Emerging Roles of Estrogen-Regulated Enhancer and Long Non-Coding RNAs.
Melina J SedanoAlana L HarrisonMina ZilaieChandrima DasRamesh ChoudhariEnrique RamosShrikanth S GadadPublished in: International journal of molecular sciences (2020)
Genome-wide RNA sequencing has shown that only a small fraction of the human genome is transcribed into protein-coding mRNAs. While once thought to be "junk" DNA, recent findings indicate that the rest of the genome encodes many types of non-coding RNA molecules with a myriad of functions still being determined. Among the non-coding RNAs, long non-coding RNAs (lncRNA) and enhancer RNAs (eRNA) are found to be most copious. While their exact biological functions and mechanisms of action are currently unknown, technologies such as next-generation RNA sequencing (RNA-seq) and global nuclear run-on sequencing (GRO-seq) have begun deciphering their expression patterns and biological significance. In addition to their identification, it has been shown that the expression of long non-coding RNAs and enhancer RNAs can vary due to spatial, temporal, developmental, or hormonal variations. In this review, we explore newly reported information on estrogen-regulated eRNAs and lncRNAs and their associated biological functions to help outline their markedly prominent roles in estrogen-dependent signaling.
Keyphrases
- long non coding rna
- single cell
- poor prognosis
- rna seq
- binding protein
- genome wide
- transcription factor
- estrogen receptor
- dna methylation
- endothelial cells
- induced pluripotent stem cells
- type diabetes
- metabolic syndrome
- copy number
- circulating tumor
- cell free
- single molecule
- skeletal muscle
- protein protein
- nucleic acid
- health information
- genome wide analysis
- amino acid
- circulating tumor cells