Evolutionary cell type mapping with single-cell genomics

被引:33
|
作者
Tanay, Amos [1 ,2 ]
Sebe-Pedros, Arnau [3 ,4 ]
机构
[1] Weizmann Inst Sci, Dept Comp Sci & Appl Math, IL-76100 Rehovot, Israel
[2] Weizmann Inst Sci, Dept Biol Regulat, IL-76100 Rehovot, Israel
[3] Ctr Genom Regulat CRG, BIST, Barcelona, Spain
[4] UPF, E-08003 Barcelona, Spain
基金
欧洲研究理事会; 欧盟地平线“2020”;
关键词
NUCLEUS RNA-SEQ; DIVERSITY; ATLAS; MOUSE; ORIGIN; DYNAMICS; GENE;
D O I
10.1016/j.tig.2021.04.008
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
A fundamental characteristic of animal multicellularity is the spatial coexistence of functionally specialized cell types that are all encoded by a single genome sequence. Cell type transcriptional programs are deployed and maintained by regulatory mechanisms that control the asymmetric, differential access to genomic information in each cell. This genome regulation ultimately results in specific cellular phenotypes. However, the emergence, diversity, and evolutionary dynamics of animal cell types remain almost completely unexplored beyond a few species. Single-cell genomics is emerging as a powerful tool to build comprehensive catalogs of cell types and their associated gene regulatory programs in non-traditional model species. We review the current state of sampling efforts across the animal tree of life and challenges ahead for the comparative study of cell type programs. We also discuss how the phylogenetic integration of cell atlases can lead to the development of models of cell type evolution and a phylogenetic taxonomy of cells.
引用
收藏
页码:919 / 932
页数:14
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