Doll T, Meichsner M, Riederer B M, Honegger P, Matus A
Friedrich Miescher Institute, Basel, Switzerland.
J Cell Sci. 1993 Oct;106 ( Pt 2):633-9. doi: 10.1242/jcs.106.2.633.
Microtubule-associated protein 2 (MAP2) exists in both high- and low-molecular mass isoforms, each of which has a tubulin-binding domain consisting of 3 imperfect tandem repeats of 31 amino acids containing a more highly conserved 18 amino acid 'core' sequence. We describe here a novel form of low molecular mass MAP2 (MAP2c) that contains an additional 4th repeat of this tubulin-binding motif. Like the 3 previously known repeat sequences, this 4th copy is highly conserved between MAP2 and the two other known members of the same gene family, tau and MAP4. In each of these three genes the additional 4th repeat is inserted between the 1st and 2nd repeats of the 3-repeat form of the molecule. Experiments with brain cell cultures, in which the relative proportions of neurons and glia had been manipulated by drug treatment, showed that 4-repeat MAP2c is associated with glial cells whereas 3-repeat MAP2c is expressed in neurons. Whereas 3-repeat MAP2c is expressed early in development and then declines, the level of 4-repeat MAP2c increases later in development, corresponding to the relatively late differentiation of glial cells compared to neurons. When transfected into non-neuronal cells, the 4-repeat version of MAP2c behaved indistinguishably from the 3-repeat form in stabilising and rearranging cellular microtubules. The presence of an additional 4th repeat of the tubulin-binding motif in all three members of the MAP2 gene family suggests that this variant arose prior to their differentiation from an ancestral gene.
微管相关蛋白2(MAP2)以高分子量和低分子量两种异构体形式存在,每种异构体都有一个微管蛋白结合结构域,该结构域由31个氨基酸的3个不完全串联重复序列组成,其中包含一个更为保守的18个氨基酸的“核心”序列。我们在此描述一种新型的低分子量MAP2(MAP2c),它包含该微管蛋白结合基序的额外第4个重复序列。与之前已知的3个重复序列一样,这个第4个拷贝在MAP2与同一基因家族的另外两个已知成员tau和MAP4之间高度保守。在这三个基因中,额外的第4个重复序列都插入到分子3重复形式的第1个和第2个重复序列之间。对脑细胞培养物进行的实验表明,通过药物处理改变了神经元和神经胶质细胞的相对比例,结果显示4重复的MAP2c与神经胶质细胞相关,而3重复的MAP2c在神经元中表达。3重复的MAP2c在发育早期表达,随后下降,而4重复的MAP2c水平在发育后期升高,这与神经胶质细胞相对于神经元较晚分化相对应。当转染到非神经元细胞中时,4重复版本的MAP2c在稳定和重排细胞微管方面与3重复形式的表现没有区别。MAP2基因家族的所有三个成员中都存在微管蛋白结合基序的额外第4个重复序列,这表明这种变体在它们从一个祖先基因分化之前就已经出现了。