Suppr超能文献

鉴定对Ⅰ型强直性肌营养不良具有治疗潜力的植物源生物碱。

Identification of Plant-derived Alkaloids with Therapeutic Potential for Myotonic Dystrophy Type I.

作者信息

Herrendorff Ruben, Faleschini Maria Teresa, Stiefvater Adeline, Erne Beat, Wiktorowicz Tatiana, Kern Frances, Hamburger Matthias, Potterat Olivier, Kinter Jochen, Sinnreich Michael

机构信息

From the Neuromuscular Research Group, Departments of Neurology and Biomedicine, University Hospital Basel, Klingelbergstrasse 50, 4056 Basel, Switzerland and.

the Division of Pharmaceutical Biology, Department of Pharmaceutical Sciences, University of Basel, Klingelbergstrasse 50, 4056 Basel, Switzerland.

出版信息

J Biol Chem. 2016 Aug 12;291(33):17165-77. doi: 10.1074/jbc.M115.710616. Epub 2016 Jun 13.

Abstract

Myotonic dystrophy type I (DM1) is a disabling neuromuscular disease with no causal treatment available. This disease is caused by expanded CTG trinucleotide repeats in the 3' UTR of the dystrophia myotonica protein kinase gene. On the RNA level, expanded (CUG)n repeats form hairpin structures that sequester splicing factors such as muscleblind-like 1 (MBNL1). Lack of available MBNL1 leads to misregulated alternative splicing of many target pre-mRNAs, leading to the multisystemic symptoms in DM1. Many studies aiming to identify small molecules that target the (CUG)n-MBNL1 complex focused on synthetic molecules. In an effort to identify new small molecules that liberate sequestered MBNL1 from (CUG)n RNA, we focused specifically on small molecules of natural origin. Natural products remain an important source for drugs and play a significant role in providing novel leads and pharmacophores for medicinal chemistry. In a new DM1 mechanism-based biochemical assay, we screened a collection of isolated natural compounds and a library of over 2100 extracts from plants and fungal strains. HPLC-based activity profiling in combination with spectroscopic methods were used to identify the active principles in the extracts. The bioactivity of the identified compounds was investigated in a human cell model and in a mouse model of DM1. We identified several alkaloids, including the β-carboline harmine and the isoquinoline berberine, that ameliorated certain aspects of the DM1 pathology in these models. Alkaloids as a compound class may have potential for drug discovery in other RNA-mediated diseases.

摘要

I型强直性肌营养不良症(DM1)是一种致残性神经肌肉疾病,目前尚无因果性治疗方法。这种疾病是由肌强直性营养不良蛋白激酶基因3'UTR中CTG三核苷酸重复序列扩增引起的。在RNA水平上,扩增的(CUG)n重复序列形成发夹结构,可隔离诸如肌肉失明样蛋白1(MBNL1)等剪接因子。缺乏可用的MBNL1会导致许多靶前体mRNA的可变剪接失调,从而导致DM1出现多系统症状。许多旨在鉴定靶向(CUG)n-MBNL1复合物的小分子的研究都集中在合成分子上。为了鉴定能从(CUG)n RNA中释放被隔离的MBNL1的新小分子,我们特别关注天然来源的小分子。天然产物仍然是药物的重要来源,在为药物化学提供新的先导化合物和药效基团方面发挥着重要作用。在一种基于DM1机制的新生化检测方法中,我们筛选了一系列分离的天然化合物以及一个包含2100多种植物和真菌菌株提取物的文库。基于高效液相色谱的活性谱分析结合光谱方法用于鉴定提取物中的活性成分。在人细胞模型和DM1小鼠模型中研究了所鉴定化合物的生物活性。我们鉴定出了几种生物碱,包括β-咔啉哈尔明和异喹啉黄连素,它们在这些模型中改善了DM1病理的某些方面。生物碱作为一类化合物在其他RNA介导的疾病的药物发现中可能具有潜力。

