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Regulation of amino acid metabolism: gene expression during seed development and the possible roles of GCN2.

Ma Junhao. / Thesis (M.Phil.)--Chinese University of Hong Kong, 2004. / Includes bibliographical references (leaves 111-123). / Abstracts in English and Chinese. / Thesis Committee --- p.i / Statement --- p.ii / Abstract --- p.iii / Acknowledgements --- p.vii / General Abbreviations --- p.ix / Abbreviations of Chemicals --- p.xi / Table of Contents --- p.xii / List of Figures --- p.xvi / List of Tables --- p.xix / Chapter 1. --- Literature review --- p.1 / Chapter 1.1 --- Importance of amino acid metabolism --- p.1 / Chapter 1.1.1 --- Rice as the important source of essential amino acids --- p.1 / Chapter 1.1.2 --- Rice seeds are nutritionally incomplete --- p.2 / Chapter 1.1.3 --- The nitrogen source for aspartate family amino acid synthesis --- p.3 / Chapter 1.1.4 --- Synthesis of aspartate family amino acids in plants --- p.4 / Chapter 1.1.5 --- Regulation of the aspartate pathway at free amino acid level --- p.12 / Chapter 1.2 --- Regulation of amino acid metabolism during seed development --- p.14 / Chapter 1.3 --- Signalling system for nitrogen metabolism --- p.17 / Chapter 1.3.1 --- Nitrogen signalling in plants --- p.18 / Chapter 1.3.2 --- GCN signalling: another nitrogen signalling pathway --- p.21 / Chapter 1.3.2.1 --- Mechanism of GCN signalling pathway in yeast --- p.21 / Chapter 1.3.2.2 --- GCN in mammalian --- p.24 / Chapter 1.3.2.3 --- GCN in higher plant --- p.24 / Chapter 1.3.3 --- Relationship between carbon and nitrogen metabolic signaling in plants --- p.26 / Chapter 1.3.4 --- Paradigm for elucidating new signal transduction pathways --- p.29 / Chapter 1.4 --- Hypothesis of this thesis work --- p.30 / Chapter 2. --- Materials and Methods --- p.32 / Chapter 2.1. --- Materials --- p.32 / Chapter 2.1.1 --- Plants --- p.32 / Chapter 2.1.2 --- Bacterial strains and vectors --- p.32 / Chapter 2.1.3 --- Chemicals and reagents --- p.33 / Chapter 2.1.4 --- Buffer,solution and gel --- p.33 / Chapter 2.1.5 --- Commercial kits --- p.33 / Chapter 2.1.6 --- Equipments and facilities used --- p.33 / Chapter 2.1.6 --- Growth medium --- p.34 / Chapter 2.2 --- Methods --- p.34 / Chapter 2.2.1 --- Profiling genes expression pattern in developing rice seeds --- p.34 / Chapter 2.2.1.1 --- Growth conditions of rice --- p.34 / Chapter 2.2.1.2 --- Collection of developing rice seeds --- p.35 / Chapter 2.2.1.3 --- Total RNA extraction from rice seeds --- p.37 / Chapter 2.2.1.4 --- Total RNA extraction from plant leaf --- p.37 / Chapter 2.2.1.5 --- Gel electrophoresis --- p.38 / Chapter 2.2.1.6 --- First strand cDNA synthesis from rice total RNA --- p.39 / Chapter 2.2.1.7 --- Search for the coding sequence of rice genes related to amino acid metabolism --- p.39 / Chapter 2.2.1.8 --- Alignment of homologous coding sequence between family member genes --- p.42 / Chapter 2.2.1.9 --- Primer design --- p.42 / Chapter 2.2.1.10 --- Quantitation of total RNA and determination of internal control --- p.45 / Chapter 2.2.1.11 --- PCR to amplify the DNA fragments --- p.45 / Chapter 2.2.1.12 --- DNA Sequencing --- p.46 / Chapter 2.2.1.13 --- Generation and testing of single-stranded DIG-labelled DNA probes --- p.46 / Chapter 2.2.1.14 --- Northern blot --- p.47 / Chapter 2.2.1.15 --- RT-PCR (Reverse-transcription polymerase chain reaction) --- p.48 / Chapter 2.2.2 --- Expression assay of selected genes in herbicide treated plants --- p.49 / Chapter 2.2.2.1 --- Growing conditions and herbicide treatments --- p.49 / Chapter 2.2.2.2 --- GCN2 homologue in Arabidopsis and rice --- p.51 / Chapter 2.2.2.3 --- RT-PCR to analyze the