Abstract

Comparative genomic studies in primates have the potential to reveal the genetic and mechanistic basis for human specific traits. These studies may also help us better understand inter-species phenotypic differences that are clinically relevant. Unfortunately, the obvious limitation on sample collection and experimentation in humans and non-human apes severely restrict our ability to perform dynamic comparative studies in primates. Induced pluripotent stem cells (iPSCs), and their corresponding differentiated cells, may provide a suitable alternative system for dynamic comparative studies. Yet, to effectively use iPSCs and differentiated cells for comparative studies, one must characterize the extent to which these systems faithfully represent biological processes in primary tissues. To do so, we compared gene expression data from primary adult heart tissue and iPSC-derived cardiomyocytes from multiple human and chimpanzee individuals. We determined that gene expression in cultured cardiomyocytes from both human and chimpanzee is most similar to that of adult hearts compared to other adult tissues. Using a comparative framework, we found that 50% of gene regulatory differences between human and chimpanzee hearts are also observed between species in cultured cardiomyocytes; conversely, inter-species regulatory differences seen in cardiomyocytes are found significantly more often in hearts than in other primary tissues. Our work provides a detailed description of the utility and limitation of differentiated cardiomyocytes as a system for comparative functional genomic studies in primates.

Highlights

  • That said, these published works do not address properties pertaining to the utility of differentiated cardiomyocytes in the context of a comparative study in primates

  • The primary goal of this work is not to test a particular hypothesis, but to develop an understanding of the degree to which Induced pluripotent stem cells (iPSCs) derived cardiomyocytes can serve as a model system for comparative functional genomic studies in primates

  • On days 20–27, a subset of cultures was treated with T3, which was shown to aid in the maturation of iPSC-derived cardiomyocytes[20,24,26]

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Summary

Introduction

To date, no study that focused on the fidelity of differentiated cells included samples from chimpanzees. To address these gaps, we performed a comparative study that was designed to allow us to effectively compare gene expression data between cultured cardiomyocytes and primary hearts from humans and chimpanzees. A key finding from previous studies pertaining to the fidelity of iPSC-derived cell types is the importance of cellular maturation after terminal differentiation. To test the effects of temporal maturation and treatment with T3, we compared gene expression profiles from human and chimpanzee iPSC-derived cardiomyocytes at day 15, day 27 (with and without T3 treatment) post induction of differentiation with data generated from primary heart tissue from both species

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