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. 2011 Dec 1;10(23):4026–4031. doi: 10.4161/cc.10.23.18578

Table 1.

Selection of enriched Gene Ontology (GO) terms associated with Ascl1 target genes in ventral telencephalon of developing mouse embryo

GO Number Biological Process Genes p value
GO:0045449 Regulation of transcription 69 1.8 × 10−8
GO:0022008 Neurogenesis 27 5.2 × 10−7
GO:0042136 Neurotransmitter biosynthetic process 3 9.2 × 10−5
GO:0051726 Regulation of cell cycle 11 9.6 × 10−5
GO:0010646 Regulation of cell communication 25 1.1 × 10−4
GO:0016337 Cell-cell adhesion 11 1.1 × 10−4
GO:0030030 Cell projection organization 17 1.2 × 10−4
GO:0009966 Regulation of signal transduction 22 1.8 × 10−4
GO:0006928 Cell motion 18 2.8 × 10−4
GO:0048663 Neuron fate commitment 6 2.8 × 10−4
GO:0007417 Central nervous system development 16 3.1 × 10−4
GO:0007411 Axon guidance 8 3.4 × 10−4
GO:0019226 Transmission of nerve impulse 13 4.0 × 10−4
GO:0007409 Axonogenesis 11 5.0 × 10−4
GO:0016568 Chromatin modification 12 5.2 × 10−4
GO:0007219 Notch signaling pathway 6 8.4 × 10−4
GO:0051960 Regulation of nervous system development 9 8.7 × 10−4
GO:0048667 Cell morphogenesis involved in neuron differentiation 11 8.8 × 10−4

Transcriptional profiling of Ascl1 gain- and loss-of-function, combined with genomic location analysis using ChIP-on-chip, was used to identify 339 direct Ascl1 trasncriptional targets.11 Enriched terms describing biological processes were identified with GoToolbox,12 using a hypergeometric distribution.