The Role of PLAG1 in Mouse Brain Development and Neurogenesis.
Jemma G GasperoniStephanie C TranSylvia V H GrommenBert De GroefSebastian DworkinPublished in: Molecular neurobiology (2024)
The pleomorphic adenoma gene 1 (Plag1) is a transcription factor involved in the regulation of growth and cellular proliferation. Here, we report the spatial distribution and functional implications of PLAG1 expression in the adult mouse brain. We identified Plag1 promoter-dependent β-galactosidase expression in various brain structures, including the hippocampus, cortex, choroid plexus, subcommisural organ, ependymal cells lining the third ventricle, medial and lateral habenulae and amygdala. We noted striking spatial-restriction of PLAG1 within the cornu ammonis (CA1) region of the hippocampus and layer-specific cortical expression, with abundant expression noted in all layers except layer 5. Furthermore, our study delved into the role of PLAG1 in neurodevelopment, focusing on its impact on neural stem/progenitor cell proliferation. Loss of Plag1 resulted in reduced proliferation and decreased production of neocortical progenitors in vivo, although ex vivo neurosphere experiments revealed no cell-intrinsic defects in the proliferative or neurogenic capacity of Plag1-deficient neural progenitors. Lastly, we explored potential target genes of PLAG1 in the cortex, identifying that Neurogenin 2 (Ngn2) was significantly downregulated in Plag1-deficient mice. In summary, our study provides novel insights into the spatial distribution of PLAG1 expression in the adult mouse brain and its potential role in neurodevelopment. These findings expand our understanding of the functional significance of PLAG1 within the brain, with potential implications for neurodevelopmental disorders and therapeutic interventions.
Keyphrases
- poor prognosis
- transcription factor
- signaling pathway
- binding protein
- induced apoptosis
- long non coding rna
- gene expression
- stem cells
- heart failure
- cerebral ischemia
- oxidative stress
- pulmonary hypertension
- resting state
- spinal cord injury
- risk assessment
- climate change
- minimally invasive
- mesenchymal stem cells
- cell death
- dna binding
- mass spectrometry
- bone marrow
- prefrontal cortex
- bioinformatics analysis
- left ventricular