Spatially resolved single-cell translatomics at molecular resolution

被引:45
|
作者
Zeng, Hu [1 ,2 ]
Huang, Jiahao [1 ,2 ]
Ren, Jingyi [1 ,2 ]
Wang, Connie Kangni [2 ]
Tang, Zefang [1 ,2 ]
Zhou, Haowen [2 ]
Zhou, Yiming [1 ,2 ,3 ]
Shi, Hailing [1 ,2 ]
Aditham, Abhishek [2 ,4 ]
Sui, Xin [1 ,2 ]
Chen, Hongyu [1 ,2 ]
Lo, Jennifer A. [2 ]
Wang, Xiao [1 ,2 ]
机构
[1] MIT, Dept Chem, Cambridge, MA 02139 USA
[2] Broad Inst MIT & Harvard, Cambridge, MA 02142 USA
[3] Broad Inst MIT & Harvard, Ctr Psychiat Res, Cambridge, MA 02142 USA
[4] MIT, Dept Biol Engn, 77 Massachusetts Ave, Cambridge, MA 02139 USA
基金
美国国家卫生研究院;
关键词
RNA TRANSLATION; DYNAMICS; PROTEIN; QUANTIFICATION;
D O I
10.1126/science.add3067
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
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.
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页码:1337 / +
页数:11
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