Cornwall G A, Orgebin-Crist M C, Hann S R
Center for Reproductive Biology Research, Vanderbilt University School of Medicine, Nashville, Tennessee 37232.
Mol Endocrinol. 1992 Oct;6(10):1653-64. doi: 10.1210/mend.6.10.1280328.
As a result of examining regional-specific gene expression in the mouse epididymis, a novel cystatin-related epididymal specific (CRES) gene was identified. Substantial homology between the CRES gene and members of the cystatin family of cysteine proteinase inhibitors was observed at the amino acid level. This homology included the presence of four highly conserved cysteine residues in exact alignment with the cystatins as well as other regions of sequence characteristic of the cystatins. However, unlike the cystatins, the CRES gene does not contain specific highly conserved sequence motifs thought to be necessary for cysteine proteinase inhibitory activity. Also, in contrast to the ubiquitous expression of the cystatin C gene, Northern blot analysis and in situ hybridization demonstrated that the CRES gene is very restricted in its expression. The 0.75-kilobase CRES transcript is dramatically restricted to the very proximal caput region of the epididymis with 15- to 20-fold less expression in the testis and no expression detected in any of the other 24 tissues examined. In addition, the CRES transcript disappears 2-3 weeks after castration, suggesting a dependence on androgens. However, its expression remained undetectable even after the administration of testosterone or dihydrotestosterone. Unilateral castration also resulted in the disappearance of the CRES mRNA from the castrate epididymis, but not from the intact epididymis, suggesting that testicular factors or hormones other than androgens may be involved in the regulation of CRES gene expression. Therefore, the unique sequence of the CRES gene as well as its highly restricted expression and unusual regulation by the testis suggests that it has a very specialized role in the epididymis.
通过检测小鼠附睾中区域特异性基因的表达,鉴定出一个新的与胱抑素相关的附睾特异性(CRES)基因。在氨基酸水平上观察到CRES基因与半胱氨酸蛋白酶抑制剂胱抑素家族成员之间存在高度同源性。这种同源性包括四个高度保守的半胱氨酸残基,它们与胱抑素精确对齐,以及胱抑素特有的其他序列区域。然而,与胱抑素不同,CRES基因不包含被认为是半胱氨酸蛋白酶抑制活性所必需的特定高度保守序列基序。此外,与胱抑素C基因的普遍表达相反,Northern印迹分析和原位杂交表明CRES基因的表达非常局限。0.75千碱基的CRES转录本显著局限于附睾的近端头部区域,在睾丸中的表达量低15至20倍,在所检测的其他24种组织中均未检测到表达。此外,去势后2至3周CRES转录本消失,表明其对雄激素有依赖性。然而,即使给予睾酮或双氢睾酮后,其表达仍未检测到。单侧去势也导致去势侧附睾中CRES mRNA消失,但完整附睾中未消失,这表明除雄激素外,睾丸因子或激素可能参与CRES基因表达的调控。因此,CRES基因的独特序列及其在附睾中高度局限的表达和睾丸的异常调控表明它在附睾中具有非常特殊的作用。