Dean W L, Seufert A C, Schultz G A, Prather R S, Simerly C, Schatten G, Pilch D R, Marzluff W F
Department of Medical Biochemistry, University of Calgary, Alberta, Canada.
Development. 1989 Jun;106(2):325-34. doi: 10.1242/dev.106.2.325.
The abundance and localization of snRNAs and snRNPs involved in processing and splicing of pre-mRNA has been studied during early mouse embryogenesis. The amount of U1, U2, U4, U5 and U6 RNA remains relatively constant between the postovulatory oocyte and 2-cell stage but increases three- to ten-fold in quantity between the 2-cell and blastocyst stages. Localization was examined by in situ hybridization with U1, U2 and U6 riboprobes and immunofluorescence microscopy using a monoclonal antibody to snRNP antigens. The snRNAs and snRNPs are primarily localized to the germinal vesicle in the preovulatory oocyte but are released and diluted within the cytoplasm of the oocyte during germinal vesicle breakdown and meiotic maturation. They subsequently relocalize to both pronuclei following fertilization and the nuclei of the 2-cell embryo following the first cleavage division. Since the amount of snRNA is constant during the first cleavage, the small amount of pre-mRNA that is synthesized at the time of transcriptional activation in the 2-cell embryo may be spliced and processed by snRNPs of maternal origin.
在小鼠早期胚胎发育过程中,对参与前体mRNA加工和剪接的小核RNA(snRNA)和小核核糖核蛋白(snRNP)的丰度及定位进行了研究。在排卵后卵母细胞和2细胞期之间,U1、U2、U4、U5和U6 RNA的量保持相对恒定,但在2细胞期和囊胚期之间数量增加了三到十倍。通过用U1、U2和U6核糖探针进行原位杂交以及使用针对snRNP抗原的单克隆抗体进行免疫荧光显微镜检查来检测定位。snRNA和snRNP主要定位于排卵前卵母细胞的生发泡,但在生发泡破裂和减数分裂成熟过程中会释放并稀释到卵母细胞的细胞质中。受精后,它们随后重新定位于两个原核,第一次卵裂分裂后定位于2细胞胚胎的细胞核。由于在第一次卵裂期间snRNA的量是恒定的,因此在2细胞胚胎转录激活时合成的少量前体mRNA可能由母源snRNP进行剪接和加工。