Variant-specific interaction of kinectin 1 with the multi-tRNA synthetase complex regulates ER sheet organization
Kinectin 1 (KTN1) is an integral endoplasmic reticulum (ER) sheet protein involved in ER organization and translation elongation. Alternative splicing introduces sequence diversity into the cytosolic region of KTN1; however, the functional significance of these variants has remained unclear. Here, we show that the multi-tRNA synthetase complex (MSC), composed of eight aminoacyl-tRNA synthetases and three nonenzymatic proteins, specifically interacts with KTN1 in a manner dependent on the alternative exon V2 and glutamine-tRNA synthetase (QARS). Using V2 exon-specific knockout cells and KTN1 knockout cells with variant-specific rescue, we found that the V2 exon is required for KTN1-mediated recruitment of the MSC to the ER, where it facilitates the formation of rough ER stacks. These findings define a variant-specific role for KTN1 in anchoring the MSC to the ER and suggest that this interaction underlies a noncanonical function of the MSC in regulating ER sheet organization.
Authors
- Masaki Hosogane (ORCID: https://orcid.org/0000-0001-5784-304X)
- Shintaro Iwasaki (ORCID: https://orcid.org/0000-0001-7724-3754)
- Masaki Matsumoto (ORCID: https://orcid.org/0000-0002-6987-0288)
- Keiko Nakayama (ORCID: https://orcid.org/0000-0003-0134-6401)
- Atsushi Hatano (ORCID: https://orcid.org/0000-0002-0386-5080)
- Yuichi Shichino (ORCID: https://orcid.org/0000-0002-0093-1185)
- Xiaoxin Huang (ORCID: https://orcid.org/0009-0003-0402-3613)
- Yasuaki Watanabe
- Siao Sue-yi
Institutions
- Pioneer (United States) (US)
- University of Tsukuba (JP)
- Tohoku University (JP)
- RIKEN (JP)
- National Institutes for Quantum Science and Technology (JP)
- Institute of Applied Biochemistry (JP)
- Niigata University (JP)
- The University of Tokyo (JP)
- Dokkyo Medical University (JP)
Publication Details
- Journal
- iScience
- Published
- 2025-12-01
- DOI
- https://doi.org/10.1016/j.isci.2025.114303
- Primary Topic
- RNA and protein synthesis mechanisms
- Type
- article
- Field-Weighted Citation Impact
- 0.00