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dc.contributor.authorFu, Yu
dc.contributor.authorYang, Yujing
dc.contributor.authorZhang, Han
dc.contributor.authorFarley, Gwen
dc.contributor.authorWang, Junling
dc.contributor.authorQuarles, Kaycee A.
dc.contributor.authorWeng, Zhiping
dc.contributor.authorZamore, Phillip D.
dc.date2022-08-11T08:09:48.000
dc.date.accessioned2022-08-23T16:44:17Z
dc.date.available2022-08-23T16:44:17Z
dc.date.issued2018-01-29
dc.date.submitted2018-02-22
dc.identifier.citation<p>Elife. 2018 Jan 29;7. pii: 31628. doi: 10.7554/eLife.31628. <a href="https://doi.org/10.7554/eLife.31628">Link to article on publisher's site</a></p>
dc.identifier.issn2050-084X (Linking)
dc.identifier.doi10.7554/eLife.31628
dc.identifier.pmid29376823
dc.identifier.urihttp://hdl.handle.net/20.500.14038/40470
dc.description.abstractWe report a draft assembly of the genome of Hi5 cells from the lepidopteran insect pest, Trichoplusia ni, assigning 90.6% of bases to one of 28 chromosomes and predicting 14,037 protein-coding genes. Chemoreception and detoxification gene families reveal T. ni-specific gene expansions that may explain its widespread distribution and rapid adaptation to insecticides. Transcriptome and small RNA data from thorax, ovary, testis, and the germline-derived Hi5 cell line show distinct expression profiles for 295 microRNA- and > 393 piRNA-producing loci, as well as 39 genes encoding small RNA pathway proteins. Nearly all of the W chromosome is devoted to piRNA production, and T. ni siRNAs are not 2 -O-methylated. To enable use of Hi5 cells as a model system, we have established genome editing and single-cell cloning protocols. The T. ni genome provides insights into pest control and allows Hi5 cells to become a new tool for studying small RNAs ex vivo.
dc.language.isoen_US
dc.relation<p><a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=29376823&dopt=Abstract">Link to Article in PubMed</a></p>
dc.rights© 2018, Fu et al. This article is distributed under the terms of the Creative Commons Attribution License permitting unrestricted use and redistribution provided that the original author and source are credited.
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subjectchromosomes
dc.subjectevolutionary biology
dc.subjectgenes
dc.subjectgenomics
dc.subjectgenome assembly
dc.subjectpiRNA
dc.subjectsiRNA
dc.subjectmiRNA
dc.subjectsex determination
dc.subjectcultured cell
dc.subject41 High Five
dc.subjectCRISPR
dc.subjectcabbage looper
dc.subjectTrichoplusia ni
dc.subjectLepidoptera
dc.subjectBiology
dc.subjectComputational Biology
dc.subjectEcology and Evolutionary Biology
dc.subjectGenetics
dc.subjectGenomics
dc.titleThe genome of the Hi5 germ cell line from Trichoplusia ni, an agricultural pest and novel model for small RNA biology
dc.typeAccepted Manuscript
dc.source.journaltitleeLife
dc.source.volume7
dc.identifier.legacyfulltexthttps://escholarship.umassmed.edu/cgi/viewcontent.cgi?article=4285&amp;context=oapubs&amp;unstamped=1
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/oapubs/3274
dc.identifier.contextkey11625481
refterms.dateFOA2022-08-23T16:44:17Z
html.description.abstract<p>We report a draft assembly of the genome of Hi5 cells from the lepidopteran insect pest, Trichoplusia ni, assigning 90.6% of bases to one of 28 chromosomes and predicting 14,037 protein-coding genes. Chemoreception and detoxification gene families reveal T. ni-specific gene expansions that may explain its widespread distribution and rapid adaptation to insecticides. Transcriptome and small RNA data from thorax, ovary, testis, and the germline-derived Hi5 cell line show distinct expression profiles for 295 microRNA- and > 393 piRNA-producing loci, as well as 39 genes encoding small RNA pathway proteins. Nearly all of the W chromosome is devoted to piRNA production, and T. ni siRNAs are not 2 -O-methylated. To enable use of Hi5 cells as a model system, we have established genome editing and single-cell cloning protocols. The T. ni genome provides insights into pest control and allows Hi5 cells to become a new tool for studying small RNAs ex vivo.</p>
dc.identifier.submissionpathoapubs/3274
dc.contributor.departmentDepartment of Biochemistry and Molecular Pharmacology
dc.contributor.departmentProgram in Bioinformatics and Integrative Biology
dc.contributor.departmentRNA Therapeutics Institute
dc.source.pages31628


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© 2018, Fu et al. This article is distributed under the terms of the Creative Commons Attribution License permitting unrestricted use and redistribution provided that the original author and source are credited.
Except where otherwise noted, this item's license is described as © 2018, Fu et al. This article is distributed under the terms of the Creative Commons Attribution License permitting unrestricted use and redistribution provided that the original author and source are credited.