Matsui Takeshi, Hayashi-Kisumi Fumie, Kinoshita Yoko, Katahira Sayaka, Morita Kazumasa, Miyachi Yoshiki, Ono Yuichi, Imai Toshio, Tanigawa Yoko, Komiya Tohru, Tsukita Shoichiro
KAN Research Institute, Inc., Shimogyo-ku, Kyoto 600-8815, Japan.
Genomics. 2004 Aug;84(2):384-97. doi: 10.1016/j.ygeno.2004.03.010.
We performed high-throughput in situ hybridization screening of sections of mouse epidermis using an equalized skin cDNA library as probes and identified a novel gene giving rise to two splicing variants, both of which are expressed in the spinous layer. This gene was mapped between two genes encoding keratinocyte-related peptides, suprabasin and keratinocyte differentiation-associated protein (Kdap), on human chromosome 19q13.1. These gene products appeared to carry functional signal sequences. We then designated these two splicing variants as dermokine-alpha and -beta. Northern blotting and quantitative RT-PCR revealed that dermokine-alpha/-beta, suprabasin, and Kdap were highly expressed in stratified epithelia. In mouse embryonic development, dermokine-alpha/-beta began to be expressed during the period of stratification. Also, in differentiating primary cultured human keratinocytes, transcription of dermokine-alpha/-beta, suprabasin, and Kdap was induced. These findings indicated that dermokine-alpha/-beta, suprabasin, and Kdap are secreted from the spinous layer of the stratified epithelia and that these genes form a novel gene complex on the chromosome.
我们使用均一化皮肤cDNA文库作为探针,对小鼠表皮切片进行了高通量原位杂交筛选,鉴定出一个产生两种剪接变体的新基因,这两种变体均在棘层表达。该基因定位于人类19号染色体q13.1上两个编码角质形成细胞相关肽的基因之间,即上层蛋白(suprabasin)和角质形成细胞分化相关蛋白(Kdap)。这些基因产物似乎携带功能性信号序列。然后,我们将这两种剪接变体命名为皮肤因子α和β。Northern印迹和定量RT-PCR显示,皮肤因子α/β、上层蛋白和Kdap在复层上皮中高表达。在小鼠胚胎发育过程中,皮肤因子α/β在分层期开始表达。此外,在分化的原代培养人角质形成细胞中,皮肤因子α/β、上层蛋白和Kdap的转录被诱导。这些发现表明,皮肤因子α/β、上层蛋白和Kdap是从复层上皮的棘层分泌的,并且这些基因在染色体上形成了一个新的基因复合体。