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. 2014 Jan 20;9(1):e85518. doi: 10.1371/journal.pone.0085518

Table 2. Ten identified midline and tracheal enhancers.

Gene Size1 Position2 Tissue Midline cells3 Tracheal cells4
CG33275 753 exon 5+ intron 5 midline glia (st. 13)
1297/265 intron 5 trachea all (st. 11)/fusion cells (st. 13)
esg 3092 ∼ 5 kb downstream midline glia, MNB and progeny (st.12)
3586 downstream trachea larval fusion cells (1st instar)
3468 ∼ 20 kb downstream trachea larval fusion cells; secondary branches (1st instar)
liprin γ 889/182 intron 1 both glia (st. 12)/glia and sporadic in MNB and progeny (st. 12) DT(st. 15)/all (st. 13)
Net 797 ∼ 10 kb downstream both mostly glia (st. 12) all but DT (st. 12)
comm 443 3′ untranslatedregion both all midline cells (st. 10) larval dorsal trunk and some secondary branches (st. 17)
moody 1221 intron 1 trachea posterior DT (st. 15)
Ect3 517 upstream of Ect3/intron 1 of Tk midline glia, MP1s, H cell and H cell sib (st. 10)

1 The size of the minimal fragment with enhancer activity,

2 the position of the enhancer relative to the gene and 3midline and 4tracheal cells that exhibit enhancer activity are indicated.

3,4 The stage of development when reporter expression is first observed is indicated in parentheses. The absence of expression in the midline or trachea is indicated with a dash.