Fay D S, Han M
Howard Hughes Medical Institute and Department of Molecular, Cellular and Developmental Biology, University of Colorado, Boulder CO 80309-0347, USA.
Development. 2000 Sep;127(18):4049-60. doi: 10.1242/dev.127.18.4049.
We have identified strong loss-of-function mutations in the C. elegans cyclin E gene, cye-1. Mutations in cye-1 lead to the underproliferation of many postembryonic blast lineages as well as defects in fertility and gut-cell endoreduplication. In addition, cye-1 is required maternally, but not zygotically for embryonic development. Our analysis of vulval development in cye-1 mutants suggests that a timing mechanism may control the onset of vulval cell terminal differentiation: once induced, these cells appear to differentiate after a set amount of time, rather than a specific number of division cycles. cye-1 mutants also show an increase in the percentage of vulval precursor cells (VPCs) that adopt vulval cell fates, indicating that cell-cycle length can play a role in the proper patterning of vulval cells. By analyzing cul-1 mutants, we further demonstrate that vulval cell terminal differentiation can be uncoupled from associated changes in vulval cell division planes.
我们已经在秀丽隐杆线虫细胞周期蛋白E基因cye-1中鉴定出功能丧失的强突变。cye-1突变导致许多胚胎后胚细胞谱系增殖不足,以及生育力和肠细胞内复制缺陷。此外,cye-1在胚胎发育中是母源必需的,但合子非必需。我们对cye-1突变体中阴门发育的分析表明,一种定时机制可能控制阴门细胞终末分化的起始:一旦被诱导,这些细胞似乎在一定时间后分化,而不是特定数量的分裂周期。cye-1突变体中采用阴门细胞命运的阴门前体细胞(VPC)百分比也增加,表明细胞周期长度可在阴门细胞的正确模式形成中发挥作用。通过分析cul-1突变体,我们进一步证明阴门细胞终末分化可以与阴门细胞分裂平面的相关变化解偶联。