Salik J, Herlands L, Hoffmann H P, Poccia D
J Cell Biol. 1981 Aug;90(2):385-95. doi: 10.1083/jcb.90.2.385.
A maternal store of histones in unfertilized sea urchin eggs is demonstrated by two independent criteria. Stored histones are identified by their ability to assemble into chromatin of male pronuclei of fertilized sea urchin eggs in the absence of protein synthesis, suggesting a minimum of at least 25 haploid equivalents for each histone present and functional in the unfertilized egg. In addition, electrophoretic analysis of proteins from acid extracts of unfertilized whole eggs and enucleated merogons reveals protein spots comigrating with cleavage stage histone standards, though not with other histone variants found in later sea urchin development or in sperm. Quantification of the amount of protein per histone spot yields an estimate of several hundred haploid DNA equivalents per egg of stored histone. The identity of some of the putative histones was verified by a highly sensitive immunological technique, involving electrophoretic transfer of proteins from the two-dimensional polyacrylamide gels to nitrocellulose filters. Proteins in amounts less than 2 x 10(-4) micrograms can be detected by this method.
通过两个独立的标准证明了未受精海胆卵中存在母源组蛋白储存。储存的组蛋白可通过在无蛋白质合成的情况下组装到受精海胆卵雄原核染色质中的能力来鉴定,这表明未受精卵中存在且具有功能的每种组蛋白至少有25个单倍体当量。此外,对未受精全卵和去核卵块酸提取物中的蛋白质进行电泳分析,发现有蛋白质斑点与卵裂期组蛋白标准品迁移一致,但与海胆后期发育或精子中发现的其他组蛋白变体不一致。对每个组蛋白斑点的蛋白质量进行定量,得出每个未受精卵储存组蛋白有数百个单倍体DNA当量的估计值。通过一种高度灵敏的免疫技术验证了一些推定组蛋白的身份,该技术包括将蛋白质从二维聚丙烯酰胺凝胶电泳转移到硝酸纤维素滤膜上。用这种方法可以检测到量少于2×10(-4)微克的蛋白质。