PKA-activated ApAF–ApC/EBP heterodimer is a key downstream effector of ApCREB and is necessary and sufficient for the consolidation of long-term facilitation

نویسندگان

  • Jin-A Lee
  • Sue-Hyun Lee
  • Changhoon Lee
  • Deok-Jin Chang
  • Yong Lee
  • Hyoung Kim
  • Ye-Hwang Cheang
  • Hyoung-Gon Ko
  • Yong-Seok Lee
  • Heejung Jun
  • Dusan Bartsch
  • Eric R. Kandel
  • Bong-Kiun Kaang
چکیده

Long-term memory requires transcriptional regulation by a combination of positive and negative transcription factors. Aplysia activating factor (ApAF) is known to be a positive transcription factor that forms heterodimers with ApC/EBP and ApCREB2. How these heterodimers are regulated and how they participate in the consolidation of long-term facilitation (LTF) has not, however, been characterized. We found that the functional activation of ApAF required phosphorylation of ApAF by PKA on Ser-266. In addition, ApAF lowered the threshold of LTF by forming a heterodimer with ApCREB2. Moreover, once activated by PKA, the ApAF-ApC/EBP heterodimer transactivates enhancer response element-containing genes and can induce LTF in the absence of CRE- and CREB-mediated gene expression. Collectively, these results suggest that PKA-activated ApAF-ApC/EBP heterodimer is a core downstream effector of ApCREB in the consolidation of LTF.

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عنوان ژورنال:
  • The Journal of Cell Biology

دوره 174  شماره 

صفحات  -

تاریخ انتشار 2006