Shimizu Atsushi, Asakawa Shuichi, Sasaki Takashi, Yamazaki Satoru, Yamagata Hidehisa, Kudoh Jun, Minoshima Shinsei, Kondo Ikuko, Shimizu Nobuyoshi
Department of Molecular Biology, Keio University School of Medicine, Tokyo, Japan.
Biochem Biophys Res Commun. 2003 Sep 12;309(1):143-54. doi: 10.1016/s0006-291x(03)01555-9.
We identified a novel giant gene encoding a transmembrane protein with CUB and sushi multiple domains on the human chromosome 8q23.3-q24.1 in which benign adult familial myoclonic epilepsy type 1 (BAFME1/FAME, OMIM:601068) has been mapped. This giant gene consists of 73 exons and spans over 1.2Mb on the genomic DNA region. It showed significant homology to two genes, CSMD1 gene on 8p23 and CSMD2 gene on 1p34, at reduced amino acid sequence level and hence we designated as CSMD3. The CSMD3 gene was expressed mainly in adult and fetal brains. We performed mutation analysis on the CSMD3 gene for seven patients with BAFME1/FAME, but no mutation was found in the coding sequence of the CSMD3 gene. Comparative genomic analysis revealed a conserved family of CSMD genes in the mouse and fugu genomes. Possible functions of the CSMD gene family are discussed.
我们在人类8号染色体q23.3 - q24.1区域鉴定出一个编码具有CUB和寿司多结构域跨膜蛋白的新型巨大基因,其中已定位了1型良性成人家族性肌阵挛癫痫(BAFME1/FAME,OMIM:601068)。这个巨大基因由73个外显子组成,在基因组DNA区域跨度超过1.2Mb。它在氨基酸序列水平上与8p23上的CSMD1基因和1p34上的CSMD2基因有显著同源性,因此我们将其命名为CSMD3。CSMD3基因主要在成人和胎儿大脑中表达。我们对7例BAFME1/FAME患者的CSMD3基因进行了突变分析,但在CSMD3基因的编码序列中未发现突变。比较基因组分析揭示了小鼠和河豚基因组中CSMD基因的保守家族。讨论了CSMD基因家族的可能功能。