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本文引用的文献

1
Mei-P26 regulates the maintenance of ovarian germline stem cells by promoting BMP signaling.Mei-P26 通过促进 BMP 信号通路调节卵巢生殖干细胞的自我更新。
Development. 2012 May;139(9):1547-56. doi: 10.1242/dev.077412. Epub 2012 Mar 21.
2
An alternative mode of microRNA target recognition.一种 miRNA 靶标识别的替代模式。
Nat Struct Mol Biol. 2012 Feb 12;19(3):321-7. doi: 10.1038/nsmb.2230.
3
HOW is required for stem cell maintenance in the Drosophila testis and for the onset of transit-amplifying divisions.它在果蝇睾丸中维持干细胞及启动过渡扩增分裂中是必需的。
Cell Stem Cell. 2010 Apr 2;6(4):348-360. doi: 10.1016/j.stem.2010.02.016.
4
Accumulation of a differentiation regulator specifies transit amplifying division number in an adult stem cell lineage.分化调节因子的积累在成体干细胞谱系中指定过渡扩增分裂次数。
Proc Natl Acad Sci U S A. 2009 Dec 29;106(52):22311-6. doi: 10.1073/pnas.0912454106. Epub 2009 Dec 14.
5
Vasa promotes Drosophila germline stem cell differentiation by activating mei-P26 translation by directly interacting with a (U)-rich motif in its 3' UTR.Vasa通过直接与mei-P26 3'UTR中的富含(U)的基序相互作用来激活其翻译,从而促进果蝇生殖系干细胞分化。
Genes Dev. 2009 Dec 1;23(23):2742-52. doi: 10.1101/gad.1820709.
6
The let-7 target gene mouse lin-41 is a stem cell specific E3 ubiquitin ligase for the miRNA pathway protein Ago2.let-7靶基因小鼠lin-41是一种针对微小RNA(miRNA)通路蛋白Ago2的干细胞特异性E3泛素连接酶。
Nat Cell Biol. 2009 Dec;11(12):1411-20. doi: 10.1038/ncb1987. Epub 2009 Nov 8.
7
eIF4A controls germline stem cell self-renewal by directly inhibiting BAM function in the Drosophila ovary.真核生物翻译起始因子4A(eIF4A)通过直接抑制果蝇卵巢中BAM的功能来控制生殖系干细胞的自我更新。
Proc Natl Acad Sci U S A. 2009 Jul 14;106(28):11623-8. doi: 10.1073/pnas.0903325106. Epub 2009 Jun 25.
8
Bam and Bgcn antagonize Nanos-dependent germ-line stem cell maintenance.Bam和Bgcn拮抗Nanos依赖的生殖系干细胞维持。
Proc Natl Acad Sci U S A. 2009 Jun 9;106(23):9304-9. doi: 10.1073/pnas.0901452106. Epub 2009 May 22.
9
The TRIM-NHL protein TRIM32 activates microRNAs and prevents self-renewal in mouse neural progenitors.TRIM-NHL蛋白TRIM32可激活微小RNA并阻止小鼠神经祖细胞的自我更新。
Cell. 2009 Mar 6;136(5):913-25. doi: 10.1016/j.cell.2008.12.024.
10
Regulation of translation initiation in eukaryotes: mechanisms and biological targets.真核生物中翻译起始的调控:机制与生物学靶点。
Cell. 2009 Feb 20;136(4):731-45. doi: 10.1016/j.cell.2009.01.042.

基于翻译控制的自我限制开关调节成年干细胞谱系中从增殖到分化的转变。

A self-limiting switch based on translational control regulates the transition from proliferation to differentiation in an adult stem cell lineage.

机构信息

Department of Developmental Biology, Stanford University School of Medicine, Stanford, CA 94305-5329, USA.

出版信息

Cell Stem Cell. 2012 Nov 2;11(5):689-700. doi: 10.1016/j.stem.2012.08.012.

DOI:10.1016/j.stem.2012.08.012
PMID:23122292
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3833810/
Abstract

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.

摘要

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。