Related Experiment Video
Updated: Aug 30, 2025

Enhanced Northern Blot Detection of Small RNA Species in Drosophila Melanogaster
Published on: August 21, 2014
Identification of Lsd1-interacting non-coding RNAs as regulators of fly oogenesis
Tzu-Ling Shao1, Ruei-Teng Ting1, Ming-Chia Lee1
1Department of Life Sciences and Institute of Genome Sciences, National Yang Ming Chiao Tung University, Taipei, Taiwan.
Abstract:
Lysine-specific demethylase 1 (Lsd1) plays a key role in balancing cell proliferation and differentiation. Lsd1 has been recently reported to associate with specific long noncoding RNAs (lncRNAs) to account for oncogenic gene expression in cancer cells. However, how lncRNA-Lsd1 interplay affects cell-specific differentiation remains elusive in vivo. Here, through Lsd1 specific RNA immunopecipitation sequencing (RIP-seq) experiments, we identify three long hairpin RNAs as Lsd1-interacting non-coding RNAs (LINRs) from fly ovaries. Knocking out LINR-1 and LINR-2 affects fly egg production, while each of the LINR deletion mutant females produce eggs with reduced hatch rate, indicating important functions of LINRs in supporting oogenesis. At the cellular level, LINR-2 regulates the differentiation of germline stem cells and follicle progenitors likely though modulating the expression and function of Lsd1 in vivo. Our identification of ovarian LINRs presents a physiological example of dynamic lncRNA-Lsd1 interplay that regulates stem cell/progenitor differentiation.
Insights
Long noncoding RNAs (lncRNAs) interact with Lysine-specific demethylase 1 (LSD1) to regulate cell differentiation. This study identifies ovarian lncRNAs (LINRs) that are crucial for oogenesis and germline stem cell differentiation in vivo.
Area of Science:
- Developmental Biology
- Epigenetics
- Molecular Biology
Background:
- Lysine-specific demethylase 1 (LSD1) is crucial for cell proliferation and differentiation.
- LSD1 interacts with long noncoding RNAs (lncRNAs) in cancer, but its role in cell-specific differentiation in vivo is unclear.
Purpose of the Study:
- To investigate the in vivo role of lncRNA-LSD1 interactions in cell differentiation.
- To identify novel lncRNAs interacting with LSD1 in ovarian tissues.
Main Methods:
- RNA immunoprecipitation sequencing (RIP-seq) to identify LSD1-interacting RNAs.
- Genetic knockout of identified lncRNAs in Drosophila melanogaster.
- Analysis of oogenesis and stem cell differentiation in mutant flies.
Main Results:
- Three LSD1-interacting non-coding RNAs (LINRs) were identified in fly ovaries.
- Knockout of LINR-1 and LINR-2 impaired fly egg production and hatch rate.
- LINR-2 regulates germline stem cell and progenitor differentiation by modulating LSD1.
Conclusions:
- Ovarian LINRs are essential for oogenesis and stem cell differentiation.
- This study reveals a physiological role for lncRNA-LSD1 interplay in regulating differentiation.
- Identified LINRs provide a model for studying dynamic lncRNA-LSD1 interactions in vivo.
Related Concept Videos
Regulation of Expression Occurs at Multiple Steps
Transcription results in the generation of precursor (pre-mRNA) that consists of both exons and introns, which needs further processing before being translated to a...
Regulation of Expression at Multiple Steps
Master Transcription Regulators
Cis-regulatory Sequences
The Ratio of X Chromosome to Autosomes
Normal male Drosophila has a ratio of one X chromosome to two sets of autosomes. In contrast, normal female...

