Proteomics

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Heterozygous mutation of NF-B innate immune response transcription factor Relish increases survival following traumatic brain injury in Drosophila


ABSTRACT: Traumatic brain injury (TBI) pathologies are caused by primary and secondary injuries. Primary injuries result from physical damage to the brain, and secondary injuries arise from cellular responses to primary injuries. A characteristic cellular response is sustained activation of inflammatory pathways commonly mediated by NF-B transcription factors. Using a Drosophila melanogaster TBI model, we previously found that the main proximal transcriptional response to primary injuries is triggered by activation of Toll and Imd innate immune response pathways that engage NF-B factors Dif and Relish (Rel), respectively. Here, we monitor the abundance of Rel protein by mass spectrometry (MS) and observe that Rel increases in fly heads at 4-8 h after TBI. To investigate the necessity of Rel for secondary injuries, we generated a null allele, Reldel, by CRISPR/Cas9 editing. Heterozygous but not homozygous Reldel mutation reduced mortality at 24 h after TBI and increased the lifespan of injured flies. Additionally, the effect of heterozygous Reldel mutation on mortality was modulated by genetic background and diet. To identify genes that facilitate effects of heterozygous Reldel mutation on TBI outcomes, we compared genome-wide mRNA expression profiles of uninjured and injured +/+, +/Reldel, and Reldel/Reldel flies at 4 h following TBI. Only a few genes changed expression more than two-fold in +/Reldel flies relative to +/+ and Reldel/Reldel flies, and they were not canonical innate immune response genes. Therefore, Rel is necessary for TBI-induced secondary injuries but in complex ways involving Rel gene dose, genetic background, diet, and possibly small changes in expression of innate immune response genes.

INSTRUMENT(S): Orbitrap Fusion Lumos

ORGANISM(S): Drosophila Melanogaster (fruit Fly)

TISSUE(S): Brain

SUBMITTER: Edna Angelica Trujillo  

LAB HEAD: Joshua J. Coon

PROVIDER: PXD021869 | Pride | 2020-12-04

REPOSITORIES: Pride

Dataset's files

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Action DRS
007227_DrosophilaMelanogaster_Uniprot_ISOFORMS_ReviewedAndUnreviewed_CONCAT_20180705.fasta Fasta
Drosophila_10_n1.raw Raw
Drosophila_10_n2.raw Raw
Drosophila_10_n3.raw Raw
Drosophila_11_n1.raw Raw
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Publications

Survival Following Traumatic Brain Injury in <i>Drosophila</i> Is Increased by Heterozygosity for a Mutation of the NF-κB Innate Immune Response Transcription Factor Relish.

Swanson Laura C LC   Trujillo Edna A EA   Thiede Gene H GH   Katzenberger Rebeccah J RJ   Shishkova Evgenia E   Coon Joshua J JJ   Ganetzky Barry B   Wassarman David A DA  

Genetics 20201027 4


Traumatic brain injury (TBI) pathologies are caused by primary and secondary injuries. Primary injuries result from physical damage to the brain, and secondary injuries arise from cellular responses to primary injuries. A characteristic cellular response is sustained activation of inflammatory pathways commonly mediated by nuclear factor-κB (NF-κB) transcription factors. Using a <i>Drosophila melanogaster</i> TBI model, we previously found that the main proximal transcriptional response to prima  ...[more]

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