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A whole genome RNAi screen identifies replication stress response genes.
Kavanaugh, Gina; Ye, Fei; Mohni, Kareem N; Luzwick, Jessica W; Glick, Gloria; Cortez, David.
Afiliación
  • Kavanaugh G; Department of Biochemistry, Vanderbilt University Medical Center, Nashville, TN 37232, USA.
  • Ye F; Department of Statistics, Vanderbilt University Medical Center, Nashville, TN 37232, USA.
  • Mohni KN; Department of Biochemistry, Vanderbilt University Medical Center, Nashville, TN 37232, USA.
  • Luzwick JW; Department of Biochemistry, Vanderbilt University Medical Center, Nashville, TN 37232, USA.
  • Glick G; Department of Biochemistry, Vanderbilt University Medical Center, Nashville, TN 37232, USA.
  • Cortez D; Department of Biochemistry, Vanderbilt University Medical Center, Nashville, TN 37232, USA. Electronic address: david.cortez@vanderbilt.edu.
DNA Repair (Amst) ; 35: 55-62, 2015 Nov.
Article en En | MEDLINE | ID: mdl-26454783
ABSTRACT
Proper DNA replication is critical to maintain genome stability. When the DNA replication machinery encounters obstacles to replication, replication forks stall and the replication stress response is activated. This response includes activation of cell cycle checkpoints, stabilization of the replication fork, and DNA damage repair and tolerance mechanisms. Defects in the replication stress response can result in alterations to the DNA sequence causing changes in protein function and expression, ultimately leading to disease states such as cancer. To identify additional genes that control the replication stress response, we performed a three-parameter, high content, whole genome siRNA screen measuring DNA replication before and after a challenge with replication stress as well as a marker of checkpoint kinase signalling. We identified over 200 replication stress response genes and subsequently analyzed how they influence cellular viability in response to replication stress. These data will serve as a useful resource for understanding the replication stress response.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Daño del ADN / Genoma Humano / ARN Interferente Pequeño / Interferencia de ARN / Replicación del ADN Límite: Humans Idioma: En Revista: DNA Repair (Amst) Asunto de la revista: BIOLOGIA MOLECULAR / BIOQUIMICA Año: 2015 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Daño del ADN / Genoma Humano / ARN Interferente Pequeño / Interferencia de ARN / Replicación del ADN Límite: Humans Idioma: En Revista: DNA Repair (Amst) Asunto de la revista: BIOLOGIA MOLECULAR / BIOQUIMICA Año: 2015 Tipo del documento: Article País de afiliación: Estados Unidos