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Studies on the control of transcriptional regulators in adaptive responses to environmental changes in Arabidopsis : 외부 환경 변화에 대한 적응 반응에서 나타나는 애기장대 전사 인자의 조절에 대한 연구

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dc.contributor.advisor박충모-
dc.contributor.author이효준-
dc.date.accessioned2017-07-14T05:54:19Z-
dc.date.available2017-07-14T05:54:19Z-
dc.date.issued2015-02-
dc.identifier.other000000025101-
dc.identifier.urihttps://hdl.handle.net/10371/125271-
dc.description학위논문 (박사)-- 서울대학교 대학원 : 화학부, 2015. 2. 박충모.-
dc.description.abstractSince the sessile nature of the plants, they have developed various adaptive systems in response to environmental changes. Transcriptional control is one of the most important regulatory systems in adaptive responses. Transcriptional regulators such as transcription factors and transcription co-factors directly or indirectly control transcription of their downstream genes. Thus, modulating the activity of transcriptional regulators is a key issue in studies on transcription. By molecular and genetic studies, transcriptional regulators that play a key role in plant adaptive responses are identified. However, how plants control their activity in response to environmental changes is still largely unknown. In this study, regulatory mechanisms of two transcriptional regulators which are critical for temperature and immune responses are identified.
In Chapter 1, a study on the modulation of PHYTOCHROME-INTERACTING FACTOR 4 (PIF4) activity under high ambient temperature conditions is described. In Arabidopsis, the basic helix-loop-helix transcription factor PIF4 regulates high temperature-induced adaptive responses by modulating auxin biosynthesis. At high temperature, PIF4 directly activates expression of YUCCA8 (YUC8), a gene encoding an auxin biosynthetic enzyme, resulting in auxin accumulation. Here, I demonstrate that the RNA-binding protein FCA attenuates the PIF4 activity by inducing its dissociation from the YUC8 promoter at high temperature. At 28oC, the auxin content is elevated in FCA-deficient mutants that exhibit elongated stems but reduced in FCA-overexpressing plants that exhibit reduced stem growth. Therefore, the proposed mechanism is that the FCA-mediated regulation of YUC8 expression tunes down the PIF4-induced architectural changes to achieve thermal adaptation of stem growth at high ambient temperature.
In Chapter 2, regulatory mechanism of NONEXPRESSER OF PR GENES 1 (NPR1) localization in response to pathogen infection is identified. In plants, necrotic lesions occur at the pathogen infection site through hypersensitive response (HR), which is followed by the activation of systemic acquired resistance (SAR) in distal tissues during defense responses. Salicylic acid (SA) plays a key role in inducing SAR by activating NPR1, but a high level of SA causes toxic effects to plant growth and development. During HR, SA biosynthesis increases in both local and systemic tissues. However, the SA level is only slightly elevated in systemic tissues, obscuring the role of SA in SAR. Here, I demonstrate that SNF1-RELATED PROTEIN KINASE 2.8 (SnRK2.8) phosphorylates NPR1 to facilitate its nuclear transport in systemic tissues which are under low SA conditions. Therefore, Arabidopsis requires the SnRK2.8-mediated activation system to induce immune responses while reducing growth defects by maintaining a low level of SA in systemic tissues.
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dc.description.tableofcontentsCONTENTS

ABSTRACT.............................................................................. i
CONTENTS............................................................................... iv
LIST OF FIGURES.................................................................viii
LIST OF TABLE.......................................................................xi
ABBREVIATIONS...................................................................xii


BACKGROUNDS
1. PIF4 mediates high ambient temperature responses in plant growth and development.......................................................................1
1.1 High ambient temperature responses in plants......................1
1.2 PIF4 is a key transcription factor in high ambient temperature responses....................................................................4
1.3 FCA functions in flowering time control.................................7
1.4 The broader role of FCA in transcriptional and post-transcriptional regulation...............................................................8
2. NPR1-mediated defense responses in plants.................................10
2.1 SA is required for inducing systemic acquired resistance...10
2.2 NPR1 is regulated by SA.........................................................11
3. The purpose of this study........................................................13

MATERIALS AND METHODS
1. Plant materials and growth conditions..........................................14
2. Analysis of gene transcript levels....................................................15
3. Measurements of free indole acetic acid (IAA) content................16
4. Bimolecular fluorescence complementation (BiFC) assay...........17
5. Preparation of recombinant proteins.............................................17
6. in vitro pull-down assay...................................................................18
7. Yeast two-hybrid assay....................................................................19
8. Chromatin immunoprecipitation (ChIP) assay.............................19
9. Coimmunoprecipitation assay........................................................21
10. Cell fractionation for subcellular localization of NPR1.............22
11. Pathogen infection assay and SA treatment................................23
12. in vitro phosphorylation assay......................................................24


CHAPTER 1: FCA mediates thermal adaptation of stem growth by attenuating auxin action in Arabidopsis

INTRODUCTION.................................................................................28

RESULTS
FCA mediates thermal acceleration of stem growth.........................31
IAA content is elevated in fca-9 at 28oC.............................................35
FCA interacts with PIF4 in thermal induction of stem growth.......39
FCA regulates PIF4 binding to YUC8 chromatin.............................43
FCA induces chromatin modification at YUC8 locus.......................48
FCA modulates dissociation of PIF4 from YUC8 chromatin..........51

