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lncRNA read-through regulates the BX-C insulator Fub-1 .

Airat N IbragimovXin Yang BingYulii V ShidlovskiiMichael LevinePavel GeorgievPaul Schedl
Published in: eLife (2023)
hough long non-coding RNAs (lncRNAs) represent a substantial fraction of the Pol II transcripts in multicellular animals, only a few have known functions. Here we report that the blocking activity of the Bithorax complex (BX-C) Fub-1 boundary is segmentally regulated by its own lncRNA. The Fub-1 boundary is located between the Ultrabithorax ( Ubx ) gene and the bxd/pbx regulatory domain, which is responsible for regulating Ubx expression in parasegment PS6/segment A1. Fub-1 consists of two hypersensitive sites, HS1 and HS2 . HS1 is an insulator while HS2 functions primarily as a lncRNA promoter. To activate Ubx expression in PS6/A1 enhancers in the bxd/pbx domain must be able to bypass Fub-1 blocking activity. We show that expression of the Fub-1 lncRNAs in PS6/A1 from the HS2 promoter inactivates Fub-1 insulating activity. Inactivation is due to readthrough as the HS2 promoter must be directed towards HS1 to disrupt blocking.
Keyphrases
  • long non coding rna
  • poor prognosis
  • dna methylation
  • transcription factor
  • gene expression
  • binding protein
  • genome wide
  • copy number
  • single molecule
  • network analysis