Paola Roncaglia, Teunis J P van Dam, Karen R Christie, Lora Nacheva, Grischa Toedt, Martijn A Huynen, Rachael P Huntley, Toby J Gibson, Jane Lomax
{"title":"真核生物纤毛和鞭毛的基因本体。","authors":"Paola Roncaglia, Teunis J P van Dam, Karen R Christie, Lora Nacheva, Grischa Toedt, Martijn A Huynen, Rachael P Huntley, Toby J Gibson, Jane Lomax","doi":"10.1186/s13630-017-0054-8","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Recent research into ciliary structure and function provides important insights into inherited diseases termed ciliopathies and other cilia-related disorders. This wealth of knowledge needs to be translated into a computational representation to be fully exploitable by the research community. To this end, members of the Gene Ontology (GO) and SYSCILIA Consortia have worked together to improve representation of ciliary substructures and processes in GO.</p><p><strong>Methods: </strong>Members of the SYSCILIA and Gene Ontology Consortia suggested additions and changes to GO, to reflect new knowledge in the field. The project initially aimed to improve coverage of ciliary parts, and was then broadened to cilia-related biological processes. Discussions were documented in a public tracker. We engaged the broader cilia community via direct consultation and by referring to the literature. Ontology updates were implemented via ontology editing tools.</p><p><strong>Results: </strong>So far, we have created or modified 127 GO terms representing parts and processes related to eukaryotic cilia/flagella or prokaryotic flagella. A growing number of biological pathways are known to involve cilia, and we continue to incorporate this knowledge in GO. The resulting expansion in GO allows more precise representation of experimentally derived knowledge, and SYSCILIA and GO biocurators have created 199 annotations to 50 human ciliary proteins. The revised ontology was also used to curate mouse proteins in a collaborative project. The revised GO and annotations, used in comparative 'before and after' analyses of representative ciliary datasets, improve enrichment results significantly.</p><p><strong>Conclusions: </strong>Our work has resulted in a broader and deeper coverage of ciliary composition and function. These improvements in ontology and protein annotation will benefit all users of GO enrichment analysis tools, as well as the ciliary research community, in areas ranging from microscopy image annotation to interpretation of high-throughput studies. 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引用次数: 0
摘要
背景:最近对纤毛结构和功能的研究为了解被称为纤毛疾病的遗传性疾病和其他与纤毛相关的疾病提供了重要线索。这些丰富的知识需要转化为计算表征,以便研究界充分利用。为此,基因本体(Gene Ontology,GO)和 SYSCILIA 联合会的成员共同努力,以改进纤毛亚结构和过程在 GO.Methods 中的表示:方法:SYSCILIA 和基因本体联盟成员建议对 GO 进行补充和修改,以反映该领域的新知识。该项目最初旨在提高纤毛部件的覆盖率,后来扩大到与纤毛相关的生物过程。讨论记录在公共跟踪器中。我们通过直接咨询和参考文献的方式让更广泛的纤毛社区参与进来。本体更新是通过本体编辑工具实现的:到目前为止,我们已经创建或修改了 127 个 GO 术语,这些术语代表了与真核生物纤毛/鞭毛或原核生物鞭毛相关的部分和过程。已知有越来越多的生物途径涉及纤毛,我们将继续把这些知识纳入 GO。由此产生的 GO 扩展可以更精确地表示实验得出的知识,SYSCILIA 和 GO 生物学家已经为 50 个人类纤毛蛋白创建了 199 个注释。在一个合作项目中,修订后的本体也被用于整理小鼠蛋白质。在对具有代表性的睫状体数据集进行 "前后 "对比分析时,修订后的 GO 和注释显著改善了富集结果:我们的工作使睫状体的组成和功能得到了更广泛、更深入的覆盖。本体和蛋白质注释方面的这些改进将使 GO 富集分析工具的所有用户以及睫状体研究界受益,包括显微镜图像注释和高通量研究解释等领域。我们欢迎反馈意见,以进一步增强纤毛生物学在 GO 中的代表性。
The Gene Ontology of eukaryotic cilia and flagella.
Background: Recent research into ciliary structure and function provides important insights into inherited diseases termed ciliopathies and other cilia-related disorders. This wealth of knowledge needs to be translated into a computational representation to be fully exploitable by the research community. To this end, members of the Gene Ontology (GO) and SYSCILIA Consortia have worked together to improve representation of ciliary substructures and processes in GO.
Methods: Members of the SYSCILIA and Gene Ontology Consortia suggested additions and changes to GO, to reflect new knowledge in the field. The project initially aimed to improve coverage of ciliary parts, and was then broadened to cilia-related biological processes. Discussions were documented in a public tracker. We engaged the broader cilia community via direct consultation and by referring to the literature. Ontology updates were implemented via ontology editing tools.
Results: So far, we have created or modified 127 GO terms representing parts and processes related to eukaryotic cilia/flagella or prokaryotic flagella. A growing number of biological pathways are known to involve cilia, and we continue to incorporate this knowledge in GO. The resulting expansion in GO allows more precise representation of experimentally derived knowledge, and SYSCILIA and GO biocurators have created 199 annotations to 50 human ciliary proteins. The revised ontology was also used to curate mouse proteins in a collaborative project. The revised GO and annotations, used in comparative 'before and after' analyses of representative ciliary datasets, improve enrichment results significantly.
Conclusions: Our work has resulted in a broader and deeper coverage of ciliary composition and function. These improvements in ontology and protein annotation will benefit all users of GO enrichment analysis tools, as well as the ciliary research community, in areas ranging from microscopy image annotation to interpretation of high-throughput studies. We welcome feedback to further enhance the representation of cilia biology in GO.