2018
DOI: 10.1111/nph.15179
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The novel cyst nematode effector protein 30D08 targets host nuclear functions to alter gene expression in feeding sites

Abstract: 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), a… Show more

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Cited by 44 publications
(33 citation statements)
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References 65 publications
(99 reference statements)
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“…Finally, a H. schachtii effector, Hs30D08, has been shown to interfere with mRNA splicing, thereby altering gene expression in feeding sites (Verma et al, 2018). RNA splicing is required to remove introns from pre-mRNA and to join the protein-coding sequences (exons) together during the translation of mRNA into protein.…”
Section: Host Cell Reprogramming Through the Modulation Of Gene Exprementioning
confidence: 99%
“…Finally, a H. schachtii effector, Hs30D08, has been shown to interfere with mRNA splicing, thereby altering gene expression in feeding sites (Verma et al, 2018). RNA splicing is required to remove introns from pre-mRNA and to join the protein-coding sequences (exons) together during the translation of mRNA into protein.…”
Section: Host Cell Reprogramming Through the Modulation Of Gene Exprementioning
confidence: 99%
“…Suppressor of Mec-8 and Unc52 2) funkcjonującym jako białko pomocnicze spliceosomu. Białko 30D08 powoduje zmiany w ekspresji 2180 genów, w tym genów związanych z obróbką, transkrypcją i wiązaniem RNA [77]. Białko efektorowe PsAvh23 z Phytophthora sojae zaburza oddziaływanie podjednostki ADA2 z podjednostką katalityczną GCN5 kompleksu acetylotransferazy histonowej.…”
Section: Zaburzanie Procesów Transkrypcji I Translacji Genówunclassified
“…Quantitative RT-PCR was first used to quantify AtMYB12 transcripts in H. schachtii and M. incognita-infected Arabidopsis roots. It must be noted that only one reference gene (Actin 8) was used in qRT-PCR [51] and that small differences in expression observed among the data are subject to potential variations in reference expression [52,53]. H. schachtii appears to induce AtMYB12 expression in Arabidopsis roots between 5-9 dpi.…”
Section: Discussionmentioning
confidence: 99%