Phloem specific responses to CLas for the identification of novel HLB resistance genes

Phloem specific responses to CLas for the identification of novel HLB resistance genes

Report Date: 03/13/2020
Project: 18-019   Year: 2020
Category: Horticultural & Management
Author: Elizabeth Rogers
Sponsor: Citrus Research and Development Foundation

Our project is examining phloem gene expression changes in response to CLas infection in HLB-susceptible sweet orange and HLB-resistant Poncirus and Carrizo (a sweet orange – Poncirus cross). We are using a recently developed methodology for woody crops that allows gene expression profiling of phloem tissues. The method leverages a translating ribosome affinity purification strategy (called TRAP) to isolate and characterize translating mRNAs from phloem specific tissues. Our approach is unlike other gene expression profiling methods in that it only samples gene transcripts that are actively being transcribed into proteins and is thus a better representation of active cellular processes than total cellular mRNA. Sweet orange, and HLB-resistant Poncirus and Carrizo (sweet orange x Poncirus) will be transformed to express the tagged ribosomal proteins under the control of characterized phloem-specific promoters; tagged ribosomal proteins under control of the nearly ubiquitous CaMV 35S promoter will be used as a control. Transgenic plants will be exposed to CLas+ or CLas- ACP and leaves sampled 1, 2, 4, 8, and 12 weeks later. Ribosome-associated mRNA will be sequenced and analyzed to identify differentially regulated genes at each time point and between each citrus cultivar. Comparisons of susceptible and resistant phloem cell responses to CLas will identify those genes that are differentially regulated during these host responses. Identified genes will represent unique phloem specific targets for CRISPR knockout or overexpression, permitting the generation of HLB-resistant variants of major citrus cultivars.During the 1st quarter of the second year of our grant, the Stover lab continues producing transgenic plants and shipping the ones that are ready to Ft. Detrick. CTV-infected plants were shipped to Ft. Detrick in February and are expressing nicely. This has allowed the post-doctoral researcher, Tami Collum, to finish optimizing citrus nucleic acid extraction protocols and perform immunoprecipitation and extraction of high quality translatome RNA from p35S::HF-RPL18 and pSUL::HF-RPL18. Another shipment of transgenic plants is anticipated in the 2nd quarter.  


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