Pera I, Derr P, Yeung C H, Cooper T G, Kirchhoff C
IHF Institute for Hormone and Fertility Research, University of Hamburg, Germany.
Mol Reprod Dev. 1997 Dec;48(4):433-41. doi: 10.1002/(SICI)1098-2795(199712)48:4<433::AID-MRD3>3.0.CO;2-R.
The regional pattern of CD52 expression in the rat epididymis was followed by Northern analyses and carbohydrate-labelling of glycoconjugates on Western blots. CD52 mRNA showed a novel aspect of regionalization, namely region-dependent length differences in its poly(A) tail. 'Short' CD52 mRNA molecules were present in all parts of this organ and also in the seminal vesicles. Additionally, the cauda epididymidis contained mRNA molecules with an extended poly(A) tail. Their appearance coincided with the occurrence of the principal M(r) approximately 26 kDa glycopeptide in the cauda region, representing the CD52 product. CD52 expression seemed to be regulated or modulated synergistically by androgens, temperature, and (an) unknown testicular factor(s), depending on the poly(A) tail length of its mRNA. Androgens alone exerted an effect only on molecules with 'short' poly(A) tails. They were down-regulated in castrated animals, and restored to normal levels upon testosterone supplementation. However, 'long' CD52 mRNA molecules were not affected. Only if combined with the exposure of the epididymis to the elevated temperature of the abdomen, castration of animals resulted in a complete loss of the CD52 mRNA, including the 'long' cauda species. Loss of 'long' CD52 mRNA molecules was also observed when the abdominal location was combined with efferent duct ligation. This combination of treatments, however, did not affect 'short' CD52 mRNA levels. Loss of the 'long' CD52 mRNA molecules by any treatment coincided with a loss of the principal M(r) approximately 26 kDa glycopeptide from caudal protein extracts.
通过Northern分析以及蛋白质免疫印迹法对糖缀合物进行碳水化合物标记,研究了大鼠附睾中CD52表达的区域模式。CD52 mRNA呈现出一种新的区域化特征,即其多聚腺苷酸尾巴存在区域依赖性的长度差异。“短”CD52 mRNA分子存在于该器官的所有部位以及精囊中。此外,附睾尾部含有多聚腺苷酸尾巴延长的mRNA分子。它们的出现与尾部区域中主要的约26 kDa糖肽(代表CD52产物)的出现相一致。CD52的表达似乎受雄激素、温度和一种未知的睾丸因子协同调节或调控,这取决于其mRNA的多聚腺苷酸尾巴长度。单独的雄激素仅对具有“短”多聚腺苷酸尾巴的分子产生影响。在去势动物中它们表达下调,补充睾酮后恢复到正常水平。然而,“长”CD52 mRNA分子不受影响。只有当附睾暴露于腹部的高温环境中时,动物去势才会导致CD52 mRNA完全丧失,包括尾部的“长”型分子。当腹部位置与输出小管结扎相结合时,也观察到“长”CD52 mRNA分子的丧失。然而,这种联合处理并不影响“短”CD52 mRNA水平。任何处理导致的“长”CD52 mRNA分子丧失都与尾部蛋白质提取物中主要的约26 kDa糖肽的丧失相一致。