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从婴儿期到成年期的小鼠多器官蛋白质组。

The mouse multi-organ proteome from infancy to adulthood.

机构信息

Department of Anesthesiology and Surgical Intensive Care Unit, Xinhua Hospital, School of Medicine and School of Biomedical Engineering, Shanghai Jiao Tong University, Shanghai, China.

State Key Laboratory of Oncogenes and Related Genes, Institute for Personalized Medicine, Shanghai Jiao Tong University, Shanghai, China.

出版信息

Nat Commun. 2024 Jul 9;15(1):5752. doi: 10.1038/s41467-024-50183-6.

Abstract

The early-life organ development and maturation shape the fundamental blueprint for later-life phenotype. However, a multi-organ proteome atlas from infancy to adulthood is currently not available. Herein, we present a comprehensive proteomic analysis of ten mouse organs (brain, heart, lung, liver, kidney, spleen, stomach, intestine, muscle and skin) at three crucial developmental stages (1-, 4- and 8-weeks after birth) acquired using data-independent acquisition mass spectrometry. We detect and quantify 11,533 protein groups across the ten organs and obtain 115 age-related differentially expressed protein groups that are co-expressed in all organs from infancy to adulthood. We find that spliceosome proteins prevalently play crucial regulatory roles in the early-life development of multiple organs, and detect organ-specific expression patterns and sexual dimorphism. This multi-organ proteome atlas provides a fundamental resource for understanding the molecular mechanisms underlying early-life organ development and maturation.

摘要

生命早期的器官发育和成熟为后期的表型奠定了基础。然而,目前还没有从婴儿期到成年期的多器官蛋白质组图谱。在此,我们使用非依赖性采集质谱法对出生后 1、4 和 8 周的 10 个小鼠器官(大脑、心脏、肺、肝脏、肾脏、脾脏、胃、肠、肌肉和皮肤)进行了全面的蛋白质组学分析。我们在这 10 个器官中检测和定量了 11,533 个蛋白质组,并获得了 115 个与年龄相关的差异表达蛋白组,这些蛋白组在婴儿期到成年期的所有器官中均有共表达。我们发现剪接体蛋白在多个器官的早期发育中普遍起着关键的调节作用,并检测到了器官特异性表达模式和性别二态性。这个多器官蛋白质组图谱为理解生命早期器官发育和成熟的分子机制提供了一个基础资源。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d5ec/11233712/12e51a37568b/41467_2024_50183_Fig1_HTML.jpg

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