果蝇胚胎发生
生物
卵母细胞
核糖核酸
卵子发生
细胞生物学
胚胎发生中的极性
胚胎
胚胎发生
极性(国际关系)
解剖
遗传学
细胞
基因
原肠化
作者
Daniel St Johnston,Wolfgang Driever,Thomas Berleth,Sibyll Richstein,Christiane Nüsslein‐Volhard
出处
期刊:Development
[The Company of Biologists]
日期:1989-04-01
卷期号:107 (Supplement): 13-19
被引量:290
标识
DOI:10.1242/dev.107.supplement.13
摘要
ABSTRACT The anterior region of the Drosophila embryonic pattern is determined by a gradient of the bicoid (bed) protein. The correct formation of this gradient requires the localization of bed RNA to the anterior pole of the egg. Here we use a wholemount in situ technique to examine the process of bed RNA localization during oogenesis and embryogenesis. While bed protein becomes distributed in a gradient that extends throughout the anterior two thirds of the early embryo, bed RNA remains restricted to a much smaller region at the anterior pole. The difference between these distributions indicates that the shape of the protein gradient must depend to some extent on the posterior movement of the protein after it has been synthesized. Four distinct phases of bed RNA localization can be distinguished during oogenesis. Between stages 6 and 9 of oogenesis, the RNA accumulates in a ring at the anterior end of the oocyte. During the second phase, in stage 9-10a follicles, the RNA also localizes to the apical regions of the nurse cells, demonstrating that the nurse cells possess an intrinsic polarity. As the nurse cells contract during stages 10b–ll, all of the bed RNA becomes localized to the cortex at the anterior end of the oocyte. During a final phase that must occur between stage 12 of oogenesis and egg deposition, the RNA becomes localized to a spherical region that occupies a slightly dorsal position at the anterior pole. Mutations in the maternal-effect genes, exuperantia (exu) and swallow (sw), lead to an almost uniform distribution of bed RNA in the early embryo, while staufen (stau) mutations produce a gradient of RNA at the anterior pole, exu mutations disrupt the second stage of bcd RNA localization during oogenesis, su’w mutations disrupt the third, and stau mutations affect the fourth phase.
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