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斑马鱼翻译核糖体亲和纯化技术的开发。

Development of translating ribosome affinity purification for zebrafish.

作者信息

Tryon Robert C, Pisat Nilambari, Johnson Stephen L, Dougherty Joseph D

机构信息

Department of Genetics, Washington University School of Medicine, St. Louis, MO 63110, USA.

出版信息

Genesis. 2013 Mar;51(3):187-92. doi: 10.1002/dvg.22363. Epub 2013 Feb 26.

Abstract

The regulation of transcription and translation by specific cell types is essential to generate the cellular diversity that typifies complex multicellular organisms. Tagging and purification of ribosomal proteins has been shown to be an innovative and effective means of characterizing the ribosome bound transcriptome of highly specific cell populations in vivo. To test the feasibility of using translating ribosome affinity purification (TRAP) in zebrafish, we have generated both a ubiquitous TRAP line and a melanocyte-specific TRAP line using the native zebrafish rpl10a ribosomal protein. We have demonstrated the capacity to capture mRNA transcripts bound to ribosomes, and confirmed the expected enrichment of melanocyte specific genes and depletion of non-melanocyte genes when expressing the TRAP construct with a cell specific promoter. We have also generated a generic EGFP-rpl10a Tol2 plasmid construct (Tol2-zTRAP) that can be readily modified to target any additional cell populations with characterized promoters in zebrafish.

摘要

特定细胞类型对转录和翻译的调控对于产生构成复杂多细胞生物体特征的细胞多样性至关重要。核糖体蛋白的标记和纯化已被证明是一种在体内表征高度特异性细胞群体核糖体结合转录组的创新且有效方法。为了测试在斑马鱼中使用翻译核糖体亲和纯化(TRAP)的可行性,我们利用天然斑马鱼核糖体蛋白rpl10a生成了一个泛在性TRAP品系和一个黑素细胞特异性TRAP品系。我们展示了捕获与核糖体结合的mRNA转录本的能力,并证实当用细胞特异性启动子表达TRAP构建体时,黑素细胞特异性基因预期会富集,而非黑素细胞基因会减少。我们还构建了一个通用的EGFP - rpl10a Tol2质粒构建体(Tol2 - zTRAP),该构建体可轻松修改,以利用斑马鱼中具有特征的启动子靶向任何其他细胞群体。

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