Tachibana K, Ishiura M, Uchida T, Kishimoto T
Biological Laboratory, Faculty of Science, Tokyo Institute of Technology, Japan.
Dev Biol. 1990 Aug;140(2):241-52. doi: 10.1016/0012-1606(90)90074-s.
During meiotic maturation and early embryonic cycles, the activity of maturation-promoting factor (MPF) cycles in exact correspondence with the mitotic cycles. For the appearance of MPF activity in starfish, protein synthesis is required except in the first meiotic cycle. In order to identify newly synthesized proteins involved in the regulation of MPF activity, we extracted poly(A)+ RNA from starfish eggs, and found that the egg poly(A)+ RNA induced germinal vesicle breakdown (GVBD) upon injection into immature oocytes of starfish and Xenopus. The molecular size of the poly(A)+ RNA responsible for GVBD was estimated to be approximately 22S by sucrose density gradient centrifugation. Since these characteristics of the starfish egg poly(A)+ RNA are similar to those of cyclin mRNAs from sea urchin and surf clam eggs, we synthesized a 50-mer antisense-cyclin oligonucleotide probe coding for a part of the sea urchin cyclin cDNA and used this to screen starfish RNA. The Northern blot analysis showed that the starfish egg RNA contained cyclin homologous transcripts. Incubation of the starfish egg poly(A)+ RNA and the antisense-cyclin oligonucleotide with RNase H completely destroyed its GVBD-inducing activity. These results indicated that starfish cyclin mRNA was the only poly(A)+ RNA responsible for GVBD. We constructed a starfish egg cDNA library to clone starfish cyclin cDNA. The longest cDNA clone containing 2190 base pairs was sequenced. The longest open reading frame consisted of 395 amino acid residues, and the predicted molecular size was 48 kDa. Comparison of the deduced amino acid sequences of starfish cyclin with known cyclins indicated that the starfish cyclin belongs to the B-type. Injection of synthetic mRNA of starfish cyclin caused GVBD in immature oocytes of starfish and Xenopus, while injection of synthetic mRNA of human CDC2 had no effect. The Northern blot analysis of starfish RNA extracted at various stages of the meiotic cycles suggested that the starfish cyclin transcript was stored in its polyadenylated form even in immature oocytes and was further polyadenylated at maturation.
在减数分裂成熟和早期胚胎发育周期中,促成熟因子(MPF)的活性与有丝分裂周期精确对应地循环变化。对于海星中MPF活性的出现,除了第一个减数分裂周期外,蛋白质合成是必需的。为了鉴定参与MPF活性调节的新合成蛋白质,我们从海星卵中提取了聚腺苷酸加尾RNA(poly(A)+ RNA),并发现卵的poly(A)+ RNA注入未成熟的海星和非洲爪蟾卵母细胞后会诱导生发泡破裂(GVBD)。通过蔗糖密度梯度离心法估计,负责GVBD的poly(A)+ RNA的分子大小约为22S。由于海星卵poly(A)+ RNA的这些特征与海胆和滨蛤卵中的细胞周期蛋白mRNA的特征相似,我们合成了一个编码海胆细胞周期蛋白cDNA一部分的50聚体反义细胞周期蛋白寡核苷酸探针,并用于筛选海星RNA。Northern印迹分析表明,海星卵RNA含有细胞周期蛋白同源转录本。将海星卵poly(A)+ RNA和反义细胞周期蛋白寡核苷酸与RNase H一起孵育,完全破坏了其诱导GVBD的活性。这些结果表明,海星细胞周期蛋白mRNA是唯一负责GVBD的poly(A)+ RNA。我们构建了一个海星卵cDNA文库以克隆海星细胞周期蛋白cDNA。对最长的包含2190个碱基对的cDNA克隆进行了测序。最长的开放阅读框由395个氨基酸残基组成,预测的分子大小为48 kDa。将海星细胞周期蛋白推导的氨基酸序列与已知的细胞周期蛋白进行比较表明,海星细胞周期蛋白属于B型。注射海星细胞周期蛋白的合成mRNA会在海星和非洲爪蟾的未成熟卵母细胞中引起GVBD,而注射人细胞周期蛋白依赖性激酶2(CDC2)的合成mRNA则没有效果。对在减数分裂周期不同阶段提取的海星RNA进行的Northern印迹分析表明,海星细胞周期蛋白转录本即使在未成熟卵母细胞中也以其聚腺苷酸化形式储存,并在成熟时进一步聚腺苷酸化。