Mpf1影响尾锚蛋白在线粒体和过氧化物酶体之间的双重分布。

IF 6 1区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY EMBO Reports Pub Date : 2025-05-01 Epub Date: 2025-04-02 DOI:10.1038/s44319-025-00440-6
Nitya Aravindan, Daniela G Vitali, Julia Breuer, Jessica Oberst, Einat Zalckvar, Maya Schuldiner, Doron Rapaport
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引用次数: 0

摘要

大多数细胞蛋白需要靶向一个独特的细胞室才能正常工作。蛋白质的一个子集分布到细胞内的两个或多个目的地,关于控制双重/多重靶向过程的机制知之甚少。在这里,我们提供了线粒体和过氧化物酶体之间蛋白质的双重靶向机制的见解。我们进行了高通量显微镜筛选,我们在几乎所有酵母基因突变的背景中可视化模型尾锚定蛋白Fis1和Gem1的位置。该筛选确定了三种蛋白质,它们的缺失导致过氧化物酶体中尾巴锚定蛋白的比例更高:两个类似的Tom70, Tom71和未表征的基因YNL144C,我们将其重新命名为线粒体和过氧化物酶体因子1 (Mpf1)。我们认为Mpf1是一种与线粒体外膜细胞质面相关的不稳定蛋白。此外,我们的研究揭示了Tom71对双重靶向调控的独特贡献。总的来说,我们的研究首次揭示了影响线粒体和过氧化物酶体之间蛋白质双重靶向的因素。
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Mpf1 affects the dual distribution of tail-anchored proteins between mitochondria and peroxisomes.

Most cellular proteins require targeting to a distinct cellular compartment to function properly. A subset of proteins is distributed to two or more destinations in the cell and little is known about the mechanisms controlling the process of dual/multiple targeting. Here, we provide insight into the mechanism of dual targeting of proteins between mitochondria and peroxisomes. We perform a high throughput microscopy screen in which we visualize the location of the model tail-anchored proteins Fis1 and Gem1 in the background of mutants in virtually all yeast genes. This screen identifies three proteins, whose absence results in a higher portion of the tail-anchored proteins in peroxisomes: the two paralogues Tom70, Tom71, and the uncharacterized gene YNL144C that we rename mitochondria and peroxisomes factor 1 (Mpf1). We characterize Mpf1 to be an unstable protein that associates with the cytosolic face of the mitochondrial outer membrane. Furthermore, our study uncovers a unique contribution of Tom71 to the regulation of dual targeting. Collectively, our study reveals, for the first time, factors that influence the dual targeting of proteins between mitochondria and peroxisomes.

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来源期刊
EMBO Reports
EMBO Reports 生物-生化与分子生物学
CiteScore
11.20
自引率
1.30%
发文量
267
审稿时长
1 months
期刊介绍: EMBO Reports is a scientific journal that specializes in publishing research articles in the fields of molecular biology, cell biology, and developmental biology. The journal is known for its commitment to publishing high-quality, impactful research that provides novel physiological and functional insights. These insights are expected to be supported by robust evidence, with independent lines of inquiry validating the findings. The journal's scope includes both long and short-format papers, catering to different types of research contributions. It values studies that: Communicate major findings: Articles that report significant discoveries or advancements in the understanding of biological processes at the molecular, cellular, and developmental levels. Confirm important findings: Research that validates or supports existing knowledge in the field, reinforcing the reliability of previous studies. Refute prominent claims: Studies that challenge or disprove widely accepted ideas or hypotheses in the biosciences, contributing to the correction and evolution of scientific understanding. Present null data: Papers that report negative results or findings that do not support a particular hypothesis, which are crucial for the scientific process as they help to refine or redirect research efforts. EMBO Reports is dedicated to maintaining high standards of scientific rigor and integrity, ensuring that the research it publishes contributes meaningfully to the advancement of knowledge in the life sciences. By covering a broad spectrum of topics and encouraging the publication of both positive and negative results, the journal plays a vital role in promoting a comprehensive and balanced view of scientific inquiry. 
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