<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>8</volume><submitter>Anbazhagan R</submitter><funding>Eunice Kennedy Shriver National Institute of Child Health and Human Development</funding><pubmed_abstract>GRTH/DDX25 is a member of the DEAD-box family of RNA helicases that play an essential role in spermatogenesis. GRTH knock-in (KI) mice with the human mutant GRTH gene (R242H) show loss of the phospho-species from cytoplasm with preservation of the non-phospho form in the cytoplasm and nucleus. GRTH KI mice are sterile and lack elongated spermatids and spermatozoa, with spermatogenic arrest at step 8 of round spermatids which contain chromatoid body (CB) markedly reduced in size. We observed an absence of phospho-GRTH in CB of GRTH KI mice. RNA-Seq analysis of mRNA isolated from CB revealed that 1,421 genes show differential abundance, of which 947 genes showed a decrease in abundance and 474 genes showed an increase in abundance in GRTH KI mice. The transcripts related to spermatid develop</pubmed_abstract><journal>Frontiers in cell and developmental biology</journal><pagination>580019</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7786181</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Role of Phosphorylated Gonadotropin-Regulated Testicular RNA Helicase (GRTH/DDX25) in the Regulation of Germ Cell Specific mRNAs in Chromatoid Bodies During Spermatogenesis.</pubmed_title><pmcid>PMC7786181</pmcid><pubmed_authors>Kavarthapu R</pubmed_authors><pubmed_authors>Coon SL</pubmed_authors><pubmed_authors>Dufau ML</pubmed_authors><pubmed_authors>Anbazhagan R</pubmed_authors></additional><is_claimable>false</is_claimable><name>Role of Phosphorylated Gonadotropin-Regulated Testicular RNA Helicase (GRTH/DDX25) in the Regulation of Germ Cell Specific mRNAs in Chromatoid Bodies During Spermatogenesis.</name><description>GRTH/DDX25 is a member of the DEAD-box family of RNA helicases that play an essential role in spermatogenesis. GRTH knock-in (KI) mice with the human mutant GRTH gene (R242H) show loss of the phospho-species from cytoplasm with preservation of the non-phospho form in the cytoplasm and nucleus. GRTH KI mice are sterile and lack elongated spermatids and spermatozoa, with spermatogenic arrest at step 8 of round spermatids which contain chromatoid body (CB) markedly reduced in size. We observed an absence of phospho-GRTH in CB of GRTH KI mice. RNA-Seq analysis of mRNA isolated from CB revealed that 1,421 genes show differential abundance, of which 947 genes showed a decrease in abundance and 474 genes showed an increase in abundance in GRTH KI mice. The transcripts related to spermatid develop</description><dates><release>2020-01-01T00:00:00Z</release><publication>2020</publication><modification>2026-04-07T20:34:33.596Z</modification><creation>2025-04-04T07:16:28.688Z</creation></dates><accession>S-EPMC7786181</accession><cross_references><pubmed>33425888</pubmed><doi>10.3389/fcell.2020.580019</doi></cross_references></HashMap>