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

  • 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

Research output: Contribution to journalArticlepeer-review

19 Scopus citations

Abstract

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.

Original languageEnglish
Pages (from-to)827-838
Number of pages12
JournalJournal of Cell Biology
Volume174
Issue number6
DOIs
StatePublished - 11 Sep 2006

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