Lareyre J J, Winfrey V P, Kasper S, Ong D E, Matusik R J, Olson G E, Orgebin-Crist M C
Department of Obstetrics and Gynecology, Vanderbilt University, Nashville, Tennessee 37232, USA.
Endocrinology. 2001 Mar;142(3):1296-308. doi: 10.1210/endo.142.3.8045.
Using transgenic mice, we have recently shown that 5 kb of the 5'-flanking region of the mouse epididymal retinoic acid-binding protein (mE-RABP) gene contains all of the information required for spatial and temporal gene expression in the epididymis. To identify the important cis-DNA regulatory element(s) involved in the tissue-, region-, and cell-specific expression of the mE-RABP gene, the 5-kb DNA fragment was sequenced. A computer analysis of the nucleotide sequence showed the presence of a new gene located 1.7 kb upstream from the mE-RABP gene transcription initiation site. The analysis of the open reading frame showed that the new gene encoded a putative 17-kDa lipocalin (named mEP17) related to mE-RABP. A 600-bp complementary DNA encoding mEP17 was cloned by rapid amplification of 3'-cDNA ends from epididymal total RNA. Two mEP17 RNA species (1 and 3.1 kb in size) were detected by Northern blot in the epididymis, but not in other tissues tested. In situ hybridization analyses showed that, unlike mE-RABP messenger RNA (mRNA), which is expressed in the distal caput epididymidis, mEP17 mRNA was detected only in the principal cells of the initial segment. The spatial expression and homology with mE-RABP suggest that mEP17 may act as a retinoid carrier protein within the epididymis. mEP17 mRNA expression disappeared 5 days postcastration. Four days after unilateral castration, mEP17 mRNA had nearly disappeared in the epididymis from the castrated side, but not from the intact side. In addition, testosterone replacement to bilaterally castrated mice failed to restore gene expression. We conclude that mEP17 gene expression is dependent on testicular factors circulating in the luminal fluid. Together our results suggest that mE-RABP and mEP17 genes were generated by duplication and that evolution led to a different region-specific gene expression and regulation in the epididymis.
利用转基因小鼠,我们最近发现小鼠附睾视黄酸结合蛋白(mE-RABP)基因5′侧翼区的5kb片段包含了附睾中基因时空表达所需的所有信息。为了鉴定参与mE-RABP基因组织、区域和细胞特异性表达的重要顺式DNA调控元件,对该5kb DNA片段进行了测序。对核苷酸序列的计算机分析显示,在mE-RABP基因转录起始位点上游1.7kb处存在一个新基因。对开放阅读框的分析表明,该新基因编码一种与mE-RABP相关的推定的17kDa脂质运载蛋白(命名为mEP17)。通过从附睾总RNA快速扩增3′-cDNA末端,克隆了一个编码mEP17的600bp互补DNA。通过Northern印迹法在附睾中检测到两种mEP17 RNA种类(大小分别为1和3.1kb),但在其他测试组织中未检测到。原位杂交分析表明,与在附睾远侧头部表达的mE-RABP信使RNA(mRNA)不同,mEP17 mRNA仅在起始段的主细胞中检测到。其空间表达及与mE-RABP的同源性表明,mEP17可能在附睾内作为类视黄醇载体蛋白发挥作用。mEP17 mRNA表达在去势后5天消失。单侧去势4天后,mEP17 mRNA在去势侧的附睾中几乎消失,但在完整侧未消失。此外,对双侧去势小鼠进行睾酮替代未能恢复基因表达。我们得出结论,mEP17基因表达依赖于管腔液中循环的睾丸因子。我们的结果共同表明,mE-RABP和mEP17基因是通过复制产生的,并且进化导致了附睾中不同的区域特异性基因表达和调控。