DISCUSSION
FCA in attenuation mechanism of high ambient temperature responses...............................................................................................58
Histone demethylation mediated by FCA..........................................58
High temperature-mediated regulation of FCA................................59
Additional role of FCA at high temperature.....................................60
FCA as a transcriptional coregulator.................................................60

ACKNOWLEDGEMENT..................................................................62


CHAPTER 2: Feedforward activation of systemic acquired resistance via NPR1 phosphorylation in Arabidopsis

INTRODUCTION.................................................................................64

RESULTS
SnRK2.8 mediates systemic acquired resistance...............................66
SnRK2.8 regulation of SAR requires SA...........................................73
SnRK2.8 phosphorylates NPR1..........................................................73
SnRK2.8 promotes NPR1 nuclear import.........................................82

DISCUSSION
Regulation of NPR1 function in systemic leaves...............................89
Convergence of SnRK2.8- and SA-mediated immune signals into NPR1.....................................................................................................90
Upstream signals of SnRK2.8..............................................................90
Crosstalk between plant growth and immune responses.................91
Post-translational regulation of NPR1...............................................92

ACKNOWLEDGEMENT..................................................................94


REFERENCES.......................................................................................95


PUBLICATION LIST........................................................................110


ABSTRACT IN KOREAN...............................................................112

















LIST OF FIGURES

Figure 1. fca mutants showed elongated hypocotyl at 28oC....................32
Figure 2. fca mutants showed increased leaf hyponasty at 28oC ............33
Figure 3. fca mutants showed increased petiole growth at 28oC............34
Figure 4. Elongated hypocotyl of fca mutants was not related with FLC..............................................................................................................36
Figure 5. Genes encoding biosynthetic enzymes of ethylene, gibberellic acid, and brassinosteroid are not influenced by high temperature........37
Figure 6. IAA29 and YUC8 are highly expressed in fca-9 mutant at 28oC..............................................................................................................38
Figure 7. Transcript levels of SAUR genes in fca-9.................................40
Figure 8. Elongated hypocotyls of fca-9 is compromised in the presence of 100 M NPA............................................................................................41
Figure 9. Measurements of free IAA content in fca-9.............................42
Figure 10. FCA interacts with PIF4..........................................................44
Figure 11. FCA-mediated regulation of hypocotyl length at 28oC is associated with PIF4...................................................................................45
Figure 12. FCA is not related with high temperature-mediated regulation of PIF4 expression and protein stability ................................46
Figure 13. FCA does not affect the transcriptional activation activity of PIF4..............................................................................................................47
Figure 14. FCA mediates dissociation of DNA binding of PIF4 at 28oC..............................................................................................................49
Figure 15. FCA mediates histone demethylation at YUC8 promoter....52
Figure 16. High temperature induces FCA-PIF4 interaction.................54
Figure 17. Schematic diagram for FCA function in transcriptional regulation of YUC8 at high temperatures.................................................56
Figure 18. FCA attenuation of PIF4 action in thermal acceleration of stem growth.................................................................................................57
Figure 19. Pathogen infection induces SnRK2.8 expression...................67
Figure 20. SnRK2.8 overexpression confers pathogen resistance...........70
Figure 21. SAR is impaired in snrk2.8 mutants.......................................71
Figure 22. PR1 expression in local and systemic leaves of snrk2.8 mutants........................................................................................................72
Figure 23. SA does not induce SnRK2.8....................................................74
Figure 24. SA biosynthesis and SA-induced PR gene expressions do not require SnRK2.8.........................................................................................75
Figure 25. SnRK2.8-mediated PR1 induction requires SA.....................76
Figure 26. SnRK2.8 interacts with NPR1.................................................78
Figure 27. SnRK2.8 phosphorylates NPR1..............................................79
Figure 28. SnRK2.8 phosphorylates T373 of NPR1................................80
Figure 29. SnRK2.8 promotes NPR1 nuclear import..............................83
Figure 30. Nucleo-cytoplasmic localization of NPR1 in snrk2.8-1 mutant..........................................................................................................86
Figure 31. Nucleo-cytoplasmic localization of NPR1 in SA-treated plant cells...............................................................................................................87
Figure 32. SnRK2.8-mediated feedforward induction of SAR...............88

















LIST OF TABLE

Table 1. Primers used in this work............................................................26
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dc.formatapplication/pdf-
dc.format.extent3389722 bytes-
dc.format.mediumapplication/pdf-
dc.language.isoen-
dc.publisher서울대학교 대학원-
dc.subjectTranscriptional regulators-
dc.subjectauxin-
dc.subjecthigh ambient temperature-
dc.subjectimmune response-
dc.subjectsystemic acquired resistance-
dc.subjectsubcellular localization-
dc.subject.ddc540-
dc.titleStudies on the control of transcriptional regulators in adaptive responses to environmental changes in Arabidopsis-
dc.title.alternative외부 환경 변화에 대한 적응 반응에서 나타나는 애기장대 전사 인자의 조절에 대한 연구-
dc.typeThesis-
dc.contributor.AlternativeAuthorHyo-Jun Lee-
dc.description.degreeDoctor-
dc.citation.pagesxvi, 114-
dc.contributor.affiliation자연과학대학 화학부-
dc.date.awarded2015-02-
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