Manes C
J Exp Zool. 1977 Aug;201(2):247-57. doi: 10.1002/jez.1402010209.
This report stems from efforts to characterize the products of transcription during the initial stages of cleavage in the rabbit embryo, since previous studies have suggested that RNA synthesis is required during this period for the continuation of normal development. Early cleaving embryos were exposed to radiolabeled precursors of nucleic acids in vitro and RNA extracted and analyzed by polyacrylamide gel electrophoresis and BD-cellulose chromatography. No unequivocal evidence of RNA synthesis could be obtained during the first three cleavage divisions; all apparent "embryonic" RNA synthesis could be ascribed to contaminating follicle cells. After the fourth cleavage, however, there is readily detectable incorporation of radioisotope into RNA by embryos which have been denuded of follicle cells. Two-thirds of the cytoplasmic RNA labeled during a 4-hour period is 25-30 X 10(3) daltons in size, and some of this low molecular weight RNA can be aminoacylated and shown to be transfer RNA. A low level of ribosomal RNA synthesis is detectable at this stage. The contribution, if any, of the rabbit embryonic genome to development prior to the 16-cell stage remains to be defined.
本报告源于对兔胚胎卵裂初期转录产物进行特性分析的研究,因为先前的研究表明,在此期间RNA合成是正常发育持续进行所必需的。将早期卵裂胚胎在体外暴露于放射性标记的核酸前体,提取RNA并通过聚丙烯酰胺凝胶电泳和BD-纤维素色谱法进行分析。在前三次卵裂过程中,未获得RNA合成的确切证据;所有明显的“胚胎”RNA合成都可归因于污染的卵泡细胞。然而,在第四次卵裂后,去除卵泡细胞的胚胎能够轻易检测到放射性同位素掺入RNA。在4小时内标记的细胞质RNA中,三分之二的大小为25 - 30×10³道尔顿,其中一些低分子量RNA可被氨酰化并显示为转运RNA。在这个阶段可检测到低水平的核糖体RNA合成。兔胚胎基因组在16细胞阶段之前对发育的贡献(如果有的话)仍有待确定。