Nuclear Receptor Coregulators, Volume 68 (Vitamins and Hormones)

by Gerald Litwack

Publisher: Academic Press

Written in English
Cover of: Nuclear Receptor Coregulators, Volume 68 (Vitamins and Hormones) | Gerald Litwack
Published: Pages: 304 Downloads: 553
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Subjects:

  • Biochemistry,
  • Medical / Nursing,
  • Medical,
  • Endocrinology & Metabolism,
  • Medical / Endocrinology & Metabolism,
  • Life Sciences - Biology - General,
  • Pharmacology
The Physical Object
FormatHardcover
Number of Pages304
ID Numbers
Open LibraryOL9283942M
ISBN 100127098682
ISBN 109780127098685

Save nuclear receptor to get e-mail alerts and updates on your eBay Feed. + 7 S 0 P O N S O A R P A 7 E E D -1 -1 U J -1 0 F J -1 -1 The Nuclear Receptor Superfamily: Methods and Protocols. / The book of opposites: The role of the nuclear receptor co-regulators in the suppression of epidermal genes by retinoic acid and thyroid hormone receptors. In: Journal of Investigative Dermatology. ; Vol. , No. 5. pp. Abstract: The pregnane X receptor (PXR) is a member of the nuclear receptor family of ligand-regulated transcription factors. Like many former orphan nuclear receptors, it contains both DNA and ligand binding domains and binds to response elements in the regulatory regions of target genes as a heterodimer with RXRα. nuclear receptors current concepts and future challenges proteins and cell regulation Posted By Jin Yong Library TEXT ID b85cf Online PDF Ebook Epub Library research laboratory planetarium place arlington tx usa search for more papers by this author subhrangsu s mandal hao zuo yihong wan in current topics in.

Endocrine therapy, and especially tamoxifen, is the most important systemic treatment of estrogen receptor (ER)-positive breast cancer at all stages. A serious obstacle, however, is intrinsic or acquired resistance to these therapies, which in the case of selective ER modulators, such as tamoxifen, involves some imbalance of their agonist versus antagonist actions. The nuclear receptor co-repressor 2 is a transcriptional coregulatory protein that contains several nuclear receptor-interacting addition, NCOR2 appears to recruit histone deacetylases to DNA promoter regions. Hence NCOR2 assists nuclear receptors in the down regulation of target gene expression. NCOR2 is also referred to as a silencing mediator for retinoid or thyroid-hormone. Robyr D, Wolffe AP, Wahli W Nuclear hormone receptor coregulators in action: diversity for shared tasks. Mol Endocrinol 14 Crossref | PubMed Google Scholar; Rochel N, Wurtz JM, Mitschler A, Klaholz B, Moras D The crystal structure of the nuclear receptor for vitamin D bound to its natural ligand. Mol Cell 5 The Yin and Yang of Nuclear Receptors: Symposium on Nuclear Receptors in Brain, Oegstgeest, The Netherlands, April , Trends in Endocrinology and Metabolism, Volume .

  Volume , Issue 4. October Pages Volume , Issue 3. July Pages Volume , Issue 2. April Pages the characterization of different human diseases in which the organization or expression of nuclear receptor coregulators is altered has further demonstrated the important physiological role of. Nuclear receptor coregulators: Judges, juries and executioners of transcriptional regulation. Molecular C McKenna, N. O'Malley, B. W. (). Combinatorial control of gene expression by nuclear receptors and coregulators. Cell , McKenna NJ and O. Androgen receptor (AR), a disease-causing protein of SBMA, is a well-characterized ligand-activated transcription factor, and androgen binding induces nuclear translocation, conformational change and recruitment of coregulators for transactivation of AR target genes. Some therapeutic strategies for SBMA are based on these native functions of AR. Nuclear receptors as drug targets: new developments in coregulators, orphan receptors and major therapeutic areas 2 Expert Opin. Ther. Targets () 7(5) Table 1. Nuclear receptors as drug targets. Abbreviation Full name Disease/function TRα,β RARα,β,γ PPARα,δ,γ RORα,β,γ LXRα,β FXR VDR PXR CAR HNF4α,γ RXRα,β,γ ERα,β ERRα.

Nuclear Receptor Coregulators, Volume 68 (Vitamins and Hormones) by Gerald Litwack Download PDF EPUB FB2

Purchase Nuclear Receptor Coregulators, Volume 68 - 1st Edition. Print Book & E-Book. ISBNBook Edition: 1. Search in this book series. Nuclear Volume 68 book Coregulators. Gerald Litwack. Vol Pages () Download full volume.

