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Publié par | westfalische_wilhelms-universitat_munster |
Publié le | 01 janvier 2006 |
Nombre de lectures | 18 |
Langue | English |
Poids de l'ouvrage | 4 Mo |
Extrait
MOLECULAR FUNCTIONAL ANALYSIS OF THE
TUMOR SUPPRESSOR GENE PDCD4
Westfälische Wilhelms-Universität and
International NRW Graduate School of Chemistry
Muenster, Deutschland
Rajeshwari Marikkannu
From
Eriyodu, Tamil Nadu, India
October-2006
Biochemie
MOLECULAR FUNCTIONAL ANALYSIS OF THE TUMOR
SUPPRESSOR GENE PDCD4
Inaugural-Dissertation
zur Erlangung des Doktorgrades
der Naturwissenschaften
in der NRW Graduate School of Chemistry
im Fachbereich Chemie und Pharmazie
der Mathematisch-Naturwissenschaftlichen Fakultät
der Westfälischen Wilhelms-Universität Münster
vorgelegt von
Rajeshwari Marikkannu
aus
Eriyodu, Tamil Nadu, Indien
Oktober-2006
Dekan : Prof. Dr. Bernhard Wünsch
Erster Gutachter : Prof. Dr. Karl-Heinz Klempnauer
Zweiter Gutachter : Prof. Dr. Hans-Joachim Galla
Tag der mündlichen Prüfung :
Tag der Promotion :
To
the nature.....
the undeniable nature..........
the four seasons........................
the rain in the four seasons.............
the transition between the four seasons...........
the human race, who continuously battle against and constantly falling and raising again.........
There was a bad blot in my day.........
There was a fine blot in my day as well.........
The Metamorphosis.............................
M.C Eischer, Dutch,1898-1972
TABLE OF CONTENTS I
TABLE OF CONTENTS
ABBREVIATIONS ---------------------------------------------------------------------IV
1 SUMMARY ---------------------------------------------------------------------------- 1
2 INTRODUCTION 3
2.1 Cancer------------------------------------------------------------------------------ 3
2.1.1 Cancer Statistics--------------------------------------------------------------------3
2.1.2 Cancer Cell Physiology -------------------------------------------------------------3
2.1.3 Cancer Cell Genetics ---------------------------------------------------------------7
2.1.4 Tumor Suppressor Genes ----------------------------------------------------------8
2.1.5 Mechanisms of Inactivation of the Tumor Suppressor Genes --------------------8
2.1.6 Cancer Therapeutics9
2.2 Pdcd4 – A Novel Putative Tumor Suppressor -------------------------------- 11
2.2.1 The Cloning of Pdcd4 11
2.2.2 The Sequence Motifs of Pdcd4--------------------------------------------------- 11
2.2.3 The Structure of Pdcd4----------------------------------------------------------- 11
2.2.4 The Subcellular Localization of Pdcd4 ------------------------------------------- 12
2.2.5 The Regulation and Expression of Pdcd4---------------------------------------- 12
2.2.6 The Cellular Functions of Pdcd4 ------------------------------------------------- 14
2.2.7 The Molecular Mechanisms of the Functions of Pdcd4-------------------------- 15
2.3 Objectives and Rationale of the Study --------------------------------------- 17
2.3.1 Pdcd4 Models --------------------------------------------------------------------- 17
2.3.2 Pdcd4 Downregulation System -------------------------------------------------- 17
2.3.3 Upregulation System------------------------------------------------------ 19
3 MATERIALS AND METHODS ------------------------------------------------------ 20
3.1 Materials------------------------------------------------------------------------- 20
3.1.1 Antibodies 20
3.1.2 Cell Culture Products------------------------------------------------------------- 20
3.1.3 Chemicals and Reagents --------------------------------------------------------- 21
3.1.4 Devices and Instruments -------------------------------------------------------- 22
3.1.5 Enzymes -------------------------------------------------------------------------- 23
3.1.6 Genotype of Escherichia coli K12 strains---------------------------------------- 24
3.1.7 Kits-------------------------------------------------------------------------------- 24
3.1.8 Plasmids and Constructs 24
