4.6 Article

Genome Expression Dynamics Reveal the Parasitism Regulatory Landscape of the Root-Knot Nematode Meloidogyne incognita and a Promoter Motif Associated with Effector Genes

Journal

GENES
Volume 12, Issue 5, Pages -

Publisher

MDPI
DOI: 10.3390/genes12050771

Keywords

genome; transcriptome; phytoparasitism; gene expression regulation; Meloidogyne; nematode

Funding

  1. BBSRC [BB/R011311/1, BB/N021908/1, BB/S006397/1]
  2. Marie Sklodowska-Curie Actions Individual Fellowships
  3. BBSRC [BB/R011311/1, BB/N021908/1, BB/S006397/1] Funding Source: UKRI

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Root-knot nematodes, especially Meloidogyne species, secrete effector proteins to manipulate host physiology and immunity, but the details of transcription regulation remain sparse. This study provides a genome-wide analysis of spatio-temporal gene expression in Meloidogyne incognita, identifying a new set of candidate effector genes for future functional analyses. The discovery of a conserved cis-regulatory motif associated with effector expression in dorsal glands, named Mel-DOG, sheds light on effector regulation in the genus Meloidogyne.
Root-knot nematodes (genus Meloidogyne) are the major contributor to crop losses caused by nematodes. These nematodes secrete effector proteins into the plant, derived from two sets of pharyngeal gland cells, to manipulate host physiology and immunity. Successful completion of the life cycle, involving successive molts from egg to adult, covers morphologically and functionally distinct stages and will require precise control of gene expression, including effector genes. The details of how root-knot nematodes regulate transcription remain sparse. Here, we report a life stage-specific transcriptome of Meloidogyne incognita. Combined with an available annotated genome, we explore the spatio-temporal regulation of gene expression. We reveal gene expression clusters and predicted functions that accompany the major developmental transitions. Focusing on effectors, we identify a putative cis-regulatory motif associated with expression in the dorsal glands, providing an insight into effector regulation. We combine the presence of this motif with several other criteria to predict a novel set of putative dorsal gland effectors. Finally, we show this motif, and thereby its utility, is broadly conserved across the Meloidogyne genus, and we name it Mel-DOG. Taken together, we provide the first genome-wide analysis of spatio-temporal gene expression in a root-knot nematode and identify a new set of candidate effector genes that will guide future functional analyses.

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