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与组蛋白茎环结合蛋白结合的mRNA的全基因组分析。

Genome-wide analysis of mRNAs bound to the histone stem-loop binding protein.

作者信息

Townley-Tilson W H Davin, Pendergrass Sarah A, Marzluff William F, Whitfield Michael L

机构信息

Department of Genetics, Dartmouth Medical School, Hanover, New Hampshire 03755, USA.

出版信息

RNA. 2006 Oct;12(10):1853-67. doi: 10.1261/rna.76006. Epub 2006 Aug 24.

Abstract

The replication-dependent histone mRNAs are cell-cycle-regulated and expressed only during S phase. In contrast to all other eukaryotic mRNAs, the histone mRNAs end in a highly conserved 16-nucleotide stem-loop rather than a poly(A) tail. The stem-loop is necessary and sufficient for the post-transcriptional regulation of histone mRNA during the cell cycle. The histone mRNA 3' stem-loop is bound by the stem-loop binding protein (SLBP) that is involved in pre-mRNA processing, translation, and stability of histone mRNA. Immunoprecipitation (IP) of RNA-binding proteins (RBPs) followed by microarray analysis has been used to identify the targets of RNA-binding proteins. This method is sometimes referred to as RIP-Chip (RNA IP followed by microarray analysis). Here we introduce a variation on the RIP-Chip method that uses a recombinant RBP to identify mRNA targets in a pool of total RNA; we call this method recombinant, or rRIP-Chip. Using this method, we show that recombinant SLBP binds exclusively to all five classes of histone mRNA. We also analyze the messages bound to the endogenous SLBP on polyribosomes by immunoprecipitation. We use two different microarray platforms to identify enriched mRNAs. Both platforms demonstrate remarkable specificity and consistency of results. Our data suggest that the replication-dependent histone mRNAs are likely to be the sole target of SLBP.

摘要

依赖复制的组蛋白mRNA在细胞周期中受到调控,仅在S期表达。与所有其他真核生物mRNA不同,组蛋白mRNA的末端是一个高度保守的16核苷酸茎环结构,而不是聚腺苷酸尾。该茎环结构对于细胞周期中组蛋白mRNA的转录后调控是必需且充分的。组蛋白mRNA 3'茎环与茎环结合蛋白(SLBP)结合,该蛋白参与前体mRNA加工、组蛋白mRNA的翻译和稳定性。通过微阵列分析对RNA结合蛋白(RBP)进行免疫沉淀(IP)已被用于鉴定RNA结合蛋白的靶标。这种方法有时被称为RIP-Chip(RNA免疫沉淀后进行微阵列分析)。在这里,我们介绍了一种RIP-Chip方法的变体,该方法使用重组RBP在总RNA池中鉴定mRNA靶标;我们将这种方法称为重组rRIP-Chip。使用这种方法,我们表明重组SLBP仅与所有五类组蛋白mRNA结合。我们还通过免疫沉淀分析了多核糖体上与内源性SLBP结合的信息。我们使用两种不同的微阵列平台来鉴定富集的mRNA。两个平台都显示出显著的特异性和结果的一致性。我们的数据表明,依赖复制的组蛋白mRNA可能是SLBP的唯一靶标。

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本文引用的文献

1
Symplekin and multiple other polyadenylation factors participate in 3'-end maturation of histone mRNAs.
Genes Dev. 2005 Nov 1;19(21):2583-92. doi: 10.1101/gad.1371105. Epub 2005 Oct 17.
2
Stable ribosome binding to the endoplasmic reticulum enables compartment-specific regulation of mRNA translation.
Mol Biol Cell. 2005 Dec;16(12):5819-31. doi: 10.1091/mbc.e05-07-0685. Epub 2005 Oct 12.
3
The polyadenylation factor CPSF-73 is involved in histone-pre-mRNA processing.
Cell. 2005 Oct 7;123(1):37-48. doi: 10.1016/j.cell.2005.08.002.
5
From birth to death: the complex lives of eukaryotic mRNAs.
Science. 2005 Sep 2;309(5740):1514-8. doi: 10.1126/science.1111443.
6
Regulated degradation of replication-dependent histone mRNAs requires both ATR and Upf1.
Nat Struct Mol Biol. 2005 Sep;12(9):794-800. doi: 10.1038/nsmb972. Epub 2005 Aug 7.
7
Translation termination is involved in histone mRNA degradation when DNA replication is inhibited.
Mol Cell Biol. 2005 Aug;25(16):6879-88. doi: 10.1128/MCB.25.16.6879-6888.2005.
8
Post-transcriptional operons and regulons co-ordinating gene expression.
Chromosome Res. 2005;13(3):327-37. doi: 10.1007/s10577-005-0848-1.
9
10
High reproducibility using sodium hydroxide-stripped long oligonucleotide DNA microarrays.
Biotechniques. 2005 Jan;38(1):121-4. doi: 10.2144/05381MT02.

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