Previous volume. Next volume. Actions for selected chapters. Select all / Deselect all. Download PDFs Export citations. Show all chapter previews Show all chapter previews. Kidney International, Vol. 68 (), pp. – PERSPECTIVES IN BASIC SCIENCE Nuclear receptors and their coregulators in kidney XIONG Z.

RUAN,ZAC VARGHESE,STEPHEN H. POWIS, and JOHN F. M OORHEAD Centre for Nephrology, Royal Free and University College Medical School, University College London, Royal Free Campus. Nuclear Receptor Coregulators (ISSN Book 68) (English Edition) ePub / PDF This is has the world's largest collection Nuclear Receptor Coregulators (ISSN Book 68) (English Edition) of ebooks for people with reading barriers.

Find the book you want for school, work, or fun. Enjoy the best books we have to offer completely free of charge. This book serves as a treasure for all those who have an interest in nuclear receptor coregulators and human diseases. Written by experts in the field, each chapter provides comprehensive, up-to-date information on the physiologic and pathologic roles of coregulators in specific organ systems, giving biomedical students; basic and clinical researchers; and educators in diverse sub-specialties.

Transcriptional coregulators (coactivators and corepressors) have emerged as the principal modulators of the functions of nuclear receptors and other transcription factors. During the decade since the discovery of steroid receptor coactivator-1 (SRC-1), the first authentic coregulator, more than coregulators have been identified and characterized, and deciphering their function has.

Keywords:nuclear receptors, transcription, ligands, lbd, dbd, domain structure, cofactors, coregulators. Abstract: The nuclear receptor superfamily comprises a large group of transcription factors that play a key regulatory role in development and homeostasis of multicellular organisms. A special feature of nuclear receptors is their ability to.

Molecular architecture of NCOAs and NCORs. (A) NCOAs are composed of the basic helix–loop–helix-PER-ARNT-SIM (HLH/PAS) domain on the N-terminus, a serine/threonine-rich (S/T) domain and a nuclear receptor interaction domain (NRID) in the middle, and 2 transactivation domains (AD) on the C-terminus.

NCORs have 3 repression domains (RD1, RD2, and RD3), a deacetylase activation domain. Volume 68 book Reviews, Vol Issue 3, 1 JunePages –, https: 68 – 70 BRG-1 SWI2/SNF2 the importance of the NR box motif is indicated by its presence in a wide variety of nuclear receptor coregulators, including E3 ubiqutin-protein ligases (Section ).

Part of the Handbook of Experimental Pharmacology book series (HEP, volume ) Abstract. Within the past two decades, coregulators have emerged as essential chromatin components of metabolic signaling by nuclear receptors and additional metabolite-sensing transcription factors.

Giudici M., Goni S., Fan R., Treuter E. () Nuclear. Nuclear Receptor Coactivators. A diverse group of proteins have emerged as potential coactivators for nuclear receptors.

Ligand-dependent recruitment of coactivators is dependent on AF-2, which consists of a short conserved helical sequence within the C terminus of the LBD ().Biochemical and expression cloning approaches have been used to identify a large number of factors that interact with.

First published inVitamins and Hormones is the longest-running serial published by Academic Press. In the early days of the Serial, the subjects of vitamins and hormones were quite distinct.

The Editorial Board now reflects expertise in the field of hormone action, vitamin action, X-ray crystal structure, physiology, and enzyme mechanisms. Under the capable and qualified. p68 is a novel nuclear AR-interacting protein in PCa cells. The conserved helicase core (amino acids –) of the p68 DEAD box RNA helicase was identified as a positive clone during a yeast two-hybrid screen for novel AR-interacting partners.

This book serves as a treasure for all those who have an interest in nuclear receptor coregulators and human diseases.

Written by experts in the field, each chapter provides comprehensive, up-to-date information on the physiologic and pathologic roles of coregulators in specific organ systems, giving biomedical students; basic and clinical. The estrogen receptor (ER), a member of the nuclear hormone receptor superfamily, is a hormone-regulated transcription factor that mediates the effects of estrogens and antiestrogens in breast cancer and other estrogen target cells.

Because of the role of estrogens in promoting the growth and progression of breast cancer, there is great interest in exploring ways to functionally inactivate the. Nuclear receptors have the ability to directly bind to DNA and regulate the expression of adjacent genes, hence these receptors are classified as transcription factors.

The regulation of gene expression by nuclear receptors generally only happens when a ligand — a molecule that affects the receptor's behavior — is present. More specifically, ligand binding to a nuclear receptor results in.

