By Frederick W. Alt
Advances in Immunology, a customary and hugely revered booklet, offers present advancements in addition to entire reports in immunology. Articles tackle the wide variety of issues that include immunology, together with molecular and mobile activation mechanisms, phylogeny and molecular evolution, and scientific modalities. Edited and authored by means of the key scientists within the box, every one quantity offers updated details and instructions for destiny * Contributions from best gurus and specialists * Informs and updates on the entire most modern advancements within the box
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Additional resources for Advances in Immunology
In the case of IkB, for example, newly synthesized IkBa protein binds to NF-kB in the cytoplasm and prevents its translocation into the nucleus. , 1995). 2. LXRs The liver X receptors LXRa (NR1H3) and LXRb (NR1H2) are regulated by endogenous oxysterol ligands and play general roles in total body cholesterol and fatty acid homeostasis. In macrophages, LXRs regulate cholesterol efflux pathways that prevent excessive cholesterol accumulation. , 2009). , 2009) (Fig. 1C), a member of TAM receptor family (Lemke and Rothlin, 2008).
The GR can also exert repressive effects by inducing the recruitment corepressors to downregulate active genes. An interesting example is provided by the ability of the GR to recruit glucocorticoid receptor interacting protein 1 (GRIP1), a member of the SRC family of nuclear receptor coregulators. The ability of GRIP1 to be converted from an activator to a repressor of transcription is dependent on a GRIP1specific repression domain, which becomes active in the context of interaction with the GR tethered to NF-kB or AP-1 (Cho and Kim, 2009) (Fig.
In contrast, the extended helices of NCoR/SMRT are too long to be accommodated by this pocket when the AF2 helix assumes the charge clamp configuration in response to ligand binding. Thus, agonist binding reduces the affinity of 26 Kaoru Saijo et al. nuclear receptors for CoRNR-box-containing corepressors and increases affinity for LXXLL-containing coactivators. This conserved biochemical strategy for cofactor recruitment also allows for selection of corepressors that are recruited to nuclear receptors in a ligand-dependent manner.