Mack K, Currie J R, Soifer D
New York State Institute for Basic Research in Developmental Disabilities, College of Staten Island, CUNY.
J Neurosci Res. 1988 May;20(1):129-36. doi: 10.1002/jnr.490200118.
A cDNA library was prepared from rabbit brain mRNA, in the expression vector, lambda gt11. The library was screened with polyclonal antibodies raised against the neurofilament protein NF-H, and a cloned cDNA (KMRH-1) was selected and characterized. The fusion protein coded for by KMRH-1 includes epitopes for two monoclonal antibodies which react with nonphosphorylated sites in the tail region of NF-H. The selected cDNA includes 891 base pairs. It hybridizes to human genomic DNA, as well as to rabbit genomic DNA, and to a rabbit brain mRNA with a size of 4.7 kilobases (kb). The sequence of KMRH-1 includes extensive repeating regions, including one duplicated 60-base segment. Within the first 196 bases, one 13-base segment is repeated 9 times. The cDNA codes for the carboxy-terminal 184 amino acid residues of NF-H, including a series of 9 serines, each surrounded by a similar group of amino acids: ..Ala.Lys.Ser.Pro.(Glu./Val.).Lys.. Comparison of the derived amino acid sequence for KMRH-1 indicates considerable divergence from the sequence information available for rodent NF-H (Robinson et al.: FEBS Lett 209:203-205, 1986). This diversity in amino acid sequence may account for the failure to induce tangles of neurofilaments in animals, such as rats, following treatment with doses of aluminum which are sufficient to induce such tangles in rabbits and to bring on seizures and behavioral pathology in both species.
利用表达载体λgt11从兔脑mRNA制备了一个cDNA文库。用针对神经丝蛋白NF-H产生的多克隆抗体筛选该文库,选择并鉴定了一个克隆的cDNA(KMRH-1)。KMRH-1编码的融合蛋白包含两种单克隆抗体的表位,这两种单克隆抗体与NF-H尾部区域的非磷酸化位点反应。所选的cDNA包含891个碱基对。它能与人基因组DNA以及兔基因组DNA杂交,也能与大小为4.7千碱基(kb)的兔脑mRNA杂交。KMRH-1的序列包含大量重复区域,包括一个重复的60碱基片段。在前196个碱基内,一个13碱基片段重复了9次。该cDNA编码NF-H的羧基末端184个氨基酸残基,包括一系列9个丝氨酸,每个丝氨酸都被一组相似的氨基酸包围:..Ala.Lys.Ser.Pro.(Glu./Val.).Lys.. 对KMRH-1推导的氨基酸序列进行比较表明,它与啮齿动物NF-H的现有序列信息有很大差异(罗宾逊等人:《欧洲生物化学学会联合会快报》209:203 - 205,1986)。氨基酸序列的这种差异可能解释了在用足以在兔中诱导神经丝缠结并在两种动物中引发癫痫和行为病理学的铝剂量处理后,大鼠等动物未能诱导神经丝缠结的原因。