Sossey-Alaoui K, Srivastava A K
J. C. Self Research Institute of Human Genetics, Greenwood Genetic Center, Greenwood, South Carolina, 29646, USA.
Genomics. 1999 Feb 15;56(1):121-6. doi: 10.1006/geno.1998.5718.
Mutations in the human doublecortin (DCX), a brain-specific putative signaling protein, cause X-linked lissencephaly and subcortical band heterotopia. A predicted 740-amino-acid protein from human brain has two distinct regions, an N-terminal 345-amino-acid region 78% similar to the DCX protein and a C-terminal 427-amino-acid region that contains two transmembrane domains and is 98% homologous to a rat Ca2+/calmodulin-dependent protein kinase. We have designated this protein DCAMKL1. It maps to chromosome 13q12.3-q13, within a 540-kb YAC clone containing markers D13S805 and D13S1164. Northern analysis detected three major transcript isoforms of the DCAMKL1 gene expressed differentially and predominantly in human fetal and adult brain and during mouse embryogenesis (11-17 dpc). These results and its homology with the DCX and Ca2+/calmodulin dependent kinase proteins suggest a likely role for DCAMKL1 transmembrane protein in developing and adult brain, possibly in a pathway of cortical development.
人类双皮质素(DCX)是一种大脑特异性的假定信号蛋白,其突变会导致X连锁无脑回畸形和皮质下带状异位。从人类大脑预测的一种740个氨基酸的蛋白质有两个不同区域,一个N端345个氨基酸的区域与DCX蛋白有78%的相似性,一个C端427个氨基酸的区域包含两个跨膜结构域,与大鼠Ca2+/钙调蛋白依赖性蛋白激酶有98%的同源性。我们将这种蛋白质命名为DCAMKL1。它定位于13号染色体q12.3-q13,在一个包含标记D13S805和D13S1164的540 kb YAC克隆内。Northern分析检测到DCAMKL1基因的三种主要转录本异构体,它们在人类胎儿和成人脑中以及小鼠胚胎发育过程(11-17天胚胎龄)中差异表达且主要表达。这些结果及其与DCX和Ca2+/钙调蛋白依赖性激酶蛋白的同源性表明,DCAMKL1跨膜蛋白在发育中的大脑和成年大脑中可能发挥作用,可能参与皮质发育途径。