{"title":"番茄黑僵菌寄生过程中长非编码 RNA 的调控与功能","authors":"Selin Ozdemir, Sobhan Bahrami Zadegan, Mst Shamira Sultana, Nicole Coffey, J Hollis Rice, Tarek Hewezi","doi":"10.1094/MPMI-10-24-0140-R","DOIUrl":null,"url":null,"abstract":"<p><p>Long non-coding RNAs (lncRNAs) are emerging as important regulators of various aspects of immune response and plant-pathogen interactions. However, the regulatory function of lncRNAs during plant-nematode interaction remain largely elusive. In this study, we investigated the differential regulation and function of lncRNAs during two different stages of tomato infection by the root-knot nematode <i>Meloidogyne incognita</i>. At the early stage of infection, 2218 and 2827 lncRNAs were regulated locally in the <i>M. incognita</i>-induced galls and systemically in the neighboring root cells, respectively. However, at the later stage of infection, the number of <i>M. incognita</i>-regulated lncRNAs was dramatically reduced with only 49 lncRNA being identified as differentially expressed. Differentially expressed lncRNAs were predicted to encode peptides with functionally annotated domains, providing insights into the potential roles of these peptides in regulating gene expression, RNA stability and splicing, and protein-protein-interactions. Among the differentially expressed lcRNAs, 55 were found to contain putative binding sites for 56 miRNAs. Overexpressing 5 of these lncRNAs significantly increased tomato resistance to <i>M. incognita</i>, supporting the functional importance of lncRNAs for establishing tomato-<i>M. incognita</i> interaction. Functional analysis of the target mimicry of lncRNAs towards miRNAs resulted in the identification of two novel regulatory modules involving miR47 and miR156e-5p and their targeted genes that regulate tomato responses to <i>M. incognita</i> parasitism. Taken together, our data provide novel insights into the transcriptional and post-transcriptional regulatory functions of lncRNA, and open a new avenue to engineer crop plants with enhanced nematode resistance by leveraging the regulatory potential of lncRNAs.</p>","PeriodicalId":19009,"journal":{"name":"Molecular Plant-microbe Interactions","volume":" ","pages":""},"PeriodicalIF":3.2000,"publicationDate":"2024-11-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Regulation and functions of long non-coding RNAs during <i>Meloidogyne incognita</i> parasitism of tomato.\",\"authors\":\"Selin Ozdemir, Sobhan Bahrami Zadegan, Mst Shamira Sultana, Nicole Coffey, J Hollis Rice, Tarek Hewezi\",\"doi\":\"10.1094/MPMI-10-24-0140-R\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Long non-coding RNAs (lncRNAs) are emerging as important regulators of various aspects of immune response and plant-pathogen interactions. However, the regulatory function of lncRNAs during plant-nematode interaction remain largely elusive. In this study, we investigated the differential regulation and function of lncRNAs during two different stages of tomato infection by the root-knot nematode <i>Meloidogyne incognita</i>. At the early stage of infection, 2218 and 2827 lncRNAs were regulated locally in the <i>M. incognita</i>-induced galls and systemically in the neighboring root cells, respectively. However, at the later stage of infection, the number of <i>M. incognita</i>-regulated lncRNAs was dramatically reduced with only 49 lncRNA being identified as differentially expressed. Differentially expressed lncRNAs were predicted to encode peptides with functionally annotated domains, providing insights into the potential roles of these peptides in regulating gene expression, RNA stability and splicing, and protein-protein-interactions. Among the differentially expressed lcRNAs, 55 were found to contain putative binding sites for 56 miRNAs. Overexpressing 5 of these lncRNAs significantly increased tomato resistance to <i>M. incognita</i>, supporting the functional importance of lncRNAs for establishing tomato-<i>M. incognita</i> interaction. Functional analysis of the target mimicry of lncRNAs towards miRNAs resulted in the identification of two novel regulatory modules involving miR47 and miR156e-5p and their targeted genes that regulate tomato responses to <i>M. incognita</i> parasitism. Taken together, our data provide novel insights into the transcriptional and post-transcriptional regulatory functions of lncRNA, and open a new avenue to engineer crop plants with enhanced nematode resistance by leveraging the regulatory potential of lncRNAs.</p>\",\"PeriodicalId\":19009,\"journal\":{\"name\":\"Molecular Plant-microbe Interactions\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":3.2000,\"publicationDate\":\"2024-11-19\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Molecular Plant-microbe Interactions\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://doi.org/10.1094/MPMI-10-24-0140-R\",\"RegionNum\":3,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"BIOCHEMISTRY & MOLECULAR BIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Molecular Plant-microbe Interactions","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1094/MPMI-10-24-0140-R","RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
Regulation and functions of long non-coding RNAs during Meloidogyne incognita parasitism of tomato.
Long non-coding RNAs (lncRNAs) are emerging as important regulators of various aspects of immune response and plant-pathogen interactions. However, the regulatory function of lncRNAs during plant-nematode interaction remain largely elusive. In this study, we investigated the differential regulation and function of lncRNAs during two different stages of tomato infection by the root-knot nematode Meloidogyne incognita. At the early stage of infection, 2218 and 2827 lncRNAs were regulated locally in the M. incognita-induced galls and systemically in the neighboring root cells, respectively. However, at the later stage of infection, the number of M. incognita-regulated lncRNAs was dramatically reduced with only 49 lncRNA being identified as differentially expressed. Differentially expressed lncRNAs were predicted to encode peptides with functionally annotated domains, providing insights into the potential roles of these peptides in regulating gene expression, RNA stability and splicing, and protein-protein-interactions. Among the differentially expressed lcRNAs, 55 were found to contain putative binding sites for 56 miRNAs. Overexpressing 5 of these lncRNAs significantly increased tomato resistance to M. incognita, supporting the functional importance of lncRNAs for establishing tomato-M. incognita interaction. Functional analysis of the target mimicry of lncRNAs towards miRNAs resulted in the identification of two novel regulatory modules involving miR47 and miR156e-5p and their targeted genes that regulate tomato responses to M. incognita parasitism. Taken together, our data provide novel insights into the transcriptional and post-transcriptional regulatory functions of lncRNA, and open a new avenue to engineer crop plants with enhanced nematode resistance by leveraging the regulatory potential of lncRNAs.
期刊介绍:
Molecular Plant-Microbe Interactions® (MPMI) publishes fundamental and advanced applied research on the genetics, genomics, molecular biology, biochemistry, and biophysics of pathological, symbiotic, and associative interactions of microbes, insects, nematodes, or parasitic plants with plants.