keyword
https://read.qxmd.com/read/23899499/trp53-activates-a-global-autophagy-program-to-promote-tumor-suppression
#21
JOURNAL ARTICLE
Daniela Kenzelmann Broz, Laura D Attardi
The mechanisms by which the TP53/TRP53 transcription factor acts as a tumor suppressor remain incompletely understood. To gain new insights into TP53/TRP53 biology, we used ChIP-seq and RNA-seq technologies to define global TRP53 transcriptional networks in primary cells subjected to DNA damage. Intriguingly, we identified a TRP53-regulated autophagy program, which can be coordinately regulated by the TRP53 family members TRP63 and TRP73 in certain settings. While autophagy is not involved in TRP53-dependent cell cycle arrest, it contributes to both TRP53-driven apoptosis in response to DNA damage and TRP53-mediated transformation suppression...
September 2013: Autophagy
https://read.qxmd.com/read/23414597/role-of-p73-in-alzheimer-disease-lack-of-association-in-mouse-models-or-in-human-cohorts
#22
JOURNAL ARTICLE
Badri Vardarajan, David Vergote, Fadel Tissir, Mark Logue, Jing Yang, Nathalie Daude, Kunie Ando, Ekaterina Rogaeva, Joseph Lee, Rong Cheng, Jean-Pierre Brion, Mahdi Ghani, Beipei Shi, Clinton T Baldwin, Satyabrata Kar, Richard Mayeux, Paul Fraser, André M Goffinet, Peter St George-Hyslop, Lindsay A Farrer, David Westaway
BACKGROUND: P73 belongs to the p53 family of cell survival regulators with the corresponding locus Trp73 producing the N-terminally distinct isoforms, TAp73 and DeltaNp73. Recently, two studies have implicated the murine Trp73 in the modulation in phospho-tau accumulation in aged wild type mice and in young mice modeling Alzheimer's disease (AD) suggesting that Trp73, particularly the DeltaNp73 isoform, links the accumulation of amyloid peptides to the creation of neurofibrillary tangles (NFTs)...
February 15, 2013: Molecular Neurodegeneration
https://read.qxmd.com/read/22454401/novel-candidate-genes-of-thyroid-tumourigenesis-identified-in-trk-t1-transgenic-mice
#23
JOURNAL ARTICLE
Katrin-Janine Heiliger, Julia Hess, Donata Vitagliano, Paolo Salerno, Herbert Braselmann, Giuliana Salvatore, Clara Ugolini, Isolde Summerer, Tatjana Bogdanova, Kristian Unger, Gerry Thomas, Massimo Santoro, Horst Zitzelsberger
For an identification of novel candidate genes in thyroid tumourigenesis, we have investigated gene copy number changes in a Trk-T1 transgenic mouse model of thyroid neoplasia. For this aim, 30 thyroid tumours from Trk-T1 transgenics were investigated by comparative genomic hybridisation. Recurrent gene copy number alterations were identified and genes located in the altered chromosomal regions were analysed by Gene Ontology term enrichment analysis in order to reveal gene functions potentially associated with thyroid tumourigenesis...
June 2012: Endocrine-related Cancer
https://read.qxmd.com/read/21661078/structural-scaffold-for-eif4e-binding-selectivity-of-4e-bp-isoforms-crystal-structure-of-eif4e-binding-region-of-4e-bp2-and-its-comparison-with-that-of-4e-bp1
#24
JOURNAL ARTICLE
Ai Fukuyo, Yasuko In, Toshimasa Ishida, Koji Tomoo
To clarify the higher eukaryotic initiation factor 4E (eIF4E) binding selectivity of 4E-binding protein 2 (4E-BP2) than of 4E-BP1, as determined by Trp fluorescence analysis, the crystal structure of the eIF4E binding region of 4E-BP2 in complex with m(7) GTP-bound human eIF4E has been determined by X-ray diffraction analysis and compared with that of 4E-BP1. The crystal structure revealed that the Pro47-Ser65 moiety of 4E-BP2 adopts a L-shaped conformation involving extended and α-helical structures and extends over the N-terminal loop and two different helix regions of eIF4E through hydrogen bonds, and electrostatic and hydrophobic interactions; these features were similarly observed for 4E-BP1...
September 2011: Journal of Peptide Science
https://read.qxmd.com/read/21635812/cyclic-regulation-of-apoptotic-gene-expression-in-the-mouse-oviduct
#25
JOURNAL ARTICLE
Myoungkun Jeoung, Phillip J Bridges
The oviduct is a dynamic structure whose function relies upon cyclic changes in the morphology of both ciliated and secretory luminal epithelial cells. Unfortunately, infection of these epithelial cells by sexually transmitted pathogens can lead to pelvic inflammatory disease, ectopic pregnancies and infertility. The disruption of normal, cyclic apoptosis in the oviducal epithelium appears to be a causal factor of oviducal pathology and therefore, these pathways represent a potential target for diagnosis and therapeutic intervention...
