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斑马鱼尾鳍再生的转录谱分析

Transcriptional profiling of caudal fin regeneration in zebrafish.

作者信息

Schebesta Michael, Lien Ching-Ling, Engel Felix B, Keating Mark T

机构信息

Howard Hughes Medical Institute, Department of Cardiology, Harvard Medical School, 320 Longwood Avenue, Boston, MA 02115, USA.

出版信息

ScientificWorldJournal. 2006 Jun 2;6 Suppl 1:38-54. doi: 10.1100/tsw.2006.326.

Abstract

Regeneration of severed limbs in adult animals is restricted to urodele amphibians. Mammals, including humans, have very limited regenerative capabilities and even with proper treatment, only the tips of our digits can grow back. Teleost fish can regenerate amputated fins, the evolutionary ancestors of limbs. To elucidate the principles of limb-fin regeneration, we performed an Affymetrix microarray screen on regenerating caudal fins 12, 24, 48, and 72 h post amputation. Approximately 15,000 zebrafish transcripts were analyzed, identifying 829 transcripts as differentially expressed during regeneration. Of those, 563 were up-regulated and 266 were down-regulated. We constructed a comprehensive database containing expression data, functional assignment, and background information from the literature for each differentially expressed transcript. In order to validate our findings, we employed three approaches: (1) microarray expression analysis of genes previously implicated in fin regeneration, (2) RT-PCR analysis of genes newly identified as differentially expressed during regeneration, and (3) in situ hybridization of the up-regulated genes bambi, dlx5A, and her6. Moreover, we show that Smad 1/5/8 proteins, effector molecules of Bmp signaling, are phosphorylated during fin regeneration. Taken together, we provide a comprehensive database of fin regeneration that will serve as an important tool for understanding the molecular mechanisms of regeneration.

摘要

成年动物断肢再生仅限于有尾两栖动物。包括人类在内的哺乳动物的再生能力非常有限,即使经过适当治疗,也只有指尖能够再生。硬骨鱼可以再生被截断的鳍,而鳍是肢体的进化祖先。为了阐明肢体-鳍再生的原理,我们在截肢后12、24、48和72小时对再生尾鳍进行了Affymetrix微阵列筛选。分析了大约15000个斑马鱼转录本,确定了829个转录本在再生过程中差异表达。其中,563个上调,266个下调。我们构建了一个综合数据库,包含每个差异表达转录本的表达数据、功能分配和来自文献的背景信息。为了验证我们的发现,我们采用了三种方法:(1)对先前涉及鳍再生的基因进行微阵列表达分析,(2)对新确定在再生过程中差异表达的基因进行RT-PCR分析,(3)对上调基因bambi、dlx5A和her6进行原位杂交。此外,我们还表明,Bmp信号的效应分子Smad 1/5/8蛋白在鳍再生过程中被磷酸化。综上所述,我们提供了一个鳍再生的综合数据库,这将成为理解再生分子机制的重要工具。

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