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miR-294/miR-302 通过可分离的机制促进增殖、抑制 G1-S 限制点,并抑制 ESC 分化。

miR-294/miR-302 promotes proliferation, suppresses G1-S restriction point, and inhibits ESC differentiation through separable mechanisms.

机构信息

Peking-Tsinghua Joint Center for Life Sciences, Institute of Molecular Medicine, Peking University, Beijing 100871, China.

出版信息

Cell Rep. 2013 Jul 11;4(1):99-109. doi: 10.1016/j.celrep.2013.05.027. Epub 2013 Jul 3.

Abstract

The miR-294 and miR-302 microRNAs promote the abbreviated G1 phase of the embryonic stem cell (ESC) cell cycle and suppress differentiation induced by let-7. Here, we evaluated the role of the retinoblastoma (Rb) family proteins in these settings. Under normal growth conditions, miR-294 promoted the rapid G1-S transition independent of the Rb family. In contrast, miR-294 suppressed the further accumulation of cells in G1 in response to nutrient deprivation and cell-cell contact in an Rb-dependent fashion. We uncovered five additional miRNAs (miR-26a, miR-99b, miR-193, miR-199a-5p, and miR-218) that silenced ESC self-renewal in the absence of other miRNAs, all of which were antagonized by miR-294 and miR-302. Four of the six differentiation-inducing miRNAs induced an Rb-dependent G1 accumulation. However, all six still silenced self-renewal in the absence of the Rb proteins. These results show that the miR-294/miR-302 family acts through Rb-dependent and -independent pathways to regulate the G1 restriction point and the silencing of self-renewal, respectively.

摘要

miR-294 和 miR-302 微 RNA 促进胚胎干细胞 (ESC) 细胞周期的缩短 G1 期,并抑制 let-7 诱导的分化。在这里,我们评估了视网膜母细胞瘤 (Rb) 家族蛋白在这些环境中的作用。在正常生长条件下,miR-294 促进了 Rb 家族独立的快速 G1-S 过渡。相比之下,miR-294 以 Rb 依赖性的方式抑制了对营养剥夺和细胞-细胞接触的进一步 G1 期细胞积累。我们发现了另外五个 miRNA(miR-26a、miR-99b、miR-193、miR-199a-5p 和 miR-218),它们在没有其他 miRNA 的情况下沉默 ESC 自我更新,所有这些都被 miR-294 和 miR-302 拮抗。在没有 Rb 的情况下,六种诱导分化的 miRNA 中有四种诱导 Rb 依赖性 G1 积累。然而,所有六种仍然沉默了自我更新。这些结果表明,miR-294/miR-302 家族通过 Rb 依赖性和非依赖性途径分别调节 G1 限制点和自我更新的沉默。

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