相似文献

1
Identification of Plant-derived Alkaloids with Therapeutic Potential for Myotonic Dystrophy Type I.
J Biol Chem. 2016 Aug 12;291(33):17165-77. doi: 10.1074/jbc.M115.710616. Epub 2016 Jun 13.
4
Systemic Evaluation of Chimeric LNA/2'-O-Methyl Steric Blockers for Myotonic Dystrophy Type 1 Therapy.
Nucleic Acid Ther. 2020 Apr;30(2):80-93. doi: 10.1089/nat.2019.0811. Epub 2019 Dec 23.
5
Colocalization of muscleblind with RNA foci is separable from mis-regulation of alternative splicing in myotonic dystrophy.
J Cell Sci. 2005 Jul 1;118(Pt 13):2923-33. doi: 10.1242/jcs.02404. Epub 2005 Jun 16.
6
Reduced cytoplasmic MBNL1 is an early event in a brain-specific mouse model of myotonic dystrophy.
Hum Mol Genet. 2017 Jun 15;26(12):2247-2257. doi: 10.1093/hmg/ddx115.
7
MBNL1 and CUGBP1 modify expanded CUG-induced toxicity in a Drosophila model of myotonic dystrophy type 1.
Hum Mol Genet. 2006 Jul 1;15(13):2138-45. doi: 10.1093/hmg/ddl137. Epub 2006 May 24.
8
Loss of MBNL1-mediated retrograde BDNF signaling in the myotonic dystrophy brain.
Acta Neuropathol Commun. 2023 Mar 15;11(1):44. doi: 10.1186/s40478-023-01540-x.
9
Furamidine Rescues Myotonic Dystrophy Type I Associated Mis-Splicing through Multiple Mechanisms.
ACS Chem Biol. 2018 Sep 21;13(9):2708-2718. doi: 10.1021/acschembio.8b00646. Epub 2018 Aug 27.
10
Pathogenic mechanisms of myotonic dystrophy.
Biochem Soc Trans. 2009 Dec;37(Pt 6):1281-6. doi: 10.1042/BST0371281.

引用本文的文献

1
Molecular genetics of myotonic dystrophy and the evolution of therapeutic approaches.
J Hum Genet. 2025 Jul 3. doi: 10.1038/s10038-025-01358-6.
2
Influence of CTG repeats from the human DM1 locus on murine gut microbiota.
Comput Struct Biotechnol J. 2025 Feb 19;27:733-743. doi: 10.1016/j.csbj.2025.02.016. eCollection 2025.
4
Antioxidant effects of bis-indole alkaloid indigo and related signaling pathways in the experimental model of Duchenne muscular dystrophy.
Cell Stress Chaperones. 2022 Jul;27(4):417-429. doi: 10.1007/s12192-022-01282-0. Epub 2022 Jun 10.
7
Increased Muscleblind levels by chloroquine treatment improve myotonic dystrophy type 1 phenotypes in in vitro and in vivo models.
Proc Natl Acad Sci U S A. 2019 Dec 10;116(50):25203-25213. doi: 10.1073/pnas.1820297116. Epub 2019 Nov 21.
8
Small Molecules Which Improve Pathogenesis of Myotonic Dystrophy Type 1.
Front Neurol. 2018 May 18;9:349. doi: 10.3389/fneur.2018.00349. eCollection 2018.
9
Inhibitory effects and mechanism of dihydroberberine on hERG channels expressed in HEK293 cells.
PLoS One. 2017 Aug 1;12(8):e0181823. doi: 10.1371/journal.pone.0181823. eCollection 2017.
10
Targeting deregulated AMPK/mTORC1 pathways improves muscle function in myotonic dystrophy type I.
J Clin Invest. 2017 Feb 1;127(2):549-563. doi: 10.1172/JCI89616. Epub 2017 Jan 9.

本文引用的文献

2
Lomofungin and dilomofungin: inhibitors of MBNL1-CUG RNA binding with distinct cellular effects.
Nucleic Acids Res. 2014 Jun;42(10):6591-602. doi: 10.1093/nar/gku275. Epub 2014 May 5.
3
Ribosome-targeting antibiotics and mechanisms of bacterial resistance.
Nat Rev Microbiol. 2014 Jan;12(1):35-48. doi: 10.1038/nrmicro3155.
4
Novel effect of berberine on thermoregulation in mice model induced by hot and cold environmental stimulation.
PLoS One. 2013;8(1):e54234. doi: 10.1371/journal.pone.0054234. Epub 2013 Jan 15.
5
A simple protocol for the subcellular fractionation of skeletal muscle cells and tissue.
BMC Res Notes. 2012 Sep 20;5:513. doi: 10.1186/1756-0500-5-513.
8
RNase H-mediated degradation of toxic RNA in myotonic dystrophy type 1.
Proc Natl Acad Sci U S A. 2012 Mar 13;109(11):4221-6. doi: 10.1073/pnas.1117019109. Epub 2012 Feb 27.
9
Rationally designed small molecules targeting the RNA that causes myotonic dystrophy type 1 are potently bioactive.
ACS Chem Biol. 2012 May 18;7(5):856-62. doi: 10.1021/cb200408a. Epub 2012 Mar 5.
10
Two high-throughput screening assays for aberrant RNA-protein interactions in myotonic dystrophy type 1.
Anal Bioanal Chem. 2012 Feb;402(5):1889-98. doi: 10.1007/s00216-011-5604-0. Epub 2012 Jan 5.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验