Nuclear receptor coregulators merge transcriptional coregulation with epigenetic regulation Shigeaki Kato1,2, Atsushi Yokoyama1,2 and Ryoji Fujiki1,2 1Institute of Molecular and Cellular Biosciences, University of Tokyo, Yayoi, Bunkyo-ku, TokyoJapan 2ERATO, Japan Science and Technology Agency, Honcho, Kawaguchishi, SaitamaJapan.

Endocrine reviews, ISSN, Vol Issue 2, pp. - Most coregulators are, by definition, rate limiting for nuclear receptor activation and repression, but do not significantly alter basal transcription. Recent data have indicated multiple modes of action of coregulators, including direct interactions with basal transcription factors and covalent modification of histones and other proteins.

Nuclear receptor pharmacology has, to a certain extent, led the way, compared with other receptor systems, in the appreciation that ligands may exert very diverse pharmacology, based on their individual chemical structure and the allosteric changes induced in the receptor/accessory protein complex.

This can lead to very selective pharmacological effects, which may not necessarily be predicted. Olivia B. Yu, Leggy A. Arnold, in Vitamin D (Fourth Edition), Abstract. Nuclear receptor coregulators (coactivators and corepressors) play an essential part in nuclear receptor-mediated transcription.

Depending on their amino acid sequence, they can bind the vitamin D receptor (VDR) in the presence or absence of ligand and enable activation or repression of gene transcription. Introduction.

The ability of nuclear receptors to alternate between activation and repression in response to specific molecular cues, is now known to be attributable in large part to a diverse group of cellular factors, collectively termed coregulators and including coactivators and study of nuclear receptors owed a debt to decades of historical endocrinology and pathology.

Get this from a library. Nuclear receptor coregulators. [Gerald Litwack;] -- First published inVitamins and Hormones is the longest-running serial published by Academic Press.

In the early days of the Serial, the subjects of vitamins and hormones were quite distinct. ISBN: OCLC Number: Description: xv, pages: illustrations ; 24 cm. Contents: 1. Gene silencing by nuclear orphan receptors structure and function of the glucocorticoid receptor ligand binding domain Nuclear receptor recruitment of histone-modifying enzymes to target gene promoters Corepressor recruitment by agonist-bound nuclear receptors   It has been only 12 years since the first nuclear receptor coactivator, SRC-1, was cloned and discovered to be a new form of transcription factor that, rather than binding to DNA, binds to nuclear receptors (NRs) and mediates the transcriptional potency of NRs (1, 2).The NR coactivators belong to a class of molecules generally termed ‘coregulators’ ().

Coregulators (coactivators and corepressors) occupy the driving seat for actions of all nuclear receptors, and consequently, selective receptor modulator drugs. The potency and selectivity for subreactions of transcription reside in the coactivators, and thus, they are critically important for tissue-selective gene function.

Each tissue has a “quantitative finger print” of coactivators. Nuclear Receptors as Drug Targets: New Developments in Coregulators, Orphan Receptors and Major Therapeutic Areas. Expert Opinion on Therapeutic Targets: Vol.

7, No. 5, pp. Introduction. Nuclear receptors (NRs) represent the largest family of metazoan transcription factors and function as ligand-dependent sensors for a diverse set of fat-soluble hormones, vitamins, and dietary lipids [].NRs and their ligands mediate the expression of genes involved in a broad range of reproductive, developmental, metabolic and immune response programs.

Nuclear Receptor Coregulators. The transcriptional activity of AR and PPAR is influenced by the recruitment of coregulator proteins. These include coactivators, which enhance receptor transcriptional activity, and corepressors, which suppress receptor-mediated transcription.

vol. 68, no. 13, pp. –, Nuclear receptors (NRs) precisely control the gene regulation throughout the development of the central nervous system, including the cerebellum. Functionally, the full activity of NRs requires their cognate coregulators to be recruited by NRs and modulate the activation or repression of target gene expression.

Recent progress of in vitro studies of NR coregulators has revealed that NR. The nuclear receptor superfamily comprises a large group of transcription factors that play a key regulatory role in development and homeostasis of multicellular organisms.

A special feature of nuclear receptors is their ability to bind to condensed chromatin templates, which makes them important initiators of gene transcription.Members of the nuclear steroid/thyroid hormone receptor (NR) gene superfamily are DNA-binding transcription factors that regulate target genes in a spatiotemporal manner, depending on the promoter context.

In vivo observations of ligand responses in NR-mediated gene regulation led to the identification of ligand-dependent coregulators that directly interact with NRs.The nuclear receptor superfamily: a personal retrospect on the first two decades.

Mol Endocrinol. ; – Crossref Medline Google Scholar; 11 O'Malley B. The Year in Basic Science: nuclear receptors and coregulators. Mol Endocrinol. ; – Crossref Medline Google Scholar.