TY - JOUR
T1 - The cytoplasmic Purkinje onconeural antigen cdr2 down-regulates c-Myc function
T2 - Implications for neuronal and tumor cell survival
AU - Okano, Hirotaka J.
AU - Park, Woong Y.
AU - Corradi, John P.
AU - Darnell, Robert B.
PY - 1999/8/15
Y1 - 1999/8/15
N2 - Paraneoplastic cerebellar degeneration (PCD) is a disorder in which breast or ovarian tumors express an onconeural antigen termed cdr2, which normally is expressed in cerebellar Purkinje neurons. This leads to an immune response to cdr2 that is associated with tumor immunity and autoimmune cerebellar degeneration. We have found that cdr2, a cytoplasmic protein harboring a helix-leucine zipper (HLZ) motif, interacts specifically with the HLZ motif of c-Myc. Both proteins colocalize in the cytoplasm of adult cerebellar Purkinje neurons, and coimmunoprecipitate from tumor cell lines and cerebellar extracts, cdr2 down-regulates c-Myc-dependent transcription in cotransfection assays, and redistributes Myc protein in the cytoplasm. Disease antisera from six of six PCD patients specifically blocked the interaction between cdr2 and c-Myc in vitro. These data indicate that cdr2 normally sequesters c-Myc in the neuronal cytoplasm, thereby down-regulating c-Myc activity, and suggest a mechanism whereby inhibition of cdr2 function by autoantibodies in PCD may contribute to Purkinje neuronal death.
AB - Paraneoplastic cerebellar degeneration (PCD) is a disorder in which breast or ovarian tumors express an onconeural antigen termed cdr2, which normally is expressed in cerebellar Purkinje neurons. This leads to an immune response to cdr2 that is associated with tumor immunity and autoimmune cerebellar degeneration. We have found that cdr2, a cytoplasmic protein harboring a helix-leucine zipper (HLZ) motif, interacts specifically with the HLZ motif of c-Myc. Both proteins colocalize in the cytoplasm of adult cerebellar Purkinje neurons, and coimmunoprecipitate from tumor cell lines and cerebellar extracts, cdr2 down-regulates c-Myc-dependent transcription in cotransfection assays, and redistributes Myc protein in the cytoplasm. Disease antisera from six of six PCD patients specifically blocked the interaction between cdr2 and c-Myc in vitro. These data indicate that cdr2 normally sequesters c-Myc in the neuronal cytoplasm, thereby down-regulating c-Myc activity, and suggest a mechanism whereby inhibition of cdr2 function by autoantibodies in PCD may contribute to Purkinje neuronal death.
KW - c-Myc function
KW - Cerebellar degeneration
KW - Leucine zipper protein
KW - Paraneoplastic neurological disease
KW - Purkinje neurons
UR - https://www.scopus.com/pages/publications/0033567137
U2 - 10.1101/gad.13.16.2087
DO - 10.1101/gad.13.16.2087
M3 - Article
C2 - 10465786
AN - SCOPUS:0033567137
SN - 0890-9369
VL - 13
SP - 2087
EP - 2097
JO - Genes and Development
JF - Genes and Development
IS - 16
ER -