Genome-wide identification of neuronal activity-regulated genes in Drosophila

Activity-regulated genes (ARGs) are important for neuronal functions like long-term memory and are well-characterized in mammals but poorly studied in other model organisms like Drosophila. Here we stimulated fly neurons with different paradigms and identified ARGs using high-throughput sequencing f...

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Main Authors: Xiao Chen, Reazur Rahman, Fang Guo, Michael Rosbash
Format: Article
Language:English
Published: eLife Sciences Publications Ltd 2016-12-01
Series:eLife
Subjects:
Online Access:https://elifesciences.org/articles/19942
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spelling doaj-cfc24e7d2de44a7faf353e4a575acb282021-05-05T00:45:04ZengeLife Sciences Publications LtdeLife2050-084X2016-12-01510.7554/eLife.19942Genome-wide identification of neuronal activity-regulated genes in DrosophilaXiao Chen0Reazur Rahman1Fang Guo2Michael Rosbash3https://orcid.org/0000-0003-3366-1780Howard Hughes Medical Institute, Brandeis University, Waltham, United States; National Center for Behavioral Genomics, Department of Biology, Brandeis University, Waltham, United StatesHoward Hughes Medical Institute, Brandeis University, Waltham, United States; National Center for Behavioral Genomics, Department of Biology, Brandeis University, Waltham, United StatesHoward Hughes Medical Institute, Brandeis University, Waltham, United States; National Center for Behavioral Genomics, Department of Biology, Brandeis University, Waltham, United StatesHoward Hughes Medical Institute, Brandeis University, Waltham, United States; National Center for Behavioral Genomics, Department of Biology, Brandeis University, Waltham, United StatesActivity-regulated genes (ARGs) are important for neuronal functions like long-term memory and are well-characterized in mammals but poorly studied in other model organisms like Drosophila. Here we stimulated fly neurons with different paradigms and identified ARGs using high-throughput sequencing from brains as well as from sorted neurons: they included a narrow set of circadian neurons as well as dopaminergic neurons. Surprisingly, many ARGs are specific to the stimulation paradigm and very specific to neuron type. In addition and unlike mammalian immediate early genes (IEGs), fly ARGs do not have short gene lengths and are less enriched for transcription factor function. Chromatin assays using ATAC-sequencing show that the transcription start sites (TSS) of ARGs do not change with neural firing but are already accessible prior to stimulation. Lastly based on binding site enrichment in ARGs, we identified transcription factor mediators of firing and created neuronal activity reporters.https://elifesciences.org/articles/19942RNA high-throughput sequencingneural firingoptogeneticschromatin accessibilityneural activity reporters
collection DOAJ
language English
format Article
sources DOAJ
author Xiao Chen
Reazur Rahman
Fang Guo
Michael Rosbash
spellingShingle Xiao Chen
Reazur Rahman
Fang Guo
Michael Rosbash
Genome-wide identification of neuronal activity-regulated genes in Drosophila
eLife
RNA high-throughput sequencing
neural firing
optogenetics
chromatin accessibility
neural activity reporters
author_facet Xiao Chen
Reazur Rahman
Fang Guo
Michael Rosbash
author_sort Xiao Chen
title Genome-wide identification of neuronal activity-regulated genes in Drosophila
title_short Genome-wide identification of neuronal activity-regulated genes in Drosophila
title_full Genome-wide identification of neuronal activity-regulated genes in Drosophila
title_fullStr Genome-wide identification of neuronal activity-regulated genes in Drosophila
title_full_unstemmed Genome-wide identification of neuronal activity-regulated genes in Drosophila
title_sort genome-wide identification of neuronal activity-regulated genes in drosophila
publisher eLife Sciences Publications Ltd
series eLife
issn 2050-084X
publishDate 2016-12-01
description Activity-regulated genes (ARGs) are important for neuronal functions like long-term memory and are well-characterized in mammals but poorly studied in other model organisms like Drosophila. Here we stimulated fly neurons with different paradigms and identified ARGs using high-throughput sequencing from brains as well as from sorted neurons: they included a narrow set of circadian neurons as well as dopaminergic neurons. Surprisingly, many ARGs are specific to the stimulation paradigm and very specific to neuron type. In addition and unlike mammalian immediate early genes (IEGs), fly ARGs do not have short gene lengths and are less enriched for transcription factor function. Chromatin assays using ATAC-sequencing show that the transcription start sites (TSS) of ARGs do not change with neural firing but are already accessible prior to stimulation. Lastly based on binding site enrichment in ARGs, we identified transcription factor mediators of firing and created neuronal activity reporters.
topic RNA high-throughput sequencing
neural firing
optogenetics
chromatin accessibility
neural activity reporters
url https://elifesciences.org/articles/19942
work_keys_str_mv AT xiaochen genomewideidentificationofneuronalactivityregulatedgenesindrosophila
AT reazurrahman genomewideidentificationofneuronalactivityregulatedgenesindrosophila
AT fangguo genomewideidentificationofneuronalactivityregulatedgenesindrosophila
AT michaelrosbash genomewideidentificationofneuronalactivityregulatedgenesindrosophila
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