Sakai K, Mitchell D J, Tsukamoto T, Steinman L
Department of Neurology and Neurological Sciences, Stanford University, CA.
Ann Neurol. 1990 Nov;28(5):692-8. doi: 10.1002/ana.410280515.
We isolated a complementary DNA clone encoding a 52-kd protein recognized by an anti-neuronal cell antibody in serum from a patient with paraneoplastic cerebellar degeneration associated with uterine carcinoma. The recombinant protein expressed in prokaryotic cells was specifically recognized by the anti-neuronal cell antibody from the patient, and its molecular weight was identical to that of antigenic proteins in the cerebellum. The deduced protein consisted of 450 amino acids dominated by hydrophilic residues, the calculated relative molecular mass was 51,238, and the predicted value of the isoelectric point was 4.99. This complementary DNA sequence and the deduced protein sequence have not been reported previously, and the sequences showed no homologies with the complimentary DNA or the amino acid sequences in the GenBank, EMBL, or NBRF databases, including the complementary DNA for a 34-kd cerebellar protein (CDR34) that is recognized by an anti-Purkinje cell antibody. Unexpectedly, the transcript of this gene was detected not only in the cerebellum and the brain stem but also in an extraneural tissue, the intestine.
我们从一名患有与子宫癌相关的副肿瘤性小脑变性患者的血清中,分离出了一个编码52-kd蛋白的互补DNA克隆,该蛋白可被抗神经元细胞抗体识别。在原核细胞中表达的重组蛋白被该患者的抗神经元细胞抗体特异性识别,其分子量与小脑中抗原性蛋白的分子量相同。推导的蛋白由450个氨基酸组成,以亲水性残基为主,计算所得的相对分子质量为51238,预测的等电点值为4.99。此前尚未报道过该互补DNA序列和推导的蛋白序列,这些序列与GenBank、EMBL或NBRF数据库中的互补DNA或氨基酸序列均无同源性,包括被抗浦肯野细胞抗体识别的34-kd小脑蛋白(CDR34)的互补DNA。出乎意料的是,该基因的转录本不仅在小脑和脑干中被检测到,还在一种神经外组织——肠道中被检测到。