3.1.9 Primers---------------------------------------------------------------------------- 27
3.1.10 Standard Buffers and Solutions ------------------------------------------------ 27
3.2 The Molecular Biology Techniques -------------------------------------------- 33
3.2.1 Media and Agar plates ----------------------------------------------------------- 33
3.2.2 Preparation of Competent E.coli cells ------------------------------------------- 33
3.2.3 Transformation of Competent Bacteria and Blue/White Screening ------------ 33
3.2.4 Plasmid DNA Isolation------------------------------------------------------------ 34
3.2.5 Quantification of DNA 35
3.2.6 Modification of DNA by Enzymes 35
3.2.7 Agarose Gel Electrophoresis ----------------------------------------------------- 36
3.2.8 Extraction of DNA Fragments from Agarose gels ------------------------------- 36
3.2.9 Ligation --------------------------------------------------------------------------- 36
3.2.10 Polymerase Chain Reaction ---------------------------------------------------- 37
TABLE OF CONTENTS II
3.2.11 T/A-cloning of PCR products with TOPO TA System--------------------------- 38
3.2.12 DNA Sequencing ---------------------------------------------------------------- 38
3.2.13 Sequencing Gel ----------------------------------------------------------------- 39
3.2.14 Isolation of Genomic DNA from the Eucaryotic cells -------------------------- 39
3.2.15 Isolation of PolyA RNA from the Eucaryotic cells ------------------------------ 40
3.2.16 Genomic DNA-Agarose gel Electrophoresis and Southern Blotting----------- 41
3.2.17 RNA-Agarose gel Electrophoresis and Northern Blotting---------------------- 41
32 33.2.18 Radioactive Labeling of DNA with α P-dCTP and with H-dUTP -------------- 42
3.2.19 Hybridization and Washing ----------------------------------------------------- 42
3.2.20 Cell Cycle Analysis by FACS Method ------------------------------------------- 43
3.3 The Cell Culture Techniques --------------------------------------------------- 44
3.3.1 Cell lines and Medium------------------------------------------------------------ 44
3.3.2 Passage and Cultivation of cells ------------------------------------------------- 44
3.3.3 Cell Counting --------------------------------------------------------------------- 45
3.3.4 Transfection and Harvesting of Adherent and Suspension Cell lines ---------- 45
3.4 The Protein Biochemical Techniques ----------------------------------------- 47
3.4.1 Reporter-gene Assays 47
3.4.2 2-Dimensional-Sodium Dodecyl Sulfate-Polyacrylamide Gel Electrophoresis - 48
3.4.3 Coomassie Brilliant Blue Staining------------------------------------------------ 51
3.4.4 Western Blotting and Immunodetection----------------------------------------- 51
353.4.5 S-Methionine Labeling---------------------------------------------------------- 51
3.4.6 Immunoprecipitation ------------------------------------------------------------- 52
4 RESULTS --------------------------------------------------------------------------- 53
4.1 Downregulation of Pdcd4 – A Knock-Down System------------------------- 53
4.1.1 Targeted Silencing of the Human Pdcd4 gene ---------------------------------- 53
4.1.2 The effect of Hpdcd4 on Cap-Dependent Translation--------------------------- 56
4.1.3 d4 on IRES-Dependentation 57
4.1.4 The search for Novel Molecular Targets of Hpdcd4 – Transcription Factors--- 61
4.1.5 The effect of Hpdcd4 on Transcription Factor C/EBP β -------------------------- 64
4.1.6 The search for Novel Molecular Targets of Hpdcd4 – A Proteomic Approach-- 67
4.1.7 The Effect of Hpdcd4 on the Biochemical Modification of CK-8 ---------------- 72
4.1.8 Expression of Pdcd4 Targets at the RNA Level---------------------------------- 74
4.1.9 The effect of Hpdcd4 on mRNA Stability ---------------------------------------- 76
4.1.10 The effect of Hpdcd4 on Nonsense-Mediated mRNA Decay------------------- 78
4.2 Downregulation of Pdcd4 – Knock-Out-System ----------------------------- 80
4.2.1 Targeted Disruption of the Chicken Pdcd4 gene -------------------------------- 80
4.2.2 The effect of the Disruption of Cpdcd