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dc.contributor.authorYoon, Yeonsoo
dc.contributor.authorRiley, Joy
dc.contributor.authorGallant, Judith
dc.contributor.authorXu, Ping
dc.contributor.authorRivera-Pérez, Jaime A.
dc.date2022-08-11T08:08:25.000
dc.date.accessioned2022-08-23T15:54:40Z
dc.date.available2022-08-23T15:54:40Z
dc.date.issued2020-10-08
dc.date.submitted2020-10-14
dc.identifier.citation<p>bioRxiv 2020.10.08.331587; doi: https://doi.org/10.1101/2020.10.08.331587. <a href="https://doi.org/10.1101/2020.10.08.331587" target="_blank">Link to preprint on bioRxiv </a></p>
dc.identifier.doi10.1101/2020.10.08.331587
dc.identifier.urihttp://hdl.handle.net/20.500.14038/29597
dc.description<p>This article is a preprint. Preprints are preliminary reports of work that have not been certified by peer review.</p>
dc.description.abstractThe period of development between the zygote and embryonic day 9.5 in mice includes multiple developmental milestones essential for embryogenesis. The preeminence of this period of development has been illustrated in loss of function studies conducted by the International Mouse Phenotyping Consortium (IMPC) which have shown that close to one third of all mouse genes are essential for survival to weaning age and a significant number of mutations cause embryo lethality before E9.5. Here we report a systematic analysis of 21 pre-E9.5 lethal lines generated by the IMPC. Analysis of pre- and post-implantation embryos revealed that the majority of the lines exhibit mutant phenotypes that fall within a window of development between implantation and gastrulation with few pre-implantation and no post-gastrulation phenotypes. Our study provides multiple genetic inroads into the molecular mechanisms that control early mammalian development and the etiology of human disease, in particular, the genetic bases of infertility and pregnancy loss. We propose a strategy for an efficient assessment of early embryonic lethal mutations that can be used to assign phenotypes to developmental milestones and outline the time of lethality.
dc.language.isoen_US
dc.rightsThe copyright holder for this preprint is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under a CC-BY-NC-ND 4.0 International license.
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.subjectDevelopmental Biology
dc.subjectmutant phenotypes
dc.subjectembryos
dc.subjectDevelopmental Biology
dc.subjectEmbryonic Structures
dc.subjectFemale Urogenital Diseases and Pregnancy Complications
dc.subjectGenetics and Genomics
dc.subjectMale Urogenital Diseases
dc.titleImplantation and Gastrulation Abnormalities Characterize Early Embryonic Lethal Mouse Lines [preprint]
dc.typePreprint
dc.source.journaltitlebioRxiv
dc.identifier.legacyfulltexthttps://escholarship.umassmed.edu/cgi/viewcontent.cgi?article=2836&amp;context=faculty_pubs&amp;unstamped=1
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/faculty_pubs/1815
dc.identifier.contextkey19816238
refterms.dateFOA2022-08-23T15:54:40Z
html.description.abstract<p>The period of development between the zygote and embryonic day 9.5 in mice includes multiple developmental milestones essential for embryogenesis. The preeminence of this period of development has been illustrated in loss of function studies conducted by the International Mouse Phenotyping Consortium (IMPC) which have shown that close to one third of all mouse genes are essential for survival to weaning age and a significant number of mutations cause embryo lethality before E9.5. Here we report a systematic analysis of 21 pre-E9.5 lethal lines generated by the IMPC. Analysis of pre- and post-implantation embryos revealed that the majority of the lines exhibit mutant phenotypes that fall within a window of development between implantation and gastrulation with few pre-implantation and no post-gastrulation phenotypes. Our study provides multiple genetic inroads into the molecular mechanisms that control early mammalian development and the etiology of human disease, in particular, the genetic bases of infertility and pregnancy loss. We propose a strategy for an efficient assessment of early embryonic lethal mutations that can be used to assign phenotypes to developmental milestones and outline the time of lethality.</p>
dc.identifier.submissionpathfaculty_pubs/1815
dc.contributor.departmentDepartment of Pediatrics, Division of Genes and Development


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The copyright holder for this preprint is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under a CC-BY-NC-ND 4.0 International license.
Except where otherwise noted, this item's license is described as The copyright holder for this preprint is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under a CC-BY-NC-ND 4.0 International license.