Data on cardiac lncRNA STX18-AS1 expression in developing human hearts and function during in vitro hESC-cardiomyocyte differentiation

Bibliographic Details
Title: Data on cardiac lncRNA STX18-AS1 expression in developing human hearts and function during in vitro hESC-cardiomyocyte differentiation
Authors: Yingjuan Liu, Mun-kit Choy, Sabu Abraham, Gennadiy Tenin, Graeme C. Black, Bernard D. Keavney
Source: Data in Brief, Vol 45, Iss , Pp 108770- (2022)
Publisher Information: Elsevier, 2022.
Publication Year: 2022
Collection: LCC:Computer applications to medicine. Medical informatics
LCC:Science (General)
Subject Terms: Long noncoding RNA, Human heart, Cardiomyocyte differentiation, CRISPR, Time-course, Cardiac development, Computer applications to medicine. Medical informatics, R858-859.7, Science (General), Q1-390
More Details: This article presents data concerning STX18-AS1, a long noncoding RNA gene identified from a Genome-wide association study of Atrial Septal Defect (ASD). The data describes its expression patterns in human tissues and functions in regulating cardiomyocyte differentiation in vitro. STX18-AS1 is a lncRNA with a higher abundance in developing tissues, including hearts. Its transcription distribution within the embryonic hearts during key heart septation stages supports STX18-AS1’s association with risk SNPs for ASD. The CRISPR stem cell pool in which STX18-AS1 was knocked down, showed reduced CM differentiation efficiency and lower expression of key cardiac transcriptional factors. This indicated its regulative role in supporting the lineage specification from cardiac mesoderm into cardiac progenitors and cardiomyocytes. These data can benefit the understanding of human embryonic heart developmental biology, and the time-course changes of cardiac transcriptional factors during in vitro cardiomyocyte differentiation from human embryonic stem cells.
Document Type: article
File Description: electronic resource
Language: English
ISSN: 2352-3409
90656490
Relation: http://www.sciencedirect.com/science/article/pii/S2352340922009738; https://doaj.org/toc/2352-3409
DOI: 10.1016/j.dib.2022.108770
Access URL: https://doaj.org/article/930e9065649040389cc5ffaff6f6abda
Accession Number: edsdoj.930e9065649040389cc5ffaff6f6abda
Database: Directory of Open Access Journals
More Details
ISSN:23523409
90656490
DOI:10.1016/j.dib.2022.108770
Published in:Data in Brief
Language:English