Nesprin-2 contains BH3-like motifs that can promote cell death
BH3-only proteins are a subgroup of the pro-apoptotic Bcl-2 family proteins. They initiate apoptosis by interacting with the multidomain pro- and anti-apoptotic Bcl-2 family proteins. SYNE2 encodes multiple nesprin-2 (Nes2) isoforms of which the most abundant and the largest is the nuclear envelope protein nesprin-2 giant (Nes2G). Nes2G is a component of the nuclear envelope Linker of Nucleoskeleton and Cytoskeleton (LINC) complex that connects the nucleus and the cytoskeleton. Previously, we showed that Nes2 has pro-apoptotic activity. We now show that Nes2G can bind multidomain pro-apoptotic and anti-apoptotic Bcl-2 family proteins and contains two BH3-like motifs near its N- and C-termini. Molecular modeling predicts that these BH3-like motifs have amphipathic α-helix structures and can dock onto the canonical groove of Bax and anti-apoptotic proteins as well as the trigger site of Bax. A chimeric tBid with its BH3 domain replaced with the C-terminal Nes2 BH3-like domain binds to Bax in cells. Furthermore, Nes2 BH3-like motif-containing fragments from the N- and the C-termini bind both pro-apoptotic and anti-apoptotic Bcl-2 proteins and promote cytochrome c release (indicative of apoptosis). Our results suggest that Nes2 acts as a BH3-only protein that regulates apoptosis by binding to the multidomain Bcl-2 family proteins.
Authors
- Reuven Stein (ORCID: https://orcid.org/0000-0002-7166-6542)
- Hila Zohar
- Nir Ben‐Tal (ORCID: https://orcid.org/0000-0001-6901-832X)
- Amit Kessel (ORCID: https://orcid.org/0000-0003-0227-0226)
- David W. Andrews (ORCID: https://orcid.org/0000-0002-9266-7157)
- Dang Nguyen (ORCID: https://orcid.org/0000-0002-3000-2053)
- Gregg G. Gundersen
- Liora Lindenboim
- Howard J. Worman
Institutions
- Sunnybrook Health Science Centre (CA)
- Tel Aviv University (IL)
- University of Toronto (CA)
- Institute of Molecular Biology and Biophysics (RU)
- Sunnybrook Research Institute
- Columbia University (US)
Publication Details
- Journal
- Cell Death Discovery
- Published
- 2025-06-03
- DOI
- https://doi.org/10.1038/s41420-025-02534-5
- Citations
- 1
- Primary Topic
- Nuclear Structure and Function
- Type
- article
- Field-Weighted Citation Impact
- 0.81
Funders
- United States - Israel Binational Science Foundation
- Israel Science Foundation
- National Institute on Aging
- National Institute of Biomedical Imaging and Bioengineering