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LIM 同源盒基因对于扁形动物体后端表达 Wnt 细胞的分化是必需的。

A LIM-homeobox gene is required for differentiation of Wnt-expressing cells at the posterior end of the planarian body.

机构信息

Genome Resource and Analysis Unit, RIKEN Center for Developmental Biology, 2-2-3 Minatojima-minamimachi, Chuo-ku, Kobe, Hyogo 650-0047, Japan.

出版信息

Development. 2011 Sep;138(17):3679-88. doi: 10.1242/dev.060194.

DOI:10.1242/dev.060194
PMID:21828095
Abstract

Planarians have high regenerative ability, which is dependent on pluripotent adult somatic stem cells called neoblasts. Recently, canonical Wnt/β-catenin signaling was shown to be required for posterior specification, and Hedgehog signaling was shown to control anterior-posterior polarity via activation of the Djwnt1/P-1 gene at the posterior end of planarians. Thus, various signaling molecules play an important role in planarian stem cell regulation. However, the molecular mechanisms directly involved in stem cell differentiation have remained unclear. Here, we demonstrate that one of the planarian LIM-homeobox genes, Djislet, is required for the differentiation of Djwnt1/P-1-expressing cells from stem cells at the posterior end. RNA interference (RNAi)-treated planarians of Djislet [Djislet(RNAi)] show a tail-less phenotype. Thus, we speculated that Djislet might be involved in activation of the Wnt signaling pathway in the posterior blastema. When we carefully examined the expression pattern of Djwnt1/P-1 by quantitative real-time PCR during posterior regeneration, we found two phases of Djwnt1/P-1 expression: the first phase was detected in the differentiated cells in the old tissue in the early stage of regeneration and then a second phase was observed in the cells derived from stem cells in the posterior blastema. Interestingly, Djislet is expressed in stem cell-derived DjPiwiA- and Djwnt1/P-1-expressing cells, and Djislet(RNAi) only perturbed the second phase. Thus, we propose that Djislet might act to trigger the differentiation of cells expressing Djwnt1/P-1 from stem cells.

摘要

涡虫具有很强的再生能力,这种能力依赖于多能成体体干细胞,即 neoblasts。最近的研究表明,经典 Wnt/β-catenin 信号通路对于尾部特化是必需的,而 Hedgehog 信号通路通过激活涡虫尾部的 Djwnt1/P-1 基因来控制前后极性。因此,各种信号分子在涡虫干细胞调控中发挥着重要作用。然而,直接参与干细胞分化的分子机制仍不清楚。在这里,我们证明了一种涡虫 LIM 同源盒基因 Djislet 对于尾部干细胞中 Djwnt1/P-1 表达细胞的分化是必需的。Djislet 的 RNA 干扰(RNAi)处理的涡虫(Djislet[RNAi])表现出无尾表型。因此,我们推测 Djislet 可能参与了尾部芽基中 Wnt 信号通路的激活。当我们通过定量实时 PCR 在尾部再生过程中仔细检查 Djwnt1/P-1 的表达模式时,我们发现了 Djwnt1/P-1 表达的两个阶段:第一个阶段在再生早期的旧组织中分化细胞中检测到,然后第二个阶段在尾部芽基中的干细胞衍生细胞中观察到。有趣的是,Djislet 在干细胞衍生的 DjPiwiA-和 Djwnt1/P-1 表达细胞中表达,而 Djislet(RNAi)仅干扰了第二个阶段。因此,我们提出 Djislet 可能作用于触发干细胞中表达 Djwnt1/P-1 的细胞的分化。

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