Schmidt Otto, Jäckle Herbert
Biologisches Institut I (Zoologie) der Albert-Ludwig-Universität, Albertstr. 21a, D-7800, Freiburg i.Br., Federal Republic of Germany.
Wilehm Roux Arch Dev Biol. 1978 Jun;184(2):143-153. doi: 10.1007/BF00848223.
RNA labelled during oogenesis or early embryogenesis was isolated from eggs of the leaf hopperEuscelis plebejus. The polyadenylated RNA fraction deposited during early oogenesis accounted for approximately 2.7% of the total RNA content of the newly laid egg. This fraction differed significantly in molecular weight (15-32 S) from poly(A)-containing RNA synthesised between early cleavage and early germ anlage stages (4-20S). Locally injectedH-uridine spread through the egg within approximately 3 h. A considerable fraction (25-35%) of label injected asH-uridine during early cleavage was recovered in DNA at subsequent stages (10-20 h later); labelled RNA was not found prior to the cellular blastoderm stage. When the yolk-endoplasm was separated from the blastoderm cells, only the latter contained demonstrable amounts of RNA synthesised by the embryo. Of the precursor incorporated into embryonic RNA, approximately 10% was found in the polyadenylated fraction at the early blastoderm stage, but only 3% at the early germ anlage stage. No differences in size distribution of polyadenylated RNA were evident between anterior and posterior halves of the early germ anlage stage.
在卵子发生或早期胚胎发生过程中标记的RNA是从叶蝉Euscelis plebejus的卵中分离出来的。早期卵子发生过程中沉积的多聚腺苷酸化RNA部分约占新产卵总RNA含量的2.7%。该部分在分子量(15 - 32S)上与在早期卵裂和早期生殖原基阶段之间合成的含poly(A)的RNA(4 - 20S)有显著差异。局部注射的H - 尿苷在大约3小时内扩散到整个卵中。在早期卵裂期间作为H - 尿苷注射的相当一部分标记(25 - 35%)在随后阶段(10 - 20小时后)在DNA中被回收;在细胞胚盘阶段之前未发现标记的RNA。当卵黄内胚层与胚盘细胞分离时,只有后者含有胚胎合成的可检测量的RNA。在早期胚盘阶段,掺入胚胎RNA的前体中约10%存在于多聚腺苷酸化部分,但在早期生殖原基阶段仅为3%。在早期生殖原基阶段的前半部分和后半部分之间,多聚腺苷酸化RNA的大小分布没有明显差异。