Journal of Integrative Agriculture
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2026, 25(1): 150-156
• Plant Protection •
toGC: A pipeline to correct gene model for functional excavation of dark GPCRs in Phytophthora sojae
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Min Qiu1,2,3*, Chun Yan1*, Huaibo Li1, Haiyang Zhao1, Siqun Tu1, Yaru Sun1, Saijiang Yong1, Ming Wang1,2,3#, Yuanchao Wang1,2,3#
Affiliations
1Sanya Institute of Nanjing Agricultural University, Department of Plant Pathology, Nanjing Agricultural University, Nanjing 210095, China
2The Key Laboratory of Plant Immunity, Nanjing Agricultural University, Nanjing 210095, China
3Key Laboratory of Soybean Disease and Pest Control (Ministry of Agriculture and Rural Affairs), Nanjing Agricultural University, Nanjing 210095, China
About Author:
Min Qiu, E-mail: minqiu@njau.edu.cn; Chun Yan, E-mail: 2022202060@stu.njau.edu.cn; #Correspondence Yuanchao Wang, E-mail: wangyc@njau.edu.cn; Ming Wang, E-mail: mwang@njau.edu.cn
* These authors contributed equally to this study.
doi: 10.1016/j.jia.2024.03.077
Outline
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 PhytophthorasojaeORFs. We applied this innovative pipeline to the GPCR-bigrams gene family, which was predicted to have 42 members in the P.sojaegenome 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-AC3and GPCR-AC4), which were previously mispredicted as a single gene. CRISPR/Cas9-mediated knockout experiments revealed the involvement of GPCR-AC4but not GPCR-AC3in oospore production, further confirming their status as two separate genes. In addition to P.sojae, the reliability of the toGC pipeline in Phytophthoracapsiciand Pythiumultimumfurther 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.
GGPPS gene family
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Osmanthus fragrans
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floral color and aroma formation
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functional characterization
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toGC:一个用于矫正大豆疫霉中GPCR基因模型的流程.
农业科学学报(英文版),
2026
, 25
(1)
: 150
-156
.
DOI: 10.1016/j.jia.2024.03.077
Min Qiu, Chun Yan, Huaibo Li, Haiyang Zhao, Siqun Tu, Yaru Sun, Saijiang Yong, Ming Wang, Yuanchao Wang.
toGC: A pipeline to correct gene model for functional excavation of dark GPCRs in Phytophthora sojae[J].
Journal of Integrative Agriculture,
2026
, 25
(1)
: 150
-156
.
DOI: 10.1016/j.jia.2024.03.077
Year 2026 volume 25 Issue 1
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doi: 10.1016/j.jia.2024.03.077