2011: Reproduction, Fertility, and Development
https://read.qxmd.com/read/21467208/ascl1-participates-in-cajal-retzius-cell-development-in-the-neocortex
#26
JOURNAL ARTICLE
Rajiv Dixit, Céline Zimmer, Ronald R Waclaw, Pierre Mattar, Tarek Shaker, Christopher Kovach, Cairine Logan, Kenneth Campbell, François Guillemot, Carol Schuurmans
Cajal-Retzius cells are essential pioneer neurons that guide neuronal migration in the developing neocortex. During development, Cajal-Retzius cells arise from distinct progenitor domains that line the margins of the dorsal telencephalon, or pallium. Here, we show that the proneural gene Ascl1 is expressed in Cajal-Retzius cell progenitors in the pallial septum, ventral pallium, and cortical hem. Using a short-term lineage trace, we demonstrate that it is primarily the Ascl1-expressing progenitors in the pallial septum and ventral pallium that differentiate into Cajal-Retzius cells...
November 2011: Cerebral Cortex
https://read.qxmd.com/read/21368881/p73-deficiency-results-in-impaired-self-renewal-and-premature-neuronal-differentiation-of-mouse-neural-progenitors-independently-of-p53
#27
JOURNAL ARTICLE
L Gonzalez-Cano, M Herreros-Villanueva, R Fernandez-Alonso, A Ayuso-Sacido, G Meyer, J M Garcia-Verdugo, A Silva, M M Marques, M C Marin
The question of how neural progenitor cells maintain its self-renewal throughout life is a fundamental problem in cell biology with implications in cancer, aging and neurodegenerative diseases. In this work, we have analyzed the p73 function in embryonic neural progenitor cell biology using the neurosphere (NS)-assay and showed that p73-loss has a significant role in the maintenance of neurosphere-forming cells in the embryonic brain. A comparative study of NS from Trp73-/-, p53KO, p53KO;Trp73-/- and their wild-type counterparts demonstrated that p73 deficiency results in two independent, but related, phenotypes: a smaller NS size (related to the proliferation and survival of the neural-progenitors) and a decreased capacity to form NS (self-renewal)...
December 16, 2010: Cell Death & Disease
https://read.qxmd.com/read/21029479/rhomboid-homologs-in-mycobacteria-insights-from-phylogeny-and-genomic-analysis
#28
JOURNAL ARTICLE
David P Kateete, Moses Okee, Fred A Katabazi, Alfred Okeng, Jeniffer Asiimwe, Henry W Boom, Kathleen D Eisenach, Moses L Joloba
BACKGROUND: Rhomboids are ubiquitous proteins with diverse functions in all life kingdoms, and are emerging as important factors in the biology of some pathogenic apicomplexa and Providencia stuartii. Although prokaryotic genomes contain one rhomboid, actinobacteria can have two or more copies whose sequences have not been analyzed for the presence putative rhomboid catalytic signatures. We report detailed phylogenetic and genomic analyses devoted to prokaryotic rhomboids of an important genus, Mycobacterium...
October 29, 2010: BMC Microbiology
https://read.qxmd.com/read/20668308/gene-expression-analysis-of-oxidative-stress-and-apoptosis-in-proton-irradiated-rat-retina
#29
JOURNAL ARTICLE
Xiao W Mao, Lora M Green, Tsehay Mekonnen, Nathan Lindsey, Daila S Gridley
UNLABELLED: The aim of this study was to examine the induction of oxidative stress and apoptosis-associated gene expression profiles in retina after proton irradiation exposure at 0.5 to 4 Gy. MATERIALS AND METHODS: One eye of each Sprague-Dawley rat (6 per group) was irradiated with a conformal proton beam to total doses of 0, 0.5, 1 and 4 Gy. Retinal tissues were isolated for characterization of gene expression profiles 6 hours after proton radiation. RESULTS: For oxidative stress, many genes responsible for regulating the production of reactive oxygen species (ROS) were significantly up-regulated (Fmo2, Gpx2, Noxa1 and Sod3) compared to controls...
