T-REX17 is a transiently expressed non-coding RNA essential for human endoderm formation.
Alexandro LandshammerAdriano BolondiHelene KretzmerChristian MuchRené BuschowAlina RoseHua-Jun WuSebastian D MackowiakBjoern BraendlPay GiesselmannRosaria TornisielloKrishna Mohan ParsiJack HueyThorsten MielkeDavid MeierhoferRené MaehrDenes HniszFranziska MichorJohn L RinnAlexander MeissnerPublished in: eLife (2023)
Long non-coding RNAs (lncRNAs) have emerged as fundamental regulators in various biological processes, including embryonic development and cellular differentiation. Despite much progress over the past decade, the genome-wide annotation of lncRNAs remains incomplete and many known non-coding loci are still poorly characterized. Here, we report the discovery of a previously unannotated lncRNA that is transcribed 230 kb upstream of the SOX17 gene and located within the same topologically associating domain. We termed it T-REX17 ( T ranscript R egulating E ndoderm and activated by so X17 ) and show that it is induced following SOX17 activation but its expression is more tightly restricted to early definitive endoderm. Loss of T-REX17 affects crucial functions independent of SOX17 and leads to an aberrant endodermal transcriptome, signaling pathway deregulation and epithelial to mesenchymal transition defects. Consequently, cells lacking the lncRNA cannot further differentiate into more mature endodermal cell types. Taken together, our study identified and characterized T-REX17 as a transiently expressed and essential non-coding regulator in early human endoderm differentiation.
Keyphrases
- genome wide
- long non coding rna
- transcription factor
- poor prognosis
- endothelial cells
- dna methylation
- stem cells
- signaling pathway
- genome wide identification
- induced apoptosis
- single cell
- high glucose
- embryonic stem cells
- rna seq
- copy number
- pluripotent stem cells
- gene expression
- small molecule
- cell cycle arrest
- long noncoding rna
- epithelial mesenchymal transition
- pi k akt
- squamous cell carcinoma
- radiation therapy
- cell death
- mesenchymal stem cells
- bone marrow
- endoplasmic reticulum stress
- binding protein
- cell proliferation
- genome wide association study