Spatially resolved single-cell translatomics at molecular resolution

The precise control of messenger RNA (mRNA) translation is a crucial step in posttranscriptional gene regulation of cellular physiology. However, it remains a challenge to systematically study mRNA translation at the transcriptomic scale with spatial and single-cell resolution. Here, we report the development of ribosome-bound mRNA mapping (RIBOmap), a highly multiplexed three-dimensional in situ profiling method to detect cellular translatome. RIBOmap profiling of 981 genes in HeLa cells revealed cell cycle-dependent translational control and colocalized translation of functional gene modules. We mapped 5413 genes in mouse brain tissues, yielding spatially resolved single-cell translatomic profiles for 119,173 cells and revealing cell type-specific and brain region-specific translational regulation, including translation remodeling during oligodendrocyte maturation. Our method detected widespread patterns of localized translation in neuronal and glial cells in intact brain tissue networks.

Errataetall:

ErratumIn: Science. 2024 Mar 8;383(6687):eado9025. - PMID 38452096

Medienart:

E-Artikel

Erscheinungsjahr:

2023

Erschienen:

2023

Enthalten in:

Zur Gesamtaufnahme - volume:380

Enthalten in:

Science (New York, N.Y.) - 380(2023), 6652 vom: 30. Juni, Seite eadd3067

Sprache:

Englisch

Beteiligte Personen:

Zeng, Hu [VerfasserIn]
Huang, Jiahao [VerfasserIn]
Ren, Jingyi [VerfasserIn]
Wang, Connie Kangni [VerfasserIn]
Tang, Zefang [VerfasserIn]
Zhou, Haowen [VerfasserIn]
Zhou, Yiming [VerfasserIn]
Shi, Hailing [VerfasserIn]
Aditham, Abhishek [VerfasserIn]
Sui, Xin [VerfasserIn]
Chen, Hongyu [VerfasserIn]
Lo, Jennifer A [VerfasserIn]
Wang, Xiao [VerfasserIn]

Links:

Volltext

Themen:

Journal Article
RNA, Messenger

Anmerkungen:

Date Completed 11.07.2023

Date Revised 07.03.2024

published: Print-Electronic

ErratumIn: Science. 2024 Mar 8;383(6687):eado9025. - PMID 38452096

Citation Status MEDLINE

doi:

10.1126/science.add3067

funding:

Förderinstitution / Projekttitel:

PPN (Katalog-ID):

NLM358859891