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Apoptotic mechanisms during competition of ribosomal protein mutant cells: roles of the initiator caspases Dronc and Dream/Strica

机译:核糖体蛋白突变细胞竞争过程中的凋亡机制:启动子caspases Dronc和Dream / Strica的作用

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Heterozygosity for mutations in ribosomal protein genes frequently leads to a dominant phenotype of retarded growth and small adult bristles in Drosophila (the Minute phenotype). Cells with Minute genotypes are subject to cell competition, characterized by their selective apoptosis and removal in mosaic tissues that contain wild-type cells. Competitive apoptosis was found to depend on the pro-apoptotic reaper, grim and head involution defective genes but was independent of p53. Rp/+ cells are protected by anti-apoptotic baculovirus p35 expression but lacked the usual hallmarks of 'undead' cells. They lacked Dronc activity, and neither expression of dominant-negative Dronc nor dronc knockdown by dsRNA prevented competitive apoptosis, which also continued in dronc null mutant cells or in the absence of the initiator caspases dredd and dream/strica. Only simultaneous knockdown of dronc and dream/strica by dsRNA was sufficient to protect Rp/+ cells from competition. By contrast, Rp/Rp cells were also protected by baculovirus p35, but Rp/Rp death was dronc-dependent, and undead Rp/Rp cells exhibited typical dronc-dependent expression of Wingless. Independence of p53 and unusual dependence on Dream/Strica distinguish competitive cell death from noncompetitive apoptosis of Rp/Rp cells and from many other examples of cell death.
机译:核糖体蛋白基因突变的杂合性经常导致果蝇生长迟缓和成年刚毛较小的显性表型(分钟表型)。具有微小基因型的细胞会遭受细胞竞争,其特征在于它们的选择性凋亡和在含有野生型细胞的镶嵌组织中的去除。发现竞争性细胞凋亡取决于促凋亡的收割者,严峻的和头部对合缺陷基因,但与p53无关。 Rp / +细胞受到抗凋亡杆状病毒p35表达的保护,但缺乏“亡灵”细胞的常见标志。他们缺乏Dronc活性,dsRNA显性阴性Dronc的表达或dronc敲除都不能阻止竞争性凋亡,在凋亡的null突变细胞中或缺少启动子的半胱氨酸蛋白酶和dream / strica的情况下,竞争性凋亡也持续存在。只有同时通过dsRNA敲除dronc和dream / strica才能保护Rp / +细胞免受竞争。相比之下,Rp / Rp细胞也受到杆状病毒p35的保护,但是Rp / Rp的死亡是依赖于dronc的,而不死的Rp / Rp细胞则表现出典型的依赖dronc的Wingless表达。 p53的独立性和对Dream / Strica的异常依赖性将竞争性细胞死亡与Rp / Rp细胞的非竞争性凋亡以及许多其他细胞死亡实例区分开来。

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