July 2010: In Vivo
https://read.qxmd.com/read/20581467/%C3%AE-np73%C3%AE-is-oncogenic-in-hepatocellular-carcinoma-by-blocking-apoptosis-signaling-via-death-receptors-and-mitochondria
#30
JOURNAL ARTICLE
André Schuster, Tobias Schilling, Vincenzo De Laurenzi, Andreas F Koch, Sarah Seitz, Frank Staib, Andreas Teufel, Snorri S Thorgeirsson, Peter Galle, Gerry Melino, Wolfgang Stremmel, Peter H Krammer, Martina Müller
BACKGROUND & AIMS: p73 belongs to the p53 family of transcription factors known to regulate cell cycle and apoptosis. The Trp73 gene has two promoters that drive the expression of two major p73 isoform subfamilies: TA and ΔN. In general, TAp73 isoforms show proapoptotic activities, whereas members of the N-terminally truncated (ΔN) p73 subfamily that lack the transactivation domain show antiapoptotic functions. We found that upregulation of ΔNp73 in hepatocellular carcinoma (HCC) correlated with reduced survival...
July 1, 2010: Cell Cycle
https://read.qxmd.com/read/18805989/tap73-knockout-shows-genomic-instability-with-infertility-and-tumor-suppressor-functions
#31
JOURNAL ARTICLE
Richard Tomasini, Katsuya Tsuchihara, Margareta Wilhelm, Masashi Fujitani, Alessandro Rufini, Carol C Cheung, Fatima Khan, Annick Itie-Youten, Andrew Wakeham, Ming-Sound Tsao, Juan L Iovanna, Jeremy Squire, Igor Jurisica, David Kaplan, Gerry Melino, Andrea Jurisicova, Tak W Mak
The Trp53 gene family member Trp73 encodes two major groups of protein isoforms, TAp73 and DeltaNp73, with opposing pro- and anti-apoptotic functions; consequently, their relative ratio regulates cell fate. However, the precise roles of p73 isoforms in cellular events such as tumor initiation, embryonic development, and cell death remain unclear. To determine which aspects of p73 function are attributable to the TAp73 isoforms, we generated and characterized mice in which exons encoding the TAp73 isoforms were specifically deleted to create a TAp73-deficient (TAp73(-/-)) mouse...
October 1, 2008: Genes & Development
https://read.qxmd.com/read/18181650/the-14-3-3-protein-affects-the-conformation-of-the-regulatory-domain-of-human-tyrosine-hydroxylase
#32
JOURNAL ARTICLE
Veronika Obsilova, Eliska Nedbalkova, Jan Silhan, Evzen Boura, Petr Herman, Jaroslav Vecer, Miroslav Sulc, Jan Teisinger, Fred Dyda, Tomas Obsil
Tyrosine hydroxylase (TH) catalyzes the first step in the biosynthesis of catecholamines. Regulation of TH enzyme activity is controlled through the posttranslational modification of its regulatory domain. The regulatory domain of TH can be phosphorylated at four serines (8, 19, 31, and 40) by a variety of protein kinases. Phosphorylation of Ser19 does not by itself increase TH activity but induces its binding to the 14-3-3 protein. That leads to the enhancement of TH activity with a still not fully understood mechanism...
February 12, 2008: Biochemistry
https://read.qxmd.com/read/17664854/association-of-genetic-polymorphisms-of-endothelin-converting-enzyme-1-gene-with-hypertension-in-a-japanese-population-and-rare-missense-mutation-in-preproendothelin-1-in-japanese-hypertensives
#33
JOURNAL ARTICLE
Mariko Banno, Hironori Hanada, Kei Kamide, Yoshihiro Kokubo, Akiko Kada, Jin Yang, Chihiro Tanaka, Shin Takiuchi, Takeshi Horio, Tetsutaro Matayoshi, Hisayo Yasuda, Junko Nagura, Hitonobu Tomoike, Yuhei Kawano, Toshiyuki Miyata
Endothelin-1 (EDN1), a 21-amino acid peptide, is a potent vasoconstrictor with various pharmacological responses. EDN1 is synthesized from a 212-amino acid precursor protein, preproEDN1, through multiple proteolytic steps. Endothelin-converting enzyme (ECE) cleaves a Trp73-Val74 peptide bond in big-EDN1 to give rise to mature EDN1. In this study, we examined the possible association of genetic variations in ECE1 with hypertension in a general Japanese population and searched for missense mutations in and around the EDN1 polypeptide...
