run_metadata: 33857
This data as json
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| 33857 | SRR30769782 | SRX26172015 | SRS22716029 | SRP534198 | PRJNA1164198 | Analysis of The Senescence Secretome During Zebrafish Retina Regeneration | GSE277792 | Transcriptome Analysis | Zebrafish possess the innate ability to regenerate any lost or damaged retinal cell type with Müller glia serving as resident stem cells. Recently we discovered that this process is aided by a population of damage induced senescent immune cells. As part of the Senescence Associated Secretory Phenotype SASP senescent cells secrete numerous factors that can play a role in the modulation of inflammation and remodeling of the retinal microenvironment during regeneration. However the identity of specific SASP factors that drive initiation and progression of retina regeneration remain unclear. Here we mined the SASP Atlas and RNAseq datasets to identify differentially expressed SASP factors post retina injury including two distinct acute damage regimens as well as a chronic genetic model of retina degeneration. We discovered a 31 factor “Regeneration associated Senescence Signature” RASS that represents SASP factors and senescence markers that are conserved across all data sets and are upregulated post damage. Among these we show that depletion of npm1a inhibits retina regeneration. Our data support the model that differential expression of SASP factors promotes regeneration post both acute and chronic retinal damage. Overall design: Adult AB zebrafish were injected with either NMDA damaging agent alone or in combination with Metformin and ABT 263 senolytic agents. Whole retinas were collected at 3 12 and 20 xxx post injury and samples were collected using Trizol based RNA extraction techniques. | pubmed:40308558 | NMDA Only 12dpi Rep 1 | GSM8530618 | source name:Retina|tissue:Retina|genotype:NMDA Damage|treatment:Control|geo loc name:missing|collection date:missing | NMDA Only 12dpi Rep 1 | Adapter sequences and low quality reads were trimmed and read files underwent paired sequence validation using Trim Galore! v0.6.10 a wrapper for CutAdapt v4.8 using the paired and illumina parameters. Trimmed reads were quantified using Salmon v1.10.3 in quasi mapping mode with the optional paramaters validateMappings and gcBias against the Ensembl release 111 Danio rerio GRCz11.111 transcriptome with the primary assembly from the same release serving as decoys. Read counts were imported to R using tximport v1.32.0 and processed using DESeq2 v1.44.0. Assembly: GRCz11.111 Supplementary files format and content: tab delimited text file with estimated relative abundance and number of reads as well as all additional output files from Salmon v1.10.3 run in quasi mapping mode | Retina | RNA was harvested using Trizol and Phenol chloroform extraction Libraries were prepared utilizing the stranded mRNA polyA selected library preparation kit | tissue:Retina|genotype:NMDA Damage|treatment:Control | GSM8530618 | GSM8530618: NMDA Only 12dpi Rep 1; Danio rerio; RNA Seq | GSM8530618 r1 | GSM8530618 | 1 | RNA was harvested using Trizol and Phenol chloroform extraction Libraries were prepared utilizing the stranded mRNA polyA selected library preparation kit | RNA-Seq | TRANSCRIPTOMIC | cDNA | PAIRED | ILLUMINA | Illumina NovaSeq X Plus | SRP534198 | 11384-GK-0007_S1_L005_R1_001.fastq.gz 11384-GK-0007_S1_L005_R2_001.fastq.gz | fastq fastq | 14797480862.0 | 48998281.0 | GSM8530618 r1 | 0:151 1:151 | A:3900528784;C:3418459440;G:3652120707;T:3823647040;N:2724891 | 151 | 151 | 3900528784 | 3418459440 | 3652120707 | 3823647040 | 2724891 | SRX26172015 | SRS22716029 | SRA1977341 | Patton Lab, Biological Sciences, Vanderbilt University | Patton Lab, Biological Sciences, Vanderbilt University | B | B | biological fallback assumption | illumina | novaseq_era | unknown | poly_a | unknown | bulk | unknown | unknown | United States | 2024-09-23 | Undetermined | Undetermined | Eye | Sensory System |