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Figure 2.9 Enhancer region modularity
Figure 2.10 Modular transcriptional regulatory regions using Pax6 as an activator
Figure 2.11 RNA polymerase is stabilized on the promoter site of the DNA by transcription factors
recruited by the enhancers
Figure 2.12 Stereoscopic model of Pax6 protein binding to its enhancer element in DNA
Figure 2.16 Silencers. Analysis of β-galactosidase staining patterns in 11.5-day embryonic mice
Figure 2.13 Pancreatic lineage and transcription factors
Zhou et al.
Figure 2.3 Nucleosome and chromatin structure (Part 1)
Figure 2.3 Nucleosome and chromatin structure (Part 2)
Figure 2.3 Nucleosome and chromatin structure (Part 3)
Figure 2.14 Three-dimensional model of the homodimeric transcription factor MITF (one protein in
red, the other in blue) binding to a promoter element in DNA (white)
Figure 2.15 Model for the role of the “pioneer” transcription factor Pbx in aligning the musclespecific transcription factor MyoD on DNA
Figure 2.17 Methylation of globin genes in human embryonic blood cells
Figure 2.18 DNA methylation can block transcription by preventing transcription factors from
binding to the enhancer region
Figure 2.24 Roles of differential RNA processing during development
Figure 2.26 Some examples of alternative RNA splicing
Figure 2.27 Alternative RNA splicing to form a family of rat α-tropomyosin proteins
Figure 2.28 The Dscam gene of Drosophila can produce 38,016 different types of proteins by
alternative nRNA splicing
Figure 2.31 Degradation of casein mRNA in the presence and absence of prolactin
Figure 2.34 Hypothetical model of the regulation of lin-14 mRNA translation by lin-4 RNAs