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Updated: Jul 31, 2025

Co-immunoprecipitation Assay Using Endogenous Nuclear Proteins from Cells Cultured Under Hypoxic Conditions
Published on: August 2, 2018
The RNA-binding protein Snd1/Tudor-SN regulates hypoxia-responsive gene expression
Juha Saarikettu1, Saara Lehmusvaara2, Marko Pesu2,3
1Institute of Biotechnology, HiLIFE Helsinki Institute of Life Sciences University of Helsinki Helsinki Finland.
The study reveals that the Snd1 protein regulates gene expression and plays a role in the body's adaptation to low oxygen conditions (hypoxia). Snd1 negatively controls hypoxia-induced microRNAs and transcription.
Area of Science:
- Molecular Biology
- Gene Regulation
- Cellular Stress Response
Background:
- Snd1 is an evolutionarily conserved RNA-binding protein involved in gene expression regulation.
- Its precise function in mammalian physiology, particularly under stress, requires further elucidation.
Purpose of the Study:
- To investigate the physiological consequences of Snd1 gene deletion in mice.
- To understand Snd1's role in cellular responses, specifically adaptation to hypoxia.
- To identify proteins interacting with Snd1.
Main Methods:
- Generation and analysis of Snd1 knockout mice.
- Transcriptomic analysis (mRNA and microRNA) in spleen and liver.
- BioID proximity ligation assay in HEK-293T cells.
Main Results:
- Snd1 knockout mice exhibited reduced fertility, body size, and myeloid cell counts.
- Gene expression changes in knockout livers mirrored hypoxia adaptation profiles.
- Upregulation of hypoxia-induced microRNAs (miR-96, -182) was observed in knockout livers.
- SND1 interactors identified via BioID were predominantly RNA-binding proteins.
Conclusions:
- Snd1 is not essential for mRNA transcription under normal conditions but is crucial for hypoxia adaptation.
- Snd1 negatively regulates hypoxia-responsive microRNAs and transcription, acting as a stress response regulator.
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