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CPEB蛋白Orb和Orb2的RNA结合图谱。

RNA-binding profiles of CPEB proteins Orb and Orb2.

作者信息

Stepien Barbara Krystyna, Oppitz Cornelia, Gerlach Daniel, Dag Ugur, Novatchkova Maria, Krüttner Sebastian, Stark Alexander, Keleman Krystyna

机构信息

The Research Institute of Molecular Pathology, 1030 Vienna, Austria;

The Research Institute of Molecular Pathology, 1030 Vienna, Austria.

出版信息

Proc Natl Acad Sci U S A. 2016 Nov 8;113(45):E7030-E7038. doi: 10.1073/pnas.1603715113. Epub 2016 Oct 24.

DOI:10.1073/pnas.1603715113
PMID:27791065
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5111685/
Abstract

Localized protein translation is critical in many biological contexts, particularly in highly polarized cells, such as neurons, to regulate gene expression in a spatiotemporal manner. The cytoplasmic polyadenylation element-binding (CPEB) family of RNA-binding proteins has emerged as a key regulator of mRNA transport and local translation required for early embryonic development, synaptic plasticity, and long-term memory (LTM). Orb and Orb2 are single members of the CPEB1 and CPEB2 subfamilies of the CPEB proteins, respectively. At present, the identity of the mRNA targets they regulate is not fully known, and the binding specificity of the CPEB2 subfamily is a matter of debate. Using transcriptome-wide UV cross-linking and immunoprecipitation, we define the mRNA-binding sites and targets of CPEBs. Both Orb and Orb2 bind linear cytoplasmic polyadenylation element-like sequences in the 3' UTRs of largely overlapping target mRNAs, with Orb2 potentially having a broader specificity. Both proteins use their RNA-recognition motifs but not the Zinc-finger region for RNA binding. A subset of Orb2 targets is translationally regulated in cultured S2 cells and fly head extracts. Moreover, pan-neuronal RNAi knockdown of these targets suggests that a number of these targets are involved in LTM. Our results provide a comprehensive list of mRNA targets of the two CPEB proteins in , thus providing insights into local protein synthesis involved in various biological processes, including LTM.

摘要

局部蛋白质翻译在许多生物学背景中至关重要,尤其是在高度极化的细胞(如神经元)中,以时空方式调节基因表达。RNA结合蛋白的细胞质聚腺苷酸化元件结合(CPEB)家族已成为早期胚胎发育、突触可塑性和长期记忆(LTM)所需的mRNA运输和局部翻译的关键调节因子。Orb和Orb2分别是CPEB蛋白的CPEB1和CPEB2亚家族的单一成员。目前,它们所调节的mRNA靶标的身份尚不完全清楚,CPEB2亚家族的结合特异性也存在争议。通过全转录组紫外线交联和免疫沉淀,我们确定了CPEB的mRNA结合位点和靶标。Orb和Orb2都结合大量重叠靶标mRNA的3'UTR中的线性细胞质聚腺苷酸化元件样序列,Orb2可能具有更广泛的特异性。两种蛋白质都利用其RNA识别基序而非锌指区域进行RNA结合。在培养的S2细胞和果蝇头部提取物中,Orb2靶标的一个子集受到翻译调控。此外,对这些靶标的全神经元RNAi敲低表明,其中许多靶标参与了长期记忆。我们的结果提供了这两种CPEB蛋白在[具体物种或细胞类型未提及]中的mRNA靶标的完整列表,从而深入了解了包括长期记忆在内的各种生物学过程中涉及的局部蛋白质合成。

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本文引用的文献

1
Amyloidogenic Oligomerization Transforms Drosophila Orb2 from a Translation Repressor to an Activator.淀粉样寡聚化将果蝇Orb2从翻译抑制因子转变为激活因子。
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Translational Control of Autophagy by Orb in the Drosophila Germline.果蝇生殖细胞中 Orb 通过翻译控制自噬
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Elevated activation of CaMKIIα in the CPEB3-knockout hippocampus impairs a specific form of NMDAR-dependent synaptic depotentiation.CPEB3基因敲除小鼠海马体中CaMKIIα的激活增强,损害了一种特定形式的NMDAR依赖性突触去增强作用。
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NDST1 missense mutations in autosomal recessive intellectual disability.常染色体隐性智力障碍中的NDST1错义突变
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8
Deletion of CPEB3 enhances hippocampus-dependent memory via increasing expressions of PSD95 and NMDA receptors.CPEB3 的缺失通过增加 PSD95 和 NMDA 受体的表达来增强海马依赖性记忆。
J Neurosci. 2013 Oct 23;33(43):17008-22. doi: 10.1523/JNEUROSCI.3043-13.2013.
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Rasputin functions as a positive regulator of orb in Drosophila oogenesis.拉斯普京在果蝇卵子发生中作为 orb 的正调控因子发挥作用。
PLoS One. 2013 Sep 12;8(9):e72864. doi: 10.1371/journal.pone.0072864. eCollection 2013.
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Specificity factors in cytoplasmic polyadenylation.细胞质多聚腺苷酸化的特异性因素。
Wiley Interdiscip Rev RNA. 2013 Jul-Aug;4(4):437-61. doi: 10.1002/wrna.1171.