The novel cyst nematode effector protein 30D08 targets host nuclear functions to alter gene expression in feeding sites. Issue 2 (4th May 2018)

• Record Type: Journal Article
• Authors: Verma, Anju; Lee, Chris; Morriss, Stephanie; Odu, Fiona; Kenning, Charlotte; Rizzo, Nancy; Spollen, William G.; Lin, Marriam; McRae, Amanda G.; Givan, Scott A.; Hewezi, Tarek; Hussey, Richard; Davis, Eric L.; Baum, Thomas J.; Mitchum, Melissa G.
• Is Part Of: New phytologist. Volume 219:Issue 2(2018)
• Page Start: 697
• Page End: 713
• Publication Date: 2018-05-04
• Subjects: alternative splicing -- cyst nematode -- effector -- Heterodera -- nucleus -- SMU2 -- spliceosome -- syncytium; Botany -- Periodicals; 580
• DOI: 10.1111/nph.15179
• Languages: English
• ISSNs: 0028-646X

Abstract

Summary: Cyst nematodes deliver effector proteins into host cells to manipulate cellular processes and establish a metabolically hyperactive feeding site. The novel 30D08 effector protein is produced in the dorsal gland of parasitic juveniles, but its function has remained unknown. We demonstrate that expression of 30D08 contributes to nematode parasitism, the protein is packaged into secretory granules and it is targeted to the plant nucleus where it interacts with SMU2 (homolog of suppressor of mec‐8 and unc‐52 2 ), an auxiliary spliceosomal protein. We show that SMU2 is expressed in feeding sites and an smu2 mutant is less susceptible to nematode infection. In Arabidopsis expressing 30D08 under the SMU2 promoter, several genes were found to be alternatively spliced and the most abundant functional classes represented among differentially expressed genes were involved in RNA processing, transcription and binding, as well as in development, and hormone and secondary metabolism, representing key cellular processes known to be important for feeding site formation. In conclusion, we demonstrated that the 30D08 effector is secreted from the nematode and targeted to the plant nucleus where its interaction with a host auxiliary spliceosomal protein may alter the pre‐mRNA splicing and expression of a subset of genes important for feeding site formation.