Non-catalytic role of SETD1A promotes gastric cancer cell proliferation through the E2F4–TAF6 axis in the cell cycle
SETD1A is a member of the KMT2 histone H3K4 methyltransferase family of mammalian proteins. Aberrant SETD1A expression is associated with a poor prognosis in patients with gastric cancer (GC). We found that the catalytic domain of SETD1A is nonessential for GC cell proliferation, whereas the non-catalytic FLOS domain is essential. The loss of SETD1A commonly reduces the expression of E2F target genes in GC cell lines from the three independent molecular subtypes. A pooled CRISPR screen and cDNA rescue experiment showed that TAF6 acts downstream of SETD1A's non-catalytic function, which is essential for GC cell proliferation. Both SETD1A and TAF6 are required for G1/S cell cycle progression in GC cells. The mRNA expression of E2F4 highly correlated with both the SETD1A and TAF6 expression in patients with GC. Notably, E2F4 supported the expression of TAF6 but not that of SETD1A, suggesting that E2F4 serves as a coregulator of SETD1A, which is involved in regulating TAF6. These results demonstrate that the non-canonical roles of SETD1A and its downstream pathways are crucial for cell cycle progression in GC.
Authors
- Genki Usui (ORCID: https://orcid.org/0000-0002-6615-8674)
- Bahityar Rahmutulla (ORCID: https://orcid.org/0000-0002-4014-2789)
- Hiroyuki Abé (ORCID: https://orcid.org/0000-0003-4513-1007)
- Tetsuo Ushiku (ORCID: https://orcid.org/0000-0002-1763-8380)
- Takayuki Hoshii (ORCID: https://orcid.org/0000-0002-5418-1981)
- Takuya Nakagawa (ORCID: https://orcid.org/0000-0003-1216-4822)
- Masaki Fukuyo (ORCID: https://orcid.org/0000-0003-2320-1529)
- Shintaro Izumi
- Atsushi Kaneda (ORCID: https://orcid.org/0000-0002-6980-5515)
- Makoto Matsumoto (ORCID: https://orcid.org/0009-0006-5365-8975)
- Ning Meng (ORCID: https://orcid.org/0000-0002-0481-9916)
- Kanako Hayashi
Institutions
- Chiba University (JP)
- The University of Tokyo (JP)
Publication Details
- Journal
- Cell Death and Disease
- Published
- 2025-08-22
- DOI
- https://doi.org/10.1038/s41419-025-07976-4
- Primary Topic
- RNA modifications and cancer
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- Novartis Foundation
- Uehara Memorial Foundation
- Japan Agency for Medical Research and Development
- Takeda Medical Research Foundation
- Kobayashi Foundation for Cancer Research
- Chiba University
- NOVARTIS Foundation (Japan) for the Promotion of Science
- Japan Society for the Promotion of Science
- Japan Science and Technology Agency
- Strategic International Collaborative Research Program
- Moonshot Research and Development Program