Boyce F M, Beggs A H, Feener C, Kunkel L M
Division of Genetics, Children's Hospital, Boston, MA 02115.
Proc Natl Acad Sci U S A. 1991 Feb 15;88(4):1276-80. doi: 10.1073/pnas.88.4.1276.
Dystrophin, the protein product of the Duchenne muscular dystrophy gene, is expressed in brain as well as muscle. The role of dystrophin in the brain is not clear, though one-third of Duchenne muscular dystrophy patients exhibit some degree of mental retardation. We have isolated the genomic region encoding the alternative 5' terminus of dystrophin used in the brain. Primer extension and polymerase chain reaction assays on RNA demonstrate that this region contains an alternative promoter for dystrophin used in the brain. Physical mapping of this region indicates that this brain promoter is located greater than 90 kilobases 5' to the promoter used in muscle and 400 kilobases from exon 2 to which it is spliced. The large physical distance between the promoters, taken together with their known tissue selectivities, suggests that in certain patients a deletion of either dystrophin promoter might give rise to reduced dystrophin expression selective to brain or muscle. We have identified one such individual with specific deletion of the dystrophin muscle promoter, giving rise to Becker muscular dystrophy, and we predict that specific loss of the brain promoter may be one cause of X chromosome-linked mental retardation.
肌营养不良蛋白是杜氏肌营养不良症基因的蛋白质产物,在大脑和肌肉中均有表达。尽管三分之一的杜氏肌营养不良症患者存在一定程度的智力迟钝,但肌营养不良蛋白在大脑中的作用尚不清楚。我们已经分离出了在大脑中使用的编码肌营养不良蛋白可变5'端的基因组区域。对RNA进行引物延伸和聚合酶链反应分析表明,该区域包含大脑中使用的肌营养不良蛋白的一个可变启动子。该区域的物理图谱显示,这个大脑启动子位于肌肉中使用的启动子的5'端超过90千碱基处,且与它所拼接的外显子2相距400千碱基。启动子之间的巨大物理距离,再加上它们已知的组织选择性,表明在某些患者中,任一肌营养不良蛋白启动子的缺失可能会导致大脑或肌肉中肌营养不良蛋白表达的选择性降低。我们已经鉴定出一名个体,其肌营养不良蛋白的肌肉启动子发生了特异性缺失,导致了贝克型肌营养不良症,并且我们预测大脑启动子的特异性缺失可能是X染色体连锁智力迟钝的一个原因。