a b s t r a c tThe C-terminally Encoded Peptide (CEP) family of regulatory peptides controls root development in vascular plants. Here, we present the first NMR structures of CEP. We show that root-knot nematode (RKN: Meloidogyne spp.) also encodes CEP, presumably to mimic plant CEP as part of their stereotypic, parasitic interaction with vascular plants. Molecular dynamics simulations of plant-and nematode-encoded CEP displaying known posttranslational modifications (PTM) provided insight into the structural effects of PTM and the conformational plasticity and rigidity of CEP. Potential mechanisms of action are discussed with respect to the structure and sampling of conformational space.
Nematodes are among the most diverse but least studied organisms. The classic morphology-based identification has proved insufficient to the study of nematode identification and diversity, mainly for lack of sufficient morphological variations among closely related taxa. Different molecular methods have been used to supplement morphology-based methods and/or circumvent these problems with various degrees of success. These methods range from fingerprint to sequence analyses of DNA- and/or protein-based information. Image analyses techniques have also contributed towards this success. In this review, we highlight what each of these methods entail and provide examples where more recent advances of these techniques have been employed in nematode identification. Wherever possible, emphasis has been given to nematodes of agricultural significance. We show that these alternative methods have aided nematode identification and raised our understanding of nematode diversity and phylogeny. We discuss the pros and cons of these methods and conclude that no one method by itself provides all the answers; the choice of method depends on the question at hand, the nature of the samples, and the availability of resources.
Cowpea [Vigna unguiculata (L.) Walp] is a multipurpose crop that provides nutrients for human and livestock diets, as well as regulates and supports ecosystem services. In developing countries, cowpea is exploited as a dual-purpose crop for its grain and fodder; it is cultivated primarily for grain and as a cover crop in industrialized countries. However, root-knot nematodes (RKNs) (Meloidogyne spp.) represent a threat to cowpea production worldwide. Thus, we screened the University of California, Riverside (UC-Riverside), cowpea mini-core collection for resistance to Meloidogyne incognita Kofoid and White (Chitwood) and M. enterolobii Yang and Eisenback to verify the potential of this collection to be used for improving RKN resistance in cowpeas. Both screenings showed significant genotypic variation and medium/high broad-sense heritability (H2) estimates for most traits, and several traits were also strongly correlated. For the M. incognita screening, 86.1% of accessions showed some level of resistance based on gall score (≤3), and 77.7% based on reproduction index (RI) (25 ≤ RI ≤ 50), whereas only 10.4% and 29.8% of accessions were resistant to M. enterolobii based on gall score (≤3) and RI (25 ≤ RI ≤ 50), respectively. These results demonstrate the greater virulence of M. enterolobii than M. incognita in cowpea, and that geographic origin of germplasm was not linked to sources of resistance. Among cultivars, only US-1136 showed resistance against both nematode species, whereas 12 wild/landrace germplasms exhibited resistance to M. incognita and M. enterolobii, and can be exploited for breeding resistant cowpeas.
Interactions between species are pervasive among plants, animals, and microbes, and identifying the molecular signals involved is an active area of research..
Intercellular signaling mediated by small peptides is critical to coordinate organ formation in animals, but whether extracellular polypeptides play similar roles in plants is unknown. Here we describe a role in Arabidopsis leaf development for two members of the CLAVATA 3/ ESR ‐ RELATED peptide family, CLE 5 and CLE 6, which lie adjacent to each other on chromosome 2. Uniquely among the CLE genes, CLE 5 and CLE 6 are expressed specifically at the base of developing leaves and floral organs, adjacent to the boundary with the shoot apical meristem. During vegetative development CLE 5 and CLE 6 transcription is regulated by the leaf patterning transcription factors BLADE ‐ ON ‐ PETIOLE 1 ( BOP 1) and ASYMMETRIC LEAVES 2 ( AS 2), as well as by the WUSCHEL ‐ RELATED HOMEOBOX ( WOX ) transcription factors WOX 1 and PRESSED FLOWER ( PRS ). Moreover, CLE 5 and CLE 6 transcript levels are differentially regulated in various genetic backgrounds by the phytohormone auxin. Analysis of loss‐of‐function mutations generated by genome engineering reveals that CLE 5 and CLE 6 independently and together have subtle effects on rosette leaf shape. Our study indicates that the CLE 5 and CLE 6 peptides function downstream of leaf patterning factors and phytohormones to modulate the final leaf morphology.
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