Soreq H, Malinger G, Zakut H
Department of Biological Chemistry, Hebrew University, Jerusalem, Israel.
Hum Reprod. 1987 Nov;2(8):689-93. doi: 10.1093/oxfordjournals.humrep.a136615.
Transcriptional activity of the human cholinesterase genes was examined in developing oocytes from mature ovaries by in-situ hybridization combined with biochemical acetylcholine hydrolysis measurements. High levels of cholinesterase mRNA could be detected in oocytes from primordial, pre-antral and antral follicles but not in atretic follicles, with transient enhancement at the pre-antral stage. Biochemical analysis of enzymatic activity identified the ovarian enzyme as 'true' acetylcholinesterase by its sensitivity to selective inhibitors. Our findings suggest that cholinergic responses may function in human oocytes independently of the surrounding follicular cells, and the pronounced synthesis of cholinesterase transcripts in oocytes suggests that the cholinesterase genes in humans are particularly good candidates for the formation and re-insertion of inheritable processed cholinesterase genes.
通过原位杂交结合生化乙酰胆碱水解测量,检测了成熟卵巢发育中卵母细胞中人胆碱酯酶基因的转录活性。在原始卵泡、窦前卵泡和窦状卵泡的卵母细胞中可检测到高水平的胆碱酯酶mRNA,但在闭锁卵泡中未检测到,在窦前阶段有短暂增强。酶活性的生化分析通过其对选择性抑制剂的敏感性将卵巢酶鉴定为“真正的”乙酰胆碱酯酶。我们的研究结果表明,胆碱能反应可能在人类卵母细胞中独立于周围卵泡细胞发挥作用,卵母细胞中胆碱酯酶转录物的显著合成表明,人类的胆碱酯酶基因是可遗传加工胆碱酯酶基因形成和重新插入的特别好的候选基因。