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TEFM 变异会损害线粒体转录,导致儿童期发病的神经退行性疾病。

TEFM variants impair mitochondrial transcription causing childhood-onset neurological disease.

机构信息

MRC Mitochondrial Biology Unit, University of Cambridge, Cambridge, CB2 0XY, UK.

Children's Hospital of Eastern Ontario Research Institute, University of Ottawa, Ottawa, ON, Canada.

出版信息

Nat Commun. 2023 Feb 23;14(1):1009. doi: 10.1038/s41467-023-36277-7.


DOI:10.1038/s41467-023-36277-7
PMID:36823193
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9950373/
Abstract

Mutations in the mitochondrial or nuclear genomes are associated with a diverse group of human disorders characterized by impaired mitochondrial respiration. Within this group, an increasing number of mutations have been identified in nuclear genes involved in mitochondrial RNA biology. The TEFM gene encodes the mitochondrial transcription elongation factor responsible for enhancing the processivity of mitochondrial RNA polymerase, POLRMT. We report for the first time that TEFM variants are associated with mitochondrial respiratory chain deficiency and a wide range of clinical presentations including mitochondrial myopathy with a treatable neuromuscular transmission defect. Mechanistically, we show muscle and primary fibroblasts from the affected individuals have reduced levels of promoter distal mitochondrial RNA transcripts. Finally, tefm knockdown in zebrafish embryos resulted in neuromuscular junction abnormalities and abnormal mitochondrial function, strengthening the genotype-phenotype correlation. Our study highlights that TEFM regulates mitochondrial transcription elongation and its defect results in variable, tissue-specific neurological and neuromuscular symptoms.

摘要

线粒体或核基因组的突变与一组多样化的人类疾病有关,这些疾病的特征是线粒体呼吸受损。在这组疾病中,越来越多的与线粒体 RNA 生物学相关的核基因突变被鉴定出来。TEFM 基因编码线粒体转录延伸因子,负责增强线粒体 RNA 聚合酶 POLRMT 的持续性。我们首次报道,TEFM 变体与线粒体呼吸链缺陷以及广泛的临床表现有关,包括具有可治疗的神经肌肉传递缺陷的线粒体肌病。从机制上讲,我们发现受影响个体的肌肉和原代成纤维细胞中,启动子远端的线粒体 RNA 转录物水平降低。最后,tefm 在斑马鱼胚胎中的敲低导致神经肌肉接头异常和线粒体功能异常,这加强了基因型-表型相关性。我们的研究强调,TEFM 调节线粒体转录延伸,其缺陷导致可变的、组织特异性的神经和神经肌肉症状。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f85/9950373/d62c692fe693/41467_2023_36277_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f85/9950373/d5624f9c03f8/41467_2023_36277_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f85/9950373/a960609d2403/41467_2023_36277_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f85/9950373/ab76abe1472a/41467_2023_36277_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f85/9950373/92c1f15847a5/41467_2023_36277_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f85/9950373/0cea060f61af/41467_2023_36277_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f85/9950373/03788a4bb2cf/41467_2023_36277_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f85/9950373/c74dd36e9366/41467_2023_36277_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f85/9950373/d62c692fe693/41467_2023_36277_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f85/9950373/d5624f9c03f8/41467_2023_36277_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f85/9950373/a960609d2403/41467_2023_36277_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f85/9950373/ab76abe1472a/41467_2023_36277_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f85/9950373/92c1f15847a5/41467_2023_36277_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f85/9950373/0cea060f61af/41467_2023_36277_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f85/9950373/03788a4bb2cf/41467_2023_36277_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f85/9950373/c74dd36e9366/41467_2023_36277_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f85/9950373/d62c692fe693/41467_2023_36277_Fig8_HTML.jpg

相似文献

[1]
TEFM variants impair mitochondrial transcription causing childhood-onset neurological disease.

Nat Commun. 2023-2-23

[2]
TEFM is a potent stimulator of mitochondrial transcription elongation in vitro.

