JmjC-domain-containing histone demethylases of the JMJD1B type as putative precursors of endogenous DSIP.
Mikhaleva. Inessa I II; Prudchenko. Igor A IA; Ivanov. Vadim T VT; Voitenkov. Vladislav B VB
Key Findings
- DSIP (WAGGDASGE) is known to protect against stress, but its natural protein precursor was unknown.
- A segment of the JMJD1B histone demethylase (WKGGNASGE) is only two amino acids different from DSIP.
- The synthetic WKGGNASGE peptide showed some activity in forced‑swim and antitoxic experiments in animals.
Practical Outcomes
- For biohackers, this work hints that the body may produce DSIP‑like peptides from JMJD1B proteins, but it does not provide new dosing guidelines or a ready‑to‑use supplement protocol. Until more data are available, the study is mainly of scientific interest rather than a direct actionable strategy.
Summary
Scientists found that a family of proteins called JMJD1B histone demethylases contains a short sequence that looks a lot like the stress‑protective peptide DSIP. They made a synthetic version of this similar peptide and saw modest effects in animal stress tests, suggesting these proteins might be natural sources of DSIP in the body.
Abstract
Delta sleep inducing peptide (WAGGDASGE, DSIP) is a well known multifunctional regulatory peptide. Numerous studies have confirmed its stress-protective and adaptive activity which is independent of the origin or nature of the stress or other harmful factors. However, the biosynthetic origin of DSIP remains obscure, since nothing is known of its protein precursor(s) and their encoding gene(s). We have performed a comprehensive analysis of available gene and protein databases for homologous peptide sites within mammalian resources including man. A family of Jumonji C (JmjC)-domain-containing histone demethylases was shown to contain a sequence fragment closely homologous to DSIP. One type of these ubiquitous and phylogenetically ancient proteins encoded by JMJD1B gene includes the WKGGNASGE sequence that differs from DSIP by only 2 amino acid residues in positions 2 and 5. The respective peptide was synthesized and its biological effects were evaluated in a preliminary way in the forced swimming and antitoxic tests. We suggest that the histone demethylases of the JmjC-group containing DSIP-related region can be considered as possible protein precursors of endogenous peptides with DSIP-like activity.
Study Information
pubmed
2011
2011-01-22T00:00:00.000Z
10.1016/j.peptides.2011.01.006
12
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