Publications by authors named "R Pocock"

Nuclear factor Y is a ubiquitous heterotrimeric transcription factor complex conserved across eukaryotes that binds to CCAAT boxes, one of the most common motifs found in gene promoters and enhancers. Over the last 30 years, research has revealed that the nuclear factor Y complex controls many aspects of brain development, including differentiation, axon guidance, homeostasis, disease, and most recently regeneration. However, a complete understanding of transcriptional regulatory networks, including how the nuclear factor Y complex binds to specific CCAAT boxes to perform its function remains elusive.

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Article Synopsis
  • Oncogenes can become activated through mechanisms like enhancer hijacking and mutations that generate new enhancers or promoters, helping researchers understand variations in noncoding cancer genomes.
  • A new mechanism is identified where the loss of an intronic element in the FTO gene causes abnormal expression of the IRX3 oncogene in T cell acute lymphoblastic leukemia (T-ALL).
  • The study suggests that 'promoter tethering' helps keep oncogenes inactive by linking them to non-functioning parts of the genome, which may act as a safeguard against tumor development.
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Fertility requires the faithful proliferation of germ cells and their differentiation into gametes. Controlling these cellular states demands precise timing and expression of gene networks. Nucleic acid binding proteins (NBPs) play critical roles in gene expression networks that influence germ cell development.

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Neurons coordinate inter-tissue protein homeostasis to systemically manage cytotoxic stress. In response to neuronal mitochondrial stress, specific neuronal signals coordinate the systemic mitochondrial unfolded protein response (UPR) to promote organismal survival. Yet, whether chemical neurotransmitters are sufficient to control the UPR in physiological conditions is not well understood.

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