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线粒体中的核转录因子:微调线粒体代谢的新范式

Nuclear Transcription Factors in the Mitochondria: A New Paradigm in Fine-Tuning Mitochondrial Metabolism.

作者信息

Sepuri Naresh Babu V, Tammineni Prasad, Mohammed Fareed, Paripati Arunkumar

机构信息

Department of Biochemistry, School of Life Sciences, University of Hyderabad, Telangana, 500046, India.

出版信息

Handb Exp Pharmacol. 2017;240:3-20. doi: 10.1007/164_2016_3.

Abstract

Noncanonical functions of several nuclear transcription factors in the mitochondria have been gaining exceptional traction over the years. These transcription factors include nuclear hormone receptors like estrogen, glucocorticoid, and thyroid hormone receptors: p53, IRF3, STAT3, STAT5, CREB, NF-kB, and MEF-2D. Mitochondria-localized nuclear transcription factors regulate mitochondrial processes like apoptosis, respiration and mitochondrial transcription albeit being nuclear in origin and having nuclear functions. Hence, the cell permits these multi-stationed transcription factors to orchestrate and fine-tune cellular metabolism at various levels of operation. Despite their ubiquitous distribution in different subcompartments of mitochondria, their targeting mechanism is poorly understood. Here, we review the current status of mitochondria-localized transcription factors and discuss the possible targeting mechanism besides the functional interplay between these factors.

摘要

近年来,几种核转录因子在线粒体中的非经典功能受到了格外关注。这些转录因子包括核激素受体,如雌激素、糖皮质激素和甲状腺激素受体;p53、IRF3、STAT3、STAT5、CREB、NF-κB和MEF-2D。定位于线粒体的核转录因子尽管起源于细胞核并具有核功能,但却能调节线粒体的过程,如细胞凋亡、呼吸作用和线粒体转录。因此,细胞允许这些多功能的转录因子在不同的操作水平上协调和微调细胞代谢。尽管它们普遍分布于线粒体的不同亚区室中,但其靶向机制却知之甚少。在此,我们综述了定位于线粒体的转录因子的研究现状,并讨论了除这些因子之间的功能相互作用外可能的靶向机制。

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