Park, Chi-HunJeoung, Young-HeeUh, KyungjunPark, Ki-EunBridge, JessicaPowell, Anne M.Li, JiePence, LaramieZhang, LuhuiLiu, TianbinSun, Hai-XiGu, YingShen, YueWu, JunBelmonte, Juan-Carlos IzpisuaTelugu, Bhanu P.2021-03-032021-03-032021-01-122213-6711http://hdl.handle.net/10919/102587Most of our current knowledge regarding early lineage specification and embryo-derived stem cells comes from studies in rodent models. However, key gaps remain in our understanding of these developmental processes from nonrodent species. Here, we report the detailed characterization of pig extraembryonic endoderm (pXEN) cells, which can be reliably and reproducibly generated from primitive endoderm (PrE) of blastocyst. Highly expandable pXEN cells express canonical PrE markers and transcriptionally resemble rodent XENs. The pXEN cells contribute both to extraembryonic tissues including visceral yolk sac as well as embryonic gut when injected into host blastocysts, and generate live offspring when used as a nuclear donor in somatic cell nuclear transfer (SCNT). The pXEN cell lines provide a novel model for studying lineage segregation, as well as a source for genome editing in livestock.application/pdfenPublic DomainArticle - Refereedhttps://doi.org/10.1016/j.stemcr.2020.11.01116133338433