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This study utilized clustered regularly interspaced short palindromic repeats\/CRISPR\u2010associated protein 9 (CRISPR\/Cas9) genome editing to assess essentiality and functionality of zebrafish (\n                    <jats:italic>Danio rerio<\/jats:italic>\n                    ) type\u2010I and type\u2010III Vtgs. A multiple CRISPR approach was employed to knockout (KO) all genes encoding type\u2010I\n                    <jats:italic>vtgs<\/jats:italic>\n                    (\n                    <jats:italic>vtg1<\/jats:italic>\n                    ,\n                    <jats:italic>4<\/jats:italic>\n                    ,\n                    <jats:italic>5<\/jats:italic>\n                    ,\n                    <jats:italic>6<\/jats:italic>\n                    , and\n                    <jats:italic>7<\/jats:italic>\n                    ) simultaneously (\n                    <jats:italic>vtg1<\/jats:italic>\n                    \u2010KO), and the type\u2010III\n                    <jats:italic>vtg<\/jats:italic>\n                    (\n                    <jats:italic>vtg3<\/jats:italic>\n                    ) individually (\n                    <jats:italic>vtg3<\/jats:italic>\n                    \u2010KO). Results of polymerase chain reaction (PCR) genotyping and sequencing, quantitative PCR, liquid chromatography\u2010tandem mass spectrometry, and Western blot analysis showed that only\n                    <jats:italic>vtg6<\/jats:italic>\n                    and\n                    <jats:italic>vtg7<\/jats:italic>\n                    escaped Cas9 editing. In fish whose remaining type\u2010I\n                    <jats:italic>vtgs<\/jats:italic>\n                    were incapacitated (\n                    <jats:italic>vtg1<\/jats:italic>\n                    \u2010KO), and in\n                    <jats:italic>vtg3<\/jats:italic>\n                    \u2010KO fish, significant increases in\n                    <jats:italic>Vtg7<\/jats:italic>\n                    transcript and protein levels occurred in liver and eggs, revealing a heretofore\u2010unknown mechanism of genetic compensation regulating Vtg homeostasis. Egg numbers per spawn were elevated more than 2\u2010fold in\n                    <jats:italic>vtg1<\/jats:italic>\n                    \u2010KO females, and egg fertility was approximately halved in\n                    <jats:italic>vtg3<\/jats:italic>\n                    \u2010KO females. Substantial mortality was evident in\n                    <jats:italic>vtg3<\/jats:italic>\n                    \u2010KO eggs\/embryos after only 8\u2009hr of incubation and in\n                    <jats:italic>vtg1<\/jats:italic>\n                    \u2010KO embryos after 5 days. Hatching rate and timing were markedly impaired in embryos from\n                    <jats:italic>vtg<\/jats:italic>\n                    mutant mothers and pericardial and yolk sac\/abdominal edema and spinal lordosis were evident in the larvae, with feeding and motor activities also being absent in\n                    <jats:italic>vtg1<\/jats:italic>\n                    \u2010KO larvae. By late larval stages,\n                    <jats:italic>vtg<\/jats:italic>\n                    mutations were either completely lethal (\n                    <jats:italic>vtg1<\/jats:italic>\n                    \u2010KO) or nearly so (\n                    <jats:italic>vtg3<\/jats:italic>\n                    \u2010KO). These novel findings offer the first experimental evidence that different types of vertebrate Vtg are essential and have disparate requisite functions at different times during both reproduction and development.\n                  <\/jats:p>","DOI":"10.1002\/mrd.23231","type":"journal-article","created":{"date-parts":[[2019,8,5]],"date-time":"2019-08-05T05:20:03Z","timestamp":1564982403000},"page":"1168-1188","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":45,"title":["Genome editing reveals reproductive and developmental dependencies on specific types of vitellogenin in zebrafish (\n                    <i>Danio rerio<\/i>\n                    )"],"prefix":"10.1002","volume":"86","author":[{"ORCID":"https:\/\/orcid.org\/0000-0002-7810-7487","authenticated-orcid":false,"given":"Ozlem","family":"Yilmaz","sequence":"first","affiliation":[{"name":"INRA, UR1037, Laboratory of Fish Physiology and Genomics Campus de Beaulieu, French National Institute for Agricultural Research  Rennes Cedex France"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Am\u00e9lie","family":"Patinote","sequence":"additional","affiliation":[{"name":"INRA, UR1037, Laboratory of Fish Physiology and Genomics Campus de Beaulieu, French National Institute for Agricultural Research  Rennes Cedex France"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Thaovi","family":"Nguyen","sequence":"additional","affiliation":[{"name":"INRA, UR1037, Laboratory of Fish Physiology and Genomics Campus de Beaulieu, French National Institute for Agricultural Research  Rennes Cedex France"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Emmanuelle","family":"Com","sequence":"additional","affiliation":[{"name":"Protim, Inserm U1085, Irset Campus de Beaulieu, Universit\u00e9 de Rennes 1, Proteomics Core Facility  Rennes Cedex France"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Charles","family":"Pineau","sequence":"additional","affiliation":[{"name":"Protim, Inserm U1085, Irset Campus de Beaulieu, Universit\u00e9 de Rennes 1, Proteomics Core Facility  Rennes Cedex France"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Julien","family":"Bobe","sequence":"additional","affiliation":[{"name":"INRA, UR1037, Laboratory of Fish Physiology and Genomics Campus de Beaulieu, French National Institute for Agricultural Research  Rennes Cedex 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