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Double-strand breaks induce short-scale DNA replication and damage amplification in the fully grown mouse oocytes.
Ma, Jun-Yu; Feng, Xie; Xie, Feng-Yun; Li, Sen; Chen, Lei-Ning; Luo, Shi-Ming; Yin, Shen; Ou, Xiang-Hong.
Afiliación
  • Ma JY; Fertility Preservation Lab, Reproductive Medicine Center, Guangdong Second Provincial General Hospital, Guangzhou 510317, China.
  • Feng X; Fertility Preservation Lab, Reproductive Medicine Center, Guangdong Second Provincial General Hospital, Guangzhou 510317, China.
  • Xie FY; The Second School of Clinical Medicine, Southern Medical University, Guangzhou 510515, China.
  • Li S; Fertility Preservation Lab, Reproductive Medicine Center, Guangdong Second Provincial General Hospital, Guangzhou 510317, China.
  • Chen LN; Fertility Preservation Lab, Reproductive Medicine Center, Guangdong Second Provincial General Hospital, Guangzhou 510317, China.
  • Luo SM; Fertility Preservation Lab, Reproductive Medicine Center, Guangdong Second Provincial General Hospital, Guangzhou 510317, China.
  • Yin S; Fertility Preservation Lab, Reproductive Medicine Center, Guangdong Second Provincial General Hospital, Guangzhou 510317, China.
  • Ou XH; College of Life Sciences, Institute of Reproductive Sciences, Qingdao Agricultural University, Qingdao 266109, China.
Genetics ; 218(2)2021 06 24.
Article en En | MEDLINE | ID: mdl-33792683
ABSTRACT
Break-induced replication (BIR) is essential for the repair of DNA double-strand breaks (DSBs) with single ends. DSBs-induced microhomology-mediated BIR (mmBIR) and template-switching can increase the risk of complex genome rearrangement. In addition, DSBs can also induce the multi-invasion-mediated DSB amplification. The mmBIR-induced genomic rearrangement has been identified in cancer cells and patients with rare diseases. However, when and how mmBIR is initiated have not been fully and deeply studied. Furthermore, it is not well understood about the conditions for initiation of multi-invasion-mediated DSB amplification. In the G2 phase oocyte of mouse, we identified a type of short-scale BIR (ssBIR) using the DNA replication indicator 5-ethynyl-2'-deoxyuridine (EdU). These ssBIRs could only be induced in the fully grown oocytes but not the growing oocytes. If the DSB oocytes were treated with Rad51 or Chek1/2 inhibitors, both EdU signals and DSB marker γH2A.X foci would decrease. In addition, the DNA polymerase inhibitor Aphidicolin could inhibit the ssBIR and another inhibitor ddATP could reduce the number of γH2A.X foci in the DSB oocytes. In conclusion, our results showed that DNA DSBs in the fully grown oocytes can initiate ssBIR and be amplified by Rad51 or DNA replication.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Reparación del ADN / Replicación del ADN / Roturas del ADN de Doble Cadena Límite: Animals Idioma: En Revista: Genetics Año: 2021 Tipo del documento: Article País de afiliación: China

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Reparación del ADN / Replicación del ADN / Roturas del ADN de Doble Cadena Límite: Animals Idioma: En Revista: Genetics Año: 2021 Tipo del documento: Article País de afiliación: China