Temporal evolution of single-cell transcriptomes of Drosophila olfactory projection neurons

Author:

Xie Qijing12ORCID,Brbic Maria3,Horns Felix45ORCID,Kolluru Sai Saroja4,Jones Robert C4ORCID,Li Jiefu1ORCID,Reddy Anay R1,Xie Anthony1,Kohani Sayeh1,Li Zhuoran1,McLaughlin Colleen N1,Li Tongchao1,Xu Chuanyun1,Vacek David1,Luginbuhl David J1,Leskovec Jure3,Quake Stephen R467ORCID,Luo Liqun1ORCID,Li Hongjie1

Affiliation:

1. Department of Biology, Howard Hughes Medical Institute, Stanford University, Stanford, United States

2. Neurosciences Graduate Program, Stanford University, Stanford, United States

3. Department of Computer Science, Stanford University, Stanford, United States

4. Department of Bioengineering, Stanford University, Stanford, United States

5. Biophysics Graduate Program, Stanford University, Stanford, United States

6. Department of Applied Physics, Stanford University, Stanford, United States

7. Chan Zuckerberg Biohub, Stanford, United States

Abstract

Neurons undergo substantial morphological and functional changes during development to form precise synaptic connections and acquire specific physiological properties. What are the underlying transcriptomic bases? Here, we obtained the single-cell transcriptomes of Drosophila olfactory projection neurons (PNs) at four developmental stages. We decoded the identity of 21 transcriptomic clusters corresponding to 20 PN types and developed methods to match transcriptomic clusters representing the same PN type across development. We discovered that PN transcriptomes reflect unique biological processes unfolding at each stage—neurite growth and pruning during metamorphosis at an early pupal stage; peaked transcriptomic diversity during olfactory circuit assembly at mid-pupal stages; and neuronal signaling in adults. At early developmental stages, PN types with adjacent birth order share similar transcriptomes. Together, our work reveals principles of cellular diversity during brain development and provides a resource for future studies of neural development in PNs and other neuronal types.

Funder

National Institutes of Health

Howard Hughes Medical Institute

Bertarelli Foundation

Wu Tsai Neurosciences Institute

Chan Zuckerberg Biohub

Publisher

eLife Sciences Publications, Ltd

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3