Lien L L, Boyce F M, Kleyn P, Brzustowicz L M, Menninger J, Ward D C, Gilliam T C, Kunkel L M
Department of Genetics, Harvard Medical School, Boston, MA 02115.
Proc Natl Acad Sci U S A. 1991 Sep 1;88(17):7873-6. doi: 10.1073/pnas.88.17.7873.
A polyclonal antiserum directed against the C-terminal domain of dystrophin was used to isolate a cDNA clone encoding an antigenically cross-reactive protein, microtubule-associated protein 1B (MAP-1B). Physical mapping of the human MAP-1B locus places its chromosomal location at 5q13, in proximity to the spinal muscular atrophy (SMA) locus. SMA is a degenerative disorder primarily affecting motor neurons. Genetic linkage analysis of SMA families using a human dinucleotide repeat polymorphism just 3' of the MAP-1B gene has shown tight linkage to SMA mutations. These mapping data together with the postulated role of MAP-1B in neuronal morphogenesis and its localization in anterior horn motor neurons suggest a possible association with SMA.
一种针对肌营养不良蛋白C末端结构域的多克隆抗血清被用于分离一个编码抗原交叉反应蛋白——微管相关蛋白1B(MAP - 1B)的cDNA克隆。人类MAP - 1B基因座的物理图谱将其染色体定位在5q13,靠近脊髓性肌萎缩症(SMA)基因座。SMA是一种主要影响运动神经元的退行性疾病。使用位于MAP - 1B基因3'端的人类二核苷酸重复多态性对SMA家系进行的遗传连锁分析表明,其与SMA突变紧密连锁。这些定位数据,连同MAP - 1B在神经元形态发生中的假定作用及其在前角运动神经元中的定位,提示其与SMA可能存在关联。