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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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 |
_version_ |
1721476097944584192 |