Combining Developmental and Perturbation-Seq Uncovers Transcriptional Modules Orchestrating Neuronal Remodeling

被引:48
作者
Alyagor, Idan [1 ]
Berkun, Victoria [1 ]
Keren-Shaul, Hadas [2 ,3 ]
Marmor-Kollet, Neta [1 ]
David, Eyal [2 ]
Mayseless, Oded [1 ]
Issman-Zecharya, Noa [1 ]
Amit, Ido [2 ]
Schuldiner, Oren [1 ]
机构
[1] Weizmann Inst Sci, Dept Mol Cell Biol, Rehovot, Israel
[2] Weizmann Inst Sci, Dept Immunol, Rehovot, Israel
[3] Weizmann Inst Sci, Life Sci Core Facil, Rehovot, Israel
基金
欧洲研究理事会; 以色列科学基金会;
关键词
B ECDYSONE RECEPTOR; UBIQUITIN-PROTEASOME; DROSOPHILA; AXON; DEGENERATION; EXPRESSION; REGULATOR; PATHWAY; METAMORPHOSIS; REQUIREMENT;
D O I
10.1016/j.devcel.2018.09.013
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Developmental neuronal remodeling is an evolutionarily conserved mechanism required for precise wiring of nervous systems. Despite its fundamental role in neurodevelopment and proposed contribution to various neuropsychiatric disorders, the underlying mechanisms are largely unknown. Here, we uncover the fine temporal transcriptional landscape of Drosophila mushroom body gamma neurons undergoing stereotypical remodeling. Our data reveal rapid and dramatic changes in the transcriptional landscape during development. Focusing on DNA binding proteins, we identify eleven that are required for remodeling. Furthermore, we sequence developing y neurons perturbed for three key transcription factors required for pruning. We describe a hierarchical network featuring positive and negative feedback loops. Superimposing the perturbation-seq on the developmental expression atlas highlights a framework of transcriptional modules that together drive remodeling. Overall, this study provides a broad and detailed molecular insight into the complex regulatory dynamics of developmental remodeling and thus offers a pipeline to dissect developmental processes via RNA profiling.
引用
收藏
页码:38 / +
页数:21
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