Mozer B A, Easwarachandran K
Laboratory of Molecular Biology, National Institutes of Neurological Diseases and Stroke, National Institutes of Health, Building 36, Room 3D02, Bethesda, Maryland 20892, USA.
Dev Biol. 1999 Sep 1;213(1):54-69. doi: 10.1006/dbio.1999.9350.
During Drosophila eye development, the posterior-to-anterior movement of the morphogenetic furrow coordinates cell cycle progression with the early events of pattern formation. The cdc25 phosphatase string (stg) has been proposed to contribute to the synchronization of retinal precursors anterior to the furrow by driving cells in G(2) through mitosis and into a subsequent G(1). Genetic and molecular analysis of Drop (Dr) mutations suggests that they represent novel cis-regulatory alleles of stg that inactivate expression in eye. Retinal precursors anterior to the furrow lacking stg arrest in G(2) and fail to enter mitosis, while cells within the furrow accumulate high levels of cyclins A and B. Although G(2)-arrested cells initiate normal pattern formation, the absence of stg results in retinal patterning defects due to the recruitment of extra photoreceptor cells. These results demonstrate a requirement for stg in cell cycle regulation and cell fate determination during eye development.
在果蝇眼睛发育过程中,形态发生沟从后向前移动,将细胞周期进程与模式形成的早期事件协调起来。有人提出,细胞周期蛋白依赖性激酶25磷酸酶“弦”(stg)通过促使处于G(2)期的细胞进入有丝分裂并进入随后的G(1)期,有助于使沟前方的视网膜前体细胞同步化。对Drop(Dr)突变的遗传和分子分析表明,它们代表stg的新型顺式调节等位基因,这些等位基因会使眼睛中的表达失活。沟前方缺乏stg的视网膜前体细胞在G(2)期停滞,无法进入有丝分裂,而沟内的细胞则积累高水平的细胞周期蛋白A和B。尽管在G(2)期停滞的细胞启动了正常的模式形成,但由于额外光感受器细胞的募集,stg的缺失导致视网膜模式形成缺陷。这些结果证明了stg在眼睛发育过程中的细胞周期调控和细胞命运决定中的必要性。