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人 MTERF3 抗体对
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人 MTERF3 抗体对

01AB02508

Mitochondrial transcription termination factor 3 (MTERF3) is a nuclear-encoded protein that localizes to the mitochondrial matrix, where it acts as a negative regulator of mitochondrial DNA (mtDNA) transcription initiation. By binding to mitochondrial promoter DNA, MTERF3 coordinates the balance between transcription, translation, and respiratory chain biogenesis. Structurally, it is a helical repeat protein that also interacts with mitochondrial 16S rRNA to promote the assembly of the large 39S mitochondrial ribosomal subunit. This dual role ensures efficient mitochondrial translation and the proper formation of respiratory complexes. MTERF3 serves as a critical checkpoint in mitochondrial gene expression; its loss leads to the overactivation of mtDNA transcription and defective ribosome biogenesis, ultimately resulting in impaired oxidative phosphorylation and significant mitochondrial dysfunction.

Human
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技术参数

靶点基因名
MTERF3
基因别名
MTERFD1
蛋白别名
mitochondrial transcription termination factor 3; MTERF3
UniProt
Q96E29
物种
Human

产品详情

靶点名称
MTERF3
蛋白名称
mitochondrial transcription termination factor 3
蛋白别名
Transcription termination factor 3; mitochondrial; Mitochondrial transcription termination factor 3; mTERF3; mTERF domain-containing protein 1; mitochondrial
靶点基因名
MTERF3
基因别名
MTERFD1
UniProt
Q96E29
来源物种
Homo sapiens (Human)
物种反应性
Human

背景介绍

Mitochondrial transcription termination factor 3 (MTERF3) is a nuclear-encoded protein that localizes to the mitochondrial matrix, where it acts as a negative regulator of mitochondrial DNA (mtDNA) transcription initiation. By binding to mitochondrial promoter DNA, MTERF3 coordinates the balance between transcription, translation, and respiratory chain biogenesis. Structurally, it is a helical repeat protein that also interacts with mitochondrial 16S rRNA to promote the assembly of the large 39S mitochondrial ribosomal subunit. This dual role ensures efficient mitochondrial translation and the proper formation of respiratory complexes. MTERF3 serves as a critical checkpoint in mitochondrial gene expression; its loss leads to the overactivation of mtDNA transcription and defective ribosome biogenesis, ultimately resulting in impaired oxidative phosphorylation and significant mitochondrial dysfunction.