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(Received for publication, June 7, 1996, and in revised form, August 15, 1996)
From the Department of Biochemistry, McGill University,
Montreal, Quebec H3G 1Y6, Canada
The aberrant phosphorylation of the neurofilament
high molecular weight subunit (NFH) in the neuronal perikaryon is a
common feature of several neurological diseases. We demonstrated a
strong correlation between hyperphosphorylation of the NFH
carboxyl-terminal domain and activation of stress-activated protein
kinase (SAPK) -
Volume 271, Number 48,
Issue of November 29, 1996
pp. 30404-30409
©1996 by The American Society for Biochemistry and Molecular Biology, Inc.
in PC12 cells. Agents that activated SAPK
in PC12
cells also caused the hyperphosphorylation of perikaryal NFH in
cultured dorsal root ganglion neurons. The NFH carboxyl-terminal domain was phosphorylated by SAPK
in vitro, and the use of
peptide substrates indicated that this event occurred preferentially at
KSPXE motifs. We propose that SAPK
, perhaps in concert
with other SAPKs, is involved in the abnormal phosphorylation of
perikaryal NFH. This finding could lead to new insights into the
etiology of several neurological diseases.
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