LIFE09200604002 Lalit Sehgal - Homi Bhabha National Institute

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such as Leukemia or lymphoma (8, 9). We hyphothesized that the the CD3+ DN cells in peripheral tissues like the spleen, may arise due to the hyperproliferation of immature T cells. This hypothesis was strengthened by the finding that 14-3-3ε binds to SLP-76 in presence of kinase HPK1 (79). These results therefore suggest that 14-3-3ε may negatively regulate the T cell activation. To further understand the role of 14-3-3ε in growth and development inducible knock down mice will be generated to test the contribution of 14-3-3ε to development in the epidermis and in the lymphoid system. 180
CHAPTER 5 DISCUSSION 181
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Generation of knockdown mice that l
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STATEMENT BY AUTHOR This dissertati
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CERTIFICATE I certify that the thes
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I am thankful to Mr Uday Dandekar f
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3.16 Isolation of Genomic DNA (gDNA
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A synopsis of thesis to be submitte
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esults in loss of 14-3-3 binding an
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and NheI (NEB) to remove tetO-CMV,
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Hanging drop and wound healing assa
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360). To generate transgenic animal
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asement of the seminiferous tubules
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normal female, pups were screened f
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14-3-3ε only in the presence of HP
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proteins are expressed in testis (3
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5. Lalit Sehgal, Srikanth B., Khyat
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Presented a poster at 33rd All Indi
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shRNA siRNA TBS-T U.V WT C IF DSG D
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List of Figures: Page No 1. Figure
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37. Figure 4.3.20: 14-3-3γ interac
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CHAPTER 1 INTRODUCTION 39
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1.1.1 Cyclin Cdk complexes Eukaryot
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1.1.1.c Cyclin A cdk complexes The
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of which are associated with acquis
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1.2.2 The G1/S DNA Damage checkpoin
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complexes. DNA damage induced degra
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cytoplasmic accumulation of cdc25 p
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14-3-3 binding site. 14-3-3 binding
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G2 arrest and induced premature chr
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emoval of S216 phosphorylation as i
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embryogenesis, a loss of cdc25A can
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dimer was essential for Raf activat
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of enhanced apoptosis of peripheral
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the generation of transgenic mice a
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CHAPTER 2 AIMS AND OBJECTIVES 67
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CHAPTER 3 MATERIALS AND METHODS 69
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Name of oligonucleotide EF1α Forwa
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cleavage sites GAAGGTATATTGCTGTTGAC
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R E1 A GAACGAATAGTGAAGCCACAGATGTA s
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100mm 25ug 225ul 250ul 500 1000ul T
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for the transgene were considered a
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solution in TBS-T containing 0.02%
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mounting agent. Confocal images wer
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3.26 Antibodies used for Western bl
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each plate was added cold 500ml of
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3.32 Hanging drop assay to determin
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3.37 Biodistribution of 18 F -FDG u
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2.5M NaCl 150mM 60ml Tween-20 (Sigm
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CHAPTER 4 RESULTS 95
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Figure 4.1.1 Generation of lentivir
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4.1.2 Generation of lentiviral vect
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transduction with the virus. Untran
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Figure 4.1.6: Application of bi-cis
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Figure 4.1.7: Application of bi-cis
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Figure 4.2.1: Infection of morulae
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Figure 4.2.2: Generation of transge
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Figure 4.2.3: EGFP-f expression in
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sequenced and the distribution amon
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4.3 Generation of 14-3-3γ knockdow
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numbering). Alignment was done usin
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presence of EGFP-f by performing po
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the mouse tested infected with vect
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Figure 4.3.7: Staging of 14-3-3γ k
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containing spermatozoa is on the Y-
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Figure 4.3.9: 14-3-3γ knockdown le
Page 129 and 130: Figure 4.3.11: 14-3-3γ knockdown i
Page 131 and 132: intercellular space (12, 110, 115,
Page 133 and 134: Figure 4.3.13: 14-3-3γ loss leads
Page 135 and 136: Figure 4.3.16: Localization of PKP3
Page 137 and 138: Figure 4.3.18: Reintroduction of sh
Page 139 and 140: A B 139
Page 141 and 142: from our laboratory demonstrated th
Page 143 and 144: Figure 4.3.21: Plakoglobin recruitm
Page 145 and 146: 4.3.23 (A and B)). These proteins g
Page 147 and 148: the desmosomal proteins recruitment
Page 149 and 150: Figure 4.3.25: Generation of stable
Page 151 and 152: KIF5B, however its reduction does n
Page 153 and 154: compared to vector control cells. (
Page 155 and 156: 4.4 Generation of 14-3-3ε knockdow
Page 157 and 158: into the interstitial spaces of the
Page 159 and 160: Figure 4.4.3: 14-3-3ε knockdown in
Page 161 and 162: Figure 4.4.4: Patchy hair loss in 1
Page 163 and 164: follicle formation marked by black
Page 165 and 166: Figure 4.4.7: Phenotypes in 14-3-3
Page 167 and 168: compared to WT lungs (indicated by
Page 169 and 170: compared to wild type (Figure 4.4.1
Page 171 and 172: and CD4 positive lyumphocyte number
Page 173 and 174: Figure 4.4.13: Bone marrow cells fr
Page 175 and 176: Figure 4.4.15: Generation of stable
Page 177 and 178: Figure 4.4.16: NIH3T3 cells lacking
Page 179: Figure 4.4.18: Generation of induci
Page 183 and 184: to generate transgenic animals expr
Page 185 and 186: transgenic research and the use of
Page 187 and 188: (reviewed in (152, 374)). Kinesins
Page 189 and 190: subtypes known to date. Type IV col
Page 191 and 192: Figure 5.1 Schematic representation
Page 193 and 194: loss of 14-3-3ε the T cell activat
Page 195 and 196: BIBLIOGRAPHY: 1. Abraham, R. T. 200
Page 197 and 198: 29. Blomer, U., L. Naldini, T. Kafr
Page 199 and 200: 58. Cheng, C. Y., and D. D. Mruk. 2
Page 201 and 202: 90. Elia, A. E., P. Rellos, L. F. H
Page 203 and 204: 118. Girard, F., U. Strausfeld, J.
Page 205 and 206: 150. Herrmann, H., M. Haner, M. Bre
Page 207 and 208: and activation of a cyclin E-cdk2 c
Page 209 and 210: 213. Liu, D., J. Bienkowska, C. Pet
Page 211 and 212: 242. Moll, R., W. W. Franke, D. L.
Page 213 and 214: 274. Pagano, M., R. Pepperkok, F. V
Page 215 and 216: 305. Russell, L. D. 1978. The blood
Page 217 and 218: inhibitor of metalloproteases-1 in
Page 219 and 220: 364. Tsunekawa, N., M. Matsumoto, S
Page 221 and 222: 397. Yashiro, M., N. Nishioka, and
Page 223: Research: Biology to Prevention to
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LIFE09200604002 Lalit Sehgal - Homi Bhabha National Institute

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