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Pregled bibliografske jedinice broj: 352233

The p53 tumor suppressor causes congenital malformations in Rpl24-deficient mice and promotes their survival


Barkić, Martina; Crnomarković, Slađana; Grabušić, Kristina; Bogetić, Ivana; Panić, Linda; Tamarut, Sanda; Cokarić, Maja; Jerić, Ines; Vidak, Sandra; Volarević, Siniša
The p53 tumor suppressor causes congenital malformations in Rpl24-deficient mice and promotes their survival // Molecular and cellular biology, 29 (2009), 10; 2489-2504 doi:10.1128/MCB.01588-08 (međunarodna recenzija, članak, znanstveni)


CROSBI ID: 352233 Za ispravke kontaktirajte CROSBI podršku putem web obrasca

Naslov
The p53 tumor suppressor causes congenital malformations in Rpl24-deficient mice and promotes their survival

Autori
Barkić, Martina ; Crnomarković, Slađana ; Grabušić, Kristina ; Bogetić, Ivana ; Panić, Linda ; Tamarut, Sanda ; Cokarić, Maja ; Jerić, Ines ; Vidak, Sandra ; Volarević, Siniša

Izvornik
Molecular and cellular biology (0270-7306) 29 (2009), 10; 2489-2504

Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni

Ključne riječi
ribosomal protein L24; cell cycle; cell growth; mouse embryonic development; p53 checkpoint control

Sažetak
Hypomorphic mutation in one allele of ribosomal protein l24 gene (Rpl24) is responsible for the Belly Spot and Tail (Bst) mouse, which suffers from defects of the eye, skeleton, and coat pigmentation. It has been hypothesized that these pathological manifestations result exclusively from faulty protein synthesis. Herein, we demonstrate that up-regulation of the p53 tumor suppressor during the restricted period of embryonic development significantly contributes to the Bst phenotype. However, in the absence of p53 a large majority of Rpl24Bst/+ embryos die. We showed that p53 promotes survival of these mice via p21-dependent mechanism. Our results imply that activation of a p53-dependent checkpoint mechanism in response to various RP deficiencies might play a role in the pathogenesis of congenital malformations in humans.

Izvorni jezik
Engleski

Znanstvena područja
Biologija

Napomena
Rad je kao poster prezentiran na skupu Congress of the Croatian Society of Biochemistry and Molecular Biology with international participation (HDBMB 2008), održanom od 17.-20.09.2008., Osijek, Hrvatska ; objavljen je u Knjizi sazetaka / Ivica Strelec ; Ljubica Glavaš-Obrovac (ur.) ; Zagreb : Croatian Society of Biochemistry and Molecular Biology, 2008 ; str. 75-75 ; ISBN 978-953-95551-2-0.



POVEZANOST RADA


Projekti:
062-1081347-0370 - Odgovor stanica sisavaca na pogrešku u sintezi ribozoma in vivo (Volarević, Siniša, MZOS ) ( CroRIS)

Ustanove:
Medicinski fakultet, Rijeka

Poveznice na cjeloviti tekst rada:

doi

Citiraj ovu publikaciju:

Barkić, Martina; Crnomarković, Slađana; Grabušić, Kristina; Bogetić, Ivana; Panić, Linda; Tamarut, Sanda; Cokarić, Maja; Jerić, Ines; Vidak, Sandra; Volarević, Siniša
The p53 tumor suppressor causes congenital malformations in Rpl24-deficient mice and promotes their survival // Molecular and cellular biology, 29 (2009), 10; 2489-2504 doi:10.1128/MCB.01588-08 (međunarodna recenzija, članak, znanstveni)
Barkić, M., Crnomarković, S., Grabušić, K., Bogetić, I., Panić, L., Tamarut, S., Cokarić, M., Jerić, I., Vidak, S. & Volarević, S. (2009) The p53 tumor suppressor causes congenital malformations in Rpl24-deficient mice and promotes their survival. Molecular and cellular biology, 29 (10), 2489-2504 doi:10.1128/MCB.01588-08.
@article{article, author = {Barki\'{c}, Martina and Crnomarkovi\'{c}, Sla\djana and Grabu\v{s}i\'{c}, Kristina and Bogeti\'{c}, Ivana and Pani\'{c}, Linda and Tamarut, Sanda and Cokari\'{c}, Maja and Jeri\'{c}, Ines and Vidak, Sandra and Volarevi\'{c}, Sini\v{s}a}, year = {2009}, pages = {2489-2504}, DOI = {10.1128/MCB.01588-08}, keywords = {ribosomal protein L24, cell cycle, cell growth, mouse embryonic development, p53 checkpoint control}, journal = {Molecular and cellular biology}, doi = {10.1128/MCB.01588-08}, volume = {29}, number = {10}, issn = {0270-7306}, title = {The p53 tumor suppressor causes congenital malformations in Rpl24-deficient mice and promotes their survival}, keyword = {ribosomal protein L24, cell cycle, cell growth, mouse embryonic development, p53 checkpoint control} }
@article{article, author = {Barki\'{c}, Martina and Crnomarkovi\'{c}, Sla\djana and Grabu\v{s}i\'{c}, Kristina and Bogeti\'{c}, Ivana and Pani\'{c}, Linda and Tamarut, Sanda and Cokari\'{c}, Maja and Jeri\'{c}, Ines and Vidak, Sandra and Volarevi\'{c}, Sini\v{s}a}, year = {2009}, pages = {2489-2504}, DOI = {10.1128/MCB.01588-08}, keywords = {ribosomal protein L24, cell cycle, cell growth, mouse embryonic development, p53 checkpoint control}, journal = {Molecular and cellular biology}, doi = {10.1128/MCB.01588-08}, volume = {29}, number = {10}, issn = {0270-7306}, title = {The p53 tumor suppressor causes congenital malformations in Rpl24-deficient mice and promotes their survival}, keyword = {ribosomal protein L24, cell cycle, cell growth, mouse embryonic development, p53 checkpoint control} }

Časopis indeksira:


  • Current Contents Connect (CCC)
  • Web of Science Core Collection (WoSCC)
    • Science Citation Index Expanded (SCI-EXP)
    • SCI-EXP, SSCI i/ili A&HCI
  • Scopus
  • MEDLINE


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