Hori T, Asakawa S, Itoh Y, Shimizu N, Mizuno S
Laboratory of Molecular Biology, Department of Molecular and Cell Biology, Graduate School of Agricultural Science, Tohoku University, Sendai 981-8555 Japan.
Mol Biol Cell. 2000 Oct;11(10):3645-60. doi: 10.1091/mbc.11.10.3645.
Two W chromosome-linked cDNA clones, p5fm2 and p5fm3, were obtained from a subtracted (female minus male) cDNA library prepared from a mixture of undifferentiated gonads and mesonephroi of male or female 5-d (stages 26-28) chicken embryos. These two clones were demonstrated to be derived from the mRNA encoding an altered form of PKC inhibitor/interacting protein (PKCI), and its gene was named Wpkci. The Wpkci gene reiterated approximately 40 times tandemly and located at the nonheterochromatic end of the chicken W chromosome. The W linkage and the moderate reiteration of Wpkci were conserved widely in Carinatae birds. The chicken PKCI gene, chPKCI, was shown to be a single-copy gene located near the centromere on the long arm of the Z chromosome. Deduced amino acid sequences of Wpkci and chPKCI showed approximately 65% identity. In the deduced sequence of Wpkci, the HIT motif, which is essential for PKCI function, was absent, but the alpha-helix region, which was conserved among the PKCI family, and a unique Leu- and Arg-rich region, were present. Transcripts from both Wpkci and chPKCI genes were present at significantly higher levels in 3- to 6-d (stages 20-29) embryos. These transcripts were detected in several embryonic tissues, including undifferentiated left and right gonads. When the green fluorescent protein-fused form of Wpkci was expressed in male chicken embryonic fibroblast, it was located almost exclusively in the nucleus. A model is presented suggesting that Wpkci may be involved in triggering the differentiation of ovary by interfering with PKCI function or by exhibiting its unique function in the nuclei of early female embryos.
从雄性或雌性5日龄(26 - 28期)鸡胚胎的未分化性腺和中肾混合物制备的消减(雌性减去雄性)cDNA文库中,获得了两个与W染色体连锁的cDNA克隆,p5fm2和p5fm3。这两个克隆被证明源自编码PKC抑制剂/相互作用蛋白(PKCI)改变形式的mRNA,其基因被命名为Wpkci。Wpkci基因串联重复约40次,位于鸡W染色体的非异染色质末端。Wpkci的W连锁和中度重复在突胸总目鸟类中广泛保守。鸡PKCI基因chPKCI被证明是位于Z染色体长臂着丝粒附近的单拷贝基因。Wpkci和chPKCI的推导氨基酸序列显示约65%的同一性。在Wpkci的推导序列中,缺少对PKCI功能至关重要的HIT基序,但存在PKCI家族中保守的α螺旋区域和独特的富含亮氨酸和精氨酸的区域。Wpkci和chPKCI基因的转录本在3至6日龄(20 - 29期)胚胎中的水平显著更高。这些转录本在包括未分化的左右性腺在内的几种胚胎组织中被检测到。当Wpkci的绿色荧光蛋白融合形式在雄性鸡胚胎成纤维细胞中表达时,它几乎完全位于细胞核中。提出了一个模型,表明Wpkci可能通过干扰PKCI功能或通过在早期雌性胚胎细胞核中发挥其独特功能来参与触发卵巢分化。