vadovič, P., Pechan, T., Luptovčiak, I., Šamajová, O., and Šamaj, J. (2016). Comparative proteomic study of Arabidopsis mutants mpk4 and mpk6. Sci. Rep. 6, 28306.
Tanaka, H., Osakabe, Y., Katsura, S., Mizuno, S., Maruyama, K., Kusakabe, K., Mizoi, J., Shinozaki, K., and Yamaguchi-Shinozaki, K. (2012). Abiotic stress-inducible receptor-like kinases negatively control ABA signaling in Arabidopsis. Plant J. Cell Mol. Biol. 70, 599–613.
Tang, W., Yuan, M., Wang, R., Yang, Y., Wang, C., Oses-Prieto, J.A., Kim, T.-W., Zhou, H.-W., Deng, Z., Gampala, S.S., et al. (2011). PP2A activates brassinosteroid-responsive gene expression and plant growth by dephosphorylating BZR1. Nat. Cell Biol. 13, 124–131.
Wang, Z.-Y. (2012). Brassinosteroids modulate plant immunity at multiple levels. Proc. Natl. Acad. Sci. U. S. A. 109, 7–8.
Wang, X., and Chory, J. (2006). Brassinosteroids regulate dissociation of BKI1, a negative regulator of BRI1 signaling, from the plasma membrane. Science 313, 1118–1122.
Wang, C., Shang, J.-X., Chen, Q.-X., Oses-Prieto, J.A., Bai, M.-Y., Yang, Y., Yuan, M., Zhang, Y.-L., Mu, C.-C., Deng, Z., et al. (2013). Identification of BZR1-interacting proteins as potential components of the Brassinosteroid signaling pathway in Arabidopsis through tandem affinity purification. Mol. Cell. Proteomics 12, 3653–3665.
Wrzaczek, M., Brosché, M., Salojärvi, J., Kangasjärvi, S., Idänheimo, N., Mersmann, S., Robatzek, S., Karpiński, S., Karpińska, B., and Kangasjärvi, J. (2010). Transcriptional regulation of the CRK/DUF26 group of receptor-like protein kinases by ozone and plant hormones in Arabidopsis. BMC Plant Biol. 10, 95.
Wu, G., Wang, X., Li, X., Kamiya, Y., Otegui, M.S., and Chory, J. (2011). Methylation of a phosphatase specifies dephosphorylation and degradation of activated brassinosteroid receptors. Sci. Signal. 4, ra29.
Xu, J., Meng, J., Meng, X., Zhao, Y., Liu, J., Sun, T., Liu, Y., Wang, Q., and Zhang, S. (2016). Pathogen-responsive MPK3 and MPK6 reprogram the biosynthesis of indole glucosinolates and their derivatives in Arabidopsis immunity. Plant Cell Online tpc.00871.2015.
Yadeta, K.A., Elmore, J.M., Creer, A.Y., Feng, B., Franco, J.Y., Rufian, J.S., He, P., Phinney, B.S., and Coaker, G.L. (2016). A cysteine-rich protein kinase associates with a membrane immune complex and is required for cell death. Plant Physiol. pp.01404.2016.
Ye, H., Li, L., and Yin, Y. (2011). Recent advances in the regulation of Brassinosteroid signaling and biosynthesis pathwaysF. J. Integr. Plant Biol. 53, 455–468.
Yeh, Y.-H., Chang, Y.-H., Huang, P.-Y., Huang, J.-B., and Zimmerli, L. (2015). Enhanced Arabidopsis pattern-triggered immunity by overexpression of cysteine-rich receptor-like kinases. Front. Plant Sci. 6.
Zhang, H., Lin, X., Han, Z., Qu, L.-J., and Chai, J. (2016). Crystal structure of PXY-TDIF complex reveals a conserved recognition mechanism among CLE peptide-receptor pairs. Cell Res. 26, 543–555.
Zhang, X., Han, X., Shi, R., Yang, G., Qi, L., Wang, R., and Li, G. (2013). Arabidopsis cysteine-rich receptor-like kinase 45 positively regulates disease resistance to Pseudomonas syringae. Plant Physiol. Biochem. 73, 383–391.
Zhang, Y., Goritschnig, S., Dong, X., and Li, X. (2003). A gain-of-function mutation in a plant disease resistance gene leads to constitutive activation of downstream signal transduction pathways in suppressor of npr1-1, constitutive 1. Plant Cell 15, 2636–2646.
Zipfel, C., Robatzek, S., Navarro, L., Oakeley, E.J., Jones, J.D.G., Felix, G., and Boller, T. (2004). Bacterial disease resistance in Arabidopsis through flagellin perception. Nature 428, 764–767.
