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Published on: April 25, 2018
lncRNA read-through regulates the BX-C insulator Fub-1
Airat Ibragimov1,2, Xin Yang Bing3, Yulii V Shidlovskii4,5
1Department of Molecular Biology, Princeton University, Princeton, United States.
Long non-coding RNAs (lncRNAs) regulate gene expression. A specific lncRNA from the Fub-1 boundary inactivates its own insulator activity, enabling Ultrabithorax gene expression in specific segments.
Area of Science:
- Developmental Biology
- Epigenetics
- RNA Biology
Background:
- Long non-coding RNAs (lncRNAs) are abundant but functionally understudied.
- The Bithorax complex (BX-C) controls segmental identity in animals.
- Insulator elements regulate gene expression by blocking enhancer-promoter interactions.
Purpose of the Study:
- To investigate the function of the lncRNA transcribed from the Fub-1 boundary.
- To understand the segmental regulation of the Ultrabithorax (Ubx) gene.
- To elucidate the mechanism by which the Fub-1 boundary's insulating activity is modulated.
Main Methods:
- Analysis of Fub-1 boundary structure and function.
- Investigation of lncRNA expression from the Fub-1 HS2 promoter.
- Functional assays to assess insulator activity and enhancer bypass.
Main Results:
- The Fub-1 boundary contains an insulator (HS1) and an lncRNA promoter (HS2).
- Expression of Fub-1 lncRNAs from HS2 inactivates the HS1 insulator activity in a segmental manner.
- This inactivation requires the HS2 promoter to be oriented towards HS1, causing read-through transcription.
Conclusions:
- Fub-1 lncRNAs play a crucial role in the segmental regulation of gene expression.
- lncRNA transcription can directly modulate the function of nearby regulatory elements like insulators.
- This provides a novel mechanism for controlling gene expression during development.
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