Brd2 is required for cell cycle exit and neuronal differentiation through the E2F1 pathway in mouse neuroepithelial cells.

To understand genetic programs controlling mammalian central nervous system (CNS) development, we have identified one transgene-inserted mutation, which showed embryonic lethality during neurulation. Determination of the transgene integration site and rescue experiments revealed that the Brd2 gene, whose products specifically bind acetylated histone H4 and can mediate transcription, was the cause of this mutation. Expression studies with specific markers demonstrated that cell cycle progression was accelerated and neuronal differentiation as well as cell cycle exit were impaired in Brd2-deficient neruoepithelial cells.

Cell surface heparan sulfate chains regulate local reception of FGF signaling in the mouse embryo.

Heparan sulfate (HS) proteoglycans modulate the activity of multiple growth factors on the cell surface and extracellular matrix. However, it remains unclear how the HS chains control the movement and reception of growth factors into targeted receiving cells during mammalian morphogenetic processes. Here, we found that HS-deficient Ext2 null mutant mouse embryos fail to respond to fibroblast growth factor (FGF) signaling.

Neurons important for the photoperiodic control of diapause in the bean bug, Riptortus pedestris.

The morphology and functions of the brain neurons projecting to the retrocerebral complex were examined in terms of photoperiodic control of adult diapause in the bean bug, Riptortus pedestris. Backfills through the nervi corporis cardiaci stained 15-20 pairs of somata in the pars intercerebralis (PI) with contralateral axons, and 14-24 pairs in the pars lateralis (PL) with ipsilateral axons to the nervi corporis cardiaci. In the PL, two clusters of somata, PL-d and PL-v, were found.

Crucial roles of Foxa2 in mouse anterior-posterior axis polarization via regulation of anterior visceral endoderm-specific genes.

Anterior visceral endoderm (AVE) plays essential roles with respect to anterior-posterior axis development in the early mouse embryo. To assess the genetic cascade involved in AVE formation, the cis-regulatory elements directing expression of vertebrate Otx2 genes in the AVE were analyzed via generation of transgenic mice. Otx2 expression in AVE is regulated directly by the forkhead transcription factor, Foxa2.