dc.identifier.urihttp://tdr.lib.ntu.edu.tw/jspui/handle/123456789/20639-
dc.description.abstract訊息胜肽調控植物的生長發育以及多種生理反應,如根部組織生長、葉形調控、防禦反應、癒合組織生長、頂端分生組織構型組成等。然而訊息胜肽如何調控植物組織之發育仍有許多未知,本研究透過比較植物在不同胜肽處理後之發育情形,篩選出阿拉伯芥CUE胜肽家族中的KottoiA/B胜肽,實驗顯示KottoiA/B會透過不同受體激酶調控葉部stomatal lineage stem cell數量以及根部之維管束發育。植物不僅能透過受體激酶感受內在訊號,也能藉由受體激酶接收環境訊息做出反應,本研究發現,富含半胱胺酸受體激酶18與絲裂原活化蛋白質激酶6能夠維持模式誘發免疫反應,使其不被菜籽類固醇訊號傳遞路徑抑制。透過對植物轉錄調控以及表型的分析發現,半胱胺酸重複受體激酶18及有絲分裂活化蛋白質激酶6會負向調控菜籽類固醇訊號傳遞路徑。因此推論半胱胺酸重複受體激酶18及有絲分裂活化蛋白質激酶6可能參與在模式誘發免疫反應抑制菜籽類固醇訊號傳遞路徑中。zh_TW
dc.description.abstractPeptide signaling molecules are increasingly known to have important and diverse roles in regulation of developmental and physiological processes in plants. Here, we found that the peptide KottoiA/B, belonging to the CLAVATA3/ESR-unlike (CUE) family, regulates two different developmental processes, namely stomatal lineage and xylem developments in Arabidopsis thaliana. We also found that Kottoi A/B is perceived by two distinct receptor-like kinases (RLKs) systems in different tissues regulating distinct developmental processes. Plant cell use RLKs as transmembrane sensors to perceive and process peptide signals. RLKs not only sense endogenous signals but also exogenous signals. Our study revealed a novel RLK, CCR18 and it upstream MPK6 maintain the activation of PTI. Notably, by transcriptional and phenotype analyses, we show that CCR18 and MPK6 negatively regulate BRs signaling and positively regulate flg22-mediated growth inhibition. Therefore, CRK18 and MPK6 may be necessary for PTI-mediated reduction of BR-signaling. Our results further provide insight into understanding the fine-tune of plant immunity and may have potential for agricultural application.en
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dc.description.tableofcontentsContents
致謝 II
Abstract III
摘要 IV
Contents V
Part 1. Abstract 1
第一部分摘要 2
Introduction 3
Materials and Methods 7
Biological materials and growth conditions 7
Chemical Treatments 7
RNA extraction and gene expression 8
Hypocotyl and Root length measurements 9
Results 9
CRK18 does not directly modulate BR signaling 10
CRK18 modulates the BR response in a flg22 -dependent manner 11
MPK6 is upstream of CRK18 in the flg22-mediated repression of BR signaling 12
MPK6 is involved in BR biosynthesis pathway in a BL-dependent manner 13
Discussion 15
Conclusions and Future Perspectives 18
Figures 19
Figure 1. BR Responses in crk18 Mutants after BL treatment 19
Figure 2. Characterization of crk18 mutants after flg22 treatment 21
Figure 3 Characterization of mpk6 mutant after flg22 treatment 23
Figure 4. mpk6 mutant is not responsive to flg22 treatment 25
Figure 5. Phenotype of mpk6 mutant after BL treatment 26
Figure 6. Characterization of mpk6 mutant after BL treatment 27
Figure S1. Characterization of CRK18 mutants and OE Lines 29
Table S1 Primer list in this study 30
Part 2. Abstract 31
第二部分摘要 32
Introduction 33
Materials and Methods 36
Plant materials and growth conditions. 36
Microscopy and quantitative analysis of the epidermis. 36
Peptide treatment on plants 38
CRISPR 38
CLE peptide treatment on plants 39
Peptide synthesis 39
VISUAL 39
Results 41
KottoiA and KottoiB are preferentially expressed in stomatal lineage precursor cells and guard cells 41
kottoiB mutants show increased cell proliferation during stomatal development 42
KottoiA/B is perceived through a novel receptor 43
Identification of KottoiB receptor HSL1 in stomatal development 44
KottoiA/B negatively regulates metaxylem formation through BAM receptors 47
Discussion 49
Conclusions and Future Perspectives 51
Figures 52
Fig. 1. Promoter activities of KottoiB and KottoiA. 52
Fig. 2. The KottoiA/B peptide negatively regulates the formation of stomatal precursor cells. 53
Fig. 3. Development of epidermal cells in the er erl1 erl2 triple mutant is sensitive to KottoiA/B. 55
Fig. 4. Effects of mutations in BAMs/CLV1 class LRR RLK genes on epidermal cell development and root elongation. 56
Fig. 5. The HSL1 receptor-like kinase is indispensable for the KottoiA/B action for regulation of stomatal development. 58
Fig. 6. KottoiA/B negatively regulates metaxylem formation through BAM receptors. 60
Fig. 7. Hypothetical model. 61
Supplementary Data 62
Fig. S1. KottoiA/B did not decrease epidermal cell number in cotyledons in spch. Number of epidermal cells in adaxial side of cotyledons were counted (n= 5). Data done by Dr.Pingping Qian. 62
Table S1. A gene and mutant list of LRR-RLK XI family used for KottoiA/B receptor screening 66
Table S2 Primer list in this study. 67
References 68
dc.language.isoen
dc.title阿拉伯芥富含半胱胺酸受體激酶18及絲裂原活化蛋白質激酶6在抗病反應抑制菜籽類固醇路徑及KottoiA/B胜肽透過不同受體調控植物氣孔和維管束之發育之功能性分析zh_TW
dc.titleFunctional Characterization of CYSTEINE-RICH RECEPTOR-LIKE Arabidopsis PTI repression of BR signaling And KottoiA/B peptide regulates development of stomata and vasculature through distinct receptorsen
dc.typeThesis
dc.date.schoolyear105-2
dc.description.degree碩士
dc.contributor.oralexamcommittee謝旭亮(Hsu-Liang Hsieh),林乃君(Nai-Chun Lin),鄭貽生(Yi-Sheng Cheng),張英?(Ing-Feng Chang)
dc.subject.keyword阿拉伯芥,免疫反應,賀爾蒙,生物逆境,zh_TW
dc.subject.keywordarabidopsis,immunity,mpk6,pti,en
dc.relation.page75
dc.identifier.doi10.6342/NTU201702431
dc.rights.note未授權
dc.date.accepted2017-08-03
dc.contributor.author-college生命科學院zh_TW
dc.contributor.author-dept植物科學研究所zh_TW
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