Nussbaum D J, Prather R S
Department of Animal Science, University of Missouri, Columbia 65211, USA.
Mol Reprod Dev. 1995 May;41(1):70-5. doi: 10.1002/mrd.1080410111.
This study was designed to evaluate the effects of cycloheximide and puromycin on activation and protein synthesis of porcine oocytes. When matured oocytes were electrostimulated, then cultured in the presence of cycloheximide (5 micrograms/ml) for 6 or 24 hr, 92% of oocytes were activated as indicated by pronuclear formation, vs. 2.8% for untreated oocytes, 5.3% for oocytes not electrostimulated but cultured with cycloheximide, and 60.0% for those only electrostimulated. When cultured with L-[35S]methionine in the presence of cycloheximide, puromycin (100 micrograms/ml), or no protein synthesis inhibitor for 24 hr, oocytes had mean radiolabeled incorporation rates of 36.5, 2.21, and 32.0 fmol/4 hr/oocyte, respectively. Thus, cycloheximide had little effect on protein synthesis after 24 hr of culture. A 1D-SDS PAGE showed that oocytes cultured with puromycin or cycloheximide are not activated, while electrostimulated oocytes are activated, as characterized by the conversion of a 25-kDa polypeptide to a 22-kDa polypeptide. The radiolabeling experiment was repeated, except that oocytes were cultured for 4 or 24 hr. At 4 hr, mean incorporation rates were lower in the cycloheximide group (2.34 fmol/4 hr/oocyte), but similar in the puromycin (15.7 fmol/4 hr/oocyte) and control groups (18.9 fmol/4 hr/oocyte). At 24 hr, the puromycin group 5.73 fmol/4 hr/oocyte) had a lower rate of incorporation, while the cycloheximide (22.6 fmol/4 hr/oocyte) and control (26.0 fmol/4 hr/oocyte) groups were similar. Cycloheximide was more effective earlier during culture, while puromycin was more effective later. When combined with ES, puromycin did have a higher rate (P = 0.10) of activation (87.8%) than with electrostimulation alone (73.0%).(ABSTRACT TRUNCATED AT 250 WORDS)
本研究旨在评估环己酰亚胺和嘌呤霉素对猪卵母细胞激活及蛋白质合成的影响。当成熟卵母细胞经电刺激后,在含有环己酰亚胺(5微克/毫升)的条件下培养6小时或24小时,92%的卵母细胞出现原核形成,表明被激活,而未处理的卵母细胞激活率为2.8%,未电刺激但用环己酰亚胺培养的卵母细胞激活率为5.3%,仅接受电刺激的卵母细胞激活率为60.0%。当在含有环己酰亚胺、嘌呤霉素(100微克/毫升)或无蛋白质合成抑制剂的情况下与L-[35S]甲硫氨酸一起培养24小时时,卵母细胞的平均放射性标记掺入率分别为36.5、2.21和32.0飞摩尔/4小时/卵母细胞。因此,培养24小时后,环己酰亚胺对蛋白质合成影响不大。一维SDS-PAGE显示,用嘌呤霉素或环己酰亚胺培养的卵母细胞未被激活,而经电刺激的卵母细胞被激活,其特征是一条25千道尔顿的多肽转化为一条22千道尔顿的多肽。重复进行放射性标记实验,但卵母细胞培养4小时或24小时。4小时时,环己酰亚胺组的平均掺入率较低(2.34飞摩尔/4小时/卵母细胞),而嘌呤霉素组(15.7飞摩尔/4小时/卵母细胞)和对照组(18.9飞摩尔/4小时/卵母细胞)相似。24小时时,嘌呤霉素组(5.73飞摩尔/4小时/卵母细胞)的掺入率较低,而环己酰亚胺组(22.6飞摩尔/4小时/卵母细胞)和对照组(26.0飞摩尔/4小时/卵母细胞)相似。环己酰亚胺在培养早期更有效,而嘌呤霉素在后期更有效。当与电刺激联合使用时,嘌呤霉素的激活率(87.8%)确实高于单独电刺激(73.0%)(P = 0.10)。(摘要截断于250字)