The mouse multi-organ proteome from infancy to adulthood.
Qingwen WangXinwen DingZhixiao XuBoqian WangAiting WangLiping WangYi DingSunfengda SongYouming ChenShuang ZhangLai JiangXianting DingPublished in: Nature communications (2024)
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.
Keyphrases
- early life
- mass spectrometry
- heart failure
- weight gain
- poor prognosis
- binding protein
- pregnant women
- electronic health record
- single cell
- protein protein
- white matter
- skeletal muscle
- amino acid
- atrial fibrillation
- small molecule
- multiple sclerosis
- liquid chromatography
- artificial intelligence
- wound healing
- high performance liquid chromatography
- gas chromatography