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Series GSE273555 Query DataSets for GSE273555
Status Public on Aug 04, 2024
Title Post-prandial cardiac hypertrophy is sustained by mechanics, epigenetic, and metabolic reprogramming in pythons [ATAC-Seq]
Organism Python regius
Experiment type Genome binding/occupancy profiling by high throughput sequencing
Summary Constricting pythons, known for their ability to consume infrequent, massive meals, exhibit rapid and reversible cardiac hypertrophy following feeding. Our primary goal was to investigate how python hearts achieve this adaptive response after feeding. Isolated myofibrils increased force after feeding without changes in sarcomere ultrastructure and without increasing energy cost. Ca2+ transients were prolonged after feeding with no changes in myofibril Ca2+ sensitivity. Feeding reduced titin-based tension, resulting in decreased cardiac tissue stiffness. Feeding also reduced the activity of sirtuins, a metabolically-linked class of histone deacetylases, and increased chromatin accessibility. A transcription factor enrichment analysis on transposase-accessible chromatin with sequencing (ATAC-Seq) revealed the prominent role of transcription factors YY1 and NRF1 in post-feeding cardiac adaptation. Gene expression was also changed in favor of translation and metabolism. Finally, metabolomics analysis and ATP production assay demonstrated that cardiac adaptation after feeding not only increased energy demand but also energy production. These findings have broader implications for our understanding of cardiac adaptation across species and hold promise for the development of innovative approaches to address cardiovascular diseases.
 
Overall design To determine the chromatin accessibility profile of post-prandial python hearts, the cardiomyocytes of fasted and 24 post fed Python regius were extracted for ATAC-sequencing analysis.
The cardiomyocytes from three fasted and three fed pythons were included in the study.
Transcription factor expression analysis (TFEA) was performed between fasted and 24 hour post fed python cardiomyocytes.
 
Contributor(s) Crocini C, Woulfe KC, Ozeroff CD, Perni S, Cardiello J, Walker CJ, Anseth KS, Allen MA, Leinwand LA
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Submission date Jul 31, 2024
Last update date Aug 05, 2024
Contact name Mary Ann Allen
E-mail(s) mary.a.allen@colorado.edu
Phone 608-209-6921
Organization name University of Colorado
Department BioFrontiers
Lab Allen
Street address UCB 596 JSCBB
City Boulder
State/province Co
ZIP/Postal code 80309
Country USA
 
Platforms (1)
GPL27701 Illumina NextSeq 500 (Python regius)
Samples (14)
GSM8432272 Python Regius, Cardiomyocytes, 28 days fasted replicate 1
GSM8432273 Python Regius, Cardiomyocytes, 28 days fasted replicate 2
GSM8432274 Python Regius, Cardiomyocytes, 28 days fasted control 1
Relations
BioProject PRJNA1142401

Download family Format
SOFT formatted family file(s) SOFTHelp
MINiML formatted family file(s) MINiMLHelp
Series Matrix File(s) TXTHelp

Supplementary file Size Download File type/resource
GSE273555_A1_pyth_cardiomyocytes_starvedmerged.open.sorted.bed.gz 310.1 Kb (ftp)(http) BED
GSE273555_A3_pyth_cardiomyocytes_fedmerged.open.sorted.bed.gz 339.5 Kb (ftp)(http) BED
GSE273555_RAW.tar 540.3 Mb (http)(custom) TAR (of BED, BEDGRAPH)
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Raw data are available in SRA

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