June 2007: Hypertension Research: Official Journal of the Japanese Society of Hypertension
https://read.qxmd.com/read/17283130/deregulated-cdc25a-expression-promotes-mammary-tumorigenesis-with-genomic-instability
#34
JOURNAL ARTICLE
Dipankar Ray, Yasuhisa Terao, Peter G Fuhrken, Zhi-Qing Ma, Francesco J DeMayo, Konstantin Christov, Nyla A Heerema, Roberta Franks, Sophia Y Tsai, Eleftherios T Papoutsakis, Hiroaki Kiyokawa
Checkpoint pathways help cells maintain genomic integrity, delaying cell cycle progression in response to various risks of fidelity, such as genotoxic stresses, compromised DNA replication, and impaired spindle control. Cancer cells frequently exhibit genomic instability, and recent studies showed that checkpoint pathways are likely to serve as a tumor-suppressive barrier in vivo. The cell cycle-promoting phosphatase CDC25A is an activator of cyclin-dependent kinases and one of the downstream targets for the CHK1-mediated checkpoint pathway...
February 1, 2007: Cancer Research
https://read.qxmd.com/read/16271312/structural-basis-for-mrna-cap-binding-regulation-of-eukaryotic-initiation-factor-4e-by-4e-binding-protein-studied-by-spectroscopic-x-ray-crystal-structural-and-molecular-dynamics-simulation-methods
#35
JOURNAL ARTICLE
Koji Tomoo, Yasunori Matsushita, Hiroyuki Fujisaki, Fumi Abiko, Xu Shen, Taizo Taniguchi, Hiroo Miyagawa, Kunihiro Kitamura, Kin-ichiro Miura, Toshimasa Ishida
Taking advantage of the Trp73 residue located close to the 4E-BP binding site of eIF4E, the interaction between the 4E-BP isoform and eIF4E was investigated by the Trp fluorescence titration method. Although no significant difference was observed among the association constants of three 4E-BP isoforms, the binding preference of 4E-BP2 over 4E-BP1 and -BP3 was shown, probably due to the effect of a 4E-BP2-specific LDRR (60-63) sequence for the binding with eIF4E. By contrast, surface plasmon resonance (SPR) analyses showed the binding preference of 4E-BP1, although the difference among the isoforms was also not significant...
December 1, 2005: Biochimica et Biophysica Acta
https://read.qxmd.com/read/15545283/ectopic-expression-of-p73alpha-but-not-p73beta-suppresses-myogenic-differentiation
#36
JOURNAL ARTICLE
Chun-Ying Li, Jiangyu Zhu, Jean Y J Wang
The TRP73 gene, a member of the p53 family, encodes several variants through differential splicing and use of alternative promoters. At the N terminus, two different promoters generate the full-length and the DeltaN isoforms, with or without the transactivating domain. At the C terminus, seven isoforms generated through alternative splicing have been cloned. Previous studies have demonstrated that DeltaN-p73 interferes with p73-induced apoptosis. However, there has been no evidence for functional diversity of the C-terminal p73 variants...
January 21, 2005: Journal of Biological Chemistry
https://read.qxmd.com/read/12446441/biochemical-and-functional-characterization-of-rab27a-mutations-occurring-in-griscelli-syndrome-patients
#37
JOURNAL ARTICLE
Gaël Menasche, Jérôme Feldmann, Anne Houdusse, Catherine Desaymard, Alain Fischer, Bruno Goud, Genèvieve de Saint Basile
Rab27a is a member of the Rab family of small GTPase proteins, and thus far is the first member to be associated with a human disease (ie, the Griscelli syndrome type 2). Mutations in the Rab27a gene cause pigment as well as cytotoxic granule transport defects, accounting for the partial albinism and severe immune disorder characteristics of this syndrome. So far, 3 Rab27a missense mutations have been identified. They open a unique opportunity to designate critical structural and functional residues of Rab proteins...
April 1, 2003: Blood
https://read.qxmd.com/read/9119020/processing-of-proendothelin-1-at-the-c-terminus-of-big-endothelin-1-is-essential-for-proteolysis-by-endothelin-converting-enzyme-1-in-vivo
#38
JOURNAL ARTICLE
T Kido, T Sawamura, H Hoshikawa, P D'Orléans-Juste, J B Denault, R Leduc, J Kimura, T Masaki
Production of endothelin-1 is thought to be a three-step process consisting of an initial proteolytic cleavage of the proendothelin-1 precursor to big endothelin-1-Lys-Arg, C-terminal trimming by a carboxypeptidase and further processing of the big endothelin-1 peptide to endothelin-1 by endothelin-converting enzyme (ECE). To further clarify the mechanism of processing in the biosynthesis of endothelin-1, we introduced a point mutation into endothelin-1 cDNA to replace the Arg in the -4 position of the recognition motifs of furin-like convertase in human preproendothelin-1 (Arg49 or Arg89) by Gly...
March 1, 1997: European Journal of Biochemistry
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