Lewis S A, Cowan N J
J Cell Biol. 1985 Mar;100(3):843-50. doi: 10.1083/jcb.100.3.843.
A 1.2-kilobase (kb) cDNA clone (NF68) encoding the mouse 68,000-mol-wt neurofilament protein is described. The clone was isolated from a mouse brain cDNA library by low-stringency cross-hybridization with a cDNA probe encoding mouse glial fibrillary acidic protein (Lewis et al., 1984, Proc. Natl. Acad. Sci. USA., 81:2743-2746). The identity of NF68 was established by hybrid selection using mouse brain polyA+ mRNA, and cell-free translation of the selected mRNA species. The cell-free translation product co-migrated with authentic 68,000-mol-wt neurofilament protein on an SDS/polyacrylamide gel, and was immunoprecipitable with a monospecific rabbit anti-bovine neurofilament antiserum. In addition, DNA sequence analysis of NF68 showed 90% homology at the amino acid level compared with the sequence of the porcine 68,000-mol-wt neurofilament protein. At high stringency, NF68 detects a single genomic sequence encoding the mouse 68,000-mol-wt neurofilament protein. Two mRNA species of 2.5 kb and 4.0 kb are transcribed from the single gene in mouse brain. The level of expression of these mRNAs remains almost constant in postnatal mouse brains of all ages and, indeed, in the adult. At reduced stringency, NF68 detects a number of mRNAs that are expressed in mouse brain, one of which encodes the 150,000-mol-wt neurofilament protein. The NF68 probe cross-hybridizes at high stringency with genomic sequences in species as diverse as human, chicken, and (weakly) frog, but not with DNA from Drosophila or sea urchin.
描述了一个编码小鼠68,000道尔顿神经丝蛋白的1.2千碱基(kb)cDNA克隆(NF68)。该克隆是通过与编码小鼠胶质纤维酸性蛋白的cDNA探针进行低严谨度交叉杂交,从小鼠脑cDNA文库中分离得到的(刘易斯等人,1984年,《美国国家科学院院刊》,81:2743 - 2746)。通过使用小鼠脑多聚腺苷酸加尾mRNA进行杂交筛选以及对所选mRNA种类进行无细胞翻译,确定了NF68的身份。无细胞翻译产物在SDS/聚丙烯酰胺凝胶上与真实的68,000道尔顿神经丝蛋白共迁移,并且能用单特异性兔抗牛神经丝抗血清进行免疫沉淀。此外,NF68的DNA序列分析表明,与猪68,000道尔顿神经丝蛋白的序列相比,其氨基酸水平具有90%的同源性。在高严谨度下,NF68检测到一个编码小鼠68,000道尔顿神经丝蛋白的单一基因组序列。在小鼠脑中,从这个单一基因转录出两种mRNA,大小分别为2.5 kb和4.0 kb。这些mRNA的表达水平在所有年龄段的出生后小鼠脑中,实际上在成体中,几乎保持恒定。在降低严谨度时,NF68检测到一些在小鼠脑中表达的mRNA,其中一种编码150,000道尔顿神经丝蛋白。NF68探针在高严谨度下与人类、鸡以及(较弱地)青蛙等不同物种的基因组序列交叉杂交,但不与果蝇或海胆的DNA杂交。