Por favor, use este identificador para citar o enlazar a este item: http://hdl.handle.net/10261/25055
COMPARTIR / EXPORTAR:
logo share SHARE logo core CORE BASE
Visualizar otros formatos: MARC | Dublin Core | RDF | ORE | MODS | METS | DIDL | DATACITE

Invitar a revisión por pares abierta
Título

Inactivation of the polycomb group protein Ring1B unveils an antiproliferative role in hematopoietic cell expansion and cooperation with tumorigenesis associated with Ink4a deletion

AutorCalés, Carmela CSIC ORCID; Román-Trufero, Mónica CSIC; Pavón, Leticia; Serrano, Iván CSIC; Melgar, Teresa CSIC
Fecha de publicaciónfeb-2008
EditorAmerican Society for Microbiology
CitaciónMolecular and Cellular Biology 28(3): 1018-1028 (2008)
ResumenPolycomb group (PcG) proteins act as positive regulators of cell proliferation. Ring1B is a PcG gene essential for embryonic development, but its contribution to cell turnover in regenerating tissues in not known. Here, we have generated a conditional mouse mutant line to study the Ring1B role in adult hematopoiesis. Mutant mice developed a hypocellular bone marrow that paradoxically contained an enlarged, hyperproliferating compartment of immature cells, with an intact differentiation potential. These alterations were associated with differential upregulation of cyclin D2, which occurred in all mutant bone marrow cells, and of p16(Ink4a), observed only in the differentiated compartment. Concurrent inactivation of Ink4a rescued the defective proliferation of maturing cells but did not affect the hyperproliferative activity of progenitors and resulted in a shortening of the onset of lymphomas induced by Ink4a inactivation. These data show that Ring1B restricts the progenitors' proliferation and promotes the proliferation of their maturing progeny by selectively altering the expression pattern of cell cycle regulators along hematopoietic differentiation. The novel antiproliferative role of Ring1B's downregulation of a cell cycle activator may play an important role in the tight control of hematopoietic cell turnover.
Descripción11 pages, 7 figures.-- et al.
Versión del editorhttp://dx.doi.org/10.1128/MCB.01136-07
URIhttp://hdl.handle.net/10261/25055
DOI10.1128/MCB.01136-07
ISSN0270-7306
Aparece en las colecciones: (CIB) Artículos
(IIBM) Artículos




Ficheros en este ítem:
Fichero Descripción Tamaño Formato
Calés -et-el-MCB_2008.pdf482,89 kBAdobe PDFVista previa
Visualizar/Abrir
Mostrar el registro completo

CORE Recommender

PubMed Central
Citations

40
checked on 01-abr-2024

SCOPUSTM   
Citations

77
checked on 16-abr-2024

WEB OF SCIENCETM
Citations

77
checked on 27-feb-2024

Page view(s)

379
checked on 18-abr-2024

Download(s)

299
checked on 18-abr-2024

Google ScholarTM

Check

Altmetric

Altmetric


Artículos relacionados:


NOTA: Los ítems de Digital.CSIC están protegidos por copyright, con todos los derechos reservados, a menos que se indique lo contrario.