Okano H J, Park W Y, Corradi J P, Darnell R B
Laboratory of Molecular Neuro-Oncology, The Rockefeller University, New York, New York 10021 USA.
Genes Dev. 1999 Aug 15;13(16):2087-97. doi: 10.1101/gad.13.16.2087.
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.
副肿瘤性小脑变性(PCD)是一种疾病,其中乳腺或卵巢肿瘤表达一种名为cdr2的肿瘤神经抗原,该抗原通常在小脑浦肯野神经元中表达。这会引发针对cdr2的免疫反应,该反应与肿瘤免疫和自身免疫性小脑变性相关。我们发现,cdr2是一种含有螺旋-亮氨酸拉链(HLZ)基序的细胞质蛋白,它与c-Myc的HLZ基序特异性相互作用。这两种蛋白在成年小脑浦肯野神经元的细胞质中共定位,并能从肿瘤细胞系和小脑提取物中共同免疫沉淀。在共转染实验中,cdr2下调c-Myc依赖性转录,并使Myc蛋白重新分布到细胞质中。来自六名PCD患者的疾病抗血清在体外特异性阻断了cdr2与c-Myc之间的相互作用。这些数据表明,cdr2通常在神经元细胞质中隔离c-Myc,从而下调c-Myc活性,并提示了一种机制,即PCD中自身抗体对cdr2功能的抑制可能导致浦肯野神经元死亡。