<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Ruthig VA</submitter><funding>NICHD NIH HHS</funding><funding>NCI NIH HHS</funding><funding>National Institutes of Health</funding><funding>DCI</funding><funding>NIGMS NIH HHS</funding><pagination>861-874</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8324984</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>104(4)</volume><pubmed_abstract>In vertebrates, the RNA-binding protein (RBP) dead end 1 (DND1) is essential for primordial germ cell (PGC) survival and maintenance of cell identity. In multiple species, Dnd1 loss or mutation leads to severe PGC loss soon after specification or, in some species, germ cell transformation to somatic lineages. Our investigations into the role of DND1 in PGC specification and differentiation have been limited by the absence of an available antibody. To address this problem, we used CRISPR/Cas9 gene editing to establish a transgenic mouse line carrying a DND1GFP fusion allele. We present imaging analysis of DND1GFP expression showing that DND1GFP expression is heterogeneous among male germ cells (MGCs) and female germ cells (FGCs). DND1GFP was detected in MGCs throughout fetal life but lost f</pubmed_abstract><journal>Biology of reproduction</journal><pubmed_title>A transgenic DND1GFP fusion allele reports in vivo expression and RNA-binding targets in undifferentiated mouse germ cells†.</pubmed_title><pmcid>PMC8324984</pmcid><funding_grant_id>F32 GM129956</funding_grant_id><funding_grant_id>R01 HD103064</funding_grant_id><funding_grant_id>R37 HD039963</funding_grant_id><funding_grant_id>P30 CA014236</funding_grant_id><pubmed_authors>Ruthig VA</pubmed_authors><pubmed_authors>Hardy J</pubmed_authors><pubmed_authors>Yokonishi T</pubmed_authors><pubmed_authors>Friedersdorf MB</pubmed_authors><pubmed_authors>Garness JA</pubmed_authors><pubmed_authors>Capel B</pubmed_authors><pubmed_authors>Keene JD</pubmed_authors><pubmed_authors>Batchvarova S</pubmed_authors></additional><is_claimable>false</is_claimable><name>A transgenic DND1GFP fusion allele reports in vivo expression and RNA-binding targets in undifferentiated mouse germ cells†.</name><description>In vertebrates, the RNA-binding protein (RBP) dead end 1 (DND1) is essential for primordial germ cell (PGC) survival and maintenance of cell identity. In multiple species, Dnd1 loss or mutation leads to severe PGC loss soon after specification or, in some species, germ cell transformation to somatic lineages. Our investigations into the role of DND1 in PGC specification and differentiation have been limited by the absence of an available antibody. To address this problem, we used CRISPR/Cas9 gene editing to establish a transgenic mouse line carrying a DND1GFP fusion allele. We present imaging analysis of DND1GFP expression showing that DND1GFP expression is heterogeneous among male germ cells (MGCs) and female germ cells (FGCs). DND1GFP was detected in MGCs throughout fetal life but lost f</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Apr</publication><modification>2026-07-11T03:19:57.454Z</modification><creation>2022-02-11T14:11:28.791Z</creation></dates><accession>S-EPMC8324984</accession><cross_references><pubmed>33394034</pubmed><doi>10.1093/biolre/ioaa233</doi></cross_references></HashMap>