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Mechanisms and consequences of aneuploidy and chromosome instability in the aging brain.
Andriani, Grasiella A; Vijg, Jan; Montagna, Cristina.
Afiliação
  • Andriani GA; Department of Genetics, Albert Einstein College of Medicine, Yeshiva University, Bronx, NY 10461, USA.
  • Vijg J; Department of Genetics, Albert Einstein College of Medicine, Yeshiva University, Bronx, NY 10461, USA; Department Ophthalmology and Visual Science, Albert Einstein College of Medicine, Yeshiva University, Bronx, NY 10461, USA; Department of Obstetrics & Gynecology and Women's Health, Albert Einstein College of Medicine, Yeshiva University, Bronx, NY 10461, USA.
  • Montagna C; Department of Genetics, Albert Einstein College of Medicine, Yeshiva University, Bronx, NY 10461, USA; Department of Pathology, Albert Einstein College of Medicine, Yeshiva University, Bronx, NY 10461, USA. Electronic address: cristina.montagna@einstein.yu.edu.
Mech Ageing Dev ; 161(Pt A): 19-36, 2017 01.
Article em En | MEDLINE | ID: mdl-27013377
Aneuploidy and polyploidy are a form of Genomic Instability (GIN) known as Chromosomal Instability (CIN) characterized by sporadic abnormalities in chromosome copy numbers. Aneuploidy is commonly linked to pathological states. It is a hallmark of spontaneous abortions and birth defects and it is observed virtually in every human tumor, therefore being generally regarded as detrimental for the development or the maturation of tissues under physiological conditions. Polyploidy however, occurs as part of normal physiological processes during maturation and differentiation of some mammalian cell types. Surprisingly, high levels of aneuploidy are present in the brain, and their frequency increases with age suggesting that the brain is able to maintain its functionality in the presence of high levels of mosaic aneuploidy. Because somatic aneuploidy with age can reach exceptionally high levels, it is likely to have long-term adverse effects in this organ. We describe the mechanisms accountable for an abnormal DNA content with a particular emphasis on the CNS where cell division is limited. Next, we briefly summarize the types of GIN known to date and discuss how they interconnect with CIN. Lastly we highlight how several forms of CIN may contribute to genetic variation, tissue degeneration and disease in the CNS.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Encéfalo / Envelhecimento / Doenças Neurodegenerativas / Instabilidade Cromossômica / Aneuploidia Idioma: En Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Encéfalo / Envelhecimento / Doenças Neurodegenerativas / Instabilidade Cromossômica / Aneuploidia Idioma: En Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Estados Unidos