# Importin Alpha Is Implicated in the Nuclear Import of Novel Duck Reovirus Protein p18

**Authors:** Dan Wang, Jiangwei Song, Jing Wang, Fangfang Guo, Rong Quan

PMC · DOI: 10.3390/v18020221 · Viruses · 2026-02-10

## TL;DR

This study finds that a duck virus protein, p18, enters the cell nucleus with the help of importin alpha proteins, and its nuclear entry does not require active viral infection.

## Contribution

The study identifies importin alpha as a key transporter for p18 nuclear import and shows that this process is independent of viral replication.

## Key findings

- p18 localizes to the nucleus in transfected cells.
- Importin α1, α3, α4, α5, and α7 interact with p18.
- The C-terminal region of p18 is essential for its nuclear localization.

## Abstract

Novel duck reovirus encodes a new nucleus-localized protein, p18. We aimed to investigate whether the nuclear entry of p18 is dependent on viral replication, identify the cellular proteins that interact with p18, and determine the transporters involved in the nuclear import. The subcellular localization of p18 was observed by confocal microscopy. Cellular proteins interacting with p18 were identified through data-independent acquisition qualitative proteomics. The interaction between p18 and importin α was determined by confocal microscopy, co-immunoprecipitation (Co-IP) and molecular docking. We observed that p18 was localized to the nucleus in transfected cells. Importin α1, α3, α4, α5, and α7 were colocalized and co-immunoprecipitated with p18. The importin α/β1 pathway inhibitor reduced the nuclear distribution of p18. The truncated form of p18, lacking the C-terminal region, was predominantly distributed in the cytoplasm. Collectively, our research suggests that the nuclear entry of p18 is independent of viral infection, importin α is implicated in the nuclear import of p18, and the C-terminal region of p18 is crucial for nuclear localization.

## Linked entities

- **Proteins:** CDKN2C (cyclin dependent kinase inhibitor 2C)

## Full-text entities

- **Genes:** HNRNPA1 (heterogeneous nuclear ribonucleoprotein A1) [NCBI Gene 3178] {aka ALS19, ALS20, HNRPA1, HNRPA1L3, IBMPFD3, MPD3}, Stmn1 (stathmin 1) [NCBI Gene 16765] {aka 19k, Lag, Lap18, Op18, P18, P19}, S100a10 (S100 calcium binding protein A10 (calpactin)) [NCBI Gene 20194] {aka 42C, CAL12, CLP11, Cal1l, p10, p11}, H3P12 (H3 histone pseudogene 12) [NCBI Gene 100689229] {aka H3F3AP3, p18}, Trp53-ps (transformation related protein 53, pseudogene) [NCBI Gene 22060], Ubl3 (ubiquitin-like 3) [NCBI Gene 24109] {aka HCG, MUB, mmMUB}, Snora73a (small nucleolar RNA, H/ACA box 73a) [NCBI Gene 100306944] {aka E1, E1-7, E1b, U17A}, KPNA1 (karyopherin subunit alpha 1) [NCBI Gene 3836] {aka IPOA5, NPI-1, RCH2, SRP1}, Transportin-1 [NCBI Gene 101839788], hnRNP K [NCBI Gene 101838781], Trim27 (tripartite motif-containing 27) [NCBI Gene 19720] {aka Gm19403, Rfp}, Hspa8 (heat shock protein family A (Hsp70) member 8) [NCBI Gene 15481] {aka 2410008N15Rik, Hsc70, Hsc71, Hsc73, Hsp73, Hspa10}, IMPA1 (inositol monophosphatase 1) [NCBI Gene 3612] {aka IMP, IMPA, MRT59}, Eif2ak2 (eukaryotic translation initiation factor 2-alpha kinase 2) [NCBI Gene 19106] {aka 2310047A08Rik, 4732414G15Rik, Pkr, Prkr, Tik}, Irf3 (interferon regulatory factor 3) [NCBI Gene 54131] {aka C920001K05Rik, IRF-3}, hnRNP H1 [NCBI Gene 101827756], Dnajc3 (DnaJ heat shock protein family (Hsp40) member C3) [NCBI Gene 100037258] {aka Dnajc3a, Dnajc3b, Prkri, mp58, p58, p58IPK}, FAM72B (family with sequence similarity 72 member B) [NCBI Gene 653820] {aka p17}, TNPO1 (transportin 1) [NCBI Gene 3842] {aka IPO2, KPNB2, MIP, MIP1, TRN}, Fam72a (family with sequence similarity 72, member A) [NCBI Gene 108900] {aka 2700049P18Rik, P17}, Tcof1 (treacle ribosome biogenesis factor 1) [NCBI Gene 21453] {aka treacle}, Gapdh (glyceraldehyde-3-phosphate dehydrogenase) [NCBI Gene 14433] {aka Gapd}, Imp alpha1 [NCBI Gene 101841518], fibrillarin [NCBI Gene 101837031], Lmnb1 (lamin B1) [NCBI Gene 16906], Copb2 (COPI coat complex subunit beta 2) [NCBI Gene 50797]
- **Diseases:** injury to (MESH:D014947), hemorrhagic-necrotic hepatitis (MESH:D006470), infection (MESH:D007239), viral infection (MESH:D014777), ARV (MESH:D012088), spleen necrosis disease (MESH:D013160)
- **Chemicals:** TritonX-100 (MESH:D017830), ACN (MESH:C032159), FA (MESH:C030544), ivermectin (MESH:D007559), DTT (MESH:D004229), SDS (MESH:D012967), iodoacetamide (MESH:D007460), H2O (MESH:D014867), Cy3 (-), DAPI (MESH:C007293), DMSO (MESH:D004121), PBS (MESH:D007854), hydrogen (MESH:D006859), Coomassie blue (MESH:C048139), paraformaldehyde (MESH:C003043), agarose (MESH:D012685), ATP (MESH:D000255), TEAB (MESH:C041737), CO2 (MESH:D002245)
- **Species:** Mus musculus (house mouse, species) [taxon 10090], Zika virus (no rank) [taxon 64320], Henipavirus (genus) [taxon 260964], Human alphaherpesvirus 1 (Herpes simplex virus type 1, no rank) [taxon 10298], Mammalian orthoreovirus 3 (no rank) [taxon 538123], Homo sapiens (human, species) [taxon 9606], Duck reovirus (no rank) [taxon 1171667], Adenoviridae (family) [taxon 10508], Orthohantavirus (genus) [taxon 1980442], Muscovy duck reovirus (no rank) [taxon 77153]
- **Mutations:** arginine (R) to alanine (A) at positions 118-121, R with A
- **Cell lines:** CCL-10 — Mus musculus (Mouse), Undefined cell line type (CVCL_M023), S2 — Drosophila melanogaster (Fruit fly), Spontaneously immortalized cell line (CVCL_Z232), BHK-21 — Mesocricetus auratus (Golden hamster), Spontaneously immortalized cell line (CVCL_RQ70)

## Full text

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## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12945130/full.md

## References

46 references — full list in the complete paper: https://tomesphere.com/paper/PMC12945130/full.md

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Source: https://tomesphere.com/paper/PMC12945130