Yang Lihui, Baker Nicholas E
Department of Molecular Genetics, Albert Einstein College of Medicine, Bronx, NY 10461, USA.
BMC Dev Biol. 2006 Feb 21;6:8. doi: 10.1186/1471-213X-6-8.
EGF receptor acts through Ras and the MAPK cascade to trigger differentiation and maintain survival of most of cell types in the Drosophila retina. Cell types are specified sequentially by separate episodes of EGFR activity. All the cell types differentiate in G1 phase of the cell cycle. Before differentiating, many cells pass through the cell cycle in the "Second Mitotic Wave" in response to Notch activity, but no cell fates are specified during the Second Mitotic Wave. It is not known how fate specification is limited to G1-arrested cells.
Competence to differentiate in response to activated RasV12 was diminished during the Second Mitotic Wave accounting for the failure to recruit cell fates from cycling cells. Competence was not restored by blocking cell cycle progression, but was restored by reduced Notch activity.
Competence to differentiate does not depend on cell cycle progression per se, but on the same receptor activity that also induces cell cycle entry. Dual effects of Notch on the cell cycle and on differentiation help ensure that only G1 phase cells undergo fate specification.
表皮生长因子受体通过Ras和丝裂原活化蛋白激酶级联反应发挥作用,以触发果蝇视网膜中大多数细胞类型的分化并维持其存活。细胞类型由表皮生长因子受体活性的不同阶段依次确定。所有细胞类型均在细胞周期的G1期分化。在分化之前,许多细胞响应Notch活性在“第二次有丝分裂波”中经历细胞周期,但在第二次有丝分裂波期间未确定任何细胞命运。尚不清楚命运指定如何仅限于G1期停滞的细胞。
在第二次有丝分裂波期间,响应活化的RasV12进行分化的能力减弱,这解释了无法从循环细胞中招募细胞命运的原因。通过阻断细胞周期进程不能恢复这种能力,但通过降低Notch活性可以恢复。
分化能力本身并不取决于细胞周期进程,而是取决于诱导细胞周期进入的相同受体活性。Notch对细胞周期和分化的双重作用有助于确保只有G1期细胞经历命运指定。