change in expression level of selected genes in herbicide treated plants --- p.53 / Chapter 2.2.3 --- Generation of transgenic Arabidopsis --- p.56 / Chapter 2.2.3.1 --- Preparation of T-vector for T-ligation --- p.56 / Chapter 2.2.3.2 --- Cloning of Arabidopsis GCN2 gene --- p.56 / Chapter 2.2.3.3 --- Transformation of the plasmid into DH5a competent cell --- p.57 / Chapter 2.2.3.4 --- Screening of right recombinants --- p.58 / Chapter 2.2.3.5 --- Construction of chimeric AtGCN2 genes --- p.59 / Chapter 2.2.3.6 --- Transformation of electro-competent Agrobacterium cell --- p.60 / Chapter 2.2.3.7 --- Transformation of Arabidopsis by vacuum infiltration --- p.61 / Chapter 2.2.3.8 --- Selection of hemizygous and homozygous transgenic plants --- p.61 / Chapter 2.2.3.9 --- Screening of the T3 transformants --- p.63 / Chapter 2.2.3.10 --- Expression analysis of homozygous AtGCN2 transgenic Arabidopsis --- p.63 / Chapter 3. --- Results --- p.63 / Chapter 3.1 --- Profiling genes expression pattern in developing rice seeds --- p.63 / Chapter 3.1.1 --- Quantification of total RNA from seeds at different developing stages --- p.63 / Chapter 3.1.2 --- DNA sequence analysis --- p.66 / Chapter 3.1.3 --- Profiling the gene expression in developing rice seeds --- p.67 / Chapter 3.1.3.1 --- Expression profiles of nitrogen assimilation related genes --- p.67 / Chapter 3.1.3.2 --- Expression profiles of aspartate pathway genes --- p.72 / Chapter 3.1.3.3 --- Expression profiles of branched-chain amino acid synthesis pathway genes --- p.78 / Chapter 3.2 --- Relationship between GCN2 and amino acid metabolism in plants --- p.82 / Chapter 3.2.1 --- GCN2 homologue in A. thaliana and rice --- p.82 / Chapter 3.2.2 --- GCN2 and amino acid starvation --- p.85 / Chapter 3.2.3 --- Effects of amino acid starvation on GCN2 expression --- p.90 / Chapter 3.2.3 --- Changes in the expression level AK and BCAT genes in herbicide treated rice and A. thaliana --- p.93 / Chapter 3.3 --- Characterization of GCN2 transgenic A. thaliana --- p.96 / Chapter 3.3.1 --- Construct of pBI121-AtGCN2 --- p.96 / Chapter 3.3.2 --- Construction of GCN2 transgenic A. thaliana --- p.96 / Chapter 3.3.3 --- Expression of GCN2 in transgenic A. thaliana --- p.97 / Chapter 3.3.4 --- Expression level changes of AK and BCAT in transgenic A. thaliana --- p.99 / Chapter 4. --- Discussions --- p.101 / Chapter 4.1 --- Expression pattern of selected metabolic genes in developing plant seeds --- p.101 / Chapter 4.1.1 --- Most genes studied displayed a similar pattern --- p.101 / Chapter 4.1.2 --- Regulation of gene expression in developing rice seeds --- p.105 / Chapter 4.2 --- GCN2 and its role in higher plants --- p.106 / Chapter 4.2.1 --- The existence of the GCN2 gene in rice --- p.106 / Chapter 4.2.2 --- GCN2 responses solely to amino acid starvation --- p.106 / Chapter 5. --- Conclusion and Prospective --- p.109 / Reference --- p.111 / Appendix I: Chemicals and reagents --- p.124 / "Appendix II: Buffer, solution and gel" --- p.126 / Appendix III: Commercial kits --- p.128 / Appendix IV: Equipments and facilities used --- p.128

Identiferoai:union.ndltd.org:cuhk.edu.hk/oai:cuhk-dr:cuhk_324935
Date January 2004
ContributorsMa, Junhao., Chinese University of Hong Kong Graduate School. Division of Biology.
Source SetsThe Chinese University of Hong Kong
LanguageEnglish, Chinese
Detected LanguageEnglish
TypeText, bibliography
Formatprint, xix, 128 leaves : ill. ; 30 cm.
RightsUse of this resource is governed by the terms and conditions of the Creative Commons “Attribution-NonCommercial-NoDerivatives 4.0 International” License (http://creativecommons.org/licenses/by-nc-nd/4.0/)

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