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dc.contributor.authorConine, Colin C
dc.contributor.authorSun, Fengyun
dc.contributor.authorRivera-Perez, Jaime A.
dc.contributor.authorRando, Oliver J.
dc.date2022-08-11T08:08:23.000
dc.date.accessioned2022-08-23T15:53:05Z
dc.date.available2022-08-23T15:53:05Z
dc.date.issued2018-04-30
dc.date.submitted2018-06-07
dc.identifier.citation<p>bioRxiv 311670; doi: https://doi.org/10.1101/311670. <a href="https://doi.org/10.1101/311670" target="_blank">Link to preprint on bioRxiv service.</a></p>
dc.identifier.doi10.1101/311670
dc.identifier.urihttp://hdl.handle.net/20.500.14038/29280
dc.description.abstractThe small RNA payload of mammalian sperm undergoes dramatic remodeling during development, as several waves of microRNAs and tRNA fragments are shipped to sperm during post-testicular maturation in the epididymis. Here, we take advantage of this developmental process to probe the function of the sperm RNA payload in preimplantation development. We generated zygotes via intracytoplasmic sperm injection (ICSI) using sperm obtained from the proximal (caput) vs. distal (cauda) epididymis, then characterized development of the resulting embryos. Embryos generated using caput sperm significantly overexpress multiple regulatory factors throughout preimplantation development, and subsequently implant inefficiently and fail soon after implantation. Remarkably, microinjection of purified cauda-specific small RNAs into caput-derived embryos not only completely rescued preimplantation molecular defects, but also suppressed the postimplantation embryonic lethality phenotype. These findings reveal an essential role for small RNA remodeling during post-testicular maturation of mammalian sperm, and identify a specific preimplantation gene expression program responsive to sperm-delivered microRNAs.
dc.language.isoen_US
dc.rightsThe copyright holder for this preprint (which was not peer-reviewed) is the author/funder. It is made available under a CC-BY-NC 4.0 International license.
dc.rights.urihttp://creativecommons.org/licenses/by-nc/4.0/
dc.subjectRNA
dc.subjectmicroRNA
dc.subjecttRNA
dc.subjectsperm
dc.subjectembryos
dc.subjectmolecular biology
dc.subjectDevelopmental Biology
dc.subjectEmbryonic Structures
dc.subjectMolecular Biology
dc.titleSmall RNAs gained during epididymal transit of sperm are essential for embryonic development in mice [preprint]
dc.typePreprint
dc.source.journaltitlebioRxiv
dc.identifier.legacyfulltexthttps://escholarship.umassmed.edu/cgi/viewcontent.cgi?article=2515&amp;context=faculty_pubs&amp;unstamped=1
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/faculty_pubs/1509
dc.identifier.contextkey12270953
refterms.dateFOA2022-08-23T15:53:05Z
html.description.abstract<p>The small RNA payload of mammalian sperm undergoes dramatic remodeling during development, as several waves of microRNAs and tRNA fragments are shipped to sperm during post-testicular maturation in the epididymis. Here, we take advantage of this developmental process to probe the function of the sperm RNA payload in preimplantation development. We generated zygotes via intracytoplasmic sperm injection (ICSI) using sperm obtained from the proximal (caput) vs. distal (cauda) epididymis, then characterized development of the resulting embryos. Embryos generated using caput sperm significantly overexpress multiple regulatory factors throughout preimplantation development, and subsequently implant inefficiently and fail soon after implantation. Remarkably, microinjection of purified cauda-specific small RNAs into caput-derived embryos not only completely rescued preimplantation molecular defects, but also suppressed the postimplantation embryonic lethality phenotype. These findings reveal an essential role for small RNA remodeling during post-testicular maturation of mammalian sperm, and identify a specific preimplantation gene expression program responsive to sperm-delivered microRNAs.</p>
dc.identifier.submissionpathfaculty_pubs/1509
dc.contributor.departmentRivera Lab
dc.contributor.departmentDepartment of Pediatrics, Division of Genes and Development
dc.contributor.departmentDepartment of Biochemistry and Molecular Pharmacology


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The copyright holder for this preprint (which was not peer-reviewed) is the author/funder. It is made available under a CC-BY-NC 4.0 International license.
Except where otherwise noted, this item's license is described as The copyright holder for this preprint (which was not peer-reviewed) is the author/funder. It is made available under a CC-BY-NC 4.0 International license.