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Hel-N1:一种自身免疫性RNA结合蛋白,对生长因子mRNA富含3'尿苷酸的非翻译区具有特异性。

Hel-N1: an autoimmune RNA-binding protein with specificity for 3' uridylate-rich untranslated regions of growth factor mRNAs.

作者信息

Levine T D, Gao F, King P H, Andrews L G, Keene J D

机构信息

Department of Microbiology and Immunology, Duke University Medical Center, Durham, North Carolina 27710.

出版信息

Mol Cell Biol. 1993 Jun;13(6):3494-504. doi: 10.1128/mcb.13.6.3494-3504.1993.

DOI:10.1128/mcb.13.6.3494-3504.1993
PMID:8497264
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC359819/
Abstract

We have investigated the RNA binding specificity of Hel-N1, a human neuron-specific RNA-binding protein, which contains three RNA recognition motifs. Hel-N1 is a human homolog of Drosophila melanogaster elav, which plays a vital role in the development of neurons. A random RNA selection procedure revealed that Hel-N1 prefers to bind RNAs containing short stretches of uridylates similar to those found in the 3' untranslated regions (3' UTRs) of oncoprotein and cytokine mRNAs such as c-myc, c-fos, and granulocyte macrophage colony-stimulating factor. Direct binding studies demonstrated that Hel-N1 bound and formed multimers with c-myc 3' UTR mRNA and required, as a minimum, a specific 29-nucleotide stretch containing AUUUG, AUUUA, and GUUUUU. Deletion analysis demonstrated that a fragment of Hel-N1 containing 87 amino acids, encompassing the third RNA recognition motif, forms an RNA binding domain for the c-myc 3' UTR. In addition, Hel-N1 was shown to be reactive with autoantibodies from patients with paraneoplastic encephalomyelitis both before and after binding to c-myc mRNA.

摘要

我们研究了人类神经元特异性RNA结合蛋白Hel-N1的RNA结合特异性,它包含三个RNA识别基序。Hel-N1是果蝇elav的人类同源物,在神经元发育中起重要作用。一种随机RNA筛选程序显示,Hel-N1更倾向于结合含有短尿苷酸片段的RNA,类似于在癌蛋白和细胞因子mRNA(如c-myc、c-fos和粒细胞巨噬细胞集落刺激因子)的3'非翻译区(3'UTR)中发现的那些片段。直接结合研究表明,Hel-N1与c-myc 3'UTR mRNA结合并形成多聚体,并且至少需要一个包含AUUUG、AUUUA和GUUUUU的特定29个核苷酸的片段。缺失分析表明,Hel-N1的一个包含87个氨基酸的片段,涵盖第三个RNA识别基序,形成了c-myc 3'UTR的RNA结合结构域。此外,在与c-myc mRNA结合之前和之后,Hel-N1都显示出与副肿瘤性脑脊髓炎患者的自身抗体发生反应。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/77bd/359819/01431a221263/molcellb00018-0390-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/77bd/359819/2bcbffad3938/molcellb00018-0386-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/77bd/359819/4075988f0d7a/molcellb00018-0387-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/77bd/359819/a2df821e441d/molcellb00018-0387-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/77bd/359819/3d8fb43fd0c7/molcellb00018-0388-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/77bd/359819/98d5ccf59008/molcellb00018-0388-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/77bd/359819/6d03cfcade08/molcellb00018-0389-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/77bd/359819/01431a221263/molcellb00018-0390-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/77bd/359819/2bcbffad3938/molcellb00018-0386-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/77bd/359819/4075988f0d7a/molcellb00018-0387-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/77bd/359819/a2df821e441d/molcellb00018-0387-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/77bd/359819/3d8fb43fd0c7/molcellb00018-0388-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/77bd/359819/98d5ccf59008/molcellb00018-0388-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/77bd/359819/6d03cfcade08/molcellb00018-0389-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/77bd/359819/01431a221263/molcellb00018-0390-a.jpg

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