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DNA damage induced during mitosis undergoes DNA repair synthesis.
Gomez Godinez, Veronica; Kabbara, Sami; Sherman, Adria; Wu, Tao; Cohen, Shirli; Kong, Xiangduo; Maravillas-Montero, Jose Luis; Shi, Zhixia; Preece, Daryl; Yokomori, Kyoko; Berns, Michael W.
Afiliação
  • Gomez Godinez V; Institute of Engineering in Medicine, University of California-San Diego, San Diego, California, United States of America.
  • Kabbara S; Department of Developmental and Cell Biology, University of California-Irvine, Irvine, California, United States of America.
  • Sherman A; Beckman Laser Institute, University of California-Irvine, Irvine, California, United States of America.
  • Wu T; Institute of Engineering in Medicine, University of California-San Diego, San Diego, California, United States of America.
  • Cohen S; Beckman Laser Institute, University of California-Irvine, Irvine, California, United States of America.
  • Kong X; Beckman Laser Institute, University of California-Irvine, Irvine, California, United States of America.
  • Maravillas-Montero JL; Department of Biomedical Engineering, University of California-Irvine, Irvine, California, United States of America.
  • Shi Z; Institute of Engineering in Medicine, University of California-San Diego, San Diego, California, United States of America.
  • Preece D; Department of Biological Chemistry, University of California-Irvine, Irvine, California, United States of America.
  • Yokomori K; Department of Physiology, University of California-Irvine, Irvine, California, United States of America.
  • Berns MW; Institute of Engineering in Medicine, University of California-San Diego, San Diego, California, United States of America.
PLoS One ; 15(4): e0227849, 2020.
Article em En | MEDLINE | ID: mdl-32343690
ABSTRACT
Understanding the mitotic DNA damage response (DDR) is critical to our comprehension of cancer, premature aging and developmental disorders which are marked by DNA repair deficiencies. In this study we use a micro-focused laser to induce DNA damage in selected mitotic chromosomes to study the subsequent repair response. Our findings demonstrate that (1) mitotic cells are capable of DNA repair as evidenced by DNA synthesis at damage sites, (2) Repair is attenuated when DNA-PKcs and ATM are simultaneously compromised, (3) Laser damage may permit the observation of previously undetected DDR proteins when damage is elicited by other methods in mitosis, and (4) Twenty five percent of mitotic DNA-damaged cells undergo a subsequent mitosis. Together these findings suggest that mitotic DDR is more complex than previously thought and may involve factors from multiple repair pathways that are better understood in interphase.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: DNA / Fase G1 / Reparo do DNA / Quebras de DNA / Mitose Limite: Animals / Humans Idioma: En Revista: PLoS One Assunto da revista: CIENCIA / MEDICINA Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: DNA / Fase G1 / Reparo do DNA / Quebras de DNA / Mitose Limite: Animals / Humans Idioma: En Revista: PLoS One Assunto da revista: CIENCIA / MEDICINA Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Estados Unidos