Department of Developmental Biology, Stanford University School of Medicine, Stanford, CA 94305-5329, USA.
Cell Stem Cell. 2012 Nov 2;11(5):689-700. doi: 10.1016/j.stem.2012.08.012.
In adult stem cell lineages, progenitor cells commonly undergo mitotic transit amplifying (TA) divisions before terminal differentiation, allowing production of many differentiated progeny per stem cell division. Mechanisms that limit TA divisions and trigger the switch to differentiation may protect against cancer by preventing accumulation of oncogenic mutations in the proliferating population. Here we show that the switch from TA proliferation to differentiation in the Drosophila male germline stem cell lineage is mediated by translational control. The TRIM-NHL tumor suppressor homolog Mei-P26 facilitates accumulation of the differentiation regulator Bam in TA cells. In turn, Bam and its partner Bgcn bind the mei-P26 3' untranslated region and repress translation of mei-P26 in late TA cells. Thus, germ cells progress through distinct, sequential regulatory states, from Mei-P26 on/Bam off to Bam on/Mei-P26 off. TRIM-NHL homologs across species facilitate the switch from proliferation to differentiation, suggesting a conserved developmentally programmed tumor suppressor mechanism.
在成人干细胞谱系中,祖细胞在终末分化前通常经历有丝分裂扩增(TA)分裂,从而允许每个干细胞分裂产生多个分化的后代。限制 TA 分裂并触发分化开关的机制可以通过防止增殖群体中致癌突变的积累来预防癌症。在这里,我们表明,果蝇雄性生殖干细胞谱系中从 TA 增殖到分化的转变是由翻译控制介导的。TRIM-NHL 肿瘤抑制因子同源物 Mei-P26 有助于 Bam 在 TA 细胞中的积累。反过来,Bam 和它的伴侣 Bgcn 结合 mei-P26 的 3'非翻译区并抑制晚期 TA 细胞中 mei-P26 的翻译。因此,生殖细胞通过不同的、连续的调节状态进展,从 Mei-P26 on/Bam off 到 Bam on/Mei-P26 off。跨物种的 TRIM-NHL 同源物促进了从增殖到分化的转变,这表明存在一种保守的发育程序化肿瘤抑制机制。