Publications by authors named "L Standaert"

Article Synopsis
  • Researchers discovered that the long noncoding RNA (lncRNA) NEAT1 is a crucial element in the p53 tumor suppressor pathway that affects how cells respond to stress.
  • When p53 is activated, it leads to the formation of paraspeckles, which are structures in the nucleus, and silencing NEAT1 makes cancer-prone cells more susceptible to cell death and reduces tumor growth.
  • Targeting NEAT1 in cancer treatments shows promise for improving the effectiveness of chemotherapy and therapies that reactivate p53, highlighting its role in cancer progression.
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Neat1 is a non-protein-coding RNA that serves as an architectural component of the nuclear bodies known as paraspeckles. Although cell-based studies indicate that Neat1 is a crucial regulator of gene expression, its physiological relevance remains unclear. Here, we find that Neat1 knockout (KO) mice stochastically fail to become pregnant despite normal ovulation.

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The lncRNA Neat1 is an essential architectural component of paraspeckle nuclear bodies. Although cell-based studies identified Neat1-paraspeckles as key regulators of gene expression through retention of hyperdited mRNAs and/or transcription factors, it is unclear under which specific physiological conditions paraspeckles are formed in vivo and whether they have any biological relevance. Herein, we show that paraspeckles are assembled in luminal epithelial cells during mammary gland development.

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Identifying master regulators of biological processes and mapping their downstream gene networks are key challenges in systems biology. We developed a computational method, called iRegulon, to reverse-engineer the transcriptional regulatory network underlying a co-expressed gene set using cis-regulatory sequence analysis. iRegulon implements a genome-wide ranking-and-recovery approach to detect enriched transcription factor motifs and their optimal sets of direct targets.

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