Nucleic Acids Res. 2015-3-11

[3]
TEFM (c17orf42) is necessary for transcription of human mtDNA.

Nucleic Acids Res. 2011-1-28

[4]
TEFM regulates both transcription elongation and RNA processing in mitochondria.

EMBO Rep. 2019-4-29

[5]
Mechanism of Transcription Anti-termination in Human Mitochondria.

Cell. 2017-11-16

[6]
TEFM facilitates transition from RNA synthesis to DNA synthesis at H-strand replication origin of mtDNA.

Commun Biol. 2025-2-8

[7]
Mitochondrial biology. Replication-transcription switch in human mitochondria.

Science. 2015-1-30

[8]
POLRMT mutations impair mitochondrial transcription causing neurological disease.

Nat Commun. 2021-2-18

[9]
TEFM facilitates uterine corpus endometrial carcinoma progression by activating ROS-NFκB pathway.

J Transl Med. 2024-12-27

[10]
Mitochondrial DNA Transcription and Its Regulation: An Evolutionary Perspective.

Trends Genet. 2018-6-23

引用本文的文献

[1]
Mitochondrial Quality Control in Health and Disease.

MedComm (2020). 2025-8-15

[2]
Structural basis for promoter recognition and transcription factor binding and release in human mitochondria.

Mol Cell. 2025-7-22

[3]
Review of 40 genes causing congenital myasthenic syndromes.

J Hum Genet. 2025-6-18

[4]
Untargeted proteomics enables ultra-rapid variant prioritisation in mitochondrial and other rare diseases.

Genome Med. 2025-5-22

[5]
Review: Utility of mass spectrometry in rare disease research and diagnosis.

NPJ Genom Med. 2025-3-31

[6]
TEFM facilitates uterine corpus endometrial carcinoma progression by activating ROS-NFκB pathway.

J Transl Med. 2024-12-27

[7]
A micro-costing study of mass-spectrometry based quantitative proteomics testing applied to the diagnostic pipeline of mitochondrial and other rare disorders.

Orphanet J Rare Dis. 2024-11-29

[8]
Illuminating mitochondrial translation through mouse models.

Hum Mol Genet. 2024-5-22

[9]
Emerging variants, unique phenotypes, and transcriptomic signatures: an integrated study of COASY-associated diseases.

Ann Clin Transl Neurol. 2024-6

[10]
Mitochondrial protein synthesis quality control.

Hum Mol Genet. 2024-5-22

本文引用的文献

[1]
Neuromuscular Junction Abnormalities in Mitochondrial Disease: An Observational Cohort Study.

Neurol Clin Pract. 2021-4

[2]
Genetic basis of mitochondrial diseases.

FEBS Lett. 2021-4

[3]
POLRMT mutations impair mitochondrial transcription causing neurological disease.

Nat Commun. 2021-2-18

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A simple and effective F0 knockout method for rapid screening of behaviour and other complex phenotypes.

Elife. 2021-1-8

[5]
The diagnostic utility of genome sequencing in a pediatric cohort with suspected mitochondrial disease.

Genet Med. 2020-7

[6]
Modulation of Agrin and RhoA Pathways Ameliorates Movement Defects and Synapse Morphology in MYO9A-Depleted Zebrafish.

Cells. 2019-8-7

[7]
Graph-based genome alignment and genotyping with HISAT2 and HISAT-genotype.

Nat Biotechnol. 2019-8-2

[8]
Salbutamol modifies the neuromuscular junction in a mouse model of ColQ myasthenic syndrome.

Hum Mol Genet. 2019-7-15

[9]
Mutations in ELAC2 associated with hypertrophic cardiomyopathy impair mitochondrial tRNA 3'-end processing.

Hum Mutat. 2019-6-18

[10]
TEFM regulates both transcription elongation and RNA processing in mitochondria.

EMBO Rep. 2019-4-29

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