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Proteome changes in autosomal recessive primary microcephaly.
Zaqout, Sami; Mannaa, Atef; Klein, Oliver; Krajewski, Angelika; Klose, Joachim; Luise-Becker, Lena; Elsabagh, Ahmed; Ferih, Khaled; Kraemer, Nadine; Ravindran, Ethiraj; Makridis, Konstantin; Kaindl, Angela M.
Afiliación
  • Zaqout S; Department of Basic Medical Sciences, College of Medicine, QU Health, Qatar University, Doha, Qatar.
  • Mannaa A; Higher Institute of Engineering and Technology, New Borg AlArab City, Alexandria, Egypt.
  • Klein O; Inserm U1192, Laboratoire Protéomique, Réponse Inflammatoire & Spectrométrie de Masse (PRISM), Université de Lille, Lille, France.
  • Krajewski A; BIH Center for Regenerative Therapies BCRT, Charité-Universitätsmedizin Berlin, Berlin, Germany.
  • Klose J; Berlin Institute of Health, Charité-Universitätsmedizin Berlin (BIH), Berlin, Germany.
  • Luise-Becker L; BIH Center for Regenerative Therapies BCRT, Charité-Universitätsmedizin Berlin, Berlin, Germany.
  • Elsabagh A; Berlin Institute of Health, Charité-Universitätsmedizin Berlin (BIH), Berlin, Germany.
  • Ferih K; Charité-Universitätsmedizin, Institute of Human Genetics, Berlin, Germany.
  • Kraemer N; Charité-Universitätsmedizin Berlin, Institute of Cell Biology and Neurobiology, Berlin, Germany.
  • Ravindran E; Charité-Universitätsmedizin Berlin, Center for Chronically Sick Children (Sozialpädiatrisches Zentrum, SPZ), Berlin, Germany.
  • Makridis K; Department of Pediatric Neurology, Charité-Universitätsmedizin, Berlin, Germany.
  • Kaindl AM; Department of Basic Medical Sciences, College of Medicine, QU Health, Qatar University, Doha, Qatar.
Ann Hum Genet ; 87(1-2): 50-62, 2023 03.
Article en En | MEDLINE | ID: mdl-36448252
BACKGROUND/AIM: Autosomal recessive primary microcephaly (MCPH) is a rare and genetically heterogeneous group of disorders characterized by intellectual disability and microcephaly at birth, classically without further organ involvement. MCPH3 is caused by biallelic variants in the cyclin-dependent kinase 5 regulatory subunit-associated protein 2 gene CDK5RAP2. In the corresponding Cdk5rap2 mutant or Hertwig's anemia mouse model, congenital microcephaly as well as defects in the hematopoietic system, germ cells and eyes have been reported. The reduction in brain volume, particularly affecting gray matter, has been attributed mainly to disturbances in the proliferation and survival of early neuronal progenitors. In addition, defects in dendritic development and synaptogenesis exist that affect the excitation-inhibition balance. Here, we studied proteomic changes in cerebral cortices of Cdk5rap2 mutant mice. MATERIAL AND METHODS: We used large-gel two-dimensional gel (2-DE) electrophoresis to separate cortical proteins. 2-DE gels were visualized by a trained observer on a light box. Spot changes were considered with respect to presence/absence, quantitative variation and altered mobility. RESULT: We identified a reduction in more than 30 proteins that play a role in processes such as cell cytoskeleton dynamics, cell cycle progression, ciliary functions and apoptosis. These proteome changes in the MCPH3 model can be associated with various functional and morphological alterations of the developing brain. CONCLUSION: Our results shed light on potential protein candidates for the disease-associated phenotype reported in MCPH3.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Microcefalia Límite: Animals / Humans Idioma: En Revista: Ann Hum Genet Año: 2023 Tipo del documento: Article País de afiliación: Qatar Pais de publicación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Microcefalia Límite: Animals / Humans Idioma: En Revista: Ann Hum Genet Año: 2023 Tipo del documento: Article País de afiliación: Qatar Pais de publicación: Reino Unido