机构:
INSERM, U964, CNRS,UdS, IGBMC,UMR 7104, BP 10142, F-67404 Illkirch Graffenstaden, Cu De Strasbour, FranceINSERM, U964, CNRS,UdS, IGBMC,UMR 7104, BP 10142, F-67404 Illkirch Graffenstaden, Cu De Strasbour, France
Kalousi, Alkmini
[1
]
Soutoglou, Evi
论文数: 0引用数: 0
h-index: 0
机构:
INSERM, U964, CNRS,UdS, IGBMC,UMR 7104, BP 10142, F-67404 Illkirch Graffenstaden, Cu De Strasbour, FranceINSERM, U964, CNRS,UdS, IGBMC,UMR 7104, BP 10142, F-67404 Illkirch Graffenstaden, Cu De Strasbour, France
Soutoglou, Evi
[1
]
机构:
[1] INSERM, U964, CNRS,UdS, IGBMC,UMR 7104, BP 10142, F-67404 Illkirch Graffenstaden, Cu De Strasbour, France
The continuous threats on genome integrity by endogenous and exogenous sources have rendered cells competent to overcome these challenges by activating DNA repair pathways. A complex network of proteins and their modifications participate in orchestrated signaling cascades, which are induced in response to DNA damage and may determine the choice of repair pathway. In this review, we summarize recent findings in the field of DNA Double Strand Break repair with regard to the positioning of the break in the highly compartmentalized nucleus. We aim to highlight the importance of chromatin state along with the nuclear position of the DNA lesions on the choice of DNA repair pathway and maintenance of genome integrity.
机构:
Loma Linda Vet Affairs Med Ctr, Res Serv 151, Loma Linda, CA 92357 USA
Loma Linda Univ, Med Ctr, Sch Med, Dept Otolaryngol & Head & Neck Surg, Loma Linda, CA USALoma Linda Vet Affairs Med Ctr, Res Serv 151, Loma Linda, CA 92357 USA
机构:
Princeton Univ, Dept Mol Biol, Lewis Thomas Lab, Washington Rd, Princeton, NJ 08544 USAPrinceton Univ, Dept Mol Biol, Lewis Thomas Lab, Washington Rd, Princeton, NJ 08544 USA
Justice, Joshua L.
Cristea, Ileana M.
论文数: 0引用数: 0
h-index: 0
机构:
Princeton Univ, Dept Mol Biol, Lewis Thomas Lab, Washington Rd, Princeton, NJ 08544 USAPrinceton Univ, Dept Mol Biol, Lewis Thomas Lab, Washington Rd, Princeton, NJ 08544 USA