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CARDIAC DEVELOPMENT LONG NON-CODING RNA (CARDEL) IS ACTIVATED DURING HUMAN HEART DEVELOPMENT AND CONTRIBUTES TO CARDIAC SPECIFICATION AND HOMEOSTASIS
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Fundação Oswaldo Cruz. Instituto Carlos Chagas. Laboratório de Biologia Básica de Células-tronco. Curitiba, PR, Brasil.
Fundação Oswaldo Cruz. Instituto Carlos Chagas. Laboratório de Biologia Básica de Células-tronco. Curitiba, PR, Brasil.
Fundação Oswaldo Cruz. Instituto Carlos Chagas. Laboratório de Biologia Básica de Células-tronco. Curitiba, PR, Brasil.
Fundação Oswaldo Cruz. Instituto Carlos Chagas. Laboratório de Biologia Básica de Células-tronco. Curitiba, PR, Brasil.
University of Minnesota. Department of Medicine. Division of Cardiology. Minneapolis, USA / University of Minnesota. Lillehei Heart Institute. Minneapolis, USA.
University of Minnesota. Lillehei Heart Institute. Minneapolis, USA / University of Minnesota. Department of Pediatrics. Minneapolis, USA.
University of Minnesota. Lillehei Heart Institute. Minneapolis, USA / University of Minnesota. Department of Pediatrics. Minneapolis, USA / University of Minnesota. Stem Cell Institute. Minneapolis, USA.
University of Minnesota. Department of Medicine. Division of Cardiology. Minneapolis, USA / University of Minnesota. Lillehei Heart Institute. Minneapolis, USA.
University of Minnesota. Lillehei Heart Institute. Minneapolis, USA / University of Minnesota. Department of Pediatrics. Minneapolis, USA.
Fundação Oswaldo Cruz. Instituto Carlos Chagas. Laboratório de Biologia Básica de Células-tronco. Curitiba, PR, Brasil.
Fundação Oswaldo Cruz. Instituto Carlos Chagas. Laboratório de Biologia Básica de Células-tronco. Curitiba, PR, Brasil.
Fundação Oswaldo Cruz. Instituto Carlos Chagas. Laboratório de Biologia Básica de Células-tronco. Curitiba, PR, Brasil.
Fundação Oswaldo Cruz. Instituto Carlos Chagas. Laboratório de Biologia Básica de Células-tronco. Curitiba, PR, Brasil.
University of Minnesota. Department of Medicine. Division of Cardiology. Minneapolis, USA / University of Minnesota. Lillehei Heart Institute. Minneapolis, USA.
University of Minnesota. Lillehei Heart Institute. Minneapolis, USA / University of Minnesota. Department of Pediatrics. Minneapolis, USA.
University of Minnesota. Lillehei Heart Institute. Minneapolis, USA / University of Minnesota. Department of Pediatrics. Minneapolis, USA / University of Minnesota. Stem Cell Institute. Minneapolis, USA.
University of Minnesota. Department of Medicine. Division of Cardiology. Minneapolis, USA / University of Minnesota. Lillehei Heart Institute. Minneapolis, USA.
University of Minnesota. Lillehei Heart Institute. Minneapolis, USA / University of Minnesota. Department of Pediatrics. Minneapolis, USA.
Fundação Oswaldo Cruz. Instituto Carlos Chagas. Laboratório de Biologia Básica de Células-tronco. Curitiba, PR, Brasil.
Abstract
Successful heart development depends on the careful orchestration of a network of transcription factors and signaling pathways. In recent years, in vitro cardiac differentiation using human pluripotent stem cells (hPSCs) has been used to uncover the intricate gene-network regulation involved in the proper formation and function of the human heart. Here, we searched for uncharacterized cardiac-development genes by combining a temporal evaluation of human cardiac specification in vitro with an analysis of gene expression in fetal and adult heart tissue. We discovered that CARDEL (CARdiac DEvelopment Long non-coding RNA; LINC00890; SERTM2) expression coincides with the commitment to the cardiac lineage. CARDEL knockout hPSCs differentiated poorly into cardiac cells, and hPSC-derived cardiomyocytes showed faster beating rates after controlled overexpression of CARDEL during differentiation. Altogether, we provide physiological and molecular evidence that CARDEL expression contributes to sculpting the cardiac program during cell-fate commitment.
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