4.5 Article

Role of topoisomerase IIβ in the expression of developmentally regulated genes

Journal

MOLECULAR AND CELLULAR BIOLOGY
Volume 26, Issue 21, Pages 7929-7941

Publisher

AMER SOC MICROBIOLOGY
DOI: 10.1128/MCB.00617-06

Keywords

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Funding

  1. NCI NIH HHS [CA102463, CA39662, R01 CA102463, R01 CA039662] Funding Source: Medline
  2. NIGMS NIH HHS [R37 GM024544, R01 GM24544, R01 GM024544] Funding Source: Medline

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Mice lacking topoisomerase II beta (TopII beta) are known to exhibit a perinatal death phenotype. In the current study, transcription profiles of the brains of wild-type and top2 beta knockout mouse embryos were generated. Surprisingly, only a small number (1 to 4%) of genes were affected in top2 beta knockout embryos. However, the expression of nearly 30% of developmentally regulated genes was either up- or down-regulated. By contrast, the expression of genes encoding general cell growth functions and early differentiation markers was not affected, suggesting that TopII beta is not required for early differentiation programming but is specifically required for the expression of developmentally regulated genes at later stages of differentiation. Consistent with this notion, immunohistochemical analysis of brain sections showed that TopII beta and histone deacetylase 2, a known TopII beta-interacting protein, were preferentially expressed in neurons which are in their later stages of differentiation. Chromatin immunoprecipitation analysis of the developing brains revealed TopII beta binding to the 5' region of a number of TopII beta-sensitive genes. Further studies of a TopII beta-sensitive gene, Kcnd2, revealed the presence of TopII beta in the transcription unit with major binding near the promoter region. Together, these results support a role of TopII beta in activation/repression of developmentally regulated genes at late stages of neuronal differentiation.

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