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Transcription overview

Figure 3 provides a very general overview of transcriptional activation in response to a PPAR ligand. Fig. 3a shows the schematic representation of a PPAR target gene in the absence of PPAR ligand. Co-repressor proteins bound to both unliganded PPAR and RXR... [Pg.940]

Figure 14.13 Overview of the concept of the antisense approach the end goal is the prevention of expression of a particular gene product (invariably a protein) by either blocking the transcription or translation of that gene... Figure 14.13 Overview of the concept of the antisense approach the end goal is the prevention of expression of a particular gene product (invariably a protein) by either blocking the transcription or translation of that gene...
Figure 21.17 Overview of the regulation of the genes that express three proteins essential for DNA synthesis. The Rb gene expresses Rb which inactivates the transcription factor by forming a complex. Phosphorylation of the Rb protein by a cell cycle kinase causes dissociation of complex and release of transcription factor, which is now active and stimulates expression of the three genes. THFR, tetra hydrofolate reductase. See chapter 20 for details of the actions of cyclins, DNA polymerase and THFR in the cell cycle. Figure 21.17 Overview of the regulation of the genes that express three proteins essential for DNA synthesis. The Rb gene expresses Rb which inactivates the transcription factor by forming a complex. Phosphorylation of the Rb protein by a cell cycle kinase causes dissociation of complex and release of transcription factor, which is now active and stimulates expression of the three genes. THFR, tetra hydrofolate reductase. See chapter 20 for details of the actions of cyclins, DNA polymerase and THFR in the cell cycle.
Finally, in this brief overview of lymphocyte defects, mention should be made of mutations affecting major histocompatibility-complex (MHC) Class II molecules. These mutations affect a multiprotein transcription factor complex that regulates the expression of MHC Class II molecules (121). Affected patients have undetectable levels of MHC Class II antigens HLA-DP, DQ, and DR on the surface of monocytes and B cells. Lack of these antigen-presenting molecules leads to impaired immune response. Affected individuals have moderate lymphopenia with a severely reduced number of CD4+ T cells and normal or increased numbers of CD8+ T cells. Since MHC molecules in the thymic epithelium play a key role in positive and negative selection of primitive T cells, selection of competent T cells is also affected in the absence of MHC Class II antigens. [Pg.259]

Fig. 9.12. Overview of the Ras signaling pathway. Signals from at least three major signaling pathways meet at the Ras protein. Activation of the Ras protein may be initiated by receptor tyrosine kinases, by G-protein-coupled receptors and by receptors with associated tyrosine kinases. The nature of the communication between the Ras protein and receptors with associated tyrosine kinase or G-protein-coupled receptors is mostly unknown. From the activated Ras protein, the signal is passed to various effector molecules including members of the MEK kinases, PI3-kinase, pl20 GAP and Ral-GEFs. The best understood is the effector function of Raf kinase, which passes a signal to the transcription level via the MAP kinase pathway. Fig. 9.12. Overview of the Ras signaling pathway. Signals from at least three major signaling pathways meet at the Ras protein. Activation of the Ras protein may be initiated by receptor tyrosine kinases, by G-protein-coupled receptors and by receptors with associated tyrosine kinases. The nature of the communication between the Ras protein and receptors with associated tyrosine kinase or G-protein-coupled receptors is mostly unknown. From the activated Ras protein, the signal is passed to various effector molecules including members of the MEK kinases, PI3-kinase, pl20 GAP and Ral-GEFs. The best understood is the effector function of Raf kinase, which passes a signal to the transcription level via the MAP kinase pathway.
Fig. 13.11. Substrates and phase-spedfic activation of CDKs in the ceU cycle. An overview is shown of the phase-specific activation of the most important CDK-cychn complexes and of selected substrates. The arrows indicate activation and phosphorylation. CDK cycMn-dependent protein kinase p53 tumor suppressor p53 pRb tumor suppressor pRb CDC25 CDC25 phosphatase TFIIIB transcription factor TFIIIB R restriction point. Fig. 13.11. Substrates and phase-spedfic activation of CDKs in the ceU cycle. An overview is shown of the phase-specific activation of the most important CDK-cychn complexes and of selected substrates. The arrows indicate activation and phosphorylation. CDK cycMn-dependent protein kinase p53 tumor suppressor p53 pRb tumor suppressor pRb CDC25 CDC25 phosphatase TFIIIB transcription factor TFIIIB R restriction point.
Kramer JA, Pettit SD, Amin RP et al. Overview on the application of transcription profiling using selected nephrotoxicants for toxicology assessment. Environ Health Perspect 2004 112 460-464. Newton RK, Aardema M, Aubrecht J. The utility of DNA microarrays for characterizing genotoxicity. Environ Health Perspect 2004 112 420 22. [Pg.349]

Transcript of an excellent talk given at the Lindesmith Center (New York) in March 2000. A straightforward overview of what MDMA is, what the potential risks of it are, what urban myths surround it, and what the therapeutic potential is. [Pg.514]

We begin by examining the interactions between proteins and DNA that are the key to transcriptional regulation. We next discuss the specific proteins that influence the expression of specific genes, first in prokaryotic and then in eukaryotic cells. Information about posttranscriptional and translational regulation is included in the discussion, where relevant, to provide a more complete overview of the rich complexity of regulatory mechanisms. [Pg.1082]

Gotte, M., Li, X., and Wainberg, M. A. (1999). HIV-1 reverse transcription A brief overview focused on structure-function relationships among molecules involved in initiation of the reaction. Arch. Biochem. Biophys. 365, 199-210. [Pg.434]

Related topics DNA replication in bacteria (F3) Transcription in DNA replication in eukaryotes (F4) prokaryotes (G2) RNA structure (Gl) Transcription in eukaryotes an overview (G5)... [Pg.147]

Overview In eukaryotes, the product of transcription of a protein-coding gene is pre-... [Pg.196]


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See also in sourсe #XX -- [ Pg.821 , Pg.822 ]




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Overview of Transcription

Overview of Transcription Initiation in Procaryotes

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