RNA Sequencing Reveals a Strong Predominance of THRA Splicing Isoform 2 in the Developing and Adult Human Brain

• Published in: International journal of molecular sciences 2024-09, Vol.25 (18), p.9883
• Main Authors: Graceffo, Eugenio, Opitz, Robert, Megges, Matthias, Krude, Heiko, Schuelke, Markus
• Format: Article
• Language: English
• Subjects: Adult; Alternative Splicing; Biological research; Biology, Experimental; Brain; Brain - growth & development; Brain - metabolism; central nervous system; Congenital diseases; Datasets; Gene expression; Genetic aspects; Hormone receptors; Hormones; Humans; Hypothyroidism; Laboratories; Metabolism; Mutation; Nervous system; organoids; Physiological aspects; Physiology; Protein Isoforms - genetics; Protein Isoforms - metabolism; RNA sequencing; RNA Splicing; Sequence Analysis, RNA; single-cell RNA analysis; Thyroid gland; thyroid hormone receptor; Thyroid Hormone Receptors alpha - genetics; Thyroid Hormone Receptors alpha - metabolism
• ISSN: 1422-0067; 1661-6596; 1422-0067
• DOI: 10.3390/ijms25189883

Thyroid hormone receptor alpha (THRα) is a nuclear hormone receptor that binds triiodothyronine (T3) and acts as an important transcription factor in development, metabolism, and reproduction. In mammals, THRα has two major splicing isoforms, THRα1 and THRα2. The better-characterized isoform, THRα1, is a transcriptional stimulator of genes involved in cell metabolism and growth. The less-well-characterized isoform, THRα2, lacks the ligand-binding domain (LBD) and is thought to act as an inhibitor of THRα1 activity. The ratio of THRα1 to THRα2 splicing isoforms is therefore critical for transcriptional regulation in different tissues and during development. However, the expression patterns of both isoforms have not been studied in healthy human tissues or in the developing brain. Given the lack of commercially available isoform-specific antibodies, we addressed this question by analyzing four bulk RNA-sequencing datasets and two scRNA-sequencing datasets to determine the RNA expression levels of human and transcripts in healthy adult tissues and in the developing brain. We demonstrate how 10X Chromium scRNA-seq datasets can be used to perform splicing-sensitive analyses of isoforms that differ at the 3'-end. In all datasets, we found a strong predominance of transcripts at all examined stages of human brain development and in the central nervous system of healthy human adults.