Closing the gap: a roadmap to single-cell regulatory genomics

被引:0
|
作者
Carnesecchi, Julie [1 ]
Lohmann, Ingrid [1 ]
机构
[1] Heidelberg Univ, Ctr Organismal Studies COS Heidelberg, Dept Dev Biol, Heidelberg, Germany
关键词
D O I
10.15252/msb.20209497
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Studying the spatiotemporal control of gene regulatory networks at the single-cell level is still a challenge, yet it is key to understanding the mechanisms driving cellular identity. In their recent study, Aerts and colleagues (Gonzalez-Blas et al, 2020) develop a new strategy to spatially map and integrate single-cell transcriptome and epigenome profiles in the Drosophila eye-antennal disc and to deduce in each cell precise enhancer-to-gene activity relationships. This opens a new era in the transcriptional regulation field, as it allows extracting from each of the thousands of cells forming a tissue the critical features driving their identity, from enhancer sequences to transcription factors to gene regulatory networks.
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