Octavina Sukarta

Ms. Octavina Sukarta


Research Focus & Metrics

Academic Career Length

11Years (2016-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 August 2016 in Seminars in Cell & Developmental Biology
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Journal Article
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OSOctavina Sukarta
Octavina Sukarta
ESErik J. Slootweg
Erik J. Slootweg
AGAska Goverse
Aska Goverse

8 March 2020 in Genes
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Journal Article
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EMEliza Martin
Eliza Martin
OSOctavina Sukarta
Octavina Sukarta
LSLaurentiu Spiridon
Laurentiu Spiridon
LGLaurentiu G. Grigore
Laurentiu G. Grigore
VCVlad Constantinescu
Vlad Constantinescu
APAndrei-Jose Petrescu
Andrei-Jose Petrescu
Leucine-rich-repeats (LRRs) belong to an archaic procaryal protein architecture that is widely involved in protein–protein interactions. In eukaryotes, LRR domains developed into key recognition modules in many innate immune receptor classes. Due to the high sequence variability imposed by recognition specificity, precise repeat delineation is often difficult especially in plant NOD-like Receptors (NLRs) notorious for showing far larger irregularities. To address this problem, we introduce here LRRpredictor, a method based on an ensemble of estimators designed to better identify LRR motifs in general but particularly adapted for handling more irregular LRR environments, thus allowing to compensate for the scarcity of structural data on NLR proteins. The extrapolation capacity tested on a set of annotated LRR domains from six immune receptor classes shows the ability of LRRpredictor to recover all previously defined specific motif consensuses and to extend the LRR motif coverage over annotated LRR domains. This analysis confirms the increased variability of LRR motifs in plant and vertebrate NLRs when compared to extracellular receptors, consistent with previous studies. Hence, LRRpredictor is able to provide novel insights into the diversification of LRR domains and a robust support for structure-informed analyses of LRRs in immune receptor functioning.

13 February 2020 in BMC Plant Biology
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Journal Article
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SWSonja Warmerdam
Sonja Warmerdam
MSMark Sterken
Mark Sterken
OSOctavina Sukarta
Octavina Sukarta
CSCasper C. van Schaik
Casper C. van Schaik
MOMarian E. P. Oortwijn
Marian E. P. Oortwijn
AGAska Goverse
Aska Goverse
Background: Root-knot nematodes transform vascular host cells into permanent feeding structures to withdraw nutrients from the host plant. Ecotypes ofArabidopsis thalianacan display large quantitative variation in susceptibility to the root-knot nematodeMeloidogyne incognita, which is thought to be independent of dominant major resistance genes. However, in an earlier genome-wide association study of the interaction between Arabidopsis andM. incognitawe identified a quantitative trait locus harboring homologs of dominant resistance genes but with minor effect on susceptibility to theM. incognitapopulation tested.Results: Here, we report on the characterization of two of these genes encoding the TIR-NB-LRR immune receptor DSC1 (DOMINANT SUPPRESSOR OF Camta 3 NUMBER 1) and the TIR-NB-LRR-WRKY-MAPx protein WRKY19 in nematode-infected Arabidopsis roots. Nematode infection studies and whole transcriptome analyses using the Arabidopsis mutants showed thatDSC1andWRKY19co-regulate susceptibility of Arabidopsis toM. incognita.Conclusion: Given the head-to-head orientation ofDSC1andWRKY19in the Arabidopsis genome our data suggests that both genes may function as a TIR-NB-LRR immune receptor pair. Unlike other TIR-NB-LRR pairs involved in dominant disease resistance in plants, DSC1 and WRKY19 most likely regulate basal levels of immunity to root-knot nematodes.