Transverse aortic constriction multi-omics analysis uncovers pathophysiological cardiac molecular mechanisms

Author:

Gjerga Enio123,Dewenter Matthias345ORCID,Britto-Borges Thiago123,Grosso Johannes34,Stein Frank67,Eschenbach Jessica123,Rettel Mandy6,Backs Johannes3458,Dieterich Christoph123ORCID

Affiliation:

1. Section of Bioinformatics and Systems Cardiology, Klaus Tschira Institute for Integrative Computational Cardiology, University Hospital Heidelberg , INF 669, Heidelberg 69120, Germany

2. Department of Internal Medicine III (Cardiology, Angiology, and Pneumology), University Hospital Heidelberg , INF 669, Heidelberg 69120, Germany

3. German Centre for Cardiovascular Research (DZHK)—Partner Site Heidelberg/Mannheim , Heidelberg 69120, Germany

4. Institute of Experimental Cardiology, Medical Faculty Heidelberg, Heidelberg University , INF 669, Heidelberg 69120, Germany

5. Internal Medicine VIII, Heidelberg University Hospital , INF 669, Heidelberg 69120, Germany

6. European Molecular Biology Laboratory , Meyerhofstrasse 1, Heidelberg 69117, Germany

7. Proteomics Core Facility, European Molecular Biology Laboratory , Meyerhofstrasse 1, Heidelberg 69117, Germany

8. Helmholtz Institute for Translational AngioCardioScience (HI-TAC), MDC at Heidelberg University , Heidelberg 69120, Germany

Abstract

Abstract Time-course multi-omics data of a murine model of progressive heart failure (HF) induced by transverse aortic constriction (TAC) provide insights into the molecular mechanisms that are causatively involved in contractile failure and structural cardiac remodelling. We employ Illumina-based transcriptomics, Nanopore sequencing and mass spectrometry-based proteomics on samples from the left ventricle (LV) and right ventricle (RV, RNA only) of the heart at 1, 7, 21 and 56 days following TAC and Sham surgery. Here, we present Transverse Aortic COnstriction Multi-omics Analysis (TACOMA), as an interactive web application that integrates and visualizes transcriptomics and proteomics data collected in a TAC time-course experiment. TACOMA enables users to visualize the expression profile of known and novel genes and protein products thereof. Importantly, we capture alternative splicing events by assessing differential transcript and exon usage as well. Co-expression-based clustering algorithms and functional enrichment analysis revealed overrepresented annotations of biological processes and molecular functions at the protein and gene levels. To enhance data integration, TACOMA synchronizes transcriptomics and proteomics profiles, enabling cross-omics comparisons. With TACOMA (https://shiny.dieterichlab.org/app/tacoma), we offer a rich web-based resource to uncover molecular events and biological processes implicated in contractile failure and cardiac hypertrophy. For example, we highlight: (i) changes in metabolic genes and proteins in the time course of hypertrophic growth and contractile impairment; (ii) identification of RNA splicing changes in the expression of Tpm2 isoforms between RV and LV; and (iii) novel transcripts and genes likely contributing to the pathogenesis of HF. We plan to extend these data with additional environmental and genetic models of HF to decipher common and distinct molecular changes in heart diseases of different aetiologies. Database URL: https://shiny.dieterichlab.org/app/tacoma

Funder

DFG, German Research Foundation

Klaus Tschira Stiftung gGmbH

Publisher

Oxford University Press (OUP)

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