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SUMOylation 通过 Hedgehog 信号通路调控涡虫干细胞增殖和区域细胞死亡。

SUMOylation controls stem cell proliferation and regional cell death through Hedgehog signaling in planarians.

机构信息

Department of Molecular and Cell Biology, University of California, 5200 North Lake Road, Merced, CA, 95343, USA.

Quantitative and Systems Biology Graduate Program, University of California, Merced, USA.

出版信息

Cell Mol Life Sci. 2018 Apr;75(7):1285-1301. doi: 10.1007/s00018-017-2697-4. Epub 2017 Nov 2.

Abstract

Mechanisms underlying anteroposterior body axis differences during adult tissue maintenance and regeneration are poorly understood. Here, we identify that post-translational modifications through the SUMO (Small Ubiquitin-like Modifier) machinery are evolutionarily conserved in the Lophotrocozoan Schmidtea mediterranea. Disruption of SUMOylation in adult animals by RNA-interference of the only SUMO E2 conjugating enzyme Ubc9 leads to a systemic increase in DNA damage and a remarkable regional defect characterized by increased cell death and loss of the posterior half of the body. We identified that Ubc9 is mainly expressed in planarian stem cells (neoblasts) but it is also transcribed in differentiated cells including neurons. Regeneration in Ubc9(RNAi) animals is impaired and associated with low neoblast proliferation. We present evidence indicating that Ubc9-induced regional cell death is preceded by alterations in transcription and spatial expression of repressors and activators of the Hedgehog signaling pathway. Our results demonstrate that SUMOylation acts as a regional-specific cue to regulate cell fate during tissue renewal and regeneration.

摘要

在成年组织维持和再生过程中,前后体轴差异的潜在机制还知之甚少。在这里,我们鉴定出,在 Lophotrocozoan 地中海扁虫 Schmidtea mediterranea 中,通过 SUMO(小泛素样修饰物)机制的翻译后修饰是进化保守的。通过 RNA 干扰唯一的 SUMO E2 连接酶 Ubc9 对成年动物进行 SUMO 化的破坏,会导致 DNA 损伤的全身性增加,并出现显著的区域性缺陷,其特征是细胞死亡增加和身体后半部分的丧失。我们鉴定出,Ubc9 主要在扁形动物干细胞(成体干细胞)中表达,但也在包括神经元在内的分化细胞中转录。Ubc9(RNAi)动物的再生受到损害,并与成体干细胞增殖减少有关。我们提供的证据表明,Ubc9 诱导的区域性细胞死亡之前,Hedgehog 信号通路的抑制剂和激活剂的转录和空间表达发生改变。我们的研究结果表明,SUMO 化作为一种区域特异性提示,在组织更新和再生过程中调节细胞命运。

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