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新陈代谢中的微小蛋白质。

Microproteins in Metabolism.

作者信息

Wadding-Lee Caris A, Makarewich Catherine A

机构信息

Division of Molecular Cardiovascular Biology, The Heart Institute, Cincinnati Children's Hospital Medical Center, Cincinnati, OH 45229, USA.

Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, OH 45229, USA.

出版信息

Cells. 2025 Jun 7;14(12):859. doi: 10.3390/cells14120859.

Abstract

Metabolism is a complex network of biochemical pathways that break down macromolecules to produce energy essential for cellular function. Disruptions in metabolic homeostasis are closely linked to noncommunicable diseases (NCDs) such as cardiovascular disease, type 2 diabetes, and cancer, which are leading causes of death worldwide. Many NCD-associated conditions, including obesity and insulin resistance, stem from metabolic dysfunction, and current therapies often fall short in preventing disease progression, highlighting the need for novel therapeutic targets. Microproteins, small proteins of ≤100-150 amino acids, have recently emerged as important regulators of metabolism. Encoded by short open reading frames (sORFs), many of these proteins were historically overlooked due to their small size and misclassification as noncoding RNAs. Advances in genomics and proteomics have revealed that these sORFs can encode functional proteins with critical roles in metabolic pathways. In this review, we highlight the microproteins involved in energy metabolism, mitochondrial function, and nutrient signaling. We discuss their emerging roles in the pathogenesis of NCDs and explore their potential as novel therapeutic targets. As microprotein biology continues to evolve, these small but powerful regulators may offer new strategies for treating metabolic dysfunction and reducing the global burden of NCDs.

摘要

新陈代谢是一个复杂的生化途径网络,它分解大分子以产生细胞功能所必需的能量。代谢稳态的破坏与心血管疾病、2型糖尿病和癌症等非传染性疾病密切相关,这些疾病是全球主要的死亡原因。许多与非传染性疾病相关的病症,包括肥胖和胰岛素抵抗,都源于代谢功能障碍,而目前的治疗方法往往在预防疾病进展方面效果不佳,这凸显了对新型治疗靶点的需求。微蛋白是一类氨基酸数量≤100 - 150的小蛋白,最近已成为新陈代谢的重要调节因子。这些蛋白由短开放阅读框(sORF)编码,由于其体积小且曾被误分类为非编码RNA,在历史上它们中的许多都被忽视了。基因组学和蛋白质组学的进展表明,这些sORF可以编码在代谢途径中起关键作用的功能性蛋白质。在这篇综述中,我们重点介绍了参与能量代谢、线粒体功能和营养信号传导的微蛋白。我们讨论了它们在非传染性疾病发病机制中的新作用,并探讨了它们作为新型治疗靶点的潜力。随着微蛋白生物学的不断发展,这些虽小但强大的调节因子可能为治疗代谢功能障碍和减轻全球非传染性疾病负担提供新策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e0ba/12190854/f1ea50c4fbef/cells-14-00859-g001.jpg

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