Literature DB >> 21435506

The role of p53 in ribosomopathies.

Stefano Fumagalli1, George Thomas.   

Abstract

Impaired ribosome biogenesis is the underlying cause of the pathological conditions collectively known as ribosomopathies. Several hypotheses have been advanced to explain the mechanisms by which deficiencies in ribosome biogenesis interfere with developmental processes leading eventually to the emergence of these diseases. In recent years it has become clear that perturbation of this process triggers a cell-cycle checkpoint that, through activation of the tumor-suppressor p53, leads to cell-cycle arrest and apoptosis. Indeed, evidence is accumulating from studies in animal models that the unscheduled activation of p53 is responsible for perturbations in tissue homeostasis that cause the development of ribosomopathies such as Treacher-Collins syndrome (TCS) and 5q(-) syndrome. These findings imply that inhibition of p53, or better, of mechanisms that specifically lead to p53 activation in response to inhibition of ribosome biogenesis, could be targeted in the treatment of ribosomopathies where activation of p53 is shown to play a pathogenic role.
Copyright © 2011 Elsevier Inc. All rights reserved.

Entities:  

Mesh:

Substances:

Year:  2011        PMID: 21435506     DOI: 10.1053/j.seminhematol.2011.02.004

Source DB:  PubMed          Journal:  Semin Hematol        ISSN: 0037-1963            Impact factor:   3.851


  47 in total

1.  Transcriptome-Wide Regulation of Key Developmental Pathways in the Mouse Neural Tube by Prenatal Alcohol Exposure.

Authors:  Karen E Boschen; Travis S Ptacek; Jeremy M Simon; Scott E Parnell
Journal:  Alcohol Clin Exp Res       Date:  2020-07-01       Impact factor: 3.455

2.  Suprainduction of p53 by disruption of 40S and 60S ribosome biogenesis leads to the activation of a novel G2/M checkpoint.

Authors:  Stefano Fumagalli; Vasily V Ivanenkov; Teng Teng; George Thomas
Journal:  Genes Dev       Date:  2012-05-15       Impact factor: 11.361

3.  CBFβ-SMMHC regulates ribosomal gene transcription and alters ribosome biogenesis.

Authors:  G Cordonnier; A Mandoli; A Radhouane; G Hypolite; L Lhermitte; M Belhocine; V Asnafi; E Macintyre; J H A Martens; S Fumagalli; J Bond
Journal:  Leukemia       Date:  2017-02-15       Impact factor: 11.528

4.  Deficiency of the ribosome biogenesis gene Sbds in hematopoietic stem and progenitor cells causes neutropenia in mice by attenuating lineage progression in myelocytes.

Authors:  Noemi A Zambetti; Eric M J Bindels; Paulina M H Van Strien; Marijke G Valkhof; Maria N Adisty; Remco M Hoogenboezem; Mathijs A Sanders; Johanna M Rommens; Ivo P Touw; Marc H G P Raaijmakers
Journal:  Haematologica       Date:  2015-07-16       Impact factor: 9.941

Review 5.  Ribosomal proteins: insight into molecular roles and functions in hepatocellular carcinoma.

Authors:  X Xie; P Guo; H Yu; Y Wang; G Chen
Journal:  Oncogene       Date:  2017-09-25       Impact factor: 9.867

6.  Conditional depletion of the RNA polymerase I subunit PAF53 reveals that it is essential for mitosis and enables identification of functional domains.

Authors:  Rachel McNamar; Zakaria Abu-Adas; Katrina Rothblum; Bruce A Knutson; Lawrence I Rothblum
Journal:  J Biol Chem       Date:  2019-11-14       Impact factor: 5.157

7.  5S ribosomal RNA is an essential component of a nascent ribosomal precursor complex that regulates the Hdm2-p53 checkpoint.

Authors:  Giulio Donati; Suresh Peddigari; Carol A Mercer; George Thomas
Journal:  Cell Rep       Date:  2013-07-03       Impact factor: 9.423

8.  Mutual protection of ribosomal proteins L5 and L11 from degradation is essential for p53 activation upon ribosomal biogenesis stress.

Authors:  Sladana Bursać; Maja Cokarić Brdovčak; Martin Pfannkuchen; Ines Orsolić; Lior Golomb; Yan Zhu; Chen Katz; Lilyn Daftuar; Kristina Grabušić; Iva Vukelić; Vedrana Filić; Moshe Oren; Carol Prives; Siniša Volarevic
Journal:  Proc Natl Acad Sci U S A       Date:  2012-11-20       Impact factor: 11.205

Review 9.  Dysregulation of RNA polymerase I transcription during disease.

Authors:  K M Hannan; E Sanij; L I Rothblum; R D Hannan; R B Pearson
Journal:  Biochim Biophys Acta       Date:  2012-11-12

10.  High-throughput transcriptome sequencing identifies candidate genetic modifiers of vulnerability to fetal alcohol spectrum disorders.

Authors:  Ana Garic; Mark E Berres; Susan M Smith
Journal:  Alcohol Clin Exp Res       Date:  2014-06-24       Impact factor: 3.455

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.