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. Author manuscript; available in PMC: 2020 Oct 3.
Published in final edited form as: Cell. 2019 Oct 3;179(2):373–391.e27. doi: 10.1016/j.cell.2019.09.004

Figure 5. NPAS4 forms excitation pathway-specific heterodimers.

Figure 5.

AD, Stimulation in the alveus.

A, WB analysis of ARNT1, ARNT2, ARNTL1, NPAS4, and β-actin from CA1 lysates. Stimulation, pharmacology, and time post-stimulation are indicated.

B, Quantification of TF expression normalized to β-actin.

C, Co-IP of NPAS4 with ARNT1, ARNT2, or ARNTL1 from lysates in (A).

D, Quantification of Co-IP normalized to IgG.

EH, As in (A–D) but with stimulation in SR.

IL, As in (A–D) but hippocampal lysates from WT mice in HC or indicated times post-EE for 5 min.

M, Schematic of injection of AAV into H11Cas9-FLAG mice and EE.

NQ, As in (I–L) but from H11Cas9-FLAG mice infected with the indicated AAV-sgRNA. Housing and time post-EE is indicated.

*p<0.05, **p<0.01 ***p<0.001. N and statistical tests indexed in Table S1. See also Figure S6.