Chapin S J, Bulinski J C
Department of Biology, University of California, Los Angeles 90024.
J Cell Sci. 1991 Jan;98 ( Pt 1):27-36. doi: 10.1242/jcs.98.1.27.
A polyclonal antiserum raised against a HeLa cell microtubule-associated protein of Mr 210,000 (210 kD MAP or MAP4), an abundant non-neuronal MAP, was used to isolate cDNA clones encoding MAP4 from a human fetal brain lambda gt11 cDNA expression library. The largest of these clones, pMAP4.245, contains an insert of 4.1 kb and encodes a 245 kD beta-galactosidase fusion protein. Evidence that pMAP4.245 encodes MAP4 sequences includes immunoabsorption of MAP4 antibodies with the pMAP4.245 fusion protein, as well as identity of protein sequences obtained from HeLa 210 kD MAP4 with amino acid sequences encoded by pMAP4.245. The MAP4.245 cDNA hybridizes to several large (approximately 6-9 kb) transcripts on Northern blots of HeLa cell RNA. DNA sequencing of overlapping MAP4 cDNA clones revealed a long open reading frame containing a C-terminal region with three imperfect 18-amino acid repeats; this region is homologous to a motif present in the microtubule (MT)-binding domain of two prominent neuronal MAPs, MAP2 and tau. The pMAP4.245 sequence also encoded a series of unrelated repeats, located in the MAP's projection domain, N-terminal to the MT-binding domain. MAP4.245 fusion proteins bound to MTs in vitro, while fusion proteins that contained only the projection domain repeats failed to bind specifically to MTs. Thus, the major human non-neuronal MAP resembles two neuronal MAPs in its MT-binding domain, while most of the molecule has sequences, and presumably functions, distinct from those of the neuronal MAPs.
一种针对分子量为210,000(210 kD MAP或MAP4)的HeLa细胞微管相关蛋白产生的多克隆抗血清,该蛋白是一种丰富的非神经元MAP,被用于从人胎儿脑λgt11 cDNA表达文库中分离编码MAP4的cDNA克隆。这些克隆中最大的pMAP4.245含有一个4.1 kb的插入片段,并编码一个245 kD的β-半乳糖苷酶融合蛋白。pMAP4.245编码MAP4序列的证据包括用pMAP4.245融合蛋白免疫吸收MAP4抗体,以及从HeLa 210 kD MAP4获得的蛋白质序列与pMAP4.245编码的氨基酸序列相同。MAP4.245 cDNA在HeLa细胞RNA的Northern印迹上与几个大的(约6 - 9 kb)转录本杂交。对重叠的MAP4 cDNA克隆进行DNA测序,发现一个长的开放阅读框,其C端区域有三个不完美的18个氨基酸的重复序列;该区域与两种主要的神经元MAP(MAP2和tau)的微管(MT)结合结构域中存在的基序同源。pMAP4.245序列还编码了一系列不相关的重复序列,位于MAP的投射结构域,在MT结合结构域的N端。MAP4.245融合蛋白在体外与MT结合,而仅包含投射结构域重复序列的融合蛋白不能特异性地与MT结合。因此,主要的人类非神经元MAP在其MT结合结构域与两种神经元MAP相似,而该分子的大部分序列以及推测的功能与神经元MAP不同。