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toGC: A pipeline to correct gene model for functional excavation of dark GPCRs in Phytophthora sojae

Min Qiu1,2,3, Chun Yan1, Huaibo Li1, Haiyang Zhao1, Siqun Tu1, Yaru Sun1, Saijiang Yong1, Ming Wang1,2,3( ), Yuanchao Wang1,2,3( )
Sanya Institute of Nanjing Agricultural University, Department of Plant Pathology, Nanjing Agricultural University, Nanjing 210095, China
The Key Laboratory of Plant Immunity, Nanjing Agricultural University, Nanjing 210095, China
Key Laboratory of Soybean Disease and Pest Control (Ministry of Agriculture and Rural Affairs), Nanjing Agricultural University, Nanjing 210095, China
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Highlights

  • Developed toGC, a new tool that corrects errors in gene annotations using RNA-seq data.

  • Experimentally validated toGC's accuracy, discovering two novel GPCR genes misannotated as one.

  • Demonstrated toGC's broad utility by applying it successfully to multiple oomycete species.

Abstract

The accuracy of genomic annotation is crucial for subsequent functional investigations; however, computational protocols used in high-throughput annotation of open reading frames (ORFs) can introduce inconsistencies. These inconsistencies, which lead to non-uniform extension or truncation of sequence ends, pose challenges for downstream analyses. Existing strategies to rectify these inconsistencies are time-consuming and labor-intensive, lacking specific approaches. To address this gap, we developed toGC, a tool that integrates genomic annotation with RNA-seq datasets to rectify annotation inconsistencies. Using toGC, we achieved an accuracy of nearly 100% accuracy in correcting inconsistencies in published Phytophthora sojae ORFs. We applied this innovative pipeline to the GPCR-bigrams gene family, which was predicted to have 42 members in the P. sojae genome but lacked experimental validation. By employing toGC, we identified 32 GPCR-bigram ORFs with inconsistencies between previous annotations and toGC-corrected sequences. Notably, among these were 5 genes (GPCR-TKL9, GPCR-TKL15, GPCR-PDE3, GPCR-AC3, and GPCR-AC4) showed substantial inconsistencies. Experimental gene annotation confirmed the effectiveness of toGC, as sequences obtained through cloning matched those annotated by toGC. Importantly, we discovered two novel GPCRs (GPCR-AC3 and GPCR-AC4), which were previously mispredicted as a single gene. CRISPR/Cas9-mediated knockout experiments revealed the involvement of GPCR-AC4 but not GPCR-AC3 in oospore production, further confirming their status as two separate genes. In addition to P. sojae, the reliability of the toGC pipeline in Phytophthora capsici and Pythium ultimum further emphasizes the robustness of this pipeline. Our findings highlight the utility of toGC for reliable gene model correction, facilitating investigations into biological functions and offering potential applications in diverse species analyses.

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Journal of Integrative Agriculture (JIA)
Pages 150-156

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Cite this article:
Qiu M, Yan C, Li H, et al. toGC: A pipeline to correct gene model for functional excavation of dark GPCRs in Phytophthora sojae. Journal of Integrative Agriculture (JIA), 2026, 25(1): 150-156. https://doi.org/10.1016/j.jia.2024.03.077

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Received: 01 January 2024
Revised: 18 February 2024
Accepted: 21 February 2024
Published: 27 March 2024
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