Skip to main content
. Author manuscript; available in PMC: 2017 Dec 1.
Published in final edited form as: Acta Neuropathol. 2016 Oct 26;132(6):859–873. doi: 10.1007/s00401-016-1637-y

Table 1.

Functional pathways of TDP-43-associated RNAs most likely to exert a meaningful effect on neurons

Gene RNA fold change (TDPKO vs. ctrl) Pathway
Cacna1b −2.5 Synaptic
Dlg3 −2.7 Synaptic
Pitpnm3 −2.4 Synaptic
Ralgps2 −2.6 Synaptic
Vps13d −2.4 Synaptic
Mrps6 −1.6 Mitochondrial
Tecpr1 −4 Autophagy
Crem −2.5 General signaling
Brms1l −2.1 Transcription/translation
Celf5 −2.4 Transcription/translation
Abr −2.9 Unclear

RNAs were selected if their absolute value fold change >1.5 in TDP-43 KO brains compared to control. Pathways in bold have been strongly implicated in the early pathogenesis of AD. The RNA sequencing data were generated from 3-month cT mice [26], and the associated functional pathways in neurons were identified using GeneCards and confirmed by the manual literature search