Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 2 de 2
Filtrar
Más filtros

Banco de datos
Tipo del documento
País de afiliación
Intervalo de año de publicación
1.
DNA Repair (Amst) ; 4(2): 203-9, 2005 Feb 03.
Artículo en Inglés | MEDLINE | ID: mdl-15590328

RESUMEN

Recently, we developed an in vitro system using human uracil DNA glycosylase (UDG), AP endonuclease (APE), DNA polymerase beta (pol beta) and rotationally positioned DNA containing a single uracil associated with a 'designed' nucleosome, to test short-patch base excision repair (BER) in chromatin. We found that UDG and APE carry out their catalytic activities with reduced efficiency on nucleosome substrates, showing a distinction between uracil facing 'out' or 'in' from the histone surface, while DNA polymerase beta (pol beta) is completely inhibited by nucleosome formation. In this report, we tested the inhibition of BER enzymes by the N-terminal 'tails' of core histones that take part in both inter- and intra-nucleosome interactions, and contain sites of post-translational modifications. Histone tails were removed by limited trypsin digestion of 'donor' nucleosome core particles and histone octamers were exchanged onto a nucleosome-positioning DNA sequence containing a single G:U mismatch. The data indicate that UDG and APE activities are not significantly enhanced with tailless nucleosomes, and the distinction between rotational settings of uracil on the histone surface is unaffected. More importantly, the inhibition of pol beta activity is not relieved by removal of the histone tails, even though these tails interact with DNA in the G:U mismatch region. Finally, inclusion of X-ray cross complement group protein 1 (XRCC1) or Werner syndrome protein (WRN) had no effect on the BER reactions. Thus, additional activities may be required in cells for efficient BER of at least some structural domains in chromatin.


Asunto(s)
Reparación del ADN , Histonas/metabolismo , Nucleosomas/metabolismo , ADN Glicosilasas/metabolismo , ADN Helicasas/metabolismo , ADN Polimerasa beta/antagonistas & inhibidores , ADN Polimerasa beta/metabolismo , ADN-(Sitio Apurínico o Apirimidínico) Liasa/metabolismo , Proteínas de Unión al ADN/metabolismo , Exodesoxirribonucleasas , Histonas/genética , Humanos , RecQ Helicasas , Uracil-ADN Glicosidasa , Helicasa del Síndrome de Werner , Proteína 1 de Reparación por Escisión del Grupo de Complementación Cruzada de las Lesiones por Rayos X
2.
J Infus Nurs ; 25(1): 45-53, 2002.
Artículo en Inglés | MEDLINE | ID: mdl-11840005

RESUMEN

Trauma, sepsis, and burns cause abnormal manifestations in the body. These manifestations can cause alterations in body metabolism, which complicates nutritional management. Goals of nutrition support with assessment modifications for a constantly changing population are reviewed. Patients in such stress states as burns, trauma, and sepsis many times need altered nutrition. This article outlines guidelines for total parenteral formula modification and monitoring, and discusses other complications such as drug interactions with parenteral formulas.


Asunto(s)
Quemaduras/metabolismo , Nutrición Parenteral , Sepsis/metabolismo , Heridas y Lesiones/metabolismo , Quemaduras/terapia , Humanos , Sepsis/terapia , Estrés Fisiológico/metabolismo , Heridas y Lesiones/terapia
SELECCIÓN DE REFERENCIAS
DETALLE DE LA BÚSQUEDA